Comparative map for mice and humans

Human c-myc onc gene is located on the region of chromosome 8 that is translocated in Burkitt lymphoma cells.

1982 • 1,746 citations

X chromosome-linked muscular dystrophy (mdx) in the mouse.

1984 • 1,678 citations

Human proto-oncogene c-kit: a new cell surface receptor tyrosine kinase for an unidentified ligand.

1987 • 1,627 citations

Genetic variants and strains of the laboratory mouse

1990 • 1,519 citations

Translocation of the c-myc gene into the immunoglobulin heavy chain locus in human Burkitt lymphoma and murine plasmacytoma cells.

1982 • 1,424 citations

The proto-oncogene c-kit encoding a transmembrane tyrosine kinase receptor maps to the mouse W locus

1988 • 1,390 citations

A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemia

1982 • 1,385 citations

The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene

1988 • 1,336 citations

Structure of the receptor for platelet-derived growth factor helps define a family of closely related growth factor receptors

1986 • 1,244 citations

A new member of the immunoglobulin superfamily—CTLA-4

1987 • 1,214 citations

The Genetic Defect Causing Familial Alzheimer's Disease Maps on Chromosome 21

1987 • 1,149 citations

Biology of the Mouse Histocompatibility-2 Complex

1975 • 1,145 citations

The major human rhinovirus receptor is ICAM-1

1989 • 1,134 citations

Multiple, Distinct Forms of Bovine and Human Protein Kinase C Suggest Diversity in Cellular Signaling Pathways

1986 • 1,044 citations

The sex-determining region of the human Y chromosome encodes a finger protein

1987 • 847 citations

Retinal degeneration in the rd mouse is caused by a defect in the β subunit of rod cGMP-phosphodiesterase

1990 • 841 citations

cDNA for the human beta 2-adrenergic receptor: a protein with multiple membrane-spanning domains and encoded by a gene whose chromosomal location is shared with that of the receptor for platelet-derived growth factor.

1987 • 687 citations

Identification of an Amplified, Highly Expressed Gene in a Human Glioma

1987 • 671 citations

Mode of proviral activation of a putative mammary oncogene (int-1) on mouse chromosome 15

1984 • 609 citations

The genomic clone G-21 which resembles a β-adrenergic receptor sequence encodes the 5-HT1A receptor

1988 • 594 citations

X-linked Gene for Testicular Feminization in the Mouse

1970 • 551 citations

Human and rat brain-derived neurotrophic factor and neurotrophin-3: Gene structures, distributions, and chromosomal localizations

1991 • 500 citations

Localization of gene for human p53 tumour antigen to band 17p13

1986 • 498 citations

Isolation and nucleotide sequence of the gene encoding human rhodopsin.

1984 • 495 citations

A new T-cell receptor gene located within the alpha locus and expressed early in T-cell differentiation

1987 • 483 citations

Distinct prion proteins in short and long scrapie incubation period mice

1987 • 482 citations

Molecular cloning of cDNA encoding a murine haematopoietic growth regulator, granulocyte—macrophage colony stimulating factor

1984 • 451 citations

A molecular map of the human major histocompatibility complex class III region linking complement genes C4, C2 and factor B

1984 • 433 citations

Identification of a cDNA encoding a parathyroid hormone-like peptide from a human tumor associated with humoral hypercalcemia of malignancy.

1988 • 431 citations

Evidence for a family of human glucose transporter-like proteins. Sequence and gene localization of a protein expressed in fetal skeletal muscle and other tissues.

1988 • 428 citations

Sequence, tissue distribution, and chromosomal localization of mRNA encoding a human glucose transporter-like protein.

1988 • 426 citations

CTLA-4 and CD28 activated lymphocyte molecules are closely related in both mouse and human as to sequence, message expression, gene structure, and chromosomal location.

1991 • 422 citations

Arrangement of human immunoglobulin heavy chain constant region genes implies evolutionary duplication of a segment containing γ, ε and α genes

1982 • 421 citations

A new family of mouse homeo box-containing genes: molecular structure, chromosomal location, and developmental expression of Hox-7.1.

1989 • 399 citations

Hypophosphatemia: mouse model for human familial hypophosphatemic (vitamin D-resistant) rickets.

1976 • 399 citations

Homologous ribosomal protein genes on the human X and Y chromosomes: Escape from X inactivation and possible implications for turner syndrome

1990 • 390 citations

The gene for human p53 cellular tumor antigen is located on chromosome 17 short arm (17p13).

1986 • 371 citations

cDNA cloning, mRNA distribution and heterogeneity, chromosomal location, and RFLP analysis of human osteopontin (OPN)

1990 • 361 citations

Human cholesterol side-chain cleavage enzyme, P450scc: cDNA cloning, assignment of the gene to chromosome 15, and expression in the placenta.

1986 • 359 citations

Molecular characterization and chromosomal mapping of melanoma growth stimulatory activity, a growth factor structurally related to beta-thromboglobulin.

1988 • 357 citations

Linkage map of the human major histocompatibility complex including the tumor necrosis factor genes.

1987 • 351 citations

The CD14 Monocyte Differentiation Antigen Maps to a Region Encoding Growth Factors and Receptors

1988 • 344 citations

Small eyes (Sey) : a homozygous lethal mutation on chromosome 2 which affects the differentiation of both lens and nasal placodes in the mouse

1986 • 344 citations

Human major histocompatibility complex contains genes for the major heat shock protein HSP70.

1989 • 336 citations

Regulation, linkage, and sequence of mouse metallothionein I and II genes.

1984 • 335 citations

Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

1982 • 334 citations

Chromosomal mapping of mouse myelin basic protein gene and structure and transcription of the partially deleted gene in shiverer mutant mice

1985 • 331 citations

En-1 and En-2, two mouse genes with sequence homology to the Drosophila engrailed gene: expression during embryogenesis.

1987 • 330 citations

Two human c-onc genes are located on the long arm of chromosome 8.

1982 • 329 citations

The adult T-cell receptor 5-chain is diverse and distinct from that of fetal thymocytes

1988 • 320 citations

Human transferrin: cDNA characterization and chromosomal localization.

1984 • 320 citations

The human HOX gene family

1989 • 317 citations

v-cbl, an oncogene from a dual-recombinant murine retrovirus that induces early B-lineage lymphomas.

1989 • 316 citations

Chromosome localization in normal human cells and neuroblastomas of a gene related to c-myc

1984 • 315 citations

Molecular cloning and chromosome mapping of a mouse DNA sequence homologous to homeotic genes of drosophila

1984 • 313 citations

Genes for the tumor necrosis factors alpha and beta are linked to the human major histocompatibility complex.

1986 • 312 citations

Human and mouse amelogenin gene loci are on the sex chromosomes

1989 • 307 citations

Chromosomal localization of human cellular homologues of two viral oncogenes

1982 • 304 citations

Androgen receptor locus on the human X chromosome: regional localization to Xq11-12 and description of a DNA polymorphism.

1989 • 301 citations

Structure of mouse metallothionein-I gene and its mRNA

1981 • 301 citations

Molecular cloning, sequencing, and mapping of EGR2, a human early growth response gene encoding a protein with "zinc-binding finger" structure.

1988 • 301 citations

A novel family of human major histocompatibility complex-related genes not mapping to chromosome 6

1986 • 297 citations

Human Ig superfamily CTLA‐4 gene: chromosomal localization and identity of protein sequence between murine and human CTLA‐4 cytoplasmic domains

1988 • 296 citations

Structure of mouse kallikrein gene family suggests a role in specific processing of biologically active peptides

1983 • 295 citations

The human met oncogene is related to the tyrosine kinase oncogenes

1985 • 295 citations

Characterization of the HST-related FGF.6 gene, a new member of the fibroblast growth factor gene family.

1989 • 294 citations

Report of the committee on comparative mapping

1979 • 293 citations

THE LINKAGE OF GENES FOR THE HUMAN INTERFERON-INDUCED ANTIVIRAL PROTEIN AND INDOPHENOL OXIDASE-B TRAITS TO CHROMOSOME G-21

1973 • 291 citations

Two HLA-linked loci controlling the fourth component of human complement.

1978 • 291 citations

Localization of the human insulin gene to the distal end of the short arm of chromosome 11.

1981 • 285 citations

Chromosomal translocation in a human leukemic stem-cell line disrupts the T-cell antigen receptor delta-chain diversity region and results in a previously unreported fusion transcript.

1989 • 285 citations

H-2 haplotypes, genes, and antigens: Second listing

1982 • 283 citations

Identification of a human gene (HCK) that encodes a protein-tyrosine kinase and is expressed in hemopoietic cells.

1987 • 278 citations

Molecular characterization of the mouse beta 3-adrenergic receptor: relationship with the atypical receptor of adipocytes.

1991 • 277 citations

The human and rodent intestinal fatty acid binding protein genes. A comparative analysis of their structure, expression, and linkage relationships.

1987 • 276 citations

Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells.

1981 • 275 citations

The β2-microglobulin gene is on chromosome 15 and not in the HL-A region

1975 • 274 citations

High-resolution chromosomal localization of human genes for amylase, proopiomelanocortin, somatostatin, and a DNA fragment (D3S1) by in situ hybridization.

1983 • 274 citations

Alpha subunit variants of the human glycine receptor: primary structures, functional expression and chromosomal localization of the corresponding genes.

1990 • 272 citations

Human chromosomal mapping of genes for insulin-like growth factors I and II and epidermal growth factor

1984 • 267 citations

Chromosomal Localization of the Human Homolog (c- sis ) of the Simian Sarcoma Virus onc Gene

1982 • 262 citations

Histocompatibility Testing 1984

1984 • 252 citations

Linkage of HL‐A and GBG¹

1974 • 242 citations

Assignment of the genes for human λ immunoglobulin chains to chromosome 22

1981 • 239 citations

The Human Gene Encoding GM-CSF Is at 5q21-q32, the Chromosome Region Deleted in the 5q ^- Anomaly

1985 • 237 citations

The yes-related cellular gene lyn encodes a possible tyrosine kinase similar to p56lck.

1987 • 236 citations

Transcriptionally active c- myc oncogene is contained within NIARD, a DNA sequence associated with chromosome translocations in B-cell neoplasia

1983 • 236 citations

Inherited structural polymorphism in human C2: evidence for genetic linkage between C2 and Bf.

1976 • 236 citations

A human protein specific for the immunoglobulin octamer DNA motif contains a functional homeobox domain

1988 • 234 citations

Assignment of the human and mouse prion protein genes to homologous chromosomes.

1986 • 233 citations

ACID HYDROLASES AS MODELS OF GENETIC CONTROL

1979 • 232 citations

Assignment of the structural gene for the third component of human complement to chromosome 19.

1982 • 229 citations

Human Aromatase: cDNA Cloning, Southern Blot Analysis, and Assignment of the Gene to Chromosome 15

1988 • 227 citations

Cloning, chromosomal assignment, and regulation of the rat thyrotropin receptor: expression of the gene is regulated by thyrotropin, agents that increase cAMP levels, and thyroid autoantibodies.

1990 • 225 citations

Gene Encoding the β Subunit of S100 Protein Is on Chromosome 21: Implications for Down Syndrome

1988 • 222 citations

Histocompatibility Testing

2000 • 219 citations

Genetic control of two electrophoretic variants of glucosephosphate isomerase in the mouse (Mus musculus)

1969 • 218 citations

Structure of the human and murine R-ras genes, novel genes closely related to ras proto-oncogenes

1987 • 216 citations

Transforming growth factor β gene maps to human chromosome 19 long arm and to mouse chromosome 7

1986 • 216 citations

Assignment of the Gene for Myelin Proteolipid Protein to the X Chromosome: Implications for X-Linked Myelin Disorders

1985 • 213 citations

Isolation of a cDNA clone and localization of the human glutathione S‐transferase 3 genes to chromosome bands 11q13 and 12q13‐14

1989 • 208 citations

Human ethanol-inducible P450IIE1: complete gene sequence, promoter characterization, chromosome mapping, and cDNA-directed expression

1988 • 207 citations

Human γ-chain genes are rearranged in leukaemic T cells and map to the short arm of chromosome 7

1985 • 205 citations

The T cell receptor β chain genes are located on chromosome 6 in mice and chromosome 7 in humans

1984 • 204 citations

Localization of the human erbB-2 gene on normal and rearranged chromosomes 17 to bands q12–21.32

1989 • 200 citations

Molecular analysis of mbcl-2: Structure and expression of the murine gene homologous to the human gene involved in follicular lymphoma

1987 • 200 citations

Human monoamine oxidase A and B genes map to xp11.23 and are deleted in a patient with norrie disease

1989 • 199 citations

Human metallothionein genes: Structure of the functional locus at 16q13

1990 • 197 citations

Mouse c-myc Oncogene Is Located on Chromosome 15 and Translocated to Chromosome 12 in Plasmacytomas

1982 • 197 citations

Chromosomal localization of the human proto-oncogene c-ets

1984 • 195 citations

Molecular genetic approach to the characterization of the ?Down syndrome region? of chromosome 21

1989 • 195 citations

Turning the Left Cheek

1973 • 194 citations

Chromosomal localization of human leukocyte, fibroblast, and immune interferon genes by means of in situ hybridization

1982 • 192 citations

Hu- ets -1 and Hu- ets -2 Genes Are Transposed in Acute Leukemias with (4;11) and (8;21) Translocations

1986 • 191 citations

Mapping of the gene for anti-Müllerian hormone to the short arm of human chromosome 19

1987 • 190 citations

Chromosomal localization of human β globin gene on human chromosome 11 in somatic cell hybrids

1978 • 189 citations

Inherited Chondrodysplasia Punctata Due to a Deletion of the Terminal Short Arm of an X Chromosome

1984 • 188 citations

cDNA sequence, protein structure, and chromosomal location of the human gene for poly(ADP-ribose) polymerase.

1987 • 181 citations

Human genes involved in lipolysis of plasma lipoproteins: Mapping of loci for lipoprotein lipase to 8p22 and hepatic lipase to 15q21

1987 • 180 citations

Localization of the human multiple drug resistance gene, MDR1, to 7q21.1

1987 • 179 citations

Characterization and Chromosome Assignment of the Human Homolog of int-2, a Potential Proto-Oncogene

1986 • 178 citations

The Human Homologs of the raf ( mil ) Oncogene Are Located on Human Chromosomes 3 and 4

1984 • 177 citations

Localization of the gene encoding the GABAA receptor beta 3 subunit to the Angelman/Prader-Willi region of human chromosome 15.

1991 • 177 citations

Trisomie 21 et superoxyde dismutase-1 (IPO-A)

1976 • 175 citations

Developmental and transformation-sensitive expression of the Sparc gene on mouse chromosome 11.

1986 • 175 citations

Investigation of genetic linkage between myosin and actin genes using an interspecific mouse back-cross

1985 • 175 citations

Linkage of human apolipoproteins A-I and C-III genes

1983 • 174 citations

Human immune interferon gene is located on chromosome 12.

1983 • 173 citations

Molecular cloning and sequence analysis of a haploid expressed gene encoding t complex polypeptide 1

1986 • 172 citations

Human tyrosinase gene, mapped to chromosome 11 (q14 → q21), defines second region of homology with mouse chromosome 7

1988 • 171 citations

Chromosomal localisation of the human homologues to the oncogenes erbA and B.

1984 • 167 citations

ASSIGNMENT OF THE GENE FOR ADRENAL P450cl7 (STEROID 17α-HYDR0XYLASE⁄17,20 LYASE) TO HUMAN CHROMOSOME 10.

1986 • 167 citations

Human cardiac myosin heavy chain genes and their linkage in the genome

1987 • 166 citations

Linkage of cystic fibrosis to two tightly linked DNA markers: joint report from a collaborative study.

1986 • 165 citations

Glucose transporter gene expression in early mouse embryos

1991 • 163 citations

Cloning and mapping of a testis-specific gene with sequence similarity to a sperm-coating glycoprotein gene

1989 • 162 citations

Human δ-aminolevulinate synthase: Assignment of the housekeeping gene to 3p21 and the erythroid-specific gene to the X chromosome

1990 • 162 citations

Human laminin B1 chain. A multidomain protein with gene (LAMB1) locus in the q22 region of chromosome 7.

1987 • 162 citations

Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).

1984 • 161 citations

The mouse homolog of the hst/k-FGF gene is adjacent to int-2 and is activated by proviral insertion in some virally induced mammary tumors.

1989 • 160 citations

Genomic organization of the selectin family of leukocyte adhesion molecules on human and mouse chromosome 1.

1990 • 160 citations

Structure, chromosome location, and expression of the human gamma-actin gene: differential evolution, location, and expression of the cytoskeletal beta- and gamma-actin genes.

1988 • 160 citations

Molecular cloning and expression of the type 1 and type 2 murine receptors for tumor necrosis factor.

1991 • 160 citations

Assignment of CSF-1 to 5q33.1: evidence for clustering of genes regulating hematopoiesis and for their involvement in the deletion of the long arm of chromosome 5 in myeloid disorders.

1987 • 158 citations

Molecular analysis of the cDNA for human SPARC/osteonectin/BM-40: Sequence, expression, and localization of the gene to chromosome 5q31-q33

1988 • 157 citations

Genetics and polymorphism of the mouse prion gene complex: control of scrapie incubation time.

1988 • 157 citations

Chromosome assignment of some human enzyme loci: mitochondrial malate dehydrogenase to 7, mannosephosphate isomerase and pyruvate kinase to 15 and probably, esterase D to 13

1975 • 156 citations

Localization of loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase and biochemical evidence of nonrandom X chromosome expression from studies of a human X-autosome translocation.

1980 • 156 citations

Structure, chromosome location, and expression of the mouse zinc finger gene Krox-20: multiple gene products and coregulation with the proto-oncogene c-fos.

1989 • 155 citations

The major human erythroid DNA-binding protein (GF-1): primary sequence and localization of the gene to the X chromosome.

1990 • 155 citations

Molecular cloning of Ly-1, a membrane glycoprotein of mouse T lymphocytes and a subset of B cells: molecular homology to its human counterpart Leu-1/T1 (CD5).

1987 • 155 citations

Chromosomal sublocalization of human c-myb and c-fes cellular onc genes

1983 • 154 citations

The structural gene coding for myelin-associated proteolipid protein is mutated in jimpy mice

1986 • 154 citations

Isolation and chromosomal localization of a novel FMS-like tyrosine kinase gene

1991 • 153 citations

Cloning, sequencing, and evolutionary analysis of the mouse erythropoietin gene.

1986 • 153 citations

Chromosomal localization of genes encoding guanine nucleotide-binding protein subunits in mouse and human.

1988 • 152 citations

Characterization and chromosomal mapping of a human steroid 5α-reductase gene and pseudogene and mapping of the mouse homologue

1991 • 151 citations

Hox-5.1 defines a homeobox-containing gene locus on mouse chromosome 2.

1988 • 151 citations

A comprehensive genetic map of murine chromosome 11 reveals extensive linkage conservation between mouse and human.

1989 • 151 citations

Characterization and chromosome assignment of the human homolog of int-2, a potential proto-oncogene.

1986 • 149 citations

cDNA cloning and characterization of three genes uniquely expressed in cerebellum by Purkinje neurons

1988 • 148 citations

X-linkage of steroid sulphatase in the mouse is evidence for a functional Y-linked allele

1985 • 147 citations

Cloning of murine TCF-1, a T cell-specific transcription factor interacting with functional motifs in the CD3-epsilon and T cell receptor alpha enhancers.

1991 • 146 citations

Human chromosomes 6 and 21 are required for sensitivity to human interferon gamma.

1987 • 146 citations

Chromosome Mapping and Expression of a Putative Testis-Determining Gene in Mouse

1989 • 146 citations

Structures and chromosomal localizations of two human genes encoding synaptobrevins 1 and 2.

1990 • 144 citations

Gene mapping in <i>Mus musculus</i>by interspecific cell hybridization: assignment of the genes for tripeptidase-1 to chromosome 10, dipeptidase-2 to chromosome 18, acid phosphatase-1 to chromosome 12, and adenylate kinase-1 to chromosome 2

1977 • 144 citations

Genetic factors controlling structure and expression of apolipoproteins B and E in mice.

1987 • 144 citations

Gene linkage analysis in the mouse by somatic cell hybridization: Assignment of adenine phosphoribosyltransferase to chromosome 8 and ?-galactosidase to the X chromosome

1975 • 144 citations

Abnormal ornithine carbamoyltransferase in mice having the sparse-fur mutation.

1976 • 144 citations

Interleukin 2 (IL2) is assigned to human chromosome 4

1984 • 143 citations

Characterization of a monoclonal antibody directed against the murine B lymphocyte receptor for IgE.

1987 • 143 citations

A group of type I keratin genes on human chromosome 17: characterization and expression.

1988 • 142 citations

Chromosomal localization of seven members of the murine TGF-β superfamily suggests close linkage to several morphogenetic mutant loci

1990 • 142 citations

Multigene Family for Sarcomeric Myosin Heavy Chain in Mouse and Human DNA: Localization on a Single Chromosome

1983 • 141 citations

The Rat Clofibrate-InducibleCYP4ASubfamily II. cDNA Sequence of IVA3, Mapping of theCyp4aLocus to Mouse Chromosome 4, and Coordinate and Tissue-Specific Regulation of theCYP4AGenes

1989 • 140 citations

The putative oncogene Spi-1: murine chromosomal localization and transcriptional activation in murine acute erythroleukemias.

1989 • 140 citations

Chromosome 8 breakpoint far 3′ of the c-myc oncogene in a Burkitt's lymphoma 2;8 variant translocation is equivalent to the murine pvt-1 locus.

1986 • 139 citations

Debrisoquine 4-Hydroxylase: Characterization of a New P450 Gene Subfamily, Regulation, Chromosomal Mapping, and Molecular Analysis of the DA Rat Polymorphism

1987 • 139 citations

The human retinal degeneration slow (RDS) gene: Chromosome assignment and structure of the mRNA

1991 • 139 citations

A complement receptor locus: genes encoding C3b/C4b receptor and C3d/Epstein-Barr virus receptor map to 1q32.

1987 • 139 citations

Characterization, mapping, and expression of the human ceruloplasmin gene.

1986 • 139 citations

Assignment of the human gene for the low density lipoprotein receptor to chromosome 19: synteny of a receptor, a ligand, and a genetic disease.

1984 • 138 citations

Characterization of cDNAs encoding human leukosialin and localization of the leukosialin gene to chromosome 16.

1989 • 138 citations

Genetic control of lipid transport in mice. II. Genes controlling structure of high density lipoproteins.

1983 • 137 citations

Dispersion of the ras family of transforming genes to four different chromosomes in man

1983 • 137 citations

X-Chromosome localization of the functional gene for the E1α subunit of the human pyruvate dehydrogenase complex

1989 • 136 citations

Isolation of a cDNA clone and localization of human glutathione S-transferase 2 genes to chromosome band 6p12.

1987 • 136 citations

Human brain glycogen phosphorylase. Cloning, sequence analysis, chromosomal mapping, tissue expression, and comparison with the human liver and muscle isozymes.

1988 • 136 citations

Studies of the locus for androgen receptor: localization on the human X chromosome and evidence for homology with the Tfm locus in the mouse.

1981 • 135 citations

Structural and functional analysis of a growth-regulated gene, the human calcyclin.

1987 • 134 citations

Evidence for two distinct c-src loci on human chromosomes 1 and 20

1984 • 134 citations

Cloning and chromosomal localization of human genes encoding the three chains of type VI collagen.

1988 • 134 citations

Cloning and characterization of a 3-methyladenine DNA glycosylase cDNA from human cells whose gene maps to chromosome 16.

1991 • 132 citations

Heritable Fragile Site on Chromosome 16: Probable Localization of Haptoglobin Locus in Man

1970 • 132 citations

Genes for skeletal muscle myosin heavy chains are clustered and are not located on the same mouse chromosome as a cardiac myosin heavy chain gene.

1985 • 130 citations

A mapped set of DNA markers for human chromosome 15

1988 • 130 citations

Chromosomal organization of adrenergic receptor genes.

1990 • 129 citations

Structure of the chromosomal gene for murine interleukin 3.

1985 • 129 citations

Chromosome assignment of genes encoding the? and? subunits of glycoprotein hormones in man and mouse

1983 • 128 citations

Report of the committee on the genetic constitution of chromosomes 7, 8, and 9.

1982 • 127 citations

Leukocyte and fibroblast interferon genes are located on human chromosome 9.

1981 • 127 citations

Mitochondrial malate dehydrogenase and malic enzyme: Mendelian inherited electrophoretic variants in the mouse

1970 • 127 citations

A fine-structure deletion map of human chromosome 11p: Analysis of J1 series hybrids

1989 • 126 citations

The cellular retinol binding protein II gene. Sequence analysis of the rat gene, chromosomal localization in mice and humans, and documentation of its close linkage to the cellular retinol binding protein gene.

1987 • 126 citations

Linkage, physical mapping, and DNA sequence analysis of pseudoautosomal loci on the human X and Y chromosomes

1987 • 126 citations

Human Ornithine Transcarbamylase Locus Mapped to Band Xp21.1 Near the Duchenne Muscular Dystrophy Locus

1984 • 126 citations

The gene for cystathionine beta-synthase (CBS) maps to the subtelomeric region on human chromosome 21q and to proximal mouse chromosome 17.

1988 • 126 citations

Assignment of the Gene for Adenine Phosphoribosyltransferase to Human Chromosome 16 by Mouse-Human Somatic Cell Hybridization

1974 • 123 citations

Chromosomal assignments of genes coding for components of the mixed-function oxidase system in mice. Genetic localization of the cytochrome P-450PCN and P-450PB gene families and the nadph-cytochrome P-450 oxidoreductase and epoxide hydratase genes.

1985 • 123 citations

Localization of human monoamine oxidase-A gene to Xp11.23-11.4 by in situ hybridization: Implications for norrie disease

1989 • 122 citations

Structure and chromosomal localization of the human renal kallikrein gene

1988 • 121 citations

Chromosomal location of structural genes encoding murine immunoglobulin lambda light chains. Genetics of murine lambda light chains.

1981 • 121 citations

Molecular genetic markers spanning mouse chromosome 10

1990 • 121 citations

Identification of a new P450 expressed in human lung: complete cDNA sequence, cDNA-directed expression, and chromosome mapping

1989 • 120 citations

Genes for serum amyloid A proteins map to Chromosome 7 in the mouse

1984 • 119 citations

Assignment of the Major Histocompatibility Complex to Chromosome No. 6 in a Family with a Pericentric Inversion

1974 • 119 citations

Twenty-five loci form a continuous linkage map of markers for human chromosome 7

1989 • 118 citations

Cloning and chromosomal assignment of a human cDNA encoding a T cell- and natural killer cell-specific trypsin-like serine protease.

1988 • 118 citations

Genetic and cytogenetic localisation of the homeo box containing genes on mouse chromosome 6 and human chromosome 7.

1986 • 118 citations

Interleukin-1 gene (IL1) assigned to long arm of human chromosome 2.

1986 • 118 citations

Molecular cloning, functional expression, and chromosomal localization of mouse hepatocyte nuclear factor 1.

1990 • 117 citations

Chromosomal assignment of the human erythropoietin gene and its DNA polymorphism.

1986 • 116 citations

Conserved chromosomal positions of dual domains of the ets protooncogene in cats, mice, and humans.

1986 • 114 citations

Genes for immunoglobulin heavy chain and serum prealbumin protein are linked in mouse

1975 • 114 citations

Conservation of autosomal gene synteny groups in mouse and man

1978 • 114 citations

CD14 is a member of the family of leucine-rich proteins and is encoded by a gene syntenic with multiple receptor genes.

1990 • 114 citations

Genetic polymorphism of C4 in man and localisation of a structural C4 locus to the HLA gene complex of chromosome 6

1976 • 114 citations

Characterization and chromosomal localization of the gene encoding the human cell adhesion molecule uvomorulin

1988 • 113 citations

The Human Gene for the β Subunit of Nerve Growth Factor Is Located on the Proximal Short Arm of Chromosome 1

1983 • 113 citations

Genetic and Developmental Regulation of the Lipoprotein Lipase Gene: Loci Both Distal and Proximal to the Lipoprotein Lipase Structural Gene Control Enzyme Expression

1989 • 113 citations

Mapping of the human retinoic acid receptor to the q21 band of chromosome 17

1988 • 112 citations

Polymorphism and linkage for mannosephosphate isomerase in Mus musculus

1973 • 112 citations

Chromosomal assignment of human cytochrome P-450 (debrisoquine/sparteine type) to chromosome 22.

1987 • 112 citations

Chromosomal location of the genes encoding the leukocyte adhesion receptors LFA-1, Mac-1 and p150,95. Identification of a gene cluster involved in cell adhesion.

1988 • 112 citations

Linkage analyses using biochemical variants in mice. III. Linkage relationships of eleven biochemical markers

1970 • 111 citations

Localization of Evi-2 to chromosome 11: linkage to other proto-oncogene and growth factor loci using interspecific backcross mice.

1988 • 111 citations

Localization of the human oestrogen receptor gene to chromosome 6q24→q27 by in situ hybridization

1986 • 111 citations

Localization of genes on human chromosomes by studies of human-Chinese hamster somatic cell hybrids

1973 • 111 citations

The pronatriodilatin gene is located on the distal short arm of human chromosome 1 and on mouse chromosome 4.

1985 • 111 citations

Glutamate oxalate transaminase (GOT) genetics in Mus musculus: Linkage, polymorphism, and phenotypes of the Got-2 and Got-1 loci

1970 • 110 citations

Structure and expression of the pulmonary surfactant protein SP-C gene in the mouse.

1990 • 108 citations

Genes coding for sensitivity to interferon (IfRec) and soluble superoxide dismutase (SOD-1) are linked in mouse and man and map to mouse chromosome 16.

1980 • 108 citations

Close genetic and physical linkage between the murine haemopoietic growth factor genes GM-CSF and Multi-CSF (IL3).

1987 • 107 citations

Human collagen genes encoding basement membrane alpha 1 (IV) and alpha 2 (IV) chains map to the distal long arm of chromosome 13.

1987 • 105 citations

Assignment by Deletion of Human Red Cell Acid Phosphatase Gene Locus to the Short Arm of Chromosome 2

1973 • 105 citations

Human metallothionein genes are clustered on chromosome 16.

1984 • 104 citations

Report of the committee on comparative mapping

1989 • 104 citations

The genes for lumor necrosis factor (TNF-alpha) and lymphotoxin (TNF-beta) are tandemly arranged on chromosome 17 of the mouse

1986 • 103 citations

The nerve growth factor receptor gene is at human chromosome region 17q12-17q22, distal to the chromosome 17 breakpoint in acute leukemias.

1986 • 103 citations

Interferon and c- ets -1 Genes in the Translocation (9;11)(p22;q23) in Human Acute Monocytic Leukemia

1986 • 103 citations

Localization of human tryptophan hydroxylase (TPH) to chromosome 11p15.3→p14 by in situ hybridization

1991 • 103 citations

Genetic mapping of the mouse c-fms proto-oncogene to chromosome 18

1988 • 103 citations

Molecular characterization of human and bovine rod photoreceptor cGMP phosphodiesterase α-subunit and chromosomal localization of the human gene

1990 • 102 citations

Assignment of the genes for thymidine kinase and galactokinase toMus musculus chromosome 11 and the preferential segregation of this chromosome in Chinese hamster/mouse somatic cell hybrids

1977 • 102 citations

Localization of the human c-sis oncogene in Ph1-positive and Ph1- negative chronic myelocytic leukemia by in situ hybridization

1984 • 101 citations

Mouse Chromosome 17

1992 • 101 citations

Refined mapping of the three DNA repair genes, ERCC1, ERCC2, and XRCC1, on human chromosome 19

1989 • 101 citations

Human microsomal xenobiotic epoxide hydrolase. Complementary DNA sequence, complementary DNA-directed expression in COS-1 cells, and chromosomal localization.

1988 • 101 citations

Human monoamine oxidase gene (MAOA): Chromosome position (Xp21-p11) and DNA polymorphism

1988 • 101 citations

Chromosomal assignment of the human homologues of feline sarcoma virus and avian myeloblastosis virus onc genes.

1982 • 100 citations

Human genes encoding prothrombin and ceruloplasmin map to 11p11?q12 and 3q21?24, respectively

1987 • 100 citations

Assignment of human ferritin genes to chromosomes 11 and 19q13.3→19qter

1985 • 100 citations

The mouse genome contains two nonallelic pro-opiomelanocortin genes.

1983 • 100 citations

Assignment of Nucleoside Phosphorylase to D-14 and Localization of X-linked Loci in Man by Somatic Cell Genetics

1973 • 99 citations

Assignment of the gene for cytoplasmic superoxide dismutase ( Sod-1 ) to a region of chromosome 16 and of Hprt to a region of the X chromosome in the mouse

1979 • 99 citations

Chromosomal assignment of the mouse kappa light chain genes.

1979 • 99 citations

The human CYP2F gene subfamily: identification of a cDNA encoding a new cytochrome P450, cDNA-directed expression, and chromosome mapping

1990 • 98 citations

Assignment of human 3-hydroxy-3-methylglutaryl coenzyme A reductase gene to q13 → q23 region of chromosome 5

1986 • 98 citations

Metallothionein gene cluster is split by chromosome 16 rearrangements in myelomonocytic leukaemia

1985 • 98 citations

Localization of the human pim oncogene (PIM) to a region of chromosome 6 involved in translocations in acute leukemias.

1986 • 98 citations

Recombinant inbred strain and interspecific backcross analysis of molecular markers flanking the murine agouti coat color locus.

1989 • 97 citations

Gene for T-Cell Growth Factor: Location on Human Chromosome 4q and Feline Chromosome B1

1984 • 97 citations

Localization of a lymphocyte-specific protein tyrosine kinase gene (lck) at a site of frequent chromosomal abnormalities in human lymphomas.

1986 • 96 citations

GENETICS OF MOUSE HEMOGLOBINS *

1974 • 96 citations

Assignment of the gene for galactokinase to human chromosome 17 and its regional localisation to band q21-22

1974 • 96 citations

Regulation, Linkage, and Sequence of Mouse Metallothionein I and II Genes

1984 • 96 citations

Intrachromosomal gene mapping in man: Assignment of nucleoside phosphorylase to region 14cen?14q21 by interspecific hybridization of cells with a t(X;14) (p22;q21) translocation

1976 • 95 citations

The myosin alkali light chains of mouse ventricular and slow skeletal muscle are indistinguishable and are encoded by the same gene.

1985 • 95 citations

Isolation of a human gene with protein sequence similarity to human and murine int-1 and the Drosophila segment polarity mutant wingless.

1988 • 95 citations

The Insulin Gene Is Located on the Short Arm of Chromosome 11 in Humans

1981 • 95 citations

Structure, expression, and genetic linkage of the mouse BCM1 (OX45 or Blast-1) antigen. Evidence for genetic duplication giving rise to the BCM1 region on mouse chromosome 1 and the CD2/LFA3 region on mouse chromosome 3.

1990 • 95 citations

Chromosomal Localization of Muscle Nicotinic Acetylcholine Receptor Genes in the Mouse

1986 • 95 citations

Menkes syndrome in a girl with X‐autosome translocation

1987 • 95 citations

Linkage of the evolutionarily-related serum albumin and alpha-fetoprotein genes within q11-22 of human chromosome 4.

1983 • 95 citations

Chromosomal Locations of the Murine T-Cell Receptor Alpha-Chain Gene and the T-Cell Gamma Gene

1985 • 95 citations

Definition of mouse chromosome 1 and 3 gene linkage groups that are conserved on human chromosome 1: Evidence that a conserved linkage group spans the centromere of human chromosome 1

1989 • 94 citations

Chromosome mapping of the growth hormone receptor gene in man and mouse

1989 • 94 citations

Comparative chromosome mapping of a conserved homoeo box region in mouse and human

1985 • 94 citations

Regional assignment of the human loci for uvomorulin (UVO) and chymotrypsinogen B (CTRB) with the help of two overlapping deletions on the long arm of chromosome 16

1989 • 93 citations

Chromosomal mapping of genes for transforming growth factors beta 2 and beta 3 in man and mouse: dispersion of TGF-beta gene family.

1988 • 93 citations

Genetic basis for a mouse model of down syndrome

1986 • 93 citations

A genetic linkage map of mouse chromosome 10: localization of eighteen molecular markers using a single interspecific backcross.

1990 • 93 citations

Chromosomal localization of the human c-fmsoncogene

1983 • 92 citations

Linkage disequilibrium of plasminogen polymorphisms and assignment of the gene to human chromosome 6q26-6q27.

1987 • 92 citations

Assignment of the alpha 1-antitrypsin gene and a sequence-related gene to human chromosome 14 by molecular hybridization.

1983 • 91 citations

A molecular genetic linkage map of mouse chromosome 7

1990 • 91 citations

Genetic linkage between lipoprotein(a) phenotype and a DNA polymorphism in the plasminogen gene

1988 • 91 citations

The human TTP protein: sequence, alignment with related proteins, and chromosomal localization of the mouse and human genes

1991 • 91 citations

Chromosomal Mapping of Genes Involved in Growth Control

1986 • 91 citations

Hereditary C2 deficiency: Genetic studies and association with the HL-A system.

1975 • 90 citations

Genes for synapsin I, a neuronal phosphoprotein, map to conserved regions of human and murine X chromosomes.

1986 • 90 citations

Random X inactivation resulting in mosaic nullisomy of region Xp21.1→p21.3 associated with heterozygosity for ornithine transcarbamylase deficiency and for chronic granulomatous disease

1984 • 89 citations

A Novel Human Gene Closely Related to the abl Proto-Oncogene

1986 • 89 citations

Mapping of genes for inhibin subunits α, βA, and βB on human and mouse chromosomes and studies of jsd mice

1989 • 89 citations

Localization of the human sex hormone-binding globulin gene (SHBG) to the short arm of chromosome 17 (17p12→p13)

1990 • 89 citations

The gene encoding the T-cell receptor α-chain maps close to the Np-2 locus on mouse chromosome 14

1985 • 89 citations

Homologous genes for enolase, phosphogluconate dehydrogenase, phosphoglucomutase, and adenylate kinase are syntenic on mouse chromosome 4 and human chromosome 1p

1978 • 89 citations

Somatic Cell Genetic Assignment of Peptidase C and the Rh Linkage Group to Chromosome A-1 in Man

1972 • 89 citations

hph-1: a mouse mutant with hereditary hyperphenylalaninemia induced by ethylnitrosourea mutagenesis.

1988 • 88 citations

Tandem arrangement of the albumin and α-fetoprotein genes in the human genome

1984 • 88 citations

A molecular genetic linkage map of mouse chromosome 4 including the localization of several proto-oncogenes

1989 • 88 citations

Liver glutathione S-transferase polymorphism in Japanese and its pharmacogenetic importance

1987 • 88 citations

Two homoeo box loci mapped in evolutionarily related mouse and human chromosomes

1985 • 88 citations

Location of the genes controlling H-Y antigen expression and testis determination on the mouse Y chromosome.

1988 • 88 citations

Genetics of Human-Mouse Somatic Cell Hybrids: Linkage of Human Genes for Lactate Dehydrogenase- A and Esterase-A ₄

1972 • 87 citations

Mapping of the gene encoding the α subunit of the stimulatory G protein of adenylyl cyclase (GNAS1) to 20q13.2 → q13.3 in human by in situ hybridization

1991 • 87 citations

Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus.

1985 • 86 citations

Actively transcribed genes in the raf oncogene group, located on the X chromosome in mouse and human.

1986 • 86 citations

Regional chromosomal localization of N-ras, K-ras-1, K-ras-2 andmyboncogenes in human cells

1983 • 86 citations

Molecular cloning of the cDNA of human X chromosomal gene (CCG1) which complements the temperature-sensitive G1 mutants, tsBN462 and ts13, of the BHK cell line.

1988 • 86 citations

Somatic cell genetic evidence for X-chromosome linkage of three enzymes in the mouse

1976 • 86 citations

Assignment of a serotonin 5HT-2 receptor gene (HTR2) to human chromosome 13q14–q21 and mouse chromosome 14

1991 • 85 citations

Cloning of a complementary DNA encoding a new mouse B lymphocyte differentiation antigen, homologous to the human B1 (CD20) antigen, and localization of the gene to chromosome 19.

1988 • 85 citations

Localization of the human progesterone receptor gene to chromosome 11q22–q23

1987 • 85 citations

Nucleotide sequence of mouse 5-aminolevulinic acid synthase cDNA and expression of its gene in hepatic and erythroid tissues

1986 • 85 citations

Genetic regulation of coumarin hydroxylase activity in mice. Evidence for single locus control on chromosome.

1979 • 85 citations

The receptors for prolactin and growth hormone are localized in the same region of human chromosome 5

1990 • 84 citations

Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this site.

1984 • 84 citations

Regional mapping of catalase and Wilms tumor?aniridia, genitourinary abnormalities, and mental retardation triad loci to the chromosome segment 11p1305?p1306

1984 • 83 citations

Assignment of a Gene for Adenosine Deaminase to Human Chromosome 20

1974 • 83 citations

Spondyloepiphyseal dysplasia congenita: genetic linkage to type II collagen (COL2AI).

1990 • 82 citations

Interleukin 4 is at 5q31 and interleukin 6 is at 7p15

1988 • 82 citations

Chromosomal assignment of retinoic acid receptor (RAR) genes in the human, mouse, and rat genomes

1991 • 82 citations

Molecular cloning and chromosomal localization of the murine homolog of the human helix-loop-helix gene SCL.

1991 • 81 citations

The alpha-spectrin gene is on chromosome 1 in mouse and man.

1985 • 81 citations

Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysis

1986 • 81 citations

cDNA cloning of human oxysterol-binding protein and localization of the gene to human chromosome 11 and mouse chromosome 19

1990 • 81 citations

Evolution of mammalian carbonic anhydrase loci by tandem duplication: Close linkage of Car-1 and Car-2 to the centromere region of chromosome 3 of the mouse

1976 • 81 citations

Human CD28 and CTLA-4 Ig superfamily genes are located on chromosome 2 at bands q33?q34

1990 • 81 citations

Assignment of defensin gene(s) to human chromosome 8p23

1989 • 80 citations

Probable Assignment of the Alpha Locus of Haptoglobin to Chromosome 16 in Man

1969 • 80 citations

A cytochrome P‐450 gene family mapped to human chromosome 19

1985 • 80 citations

Regulation of expression of liver‐specific enzymes

1982 • 80 citations

Human cytochrome P-450 PB-1: a multigene family involved in mephenytoin and steroid oxidations that maps to chromosome 10.

1988 • 80 citations

Eight closely linked loci place the Wilson disease locus within 13q14-q21.

1988 • 80 citations

A genetic linkage map of 27 markers on human chromosome 21

1991 • 79 citations

Molecular cloning and nucleotide sequence of the cDNA for sperm-specific lactate dehydrogenase-C from mouse

1987 • 79 citations

Identification of a novel P450 expressed in rat lung: cDNA cloning and sequence, chromosome mapping, and induction by 3-methylcholanthrene

1989 • 79 citations

Yeast artificial chromosome cloning of a two-megabase-size contig within chromosomal band 18q21 establishes physical linkage between BCL2 and plasminogen activator inhibitor type-2

1991 • 79 citations

Chromosomal localization of three humanras genes by in situ molecular hybridization

1985 • 79 citations

Isolation of Duplicated Human c-src Genes Located on Chromosomes 1 and 20

1985 • 78 citations

Chromosomal location of the gene encoding the neural cell adhesion molecule (N-CAM) in the mouse.

1985 • 78 citations

Assignment of the human thyroid stimulating hormone receptor (TSHR) gene to chromosome 14q31

1990 • 78 citations

Genetic polymorphisms for a phenobarbital-inducible cytochrome P-450 map to the Coh locus in mice.

1983 • 78 citations

The murine Ah locus: a new allele and mapping to chromosome 12.

1987 • 78 citations

Localization of the panhypopituitary dwarf mutation (df) on mouse chromosome 11 in an intersubspecific backross

1991 • 78 citations

Linkage of isozyme loci in the mouse: Phosphoglucomutase-2 (Pgm-2), mitochondrial NADP malate dehydrogenase (Mod-2), and dipeptidase-1 (Dip-1)

1971 • 77 citations

Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardation.

1987 • 77 citations

Chromosomal location of human genes encoding major heat-shock protein HSP70

1987 • 77 citations

Assignment of the genes for malate oxidoreductase decarboxylating to chromosome 6 and peptidase B and lactate dehydrogenase B to chromosome 12 in man.

1973 • 77 citations

Genes for two autosomal recessive forms of chronic granulomatous disease assigned to 1q25 (NCF2) and 7q11.23 (NCF1).

1990 • 77 citations

Additional Data and Summary for Albumin-Gc Linkage in Man

1970 • 77 citations

Comparison of nonerythroid alpha-spectrin genes reveals strict homology among diverse species.

1988 • 77 citations

Proviral Integration Site Mis-1 in Rat Thymomas Corresponds to the pvt-1 Translocation Breakpoint in Murine Plasmacytomas

1986 • 77 citations

The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophy.

1990 • 77 citations

Assignment of a human DNA-repair gene associated with sister-chromatid exchange to chromosome 19

1986 • 76 citations

Murine Ly-6 multigene family is located on chromosome 15.

1987 • 76 citations

Human Luteinizing hormone-releasing hormone gene (LHRH) is located on short arm of chromosome 8 (region 8p11.2 → p21)

1986 • 76 citations

Sex, strain, and species differences affect recombination across an evolutionarily conserved segment of mouse chromosome 16

1990 • 76 citations

Thyroid Peroxidase: Rat cDNA Sequence, Chromosomal Localization in Mouse, and Regulation of Gene Expression by Comparison to Thyroglobulin in Rat FRTL-5 Cells

1989 • 76 citations

Chromosomal location of the co-expressed human skeletal and cardiac actin genes.

1984 • 76 citations

Chromosomal localization of human Na+,K+-ATPase α- and β-subunit genes

1988 • 76 citations

X linkage of phosphoglycerate kinase in the mouse

1974 • 76 citations

Comparative mapping of DNA markers from the familial Alzheimer disease and Down syndrome regions of human chromosome 21 to mouse chromosomes 16 and 17.

1988 • 76 citations

Chromosomal Location of Human Metallothionein Genes: Implications for Menkes' Disease

1984 • 76 citations

Regional assignment of catalase (CAT) gene to band 11p13. Association with the aniridia-Wilms' tumor-Gonadoblastoma (WAGR) complex.

1980 • 76 citations

The human homeobox gene HOX7 maps to chromosome 4p16.1 and may be implicated in Wolf-Hirschhorn syndrome

1990 • 75 citations

Human c-Ki- ras 2 Proto-Oncogene on Chromosome 12

1983 • 75 citations

The human homolog of murine Evi-2 lies between two von Recklinghausen neurofibromatosis translocations

1990 • 75 citations

Polymorphic Human Glucose Transporter Gene (GLUT) is on Chromosome 1p31.3→p35

1987 • 74 citations

Mapping of the gene encoding the beta-amyloid precursor protein and its relationship to the Down syndrome region of chromosome 21.

1988 • 74 citations

Ankyrin and the hemolytic anemia mutation, nb, map to mouse chromosome 8: presence of the nb allele is associated with a truncated erythrocyte ankyrin.

1990 • 74 citations

The interleukin-4 receptor gene (IL4R) maps to 16p11.2–16p12.1 in human and to the distal region of mouse chromosome 7

1991 • 74 citations

Mouse mammary tumor virus integration regions int-1 and int-2 map on different mouse chromosomes.

1984 • 74 citations

The human homologue of the mouse t-complex gene, TCP1, is located on chromosome 6 but is not near the HLA region.

1987 • 74 citations

The acute phase response of mouse liver. Genetic analysis of the major acute phase reactants.

1984 • 74 citations

Chromosomal mapping of the gene for the type II insulin-like growth factor receptor/cation-independent mannose 6-phosphate receptor in man and mouse

1988 • 73 citations

Structure of human cholecystokinin gene and its chromosomal location

1986 • 73 citations

Genetics and biology of human ovarian teratomas

1992 • 73 citations

Localization of the polymorphic human calcitonin gene on chromosome 11

1984 • 73 citations

The CD14 monocyte differentiation antigen maps to a region encoding growth factors and receptors

1988 • 73 citations

Human homeo box-containing genes located at chromosome regions 2q31----2q37 and 12q12----12q13.

1987 • 73 citations

EVX2, a human homeobox gene homologous to the even-skipped segmentation gene, is localized at the 5′ end of HOX4 locus on chromosome 2

1991 • 72 citations

Linkage of theleuS, emtB, andchr genes on chromosome 5 in humans and expression of human genes encoding protein synthetic components in human-Chinese hamster hybrids

1982 • 72 citations

Mathematical models of gene amplification with applications to cellular drug resistance and tumorigenicity.

1990 • 72 citations

Chromosomal assignments of human type I and type II cytokeratin genes to different chromosomes

1988 • 72 citations

Definition of subchromosomal intervals around the myotonic dystrophy gene region at 19q

1989 • 72 citations

Chromosome assignment of a murine glucocorticoid receptor gene (Grl-1) using intraspecies somatic cell hybrids

1980 • 72 citations

Complete sequence of human vinculin and assignment of the gene to chromosome 10.

1990 • 72 citations

Sequence and organization of the mouse poly (ADP-ribose) polymerase gene

1989 • 72 citations

HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and genitourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band 11p13.

1987 • 72 citations

Cloning of human hepatic nuclear factor 1 (HNF1) and chromosomal localization of its gene in man and mouse

1990 • 71 citations

The AKT1 proto-oncogene maps to human chromosome 14, band q32

1988 • 71 citations

A molecular genetic linkage map of mouse chromosome 2

1990 • 71 citations

The human c-ros gene (ROS) is located at chromosome region 6q16----6q22.

1986 • 71 citations

Opioid-Noradrenergic Interactions in the Neurohypophysis

1988 • 71 citations

Murine complement component 3: genetic variation and linkage to H-2.

1978 • 71 citations

Gene dose effect: intraband mapping of the <i>LDH A </i>locus using cells from four individuals with different interstitial deletions of 11p

1977 • 71 citations

Chromosomal assignment of the human genes coding for the major proteins of the desmosome junction, desmoglein DGI (DSG), desmocollins DGIIIII (DSC), desmoplakins DPIII (DSP), and plakoglobin DPIII (JUP)

1991 • 70 citations

Inherited and de novo deletion of the tyrosine aminotransferase gene locus at 16q22.1 ? q22.3 in a patient with tyrosinemia type II

1987 • 70 citations

Chromosomal localization of the genes encoding two forms of the G protein β polypeptide, β1 and β3, in man

1990 • 70 citations

Bone morphogenetic protein: Chromosomal localization of human genes for BMP1, BMP2A, and BMP3

1991 • 70 citations

Nucleotide sequence, chromosomal localization and developmental expression of the mouse int-1-related gene

1989 • 70 citations

The serotonin receptor subtype 2 locusHTR2 is on human chromosome 13 near genes for esterase D and retinoblastoma-1 and on mouse chromosome 14

1990 • 70 citations

Characterization of a murine cDNA encoding a member of the carboxylesterase multigene family

1991 • 70 citations

Nineteen of 26 cellular oncogenes precisely localized in the human genome map to one of the 83 bands involved in primary cancer-specific rearrangements

1987 • 70 citations

Mapping of nucleoside phosphorylase (Np-1) and esterase 10 (Es-10) on mouse chromosome 14

1977 • 70 citations

Insulin-Degrading Enzyme: Stable Expression of the Human Complementary DNA, Characterization of its Protein Product, and Chromosomal Mapping of the Human and Mouse Genes

1990 • 69 citations

Physical mapping of the von Recklinghausen neurofibromatosis region on chromosome 17.

1989 • 69 citations

Molecular and cytogenetic evidence for the location of Tdy and Hya on the mouse Y chromosome short arm.

1988 • 69 citations

The genes coding for the muscle contractile proteins, myosin heavy chain, myosin light chain 2, and skeletal muscle actin are located on three different mouse chromosomes.

1982 • 69 citations

The coding sequence for the 32,000-dalton pulmonary surfactant-associated protein A is located on chromosome 10 and identifies two separate restriction-fragment-length polymorphisms.

1987 • 69 citations

Localisation of a dystrophin-related autosomal gene to 6q24 in man, and to mouse chromosome 10 in the region of the dystrophia muscularis (dy) locus

1990 • 69 citations

Interleukin-1 ? and ? genes: linkage on chromosome 2 in the mouse

1987 • 69 citations

Assignment of the human 2,3,7,8-tetrachlorodibenzo-p-dioxin-inducible cytochrome P₁-450 gene to chromosome 15

1985 • 68 citations

Localisation of genetic markers and orientation of the linkage group on chromosome 19

1984 • 68 citations

Structural organization and chromosomal assignment of the parvalbumin gene.

1987 • 68 citations

Location on chromosome 1 of Rnr, a gene that regulates renin in the submaxillary gland of the mouse.

1978 • 68 citations

The murine homologue of the T lymphocyte CD2 antigen: molecular cloning, chromosome assignment and cell surface expression

1987 • 68 citations

Mapping of Col3a1 and Col6a3 to proximal murine chromosome 1 identifies conserved linkage of structural protein genes between murine chromosome 1 and human chromosome 2q

1990 • 68 citations

A primary map of ten DNA markers and two serological markers for human chromosome 19

1988 • 67 citations

Structure, chromosome mapping and expression of the murine Fgf-6 gene.

1990 • 67 citations

New Murine Homeoboxes: Structure, Chromosomal Assignment, and Differential Expression in Adult Erythropoiesis

1987 • 67 citations

Gene for a major cell surface glycoprotein of mouse macrophages and other phagocytic cells is on chromosome 2.

1982 • 67 citations

Chromosomal Mapping of the Prolactin/Growth Hormone Gene Family in the Mouse*

1988 • 67 citations

Linkage analysis of multiple endocrine neoplasia type 1 with INT2 and other markers on chromosome 11

1989 • 67 citations

Human ornithine decarboxylase sequences map to chromosome regions 2pter→p23 and 7cen→qter but are not coamplified with the NMYC oncogene

1986 • 67 citations

Physical mapping of human chromosome 17 using fragment-containing microcell hybrids

1989 • 66 citations

A new allele of the sparse fur gene in the mouse

1974 • 66 citations

c-src is consistently conserved in the chromosomal deletion (20q) observed in myeloid disorders.

1985 • 66 citations

Localization of a human heat-shock HSP 70 gene sequence to chromosome 6 and detection of two other loci by somatic-cell hybrid and restriction fragment length polymorphism analysis

1987 • 66 citations

Clustering of cytokine genes on mouse chromosome 11.

1990 • 66 citations

Chromosomal assignment of the genes for human aldehyde dehydrogenase-1 and aldehyde dehydrogenase-2.

1986 • 66 citations

Molecular cloning and chromosomal mapping of a human locus related to the transforming gene of Moloney murine sarcoma virus.

1982 • 66 citations

Conservation and reorganization of loci on the mammalian X chromosome: A molecular framework for the identification of homologous subchromosomal regions in man and mouse

1988 • 65 citations

A mapped set of genetic markers for human chromosome 9

1988 • 65 citations

Genetic polymorphism of ?2-microglobulin (B2m) maps to the H-3 region of chromosome 2

1981 • 65 citations

The murine Il-6 gene maps to the proximal region of chromosome 5.

1989 • 65 citations

Assignment of human alpha 1-antitrypsin to chromosome 14 by somatic cell hybrid analysis.

1982 • 65 citations

Chromosomal locations of the human and mouse genes for precursors of epidermal growth factor and the beta subunit of nerve growth factor.

1985 • 65 citations

Ly-4 , A New Locus Determining a Lymphocyte Cell-Surface Alloantigen in Mice

1973 • 65 citations

Partial trisomy 21

1973 • 65 citations

Autosomal phosphoglycerate kinase linked to mouse major histocompatibility complex

1978 • 65 citations

The metallothionein-I gene maps to mouse chromosome 8: implications for human Menkes' disease

1983 • 65 citations

Murine?-fetoprotein and albumin: Two evolutionarily linked proteins encoded on the same mouse chromosome

1981 • 65 citations

Chromosomal location of the octamer transcription factors, Otf-1, Otf-2, and Otf-3, defines multiple Otf-3-related sequences dispersed in the mouse genome

1991 • 64 citations

G protein Gsα (GNAS1), the probable candidate gene for albright hereditary osteodystrophy, is assigned to human chromosome 20q12–q13.2

1991 • 64 citations

The myelin-associated glycoprotein gene: Mapping to human chromosome 19 and mouse chromosome 7 and expression in quivering mice

1987 • 64 citations

Characterization and chromosomal mapping of a cDNA encoding tryptophan hydroxylase from a mouse mastocytoma cell line

1990 • 64 citations

Establishment of a molecular genetic map of distal mouse chromosome 1: Further definition of a conserved linkage group syntenic with human chromosome 1q

1988 • 63 citations

Identification of a Human Gene (HCK) that Encodes a Protein-Tyrosine Kinase and is Expressed in Hemopoietic Cells

1987 • 63 citations

Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26?q27

1987 • 63 citations

Comparative gene mapping: order of loci on the X chromosome is different in mice and humans.

1980 • 63 citations

Genomic organization of adrenergic and serotonin receptors in the mouse: Linkage mapping of sequence-related genes provides a method for examining mammalian chromosome evolution

1991 • 63 citations

Assignment of human porphobilinogen deaminase to 11q24.1→q24.2 by in situ hybridization and gene dosage studies

1991 • 63 citations

Location of the retinoblastoma susceptibility gene(s) and the human esterase D locus.

1984 • 63 citations

IL9 maps to mouse chromosome 13 and human chromosome 5

1990 • 63 citations

Chromosome assignments of genes in man using mouse-human somatic cell hybrids: Mitochondrial superoxide dismutase (indophenol oxidase-B, tetrameric) to chromosome 6

1973 • 62 citations

Multilocus molecular mapping of the mouse X chromosome

1988 • 62 citations

Physical mapping studies on the human X chromosome in the region Xq27-Xqter

1987 • 62 citations

Genetic analysis of the dominant white-spotting (W) region on mouse chromosome 5: identification of cloned DNA markers near W.

1988 • 62 citations

Assignment of the humanhap retinoic acid receptor RARβ gene to the p24 band of chromosome 3

1988 • 62 citations

Direct regional assignment of the gene for vitamin D binding protein (Gc-globulin) to human chromosome 4q11-q13 and identification of an associated DNA polymorphism

1986 • 62 citations

cDNA cloning and assignment to chromosome 21 ofIFI-78K gene, the human equivalent of murineMx gene

1988 • 62 citations

The gene encoding the T-cell surface protein T4 is located on human chromosome 12.

1986 • 62 citations

Related calcium-binding proteins map to the same subregion of chromosome 1q and to an extended region of synteny on mouse chromosome 3

1990 • 62 citations

Assignment of the gene coding for the T3-delta subunit of the T3-T-cell receptor complex to the long arm of human chromosome 11 and to mouse chromosome 9.

1985 • 62 citations

Genetic mapping of <i>Prm-1, Igl-1, Smst, Mtv-6, Sod-1,</i> and <i>Ets-2</i>and localization of the Down syndrome region on mouse chromosome 16

1987 • 62 citations

The genes coding for A alpha-, B beta-, and gamma-chains of fibrinogen map to 4q2.

1984 • 62 citations

Comparison of linkage maps of mouse chromosome 12 derived from laboratory strain intraspecific and Mus spretus interspecific backcrosses

1989 • 62 citations

Human tyrosine hydroxylase and insulin genes are contiguous on chromosome 11.

1988 • 62 citations

The gene encoding the epsilon subunit of the T3/T-cell receptor complex maps to chromosome 11 in humans and to chromosome 9 in mice.

1987 • 61 citations

Linkage between the loci for the Lp(a) lipoprotein (LP) and plasminogen (PLG)

1988 • 61 citations

Localization of the human JUN protooncogene to chromosome region 1p31-32.

1988 • 61 citations

cDNA cloning, sequencing and chromosome mapping of a non-erythroid spectrin, human α-fodrin

1987 • 61 citations

A 6000 kb segment of chromosome 1 is conserved in human and mouse.

1989 • 61 citations

Lambda lg constant region genes are translocated to chromosome 8 in Burkitt's lymphoma with t(8:22

1983 • 61 citations

Localization of heat shock protein 70 genes inside the rat major histocompatibility complex close to class III genes

1989 • 61 citations

The GABAA receptor β3 subunit gene: Characterization of a human cDNA from chromosome 15q11q13 and mapping to a region of conserved synteny on mouse chromosome 7

1991 • 61 citations

Cognate homeo-box loci mapped on homologous human and mouse chromosomes.

1986 • 60 citations

Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers

1988 • 60 citations

Report of the committee on the genetic constitution of chromosomes 17, 18 and 19

1985 • 60 citations

Assignment by in situ hybridization of the angiotensinogen gene to chromosome band 1q4, the same region as the human renin gene

1990 • 60 citations

Selective Linkage Disruption in Human-Chinese Hamster Cell Hybrids: Deletion Mapping of the leuS, hexB, emtB, and chr Genes on Human Chromosome 5

1982 • 60 citations

Human proto-oncogene c-mos maps to 8q11.

1985 • 60 citations

Gene for the human T cell differentiation antigen Leu-2/T8 is closely linked to the kappa light chain locus on chromosome 2.

1985 • 60 citations

Linkage analysis of the human HMG14 gene on chromosome 21 using a GT dinucleotide repeat as polymorphic marker

1990 • 60 citations

Chromosomal location of three spectrin genes: relationship to the inherited hemolytic anemias of mouse and man.

1988 • 60 citations

Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13.

1987 • 60 citations

Twenty-eight loci form a continuous linkage map of markers for human chromosome 1

1989 • 60 citations

Orientation and molecular map position of the complement genes in the mouse MHC.

1987 • 59 citations

Localization of the mouse gene for secreted phosphoprotein 1 (Spp-1) (2ar, osteopontin, bone sialoprotein 1, 44-kDa bone phosphoprotein, tumor-secreted phosphoprotein) to chromosome 5, closely linked to Ric (Rickettsia resistance)

1989 • 59 citations

Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome region.

1989 • 59 citations

Mapping of the MYC gene to band 8q24.12→q24.13 by R-banding and distal to fra(8)(q24.11), FRA8E, by fluorescence in situ hybridization

1991 • 59 citations

Refined linkage map of chromosome 7 in the region of the cystic fibrosis gene.

1988 • 59 citations

A genetic linkage map of 27 loci from PND to FY on the short arm of human chromosome I.

1988 • 59 citations

Genetics and ontogeny of alcohol dehydrogenase isozymes in the mouse: Evidence for a cis-acting regulator gene (Adt-1) controlling C2 isozyme expression in reproductive tissues and close linkage of Adh-3 and Adt-1 on chromsome 3

1979 • 59 citations

The yes-Related Cellular Gene lyn Encodes a Possible Tyrosine Kinase Similar to p56^lck

1987 • 59 citations

Report of the committee on the genetic constitution of chromosome 3

1988 • 58 citations

Murine hematopoietic cell surface antigen expression

1988 • 58 citations

Interferon-regulated influenza virus resistance gene Mx is localized on mouse chromosome 16

1986 • 58 citations

A novel human cytochrome P4S0 gene (P450IIB): chromosomal localization and evidence for alternative splicing

1988 • 58 citations

Chromosomal Assignment of the Endogenous Proto-Oncogene C- abl

1982 • 58 citations

Formation and drainage of aqueous humour in cats

1966 • 58 citations

A complex of serine protease genes expressed preferentially in cytotoxic T-lymphocytes is closely linked to the T-cell receptor α- and δ-chain genes on mouse chromosome 14

1990 • 58 citations

Synaptophysin: structure of the human gene and assignment to the X chromosome in man and mouse.

1990 • 58 citations

Mouse proacrosin gene: Nucleotide sequence, diploid expression, and chromosomal localization

1991 • 58 citations

Chromosomal localisation of a developmental gene in man: Direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13

1988 • 58 citations

Assignment of the lactotransferrin gene to human chromosome 3 and to mouse chromosome 9

1987 • 57 citations

Mapping of haploid expressed genes: Genes for both mouse protamines are located on chromosome 16

1986 • 57 citations

Chromosome assignments of four mouse cellular homologs of sarcoma and leukemia virus oncogenes.

1984 • 57 citations

Localization of human thyrotropin receptor gene to chromosome region 14q31 by in situ hybridization

1990 • 57 citations

Genetics and Polymorphism of the Mouse Prion Gene Complex: Control of Scrapie Incubation Time

1988 • 57 citations

The gene for human leukemia inhibitory factor (LIF) maps to 22q12.

1989 • 57 citations

Argininosuccinic aciduria: assignment of the argininosuccinate lyase gene to the pter to q22 region of human chromosome 7 by bioautography.

1978 • 57 citations

Detailed ordering of markers localizing to the Xq26-Xqter region of the human X chromosome by the use of an interspecific Mus spretus mouse cross.

1987 • 57 citations

The Alzheimer amyloid precursor protein maps to human chromosome 21 bands q21.105–q21.05

1989 • 57 citations

TheIL-4 andIL-5 genes are closely linked and are part of a cytokine gene cluster on mouse chromosome 11

1989 • 57 citations

Chromosome assignment, biochemical and immunological studies on a human aldehyde dehydrogenase, ALDH3

1985 • 57 citations

Human apolipoprotein A-I and C-III genes reside in the p11 → q13 region of chromosome 11

1984 • 56 citations

Genomic organization and complete sequence of the human gene encoding the β-subunit of the cGMP phosphodiesterase and its localisation to 4p16.3

1991 • 56 citations

A reordering of human chromosome 19 long-arm DNA markers and identification of markers flanking the myotonic dystrophy locus

1989 • 56 citations

Gene for lymphoid enhancer-binding factor 1 (LEF1) mapped to human chromosome 4 (q23–q25) and mouse chromosome 3 near Egf

1991 • 56 citations

Glyoxalase I Polymorphism in the Mouse: A New Genetic Marker Linked to H-2

1977 • 56 citations

Murine epidermal growth factor: heterogeneity on high resolution ion-exchange chromatography.

1983 • 56 citations

A genetic linkage map of chromosome 17

1990 • 56 citations

<i>NRAS </i>transforming gene maps to region p11→p13 on chromosome 1 by in situ hybridization

1984 • 55 citations

Mapping of aminoacylase-1 and beta-galactosidase-A to homologous regions of human chromosome 3 and mouse chromosome 9 suggests location of additional genes.

1982 • 55 citations

Variations among Sublines of Inbred AKR Mice

1973 • 55 citations

Regional chromosomal assignment of the human glucocorticoid receptor gene to 5q31

1989 • 55 citations

Chromosomal location of the genes encoding complement components C5 and factor H in the mouse.

1986 • 55 citations

Genetic analysis of NF1: Identification of close flanking markers on chromosome 17

1987 • 55 citations

Specific detection of neuronal cell bodies: in situ hybridization with a biotin-labeled neurofilament cDNA probe.

1986 • 55 citations

Chromosomal localization of the human apoprotein ci gene and of a polymorphic apoprotein AII gene

1984 • 55 citations

Comparison between Mice Chimaeric and Heterozygous for the X-linked Gene tabby

1973 • 55 citations

Genetics and biology of human ovarian teratomas. II. Molecular analysis of origin of nondisjunction and gene-centromere mapping of chromosome I markers.

1990 • 54 citations

Structure and chromosomal localization of the human thrombospondin gene

1990 • 54 citations

Chromosomal Location of Human T-Cell Receptor Gene T _i β

1984 • 54 citations

Genetic Control of Mitochondrial Enzymes in Human–Mouse Somatic Cell Hybrids

1973 • 54 citations

The human T-cell receptor α-chain gene maps to chromosome 14

1985 • 54 citations

Preferential but Nonexclusive Expression of Macromolecular Antigens on B‐Lineage Cells

1983 • 54 citations

Characterization of the cDNA coding for mouse plasminogen and localization of the gene to mouse chromosome 17

1990 • 54 citations

Evidence for placing the Neu-1 locus within the mouse H-2 complex.

1982 • 54 citations

Genetic Polymorphism of Murine C3 Controlled by a Single Co-Dominant Locus on Chromosome 17

1978 • 54 citations

The DNF15S2 locus at 3p21 is transcribed in normal lung and small cell lung cancer

1989 • 54 citations

Isolation of duplicated human c-src genes located on chromosomes 1 and 20.

1985 • 54 citations

Genetic analysis of the 15;17 chromosome translocation associated with acute promyelocytic leukemia.

1983 • 53 citations

Multiple restriction fragment length polymorphisms at the insulin receptor locus: a highly informative marker for linkage analysis.

1986 • 53 citations

Frequent recombination is observed in the distal end of the long arm of chromosome 14

1989 • 53 citations

Toward a physical map of the Xq28 region in man: Linking color vision, G6PD, and coagulation factor VIII genes to an X-Y homology region

1989 • 53 citations

Chromosomal location of Evi-1, a common site of ecotropic viral integration in AKXD murine myeloid tumors.

1988 • 53 citations

Comparison of the chromosomal localization of murine and human glucocerebrosidase genes and of the deduced amino acid sequences.

1989 • 53 citations

Localization of the region homologous to the Duchenne muscular dystrophy locus on the mouse X chromosome

1987 • 53 citations

A molecular genetic linkage map of mouse chromosome 9 with regional localizations for the Gsta, T3g, Ets-1 and Ldlr loci.

1989 • 53 citations

Polymorphism and linkage of glutathione reductase in Mus musculus

1975 • 52 citations

Regional localization of human gene loci on chromosome 9: studies of somatic cell hybrids containing human translocations.

1979 • 52 citations

Ribonucleotide reductase M2 subunit sequences mapped to four different chromosomal sites in humans and mice: Functional locus identified by its amplification in hydroxyurea-resistant cell lines

1987 • 52 citations

Genomic organization and chromosomal localization of the TAPA-1 gene.

1991 • 52 citations

A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19

1989 • 52 citations

Linkage of amelogenin (Amel) to the distal portion of the mouse X chromosome

1991 • 52 citations

Fim-1, Fim-2/c-fms, and Fim-3, three common integration sites of Friend murine leukemia virus in myeloblastic leukemias, map to mouse chromosomes 13, 18, and 3, respectively

1988 • 52 citations

The gene that encodes the human CD20 (B1) differentiation antigen is located on chromosome 11 near the t(11;14)(q13;q32) translocation site.

1989 • 52 citations

Murine T cell receptor beta chain is encoded on chromosome 6.

1984 • 51 citations

Three patients with structurally abnormal X chromosomes, each with Xq13 breakpoints and a history of idiopathic acquired sideroblastic anemia

1982 • 51 citations

Human c-fos oncogene mapped within chromosomal region 14q21----q31.

1984 • 51 citations

Evidence for the assignment of the loci AK₁, AK₃ and ACON_s to chromosome 9 in man

1976 • 51 citations

Genetic mapping of the Mx influenza virus resistance gene within the region of mouse chromosome 16 that is homologous to human chromosome 21

1988 • 51 citations

Localization of human SAA gene(s) to chromosome 11 and detection of DNA polymorphisms

1986 • 51 citations

Localization of murine X and autosomal sequences homologous to the human Y located testis-determining region.

1989 • 51 citations

Chromosomal assignment and trans regulation of the tyrosine aminotransferase structural gene in hepatoma hybrid cells.

1985 • 51 citations

The human C-reactive protein gene (CRP) and serum amyloid P component gene (APCS) are located on the proximal long arm of chromosome 1

1986 • 51 citations

Activation of multiple genes by provirus integration in the Mlvi-4 locus in T-cell lymphomas induced by Moloney murine leukemia virus

1990 • 50 citations

Preferential expression of cellular retinoic acid binding protein in a subpopulation of neural cells in the developing mouse embryo

1989 • 50 citations

The genes coding for the cardiac muscle actin, the skeletal muscle actin and the cytoplasmic beta-actin are located on three different mouse chromosomes.

1983 • 50 citations

Human apolipoprotein A-II: Nucleotide sequence of a cloned cDNA, and localization of its structural gene on human chromosome 1

1984 • 50 citations

Mapping of the oncogenes <i>Myc, Sis, </i>and <i>int-1</i> to the distal part of mouse chromosome 15

1987 • 50 citations

Distribution of genes for gap junction membrane channel proteins on human and mouse chromosomes

1991 • 50 citations

Rhabdomyosarcoma-associated locus and MYOD1 are syntenic but separate loci on the short arm of human chromosome 11.

1990 • 50 citations

Structure, Chromosome Location, and Expression of the Human γ-Actin Gene: Differential Evolution, Location, and Expression of the Cytoskeletal β- and γ-Actin Genes

1988 • 50 citations

Linkage analyses using biochemical variants in mice. II. Levulinate dehydratase and autosomal glucose 6-phosphate dehydrogenase

1969 • 50 citations

Localization of the cryptdin locus on mouse chromosome 8

1989 • 50 citations

A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11

1989 • 49 citations

The genetics of sex-linked anaemia in the mouse

1962 • 49 citations

A genetic map of mouse chromosome 12 composed of polymorphic DNA fragments.

1984 • 49 citations

New assignment of the adenosine deaminase gene locus to chromosome 20q13 X 11 by study of a patient with interstitial deletion 20q.

1987 • 49 citations

The family of mouse phosphoglycerate kinase genes and pseudogenes

1988 • 49 citations

Chromosomal localization of ZFX—A human gene that escapes X inactivation—and its murine homologs

1990 • 49 citations

REARRANGEMENT OF GENES LOCATED ON HOMOLOGOUS CHROMOSOMAL SEGMENTS IN MOUSE AND MAN: THE LOCATION OF GENES FOR ALPHA-AND BETA-INTERFERON, ALPHA-1 ACID GLYCOPROTEIN-1 AND -2, AND AMINOLEVULINATE DEHYDRATASE ON MOUSE CHROMOSOME 4

1986 • 49 citations

A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus.

1990 • 49 citations

The proopiocortin (adrenocorticotropin/?-lipotropin) gene is located on chromosome 2 in humans

1981 • 49 citations

Gene family of male-specific testosterone 16α-hydroxylase (C-P-45016α) in mice

1989 • 49 citations

Mapping of human chromosome 22 with a panel of somatic cell hybrids

1991 • 49 citations

Assignment of 12 loci to rat chromosome 5: Evidence that this chromosome is homologous to mouse chromosome 4 and to human chromosomes 9 and 1 (1p Arm)

1990 • 49 citations

Linkage of GLO with HLA and Bf. Effect of Population and Sex on Recombination Frequency*

1976 • 48 citations

Gene order, amplification, and rearrangement of chromosome band 11q23 in hematologic malignancies

1989 • 48 citations

Regional localization of the human genes for S-adenosylhomocysteine hydrolase (cen?q131) and adenosine deaminase (q131?qter) on chromosome 20

1984 • 48 citations

The polymorphic locus for glycogen storage disease VI (liver glycogen phosphorylase) maps to chromosome 14.

1987 • 48 citations

Localization of the human myelin basic protein gene <i>(MBP)</i> to region 18q22→qter by in situ hybridization

1985 • 48 citations

Chromosomal localization of human genes governing the interferon-induced antiviral state.

1975 • 48 citations

The localization of the human myeloperoxidase gene is in close proximity to the translocation breakpoint in acute promyelocytic leukemia.

1987 • 48 citations

Assignment of the genes for the alpha and beta subunits of thyrotropin to different mouse chromosomes.

1984 • 48 citations

The HOX-5 and surfeit gene clusters are linked in the proximal portion of mouse chromosome 2

1990 • 48 citations

Shiverer gene maps near the distal end of chromosome 18 in the house mouse

1985 • 48 citations

Genetics of beta-2 microglobulin in the mouse

1983 • 47 citations

Localization of the properdin structural locus to Xp11.23–Xp21.1

1989 • 47 citations

Regional localization of the human genes for aldehyde dehydrogenase-1 and aldehyde dehydrogenase-2

1988 • 47 citations

Location of the gene involving the Small eye mutation on mouse chromosome 2 suggests homology with human aniridia 2 (AN2)

1990 • 47 citations

Polymorphism of kidney pyruvate kinase in the mouse is determined by a gene, Pk-3, on chromosome 9

1981 • 47 citations

Sublocalization on chromosome 21 of human interferon-alpha receptor gene and the gene for an interferon-gamma response protein

1990 • 47 citations

Assignment of the DIA₁ locus to chromosome 22

1977 • 47 citations

Trisomy 8 in the bone marrow associated with high red cell glutathione reductase activity

1976 • 47 citations

Human tissue-type plasminogen activator gene located near chromosomal breakpoint in myeloproliferative disorder.

1986 • 47 citations

Brief report: Linkage between G6PD and fragile‐X syndrome

1983 • 46 citations

Human Glyceraldehyde-3-Phosphate Dehydrogenase in Man-Rodent Somatic Cell Hybrids

1976 • 46 citations

The gene encoding the human class II antigen-associated ? chain is located on chromosome 5

1984 • 46 citations

Proviral integration site Mis-1 in rat thymomas corresponds to the pvt-1 translocation breakpoint in murine plasmacytomas.

1986 • 46 citations

Mapping of the mouse fibronectin gene (Fn-1) to chromosome 1: Conservation of the Idh-1-Cryg-Fn-1 synteny group in mammals

1987 • 46 citations

A molecular genetic linkage map of mouse chromosome 13 anchored by the beige (bg) and satin (sa) loci

1990 • 46 citations

Human ?-aminolevulinate dehydratase: chromosomal localization to 9q34 by in situ hybridization

1987 • 46 citations

Chromosomal organization of the cytochrome P450-2C gene family in the mouse: a locus associated with constitutive aryl hydrocarbon hydroxylase.

1988 • 45 citations

Genomic organization and chromosomal assignment for a serine protease gene (CSPB) expressed by human cytotoxic lymphocytes

1989 • 45 citations

Localization of the muscle, liver, and brain glycogen phosphorylase genes on linkage maps of mouse chromosomes 19, 12, and 2, respectively

1989 • 45 citations

New alleles of C4-binding protein and factor H and further linkage data in the regulator of complement activation (RCA) gene cluster in man

1987 • 45 citations

Chromosomal mapping of a human phenol UDP‐glucuronosyltransferase, GNT1

1990 • 45 citations

Chromosome assignment of a human gene for argininosuccinate synthetase expression in Chinese hamster X human somatic cell hybrids

1977 • 45 citations

Polymorphic gene for human carbonic anhydrase II: a molecular disease marker located on chromosome 8.

1983 • 45 citations

Maps of mouse chromosome 17: First report

1991 • 45 citations

The polymorphic Fc? receptor II gene maps to human chromosome 1q

1989 • 44 citations

Mapping of the two mouse engrailed-like genes: Close linkage of En-1 to dominant hemimelia (Dh) on chromosome 1 and of En-2 to hemimelic extra-toes (Hx) on chromosome 5

1990 • 44 citations

A primary map of 24 loci on human chromosome 16

1990 • 44 citations

The mouse homolog of the human amyloid β protein (AD-AP) gene is located on the distal end of mouse chromosome 16: Further extension of the homology between human chromosome 21 and mouse chromosome 16

1987 • 44 citations

Localisation of the human N-ras oncogene to chromosome 1cen - p21 by in situ hybridisation.

1983 • 44 citations

A new oncogene, c-raf, is located on mouse chromosome 6

1984 • 44 citations

Linkage of the Steroid Sulfatase Gene to the Sex-Reversed Mutation in the Mouse

1987 • 44 citations

LINKAGE OF GENETIC DETERMINANTS FOR MOUSE β-GALACTOSIDASE ELECTROPHORESIS AND ACTIVITY

1977 • 43 citations

Localization of the cellular oncogenes <i>ABL, SIS,</i> and <i>FES </i>on human germ-line chromosomes

1984 • 43 citations

THE LOCUS ENCODING αA-CRYSTALLIN IS CLOSELY LINKED TO H-2K ON MOUSE CHROMOSOME 17

1985 • 43 citations

Regional localization of DNA probes on the short arm of chromosome 11 using aniridia-Wilms' tumor-associated deletions

1987 • 43 citations

Quantitative variations of the C3b/C4b receptor (CR1) in human erythrocytes are controlled by genes within the regulator of complement activation (RCA) gene cluster.

1986 • 43 citations

A glutaminase (Gls) gene maps to mouse chromosome 1, rat chromosome 9, and human chromosome 2*1

1989 • 43 citations

The congenital goiter mutation is linked to the thyroglobulin gene in the mouse.

1987 • 43 citations

Physical mapping of a family of interferon-activated genes, serum amyloid P-component, and α-spectrin on mouse chromosome 1

1989 • 43 citations

Reassignment of the human CSF1 gene to chromosome 1p13-p21

1991 • 43 citations

Linkage of TNF genes to the HLA-B locus

1987 • 43 citations

Localization of the genes for tumor necrosis factor and lymphotoxin between the HLA class I and III regions by field inversion gel electrophoresis

1988 • 43 citations

The gene encoding human vimentin is located on the short arm of chromosome 10.

1987 • 43 citations

Isolation of a human cytochrome P‐450 reductase cDNA clone and localization of the corresponding gene to chromosome 7q11.2

1989 • 43 citations

Localization of the thyroglobulin gene by in situ hybridization to human chromosomes

1985 • 42 citations

A new location for the human adenine phosphoribosyltransferase gene (<i>APRT</i>) distal to the haptoglobin (<i>HP</i>) and fra(16)(q23) (<i>FRA16D</i>) loci

1986 • 42 citations

The human desmin and vimentin genes are located on different chromosomes

1985 • 42 citations

Lymphocyte antigens: Ly-4, Ly-6, and Ly-7.

1977 • 42 citations

The structural gene for the M1 subunit of ribonucleotide reductase maps to chromosome 11, band p15, in human and to chromosome 7 in mouse

1988 • 42 citations

The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (region 16q22?q24) by somatic cell hybrid analysis and in situ hybridization

1986 • 42 citations

cDNA and genomic cloning of HRC, a human sarcoplasmic reticulum protein, and localization of the gene to human chromosome 19 and mouse chromosome 7

1991 • 42 citations

Isolation, characterization, and chromosomal mapping of mouse P450 17α-hydroxylase/C17–20 lyase

1991 • 42 citations

Location of a gene controlling electrophoretic variation in mouse γ-crystallins

1982 • 42 citations

The Putative Oncogene Pim-1 in the Mouse: Its Linkage and Variation Among t Haplotypes

1987 • 42 citations

Localization of human U1 small nuclear RNA genes to band p36.3 of chromosome 1 by in situ hybridization

1984 • 42 citations

Genetic variation in mouse salivary amylase rate of synthesis

1979 • 42 citations

Segregation of ABO, AK₁ and ACON_S in families with abnormalities of chromosome 9

1978 • 42 citations

A genetic map of mouse chromosome 1 near the Lsh-Ity-Bcg disease resistance locus

1990 • 42 citations

An interspecific backcross linkage map of the proximal half of mouse chromosome 14

1990 • 42 citations

The human galactosyltransferase gene is on chromosome 9 at band p13

1986 • 41 citations

The gene for human carbonic anhydrase II (CA2) is located at chromosome 8q22

1987 • 41 citations

Chromosomal localization of the human interleukin 1α (IL-1α) gene

1988 • 41 citations

Linkage of tyrosine hydroxylase to four other markers on the short arm of chromosome 11

1986 • 41 citations

? 2-Microglobulin locus on human chromosome 15

1976 • 41 citations

Location of the Gene for Theta Antigen in the Mouse

1972 • 41 citations

Sequences homologous to glutamic acid decarboxylase cDNA are present on mouse chromosomes 2 and 10

1990 • 41 citations

Linkage analysis with RFLPs in families with androgen resistance syndromes: evidence for close linkage between the androgen receptor locus and the DXS1 segment

1987 • 41 citations

Involvement of a gene on chromosome 9 in human fibroblast Interferon production

1979 • 41 citations

Δ‐Aminolevulinatedehydrase: synteny with ABO‐AK1‐ORM (and assignment to chromosome 9)

1983 • 41 citations

A human T-cell antigen receptor beta chain gene maps to chromosome 7.

1984 • 40 citations

Localization of a mouse heat shock Hsp70 gene within the H-2 complex

1990 • 40 citations

Localization of the villin gene on human chromosome 2q35-q36 and on mouse chromosome 1

1988 • 40 citations

Construction of a genetic map of human chromosome 17 by use of chromosome-mediated gene transfer.

1988 • 40 citations

Mapping the human CAS2 gene, the homologue of the mouse brown (b) locus, to human Chromosome 9p22-pter

1991 • 40 citations

Complementation mapping in microcell hybrids: Localization ofFpgs andAk-1 onmus musculus chromosome 2

1983 • 40 citations

Chromosomal assignment of genes encoding the α, β, and γ subunits of human complement protein C8: Identification of a close physical linkage between the α and the β loci

1989 • 40 citations

Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X site

1985 • 40 citations

Chromosomal localization of the human genes for lipocortin I and lipocortin II.

1988 • 40 citations

Chromosomal mapping of brain-derived neurotrophic factor and neurotrophin-3 genes in man and mouse

1991 • 40 citations

Chromosomal localization of the human homeo box-containing genes, EN1 and EN2

1989 • 40 citations

Molecular detection of chromosomal translocations that disrupt the putative retinoblastoma susceptibility locus.

1989 • 39 citations

A long-range restriction map of the interleukin-4 and interleukin-5 linkage group on chromosome 5

1990 • 39 citations

The human apolipoprotein A-II gene is located on chromosome 1

1984 • 39 citations

Chromosomal assignment of the murine gene encoding the transformation-related protein p53.

1984 • 39 citations

Chromosomal location of the human tumor necrosis factor receptor genes

1991 • 39 citations

Assignment of the erythropoietin receptor (EPOR) gene to mouse chromosome 9 and human chromosome 19

1990 • 39 citations

An interspecific backcross linkage map of mouse chromosome 8

1990 • 39 citations

Proximity of the CTLA-1 serine esterase and Tcr ? loci in mouse and man

1988 • 39 citations

Selective linkage disruption in human-Chinese hamster cell hybrids: deletion mapping of the leuS, hexB, emtB, and chr genes on human chromosome 5.

1982 • 39 citations

GENETICS OF ALDEHYDE DEHYDROGENASE ISOZYMES IN THE MOUSE: EVIDENCE FOR MULTIPLE LOCI AND LOCALIZATION OF Ahd-2 ON CHROMOSOME 19

1981 • 39 citations

The gene CYP3 encoding P450pcn1 (nifedipine oxidase) is tightly linked to the gene COL1A2 encoding collagen type 1 alpha on 7q21-q22.1.

1988 • 39 citations

Inactivation of the Rps4 gene on the mouse X chromosome

1991 • 39 citations

Cd28 and Ctla-4, two related members of the Ig supergene family, are tightly linked on proximal mouse chromosome 1

1991 • 39 citations

Cloning, Sequencing, and Evolutionary Analysis of the Mouse Erythropoietin Gene

1986 • 39 citations

Mouse lipocortin I gene structure and chromosomal assignment: Gene duplication and the origins of a gene family

1991 • 39 citations

Localization of cytochrome P1-450 and P3-450 genes to mouse chromosome 9.

1984 • 39 citations

Mouse alcohol dehydrogenase isozymes: Products of closely localized duplicated genes exhibiting divergent kinetic properties

1981 • 38 citations

The murine retinoblastoma homolog maps to chromosome 14 near Es-10

1989 • 38 citations

The gene encoding the Ia antigen-associated invariant chain (Ii) is not linked to the H–2 complex

1983 • 38 citations

Irradiation-reduced human chromosome 21 hybrids

1988 • 38 citations

Chromosomal localization and structure of the human P1 protamine gene

1989 • 38 citations

The human myelin-basic-protein gene: chromosomal localization and RFLP analysis.

1987 • 38 citations

Regional localization of α-galactosidase (<i>GLA</i>) to Xpter→q22, hexosaminidase B (<i>HEXB</i>) to 5q13→qter, and arylsulfatase B (<i>ARSB</i>) to 5pter→q13

1984 • 38 citations

The human neurofilament gene (NEFL) is located on the short arm of chromosome 8

1987 • 38 citations

Chromosomal mapping of the mouse IL-4 and human IL-5 genes

1989 • 38 citations

Assignment of the genes for human peptidase A to chromosome 18 and cytoplasmic glutamic oxaloacetate transaminase to chromosome 10 using somatic-cell hybrids

1973 • 38 citations

Structure, Chromosome Location, and Expression of the Mouse Zinc Finger Gene Krox-20: Multiple Gene Products and Coregulation with the Proto-Oncogene c-fos

1989 • 38 citations

Mapping of mouse gamma crystallin genes on chromosome 1

1988 • 38 citations

The syntenic relationship of proximal mouse chromosome 7 and the myotonic dystrophy gene region on human chromosome 19q

1990 • 38 citations

Comparative analysis of mouse-human hybrids with rearranged chromosomes 1 by in situ hybridization and southern blotting: High-resolution mapping of NRAS, NGFB, and AMY on human chromosome 1

1984 • 38 citations

Evidence for Linkage between Human Loci for 6-Phosphogluconate Dehydrogenase and Phosphoglucomutase1 in Man–Chinese Hamster Somatic Cell Hybrids

1972 • 38 citations

A Group of Type I Keratin Genes on Human Chromosome 17: Characterization and Expression

1988 • 38 citations

Assignment of the human gene for galactose-1-phosphate uridyltransferase to chromosome 9: studies with Chinese hamster-human somatic cell hybrids.

1977 • 38 citations

Mapping of multiple subunits of the neuronal nicotinic acetylcholine receptor to chromosome 15 in man and chromosome 9 in mouse

1991 • 37 citations

The gene for the RNA component of the mitochondrial RNA-processing endoribonuclease is located on human chromosome 9p and on mouse chromosome 4

1990 • 37 citations

Regional linkage analysis of the dioxin-inducible P-450 gene family on mouse chromosome 9

1985 • 37 citations

Mapping of the thrombospondin gene to human chromosome 15 and mouse chromosome 2 by in situ hybridization

1990 • 37 citations

Three brain sodium channel α-subunit genes are clustered on the proximal segment of mouse chromosome 2

1991 • 37 citations

Chromosomal localization of zinc finger protein genes in man and mouse

1989 • 37 citations

Assignment of the human homologue of Pim-1, a mouse gene implicated in leukemogenesis, to the pter-q12 region of chromosome 6

1986 • 37 citations

Receptors for Fc epsilon and Fc gamma are linked on mouse chromosome 1.

1988 • 37 citations

Genetics and evolution of the acute phase proteins in mice

1985 • 37 citations

Assignment of the Ly-6--Ril-1--Sis--H-30--Pol-5/Xmmv-72--Ins-3--Krt-1--Int-1--Gdc-1 region to mouse chromosome 15

1987 • 37 citations

ELECTROPHORETIC VARIATION FOR X CHROMOSOME-LINKED HYPOXANTHINE PHOSPHORIBOSYL TRANSFERASE (HPRT) IN WILD-DERIVED MICE

1983 • 37 citations

Linkage of HL-A and GBG

1974 • 37 citations

Localization of the ornithine aminotransferase gene and related sequences on two human chromosomes

1987 • 37 citations

Genetic mapping ofPim-1 putative oncogene to mouse chromosome 17

1986 • 36 citations

Chromosomal localization of the human gene for brain Ca2+calmodulin-dependent protein kinase type IV

1989 • 36 citations

Ribosomal protein gene sequences map to human chromosomes 5, 8, and 17

1986 • 36 citations

Mouse serum amyloid P-component (SAP) levels controlled by a locus on chromosome 1

1985 • 36 citations

Molecular Cloning and Expression of the Type 1 and Type 2 Murine Receptors for Tumor Necrosis Factor

1991 • 36 citations

Development of a hemolytic assay for mouse C2 and determination of its genetic control.

1980 • 36 citations

The gene for the type II (p75) tumor necrosis factor receptor (TNF-RII) is localized on band 1p36.2?p36.3

1991 • 36 citations

Regional localization of the human glutaminase (GLS) and interleukin-9 (IL9) genes by in situ hybridization

1991 • 36 citations

Chromosome 1 localization of the human alpha-L-fucosidase structural gene with a homologous site on chromosome 2

1986 • 36 citations

Genetic Mapping of the Mouse Proto-Oncogene c- sis to Chromosome 15

1983 • 36 citations

Further linkage data on cystic fibrosis: the Utah Study.

1986 • 36 citations

Assignment of the gene coding for human FcRII (CD32) to bands g23g24 on chromosome 1

1988 • 36 citations

THE GENETICS OF α-HYDROXYACID OXIDASE AND ALCOHOL DEHYDROGENASE IN THE MOUSE: EVIDENCE FOR MULTIPLE GENE LOCI AND LINKAGE BETWEEN Hao-2 AND Adh-3

1977 • 36 citations

Localization of the human glucagon gene (<i>GCG</i>) to chromosome segment 2q36→37

1984 • 36 citations

Myc-1 is centromeric to the linkage group Ly-6--Sis--Gdc-1 on mouse chromosome 15

1988 • 36 citations

The human PGM-2 and its chromosomal localization in man-mouse hybrids

1977 • 36 citations

The genetics and developmental regulation of L-glycerol 3-phosphate dehydrogenase

1975 • 36 citations

Mapping of PRM 1 to Human Chromosome 16 and Tight Linkage of Prm-1 and Prm-2 on Mouse Chromosome 16

1989 • 35 citations

Molecular and genetic mapping of the mouse mdx locus

1988 • 35 citations

Mapping anti-müllerian hormone (amh) and related sequences in the mouse: Identification of a new region of homology between MMU10 and HSA19p

1991 • 35 citations

The interspecific and evolutionary relationships of Triticum ovatum

1988 • 35 citations

Localization of the gene encoding human Factor V to chromosome 1q21–25

1988 • 35 citations

Murine complement receptor gene family. II. Identification and characterization of the murine homolog (Cr2) to human CR2 and its molecular linkage to Crry.

1989 • 35 citations

Localization of the gene encoding human erythroid-potentiating activity to chromosome region Xp11.1----Xp11.4.

1986 • 35 citations

Human homologs of two testes-expressed loci on mouse chromosome 17 map to opposite arms of chromosome 6

1989 • 35 citations

The ETS genes on chromosome 21 are distal to the breakpoint of the acute myelogenous leukemia translocation (8;21)

1988 • 35 citations

Genetic variation between mice in their metabolism of coumarin and its derivatives

1978 • 35 citations

The human chromosome 19 linkage group FUT1 (H), FUT2 (SE), LE, LU, PEPD, C3, APOC2, D19S7 and D19S9

1991 • 35 citations

Mouse immune interferon (IFN-?) gene is on chromosome 10

1984 • 35 citations

The loci for parathyroid hormone and ?-globin are closely linked and map to chromosome 15 in cattle

1988 • 35 citations

Mapping of human lactate dehydrogenase-A, -B, and -C genes and their related sequences: the gene for LDHC is located with that for LDHA on chromosome 11

1988 • 35 citations

The gene for the α-subunit of retinal rod transducin is on mouse chromosome 9

1989 • 35 citations

Chromosomal locations of genes encoding 2′,3′ cyclic nucleotide 3′‐phosphodiesterase and glial fibrillary acidic protein in the mouse

1988 • 35 citations

Cloning of the human genomic amiloride-sensitive Na+H+ antiporter gene, identification of genetic polymorphisms, and localization on the genetic map of chromosome 1p

1990 • 35 citations

The Map Position of the rds Gene on the 17th Chromosome of the Mouse

1979 • 35 citations

Assignment of human phosphoribosylglycinamide synthetase locus to region 21q221

1984 • 35 citations

Mapping the human amylase gene cluster on the proximal short arm of chromosome 1 using a highly informative (CA)n repeat

1990 • 35 citations

His-1 and His-2: identification and chromosomal mapping of two commonly rearranged sites of viral integration in a myeloid leukemia.

1991 • 35 citations

Amplified DNA in Y1 mouse adrenal tumor cells: isolation of cDNAs complementary to an amplified c-Ki-rasgene and localization of homologous sequences to mouse chromosome 6

1984 • 34 citations

Polymorphisms at the estrogen receptor (ESR) locus and linkage relationships on chromosome 6q

1989 • 34 citations

Genetic mapping of the mouse interleukin 3 gene to chromosome 11.

1987 • 34 citations

Localization of mouse Pgk‐2 gene at the D end of the H‐2 complex

1978 • 34 citations

Role of human chromosome 11 in determining surface antigenic phenotype of normal and malignant cells. Somatic cell genetic analysis of eight antigens, including putative human Thy-1.

1985 • 34 citations

Regional mapping of ADA and ITP on human chromosome 20: cytogenetic and somatic cell studies in an X/20 translocation

1980 • 34 citations

Cellular homologs of the avian erythroblastosis virus erb-A and erb-B genes are syntenic in mouse but asyntenic in man.

1984 • 34 citations

The structural gene for lecithin:cholesterol acyl transferase (LCAT) maps to 16q22

1987 • 34 citations

Genetic polymorphism of microsomal epoxide hydrolase activity in the mouse.

1980 • 34 citations

Cloning and comparative mapping of a human class III (χ) alcohol dehydrogenase cDNA

1989 • 34 citations

Chromosome localization and cDNA sequence of murine and human genes forras p21 GTPase activating protein (GAP)

1989 • 34 citations

Regional localization of the gene for thyroid peroxidase to human chromosome 2pter→p12

1988 • 34 citations

GLUTAMATE OXALOACETATE TRANSAMINASE (GOT) GENETICS IN THE MOUSE: POLYMORPHISM OF GOT-1

1972 • 34 citations

Localization of the human haptoglobin genes distal to the fragile site at 16q22 using in situ hybridization

1986 • 33 citations

c-Ha-ras-1 oncogene lies between beta-globin and insulin loci on human chromosome 11p.

1984 • 33 citations

Human pepsinogen C (progastricsin) polymorphism: Evidence for a single locus located at 6p21.1-pter

1989 • 33 citations

Multilocus linkage analysis with the human argininosuccinate synthetase gene

1989 • 33 citations

The N-rasoncogene assigned to the short arm of human chromosome 1

1983 • 33 citations

EVIDENCE FOR X-LINKAGE OF STEROID SULFATASE IN THE MOUSE: STEROID SULFATASE LEVELS IN OOCYTES OF XX AND XO MICE

1983 • 33 citations

Regional assignment of human amylase (AMY) to p22 ? p21 of chromosome 1

1984 • 33 citations

The human amiloride-sensitive Na<sup>+</sup>/H<sup>+</sup> antiporter: localization to chromosome 1 by in situ hybridization

1988 • 33 citations

The gene for the muscle-specific enolase is on the short arm of human chromosome 17

1990 • 33 citations

The mouseCD3-?, -?, and -? genes reside within 50 kilobases on chromosome 9, whereasCD3-? maps to chromosome 1, band H

1989 • 33 citations

Localization of the Murine Leukemia Inhibitory Factor Gene Near the Centromere on Chromosome 11

1990 • 33 citations

Regional assignment of human genes <i>TP</i><i>I</i><sub>1</sub>, <i>GAPD</i><i>H</i>, <i>LDH</i><sub>B</sub>, <i>SHMT</i>, and <i>PEPB</i> on chromosome 12

1979 • 33 citations

Human laminin a chain (LAMA) gene: Chromosomal mapping to locus 18p11.3

1989 • 33 citations

Mapping and conservation of the group-specific component gene in mouse

1990 • 33 citations

Mapping studies and expression of genes located on human chromosome 11, band q23

1988 • 33 citations

Prp (proline-rich protein) genes linked to markers Es-12 (esterase-12), Ea-10 (erythrocyte alloantigen), and loci on distal mouse chromosome 6

1989 • 33 citations

The gene for the ubiquitous octamer-binding protein Oct-1 is on human chromosome 1, region cen-q32, and near Ly-22 and Ltw-4 on mouse chromosome 1

1990 • 33 citations

Isolation, characterization and chromosomal mapping of the mouse tyrosine aminotransferase gene

1985 • 32 citations

Comparison of the physical and recombination maps of the mous X chromosome

1989 • 32 citations

Assignment ofLIPA, associated with human acid lipase deficiency, to human chromosome 10 and comparative assignment to mouse chromosome 19

1981 • 32 citations

The murine <i>Hox-2</i> cluster of homeo box containing genes maps distal on chromosome 11 near the tail-short (<i>Ts</i>) locus

1986 • 32 citations

Assignment of the structural genes for the ? subunit of hexosaminidase A, mannosephosphate isomerase, and pyruvate kinase to the region q22-qter of human chromosome 15

1977 • 32 citations

Chromosomal mapping of murine c-fes and c-src genes.

1984 • 32 citations

The human calbindin D28k (CALB1) and calretinin (CALB2) genes are located at 8q21.3→q22.1 and 16q22→q23, respectively, suggesting a common duplication with the carbonic anhydrase isozyme loci

1991 • 32 citations

Genetics of ocular NAD+-dependent alcohol dehydrogenase and aldehyde dehydrogenase in the mouse: Evidence for genetic identity with stomach isozymes and localization ofAhd-4 on chromosome 11 near trembler

1988 • 32 citations

Refined sublocalization of the human gene encoding the β subunit of the S100 protein (S100B) and confirmation of a subtle t(9;21) translocation using in situ hybridization

1989 • 32 citations

Mapping of the human type II collagen gene (COL2A1) proximal to fra(12)(q13.1) by nonisotopic in situ hybridization

1990 • 32 citations

Synteny of the genes for thymidine kinase and galactokinase in the mouse and their assignment to mouse chromosome 11

1977 • 32 citations

A mouse chromosome 17 gene encodes a testes-specific transcript with unusual properties

1989 • 32 citations

Human and mouse cellularmyc protooncogenes reside on chromosomes involved in numerical and structural aberrations in cancer 1

1983 • 32 citations

Chromosomal protein HMG-14 gene maps to the Down syndrome region of human chromosome 21 and is overexpressed in mouse trisomy 16.

1990 • 32 citations

Localization of a human brain sodium channel gene (SCN2A) to chromosome 2

1989 • 32 citations

Genetic linkage map of 46 DNA markers on human chromosome 16.

1990 • 32 citations

Human differentiation-stimulating factor (leukemia inhibitory factor, human interleukin DA) gene maps distal to the Ewing sarcoma breakpoint on 22q

1989 • 32 citations

Localization of the multidrug resistance-associated 170 kDa P-glycoprotein gene to mouse chromosome 5 and to homogeneously staining regions in multidrug-resistant mouse cells by in situ hybridization

1987 • 32 citations

Human aminoacylase-1: Cloning, regional assignment to distal chromosome 3p21.1, and identification of a cross-hybridizing sequence on chromosome 18

1990 • 32 citations

The FGF-related oncogene, K-FGF, maps to human chromosome region 11q13, possibly near int-2.

1988 • 32 citations

The Structural Genes Encoding P450_sccand P450_aromAre Closely Linked on Mouse Chromosome 9*

1989 • 32 citations

A human homolog of the mouse CD8 molecule, Lyt-3: genomic sequence and expression

1987 • 32 citations

Human ?-glucuronidase: Assignment of the structural gene to chromosome 7 using somatic cell hybrids

1977 • 31 citations

Localization of the human angiogenin gene to chromosome band 14q11, proximal to the T cell receptor alpha/delta locus.

1990 • 31 citations

The human calbindin 27-kDa gene: Structural organization of the 5′ and 3′ regions, chromosomal assignment, and restriction fragment length polymorphism

1989 • 31 citations

Mouse mitochondrial superoxide dismutase locus is on chromosome 17

1981 • 31 citations

The gene encoding the hydrophobic surfactant protein SP-C is located on 8p and identifies an EcoRI RFLP.

1988 • 31 citations

Long-range restriction site mapping of a syntenic segment conserved between human chromosome 1 and mouse chromosome 3

1990 • 31 citations

Human embryonic/atrial myosin alkali light chain gene: Characterization, sequence, and chromosomal location

1990 • 31 citations

Chromosomal mapping of the structural gene coding for the mouse cell adhesion molecule uvomorulin.

1988 • 31 citations

Chromosomal localization of the three members of the jun proto-oncogene family in mouse and man.

1990 • 31 citations

Genetic linkage between a locus for 6-PGD and the Rh locus: evaluation of possible heterogeneity in the recombination fraction between sexes and among families.

1971 • 31 citations

Characterization of a Family of Gamma-Ray-Induced CHO Mutants Demonstrates that the ldlA Locus Is Diploid And Encodes the Low-Density Lipoprotein Receptor

1986 • 31 citations

Chromosomal localization of ceruoplasmin and transferrin genes in laboratory rats, mice and in man by hybridization with specific DNA probes

1987 • 31 citations

Chromosomal localization of the Moloney sarcoma virus mouse cellular (c-mos) sequence

1982 • 31 citations

Assignment of NADH-cytochrome b5 reductase (DIA1 locus) to human chromosome 22

1978 • 31 citations

Mapping parathyroid hormone, ?-globin, insulin, and LDH-A genes within the human chromosome 11 short arm by spot blotting sorted chromosomes

1985 • 31 citations

Chromosomal localization and racial distribution of the polymorphic human dihydrofolate reductase pseudogene (DHFRP1).

1988 • 31 citations

Locus determining the human sperm‐specific lactate dehydrogenase, LDHC, is syntenic with LDHC

1987 • 31 citations

Human renin gene is on chromosome 1

1984 • 31 citations

Evidence for distinguishable transcripts of the putative testis determining gene (ZFY) and mapping of homologous cDNA sequences to chromosomes X,Y and 9

1989 • 31 citations

Regional assignment of the <i>ADA </i>locus on 20q13.2→qter by gene dosage studies

1980 • 30 citations

CONSERVED LINKAGE WITHIN A 4-cM REGION OF MOUSE CHROMOSOME 9 AND HUMAN CHROMOSOME 11

1984 • 30 citations

Mapping polypeptide hormone genes in the mouse: somatostatin, glucagon, calcitonin, and parathyroid hormone

1987 • 30 citations

The 1987 Catalog of Mapped Genes and Report of the Nomenclature Committee (Part 1 of 4)

1987 • 30 citations

Human apoB-100 gene resides in the p23 → pter region of chromosome 2

1985 • 30 citations

Chromosomal assignment of the alcohol dehydrogenase cluster locus to human chromosome 4q21–23 by in situ hybridization

1989 • 30 citations

Three-point linkage analysis employing C3 and 19cen markers assigns the myotonic dystrophy gene to 19q

1987 • 30 citations

DNA sequences of chromosome 21-specific YAC detect the t(8;21) breakpoint of acute myelogenous leukemia

1991 • 30 citations

Localization of the murine macrophage colony-stimulating factor gene to chromosome 3 using interspecific backcross analysis

1989 • 30 citations

Molecular cloning and genetic mapping of the t complex responder candidate gene family.

1990 • 30 citations

Relationship of the genes for Chediak-Higashi syndrome (beige) and the T-cell receptor γ chain in mouse and man

1987 • 30 citations

Linkage of genes for laminin B1 and B2 subunits on chromosome 1 in mouse

1985 • 30 citations

Gene for human CD59 (likely Ly-6 homologue) is located on the short arm of chromosome 11

1989 • 30 citations

Relationship of the human protooncogene CBL2 on 11q23 to the t(4;11), t(11;22), and t(11;14) breakpoints

1991 • 30 citations

Polymorphism of DNA sequence in the human pro alpha 2(I) collagen gene.

1985 • 30 citations

A Sequence Homologous to Rous Sarcoma Virus v-src is on Human Chromosome 20

1983 • 30 citations

Recombination between kappa chain genetic markers and the Lyt-3 locus

1983 • 30 citations

Assignment of the gene for adenosine kinase to chromosome 14 in <i>Mus musculus</i> by somatic cell hybridization

1978 • 30 citations

Identification of two murine loci homologous to the v-cbl oncogene

1989 • 30 citations

Mouse Alloantigen System Ly-m22 Predominantly Expressed on T Lymphocytes and Controlled by a Gene Linked to M1s Region on Chromosome 1

1983 • 30 citations

Mouse Interferon Alpha Beta Genes Are Linked at the Centromere Proximal Region of Chromosome 4

1985 • 30 citations

An endogenous mouse mammary tumor virus genome common in inbred mouse strains is located on chromosome 6