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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
1989-5-26
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pubmed:abstractText |
mdx is an X-linked muscular dystrophy mutant of the mouse and a putative homolog of the human X-linked muscular dystrophy locus--Duchenne muscular dystrophy (DMD). Utilizing a C57BL/10/Mus Spretus interspecific cross in which the mdx mutation was segregating, we have constructed a detailed genetic map around the mdx locus on the mouse X chromosome. We were unable to detect recombinants between mdx and exonic probes derived from the human DMD gene. These genetic data support the contention from biochemical studies (E.P. Hoffman, R. H. Brown, and L. M. Kunkel, 1987, Cell 51: 919-928) that DMD and mdx are homologous genes.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0888-7543
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
3
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
337-41
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:3243547-Animals,
pubmed-meshheading:3243547-Blotting, Southern,
pubmed-meshheading:3243547-Chromosome Mapping,
pubmed-meshheading:3243547-Female,
pubmed-meshheading:3243547-Genes,
pubmed-meshheading:3243547-Genetic Markers,
pubmed-meshheading:3243547-Haplotypes,
pubmed-meshheading:3243547-Humans,
pubmed-meshheading:3243547-Male,
pubmed-meshheading:3243547-Mice,
pubmed-meshheading:3243547-Mice, Inbred C57BL,
pubmed-meshheading:3243547-Muscular Dystrophies,
pubmed-meshheading:3243547-Muscular Dystrophy, Animal,
pubmed-meshheading:3243547-X Chromosome
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pubmed:year |
1988
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pubmed:articleTitle |
Molecular and genetic mapping of the mouse mdx locus.
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pubmed:affiliation |
Department of Biochemistry and Molecular Genetics, St. Mary's Hospital Medical School, London, United Kingdom.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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