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

Construction of a genetic linkage map in man using restriction fragment length polymorphisms.

1980 • 8,270 citations

[9] Gel electrophoresis of restriction fragments

1979 • 653 citations

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

1964 • 607 citations

Characterization of cloned cDNA representing rat myelin basic protein: Absence of expression in brain of shiverer mutant mice

1983 • 382 citations

Ancient Linkage Groups and Frozen Accidents

1973 • 338 citations

Report of the committee on human gene mapping by recombinant DNA techniques

1984 • 274 citations

Isolation and characterization of a major tandem repeat family from the human X chromosome

1983 • 258 citations

Compact myelin exists in the absence of basic protein in the shiverer mutant mouse

1980 • 224 citations

Immunochemical studies of myelin basic protein in shiverer mouse devoid of major dense line of myelin

1979 • 210 citations

Chromosome-specific alpha satellite DNA: nucleotide sequence analysis of the 2.0 kilobasepair repeat from the human X chromosome

1985 • 188 citations

EVOLUTION OF SEX CHROMOSOMES IN MAMMALS

1969 • 164 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

Isolation of human fibroblast catalase cDNA clones. Sequence of clones derived from spliced and unspliced mRNA.

1984 • 90 citations

A neurological mutation (msd) of the mouse causing a deficiency of myelin synthesis

1970 • 87 citations

Brain proteolipids in neurological mutant mice

1973 • 82 citations

Amino acid sequence of bovine white matter proteolipid

1983 • 70 citations

Study of the expression of myelin proteolipid protein (lipophilin) using a cloned complementary DNA

1985 • 63 citations

Regional localization of the phosphoglycerate kinase gene and pseudogene on the human X chromosome and assignment of a related DNA sequence to chromosome 19

1985 • 63 citations

The human genome through the eyes of a clinical geneticist

1982 • 63 citations

Intraspecies transfer via total cellular DNA of the gene for hypoxanthine phosphoribosyltransferase into cultured mouse cells

1979 • 62 citations

EARLY LESION OF PELIZAEUS-MERZBACHER DISEASE

1973 • 53 citations

The specific organisation of satellite DNA sequences on the X-chromosome of Mus musculus: partial independence of chromosome evolution.

1980 • 46 citations

The William Allan Memorial Award address: Reverse genetics and beyond.

1984 • 46 citations

Molecular cloning and chromosomal localization of DNA sequences associated with a human DNA repair gene.

1985 • 45 citations

Use of chimeras to transmit lethal genes in the mouse and to demonstrate allelism of the two X‐linked male lethal genes jp and msd

1973 • 44 citations

Connatal Pelizaeus-Merzbacher Disease with congenital stridor in two maternal cousins

1981 • 42 citations

Congenital failure of myelinization

1971 • 41 citations

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

1969 • 41 citations

Assignment of human gamma crystallin multigene family to chromosome 2

1985 • 41 citations

Congenital Nervous Diseases of Pigs: A Review

1968 • 39 citations

Introduction

1984 • 31 citations

Genetic analysis of the human cell surface: antigenic marker for the human X chromosome in human-mouse hybrids.

1978 • 30 citations

A sensitive and dependable assay for distinguishing hamster and human X-linked steroid sulfatase activity in somatic cell hybrids

1984 • 28 citations

Enzymic and chemical fragmentation of the apoprotein of the major rat brain myelin proteolipid

1983 • 28 citations

NEEDLE BIOPSY OF SKELETAL MUSCLE

1969 • 24 citations

Gene duplication in bovine brain myelin proteolipid and homology with related proteins

1983 • 20 citations

X;14 translocation: An exception to the critical region hypothesis on the human X‐chromosome

1985 • 16 citations

An (X;14) translocation, balanced, 47 chromosomes

1973 • 13 citations

Disturbances of rapid‐eye‐movement sleep in 3 brothers with Pelizaeus‐Merzbacher disease

1979 • 13 citations

METABOLISM IN VIVO OF BRAIN GALACTOLIPIDS: THE JIMPY MUTANT

1972 • 12 citations