X-Linked genetic homologies between mouse and man

The Metabolic Basis of Inherited Disease.

1988 • 7,933 citations

The Metabolic Basis of Inherited Disease.

1983 • 2,885 citations

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

1984 • 1,678 citations

The Metabolic Basis of Inherited Disease.

1972 • 1,407 citations

The Primary Immunodeficiencies

1984 • 1,111 citations

Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene

1986 • 1,033 citations

Mutant Mice (Quaking and Jimpy) with Deficient Myelination in the Central Nervous System

1964 • 607 citations

Lengths of chromosomal segments conserved since divergence of man and mouse.

1984 • 599 citations

X-linked Gene for Testicular Feminization in the Mouse

1970 • 551 citations

Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy

1986 • 468 citations

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

1976 • 399 citations

Report of the committee on the genetic constitution of the X and Y chromosomes

1985 • 369 citations

A system of nomenclature for band patterns of mouse chromosomes

1973 • 368 citations

Genetic Variants and Strains of the Laboratory Mouse

1990 • 327 citations

Primary defect in copper transport underlies mottled mutants in the mouse

1974 • 318 citations

Muscle development in mdx mutant mice

1984 • 315 citations

A gradient of sex linkage in the pseudoautosomal region of the human sex chromosomes

1986 • 307 citations

The CBA/N Mouse Strain: An Experimental Model Illustration the Influence of the X-Chromosome on Immunity

1982 • 305 citations

The Primary Immunodeficiencies

1984 • 288 citations

The Genetic Linkage Map of the Human X Chromosome

1985 • 220 citations

Jimpy mutant mouse: a 74-base deletion in the mRNA for myelin proteolipid protein and evidence for a primary defect in RNA splicing.

1986 • 219 citations

Non-inactivation of an X-Chromosome Locus in Man

1979 • 216 citations

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

1985 • 213 citations

A Pseudoautosomal Gene in Man

1986 • 210 citations

X-chromosome deletions in embryo-derived (EK) cell lines associated with lack of X-chromosome inactivation

1985 • 208 citations

X-linked B-lymphocyte immune defect in CBA/N mice. II. Studies of the mechanisms underlying the immune defect.

1975 • 200 citations

X-autosome ratio and the behavior pattern of individual X-chromosomes in placental mammals

1964 • 180 citations

EVOLUTION OF SEX CHROMOSOMES IN MAMMALS

1969 • 164 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

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

1986 • 154 citations

Regional assignment of the steroid sulfatase—X-linked ichthyosis locus: Implications for a noninactivated region on the short arm of human X chromosome

1979 • 150 citations

Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223

1980 • 148 citations

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

1985 • 147 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

Primary immunodeficiency diseases

1983 • 141 citations

Differential expression of steroid sulphatase locus on active and inactive human X chromosome

1982 • 135 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

Evidence for X-Linked Dominant Inheritance of Ornithine Transcarbamylase Deficiency

1973 • 128 citations

The Gy mutation: another cause of X-linked hypophosphatemia in mouse.

1986 • 127 citations

Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphism.

1986 • 123 citations

Assignment of the gene for dyskeratosis congenita to Xq28

1986 • 122 citations

Altered copper metabolism in cultured cells from human Menkes' syndrome and mottled mouse mutants

1980 • 121 citations

ELECTROPHORETIC VARIATION FOR X-CHROMOSOME-LINKED PHOSPHOGLYCERATE KINASE (PGK-1) IN THE MOUSE

1977 • 116 citations

Tissue-specific expression of the rat albumin gene: genetic control of its extinction in microcell hybrids.

1986 • 100 citations

Decreased lysyl oxidase activity in the aneurysm-prone, mottled mouse.

1977 • 98 citations

Expression of an X-linked gene from an inactive human X chromosome in mouse-human hybrid cells: further evidence for the noninactivation of the steroid sulfatase locus in man.

1980 • 95 citations

The glandular aspects of the tabby syndrome in the mouse.

1971 • 93 citations

Report of the committee on comparative mapping

1985 • 90 citations

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

1986 • 90 citations

Two cases of X/autosome translocation in females with incontinentia pigmenti

1985 • 88 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

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

1976 • 86 citations

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

1986 • 86 citations

Structural anomalies of the X chromosome and inactivation center

1981 • 82 citations

Linkage of the Wiskott-Aldrich syndrome with polymorphic DNA sequences from the human X chromosome.

1987 • 77 citations

X linkage of phosphoglycerate kinase in the mouse

1974 • 76 citations

The gene encoding for the major brain proteolipid (PLP) maps on the q-22 band of the human X chromosome

1986 • 74 citations

Myelin proteolipid protein (PLP and DM-20) transcripts are deleted in jimpy mutant mice.

1986 • 71 citations

THE X CHROMOSOMES OF MAMMALS: KARYOLOGICAL HOMOLOGY AS REVEALED BY BANDING TECHNIQUES

1974 • 69 citations

The mapping of a cDNA from the human X-linked Duchenne muscular dystrophy gene to the mouse X chromosome

1987 • 67 citations

Human Regulatory Gene for Inducible Tyrosine Aminotransferase in Rat-Human Hybrids

1973 • 66 citations

Isolation of a cDNA clone corresponding to an X-linked gene family (XLR) closely linked to the murine immunodeficiency disorder xid

1985 • 65 citations

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

1980 • 63 citations

Mapping of the X-linked immune deficiency mutation (xid) of CBA/N mice.

1980 • 62 citations

Position of the human X inactivation center on Xq

1979 • 62 citations

HISTOINCOMPATIBILITY ASSOCIATED WITH THE X CHROMOSOME IN MICE

1963 • 61 citations

Microdissection and microcloning of the mouse X chromosome.

1985 • 61 citations

Genetic control over the inactivation of autosomal genes attached to the X-chromosome

1965 • 60 citations

The glandular aspects of the tabby syndrome in the mouse

1971 • 60 citations

Steroid Sulfatase Deficiency and the Genetics of the Short Arm of the Human X Chromosome

1985 • 60 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 X-chromosome and the enzymes controlling muscle glycogen: Phosphorylase kinase

1970 • 54 citations

Expression of an X-linked gene family (XLR) in late-stage B cells and its alteration by the xid mutation

1985 • 54 citations

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

1987 • 53 citations

Sex chromosomes: Mammalian X and Y crossover

1986 • 52 citations

The genetics of sex-linked anaemia in the mouse

1962 • 49 citations

X-linked Recessive Inheritance in the Ehlers-Danlos Syndrome

1968 • 48 citations

Hereditary, X-Linked, Sideroachrestic Anemia. The Isolation of Two Erythrocyte Populations Differing in Xga Blood Type and Porphyrin Content

1968 • 47 citations

Evidence That the Human Y Chromosome Does Not Contain Clustered DNA Sequences (Bkm) Associated with Heterogametic Sex Determination in Other Vertebrates

1985 • 47 citations

Controlling elements in the mouse X-chromosome

1970 • 46 citations

An ultrastructural study on the cerebellum of the brindled mouse

1980 • 45 citations

Anhidrosis and Absence of Sweat Glands in Mice Hemizygous for the Tabby Gene; Supportive Evidence for the Hypothesis of Homology Between Tabby and Human Anhidrotic (Hypohidrotic) Ectodermal Dysplasia (Christ-Siemens-Touraine Syndrome)

1986 • 42 citations

Emery-Dreifuss muscular dystrophy: localisation to Xq27.3----qter confirmed by linkage to the factor VIII gene.

1986 • 41 citations

Absence of cerebral myelin sheaths in a case of presumed Pelizaeus-Merzbacher disease. Electron microscopic and biochemical studies.

1969 • 41 citations

Bare-patches, a new sex-linked gene in the mouse, associated with a high production of XO females: I. A preliminary report of breeding experiments

1973 • 41 citations

A re-examination of the case for homology between the X and Y chromosomes of mouse and man

1984 • 38 citations

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

1983 • 37 citations

Hereditary sideroblastic anemia and glucose-6-phosphate dehydrogenase deficiency in a negro family

1968 • 35 citations

Gene localisation of X-linked hypohidrotic ectodermal dysplasia (C-S-T syndrome)

1986 • 34 citations

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

1983 • 33 citations

ABSENCE OF CEREBRAL MYELIN SHEATHS IN A CASE OF PRESUMED PELIZAEUS—MERZBACHER DISEASE

1969 • 30 citations

Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qter

1987 • 29 citations

Fine mapping of the distal short arm of the human X chromosome using X/Y translocations.

1986 • 29 citations

Lipophilin (PLP) Gene in X‐linked myelin disorders

1986 • 29 citations

Genetic diseases of copper metabolism.

1986 • 29 citations

X-linked control of hemoglobin production in somatic hybrids of mouse erythroleukemic cells and mouse lymphoma or bone marrow cells

1977 • 29 citations

Genetic Mapping of the Human X Chromosome: Linkage Analysis of the q26-q28 Region That Includes the Fragile X Locus and Isolation of Expressed Sequences

1986 • 28 citations

A study of the copper-binding proteins in liver and kidney tissue of neonatal normal and mottled mutant mice

1979 • 26 citations

Glycogen-storage disease associated with phosphorylase kinase deficiency: evidence for X inactivation.

1974 • 24 citations

Variation in regulation of steroid sulphatase locus in mammals

1983 • 22 citations

Localization of the <i>Hprt </i>locus by in situ hybridization and distribution of loci on the mouse X-chromosome

1987 • 22 citations

Localization of glucose-6-phosphate dehydrogenase in mouse and man by in situ hybridization: evidence for a single locus and transposition of homologous X-linked genes

1985 • 20 citations

Copper utilization in cultured skin fibroblasts of the mottled mouse, an animal model for Menkes' kinky hair syndrome

1984 • 17 citations

X-linked polydactyly (Xpl), a new mutation in the mouse

1980 • 15 citations

No extinction of tyrosine aminotransferase inducibility in rat hepatoma-human fibroblast hybrids containing the human X chromosome

1981 • 14 citations

Antibody against T cell-replacing factor acceptor site(s) augments in vivo primary IgM responses to suboptimal doses of heterologous erythrocytes

1981 • 14 citations

A-raf oncogene localizes on mouse X chromosome to region some 10–17 centimorgans proximal to hypoxanthine phosphoribosyltransferase gene

1987 • 13 citations

Aminolevulinic acid synthetase activity in erythroblasts of patients with primary sideroblastic anemia.

1973 • 13 citations

Role of Heterophoria in Binocular Disharmony

1937 • 13 citations

X-LINKED AND AUTOSOMAL GENES CONTROLLING MOUSE α-GALACTOSIDASE EXPRESSION

1978 • 11 citations

Location of phosphorylase kinase (Phk) in the mouse X chromosome

1973 • 8 citations

Pre-B cells in X-linked agammaglobulinemia.

1983 • 3 citations

[Cutaneous signs and symptoms of X-linked chondrodysplasia punctata in man and mouse].

1983 • 3 citations

Deleted Work

1955 • 0 citations