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

Production of monoclonal antibodies to group A erythrocytes, HLA and other human cell surface antigens-new tools for genetic analysis

1978 • 1,954 citations

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

1983 • 1,952 citations

Rapid and efficient cosmid cloning

1981 • 1,897 citations

Disruption of the proto-oncogene int-2 in mouse embryo-derived stem cells: a general strategy for targeting mutations to non-selectable genes

1988 • 1,690 citations

Actions of Radiations on Living Cells

1955 • 1,242 citations

Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries

1988 • 1,171 citations

A genetic linkage map of the human genome

1987 • 913 citations

Isolation of a transforming sequence from a human bladder carcinoma cell line

1982 • 776 citations

The radiobiology of cultured mammalian cells

1967 • 687 citations

The "beta-like-globin" gene domain in human erythroid cells.

1985 • 634 citations

SEGMENTAL ANEUPLOIDY AND THE GENETIC GROSS STRUCTURE OF THE DROSOPHILA GENOME

1972 • 609 citations

Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism

1985 • 555 citations

FINE STRUCTURE OF A GENETIC REGION IN BACTERIOPHAGE

1955 • 524 citations

Specific chromosomal translocations and the genesis of B-cell-derived tumors in mice and men

1983 • 517 citations

Simple and rapid fluorimetric method for DNA microassay

1977 • 491 citations

A closely linked genetic marker for cystic fibrosis

1985 • 463 citations

Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion.

1985 • 455 citations

Characterization of a monoclonal antibody (4F2) that binds to human monocytes and to a subset of activated lymphocytes.

1981 • 453 citations

Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

1989 • 448 citations

New chromosomal translocations correlate with specific immunophenotypes of childhood acute lymphoblastic leukemia

1984 • 365 citations

A deletion map of the human Y chromosome based on DNA hybridization.

1986 • 337 citations

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

1982 • 334 citations

Cloning and sequence analysis of cDNA for human cathepsin D.

1985 • 318 citations

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.

1989 • 306 citations

Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature

1986 • 300 citations

Report of the committee on comparative mapping

1979 • 293 citations

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

1981 • 285 citations

Genetic Analysis with Human—Mouse Somatic Cell Hybrids

1969 • 273 citations

Abnormality of chromosome 11 in patients withfeatures of Beckwith-Wiedemann syndrome

1983 • 236 citations

Cloning specific segments of the mammalian genome: bacteriophage lambda containing mouse globin and surrounding gene sequences.

1977 • 229 citations

Isolation and localization of DNA segments from specific human chromosomes

1980 • 220 citations

Isolation of the human insulin-like growth factor genes: insulin-like growth factor II and insulin genes are contiguous.

1985 • 212 citations

Nucleotide sequence of the human parathyroid hormone gene.

1983 • 206 citations

Apolipoprotein A-I Gene Polymorphism Associated with Premature Coronary Artery Disease and Familial Hypoalphalipoproteinemia

1986 • 206 citations

Deletion in Chromosome 11p Associated with a Hepatitis B Integration Site in Hepatocellular Carcinoma

1985 • 199 citations

Actions of radiations on living cells. 2nd edition

1956 • 199 citations

Full-length cDNA for rabbit tryptophan hydroxylase: functional domains and evolution of aromatic amino acid hydroxylases.

1987 • 180 citations

A cloned sequence, p82H, of the alphoid repeated DNA family found at the centromeres of all human chromosomes

1985 • 162 citations

The gene, MIC4, which controls expression of the antigen defined by monoclonal antibody F10.44.2, is on human chromosome 11

1982 • 157 citations

A highly polymorphic locus very tightly linked to the Huntington's disease gene

1988 • 149 citations

A highly polymorphic locus in human DNA revealed by cosmid-derived probes.

1985 • 134 citations

DNA Sequence and Regional Assignment of the Human Follicle-Stimulating Hormone β-Subunit Gene to the Short Arm of Human Chromosome 11

1987 • 131 citations

Gene encoding the alpha chain of the T-cell receptor is moved immediately downstream of c-myc in a chromosomal 8;14 translocation in a cell line from a human T-cell leukemia.

1986 • 131 citations

A cluster of chromosome 11p13 translocations found via distinct D-D and D-D-J rearrangements of the human T cell receptor delta chain gene.

1988 • 127 citations

Assignment of Three Human Genes to Chrosomes (LDH-A to 11, TK to 17, and IDH to 20) and Evidence for Translocation between Human and Mouse Chrosomes in Somatic Cell Hybrids

1972 • 124 citations

Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome.

1985 • 122 citations

Genetics of Somatic Mammalian Cells: Lethal Antigens as Genetic Markers for Study of Human Linkage Groups

1971 • 121 citations

Genetics of somatic mammalian cells: genetic, immunologic, and biochemical analysis with Chinese hamster cell hybrids containing selected human chromosomes.

1976 • 120 citations

The β-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus

1986 • 118 citations

ANALYSIS OF THE ALBINO-LOCUS REGION OF THE MOUSE: IV. CHARACTERIZATION OF 34 DEFICIENCIES

1982 • 113 citations

Construction of Human Chromosome-specific DNA Libraries from Flow-sorted Chromosomes

1986 • 110 citations

Two regulatory domains flank the mouse H19 gene.

1988 • 110 citations

Gene transfer by means of cell fusion : I. statistical mapping of the human X-chromosome by analysis of radiation-induced gene segregation

1977 • 102 citations

A locus on chromosome 11p with multiple restriction site polymorphisms.

1984 • 99 citations

Breakpoints in the human T-cell antigen receptor α-chain locus in two T-cell leukaemia patients with chromosomal translocations

1985 • 93 citations

A systematic approach for detecting high-frequency restriction fragment length polymorphisms using large genomic probes.

1985 • 93 citations

Linkage map of the short arm of human chromosome 11: location of the genes for catalase, calcitonin, and insulin-like growth factor II.

1985 • 92 citations

Long range physical map of the Wilms' tumor-aniridia region on human chromosome 11

1988 • 91 citations

Cloning, characterization, expression, and chromosomal localization of a human ferritin heavy-chain gene.

1986 • 83 citations

Isolation of microcell hybrid clones containing retroviral vector insertions into specific human chromosomes.

1987 • 82 citations

Familial aniridia and translocation t(4;11)(q22;p13) without Wilms' tumor

1983 • 81 citations

Regional localization of the autosomal dominant polycystic kidney disease locus

1988 • 74 citations

Identification and regional localization of DNA markers on chromosome 7 for the cloning of the cystic fibrosis gene.

1988 • 73 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

Characterization of banding patterns of metaphase-prophase G-banded chromosomes and their use in gene mapping

1978 • 69 citations

Localization of the human tyrosine hydroxylase gene to 11p15: gene duplication and evolution of metabolic pathways

1986 • 69 citations

Localization of the beta-globin gene by chromosomal in situ hybridization.

1984 • 65 citations

TYPES AND FREQUENCIES OF HUMAN CHROMOSOME ABERRATIONS INDUCED BY X-RAYS

1961 • 64 citations

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

1988 • 62 citations

Two Anonymous DNA Segments Distinguish the Wilms' Tumor and Aniridia Loci

1988 • 59 citations

Genetic fine-structure mapping in human chromosome 11 by use of repetitive DNA sequences.

1982 • 57 citations

Chromosome mapping of genes on the short arm of human chromosome 11: parathyroid hormone gene is at 11p15 together with the genes for insulin, c-Harvey-<i>ras</i> 1, and β-hemoglobin

1985 • 55 citations

Familial isolated aniridia associated with a translocation involving chromosomes 11 and 22 [t(11;22)(p13;q12.2)]

1986 • 53 citations

A DELETION MAP OF cyc1 MUTANTS AND ITS CORRESPONDENCE TO MUTATIONALLY ALTERED ISO-1-CYTOCHROMES c OF YEAST

1975 • 53 citations

Selective Systems in Somatic Cell Genetics

1976 • 52 citations

DEFICIENCY

1917 • 52 citations

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

1986 • 51 citations

THE INTERACTION OF MAMMALIAN CELLS WITH ANTIBODIES. I

1961 • 48 citations

Genetics of cell-surface antigens: Regional mapping of three components of the human cell-surface antigen complex, Al, on chromosome 11

1977 • 48 citations

Regional mapping of the gene for human lysosomal acid phosphatase (ACP2) using a hybrid clone panel containing segments of human chromosome 11

1978 • 47 citations

Molecular Cell Genetics

1986 • 45 citations

The human calcitonin gene is located on the short ARM of chromosome 11

1984 • 42 citations

Genetics of somatic cell surface antigens. III. Further analysis of the AL marker

1975 • 38 citations

Relationships between genes on human chromosome 11 encoding cell-surface antigens

1984 • 37 citations

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

1984 • 33 citations

SURFACE ANTIGENS OF MAMMALIAN CELLS AS GENETIC MARKERS. II

1973 • 33 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

Genetic analysis of tumorigenesis: a conserved region in the human and Chinese hamster genomes contains genetically identified tumor-suppressor genes.

1987 • 27 citations

Genetic and biochemical analysis of the a1 cell-surface antigen associated with human chromosome 11.

1979 • 27 citations

Somatic cell hybrid mapping panels

1984 • 27 citations

Accurate and superaccurate gene mapping.

1985 • 26 citations

Further studies on hybrid cell-surface antigens associated with human chromosome 11

1977 • 25 citations

Wilms' tumor-aniridia association: Segregation of affected chromosome in somatic cell hybrids, identification of cell surface antigen associated with deleted area, and regional mapping of c-Ha-ras-1 oncogene, insulin gene, and beta-globin gene

1984 • 25 citations

Report of the committee on comparative mapping

1987 • 25 citations

Four new DNA markers are assigned to the WAGR region of 11p13: Isolation and regional assignment of 112 chromosome 11 anonymous DNA segments

1988 • 23 citations

Analysis of human chromosome 11 by somatic cell genetics: Reexamination of derivatives of human-hamster cell line J1

1987 • 19 citations

Localization of the ?-globin gene to 11p15 by in situ hybridization: Utilization of chromosome 11 rearrangements

1985 • 16 citations

A highly polymorphic locus cloned from the breakpoint of a chromosome 11p13 deletion associated with the WAGR syndrome

1989 • 14 citations

Assignment of gene coding for cell surface glycoprotein with a molecular weight of 75,000 to human chromosome 11

1983 • 13 citations

Localization of the LDHA gene to 11p14?11p15 by in situ hybridization of an LDHA cDNA probe to two translocations with breakpoints in 11p13

1986 • 12 citations

Localization of the human catalase and apolipoprotein A-I genes to chromosome 11

1987 • 12 citations

Human muscle cell surface antigen 16.3A5 is encoded by a gene on chromosome 11

1984 • 11 citations

Molecular Genetics of Tyrosine Hydroxylase

1986 • 10 citations

Expression of human chromosome 11-encoded cell-surface antigens by DNA-mediated transfectants

1986 • 9 citations

Definition of selectable cell surface markers for human chromosomes and chromosome segments in rodent-human hybrids

1988 • 9 citations

Molecular cloning of MER-2, a human chromosome-11-encoded red blood cell antigen, using linkage of cotransfected markers

1987 • 7 citations

The anonymous RFLP locus D11S16 is tightly linked to catalase on 11p

1987 • 7 citations

Regional assignment of genes on human chromosomes 11 and 12

1978 • 7 citations

Abstracts of workshop presentations (Part 6 of 13)

1985 • 1 citations