Mouse myodystrophy (myd) mutation: Refined mapping in an interval flanked by homology with distal human 4q-Reference-Cited by-同舟云学术

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Mouse myodystrophy (myd) mutation: Refined mapping in an interval flanked by homology with distal human 4q

Published:1995 Issue:S13 Volume:18 Page:S98-S102
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Mathews Katherine D.,Mills Kathleen A.,Bailey Holly L.,Schelper Robert L.,Murray Jeffrey C.

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

Reference17 articles.

1. Gene structure and chromosomal localization of plasma kallikrein

2. Hearing loss in facioscapulohumeral muscular dystrophy

3. Mouse chromosome 8

4. A genetic map of the mouse suitable for typing intraspecific crosses.

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Defects in Glycosylation Impair Satellite Stem Cell Function and Niche Composition in the Muscles of the Dystrophic Large myd Mouse;STEM CELLS;2012-09-20

2. Mutation of Large, which encodes a putative glycosyltransferase, in an animal model of muscular dystrophy;Biochimica et Biophysica Acta (BBA) - General Subjects;2002-12

3. Mutant glycosyltransferase and altered glycosylation of α-dystroglycan in the myodystrophy mouse;Nature Genetics;2001-06

4. The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8;Mammalian Genome;1997-06

5. Fath, the murine homolog of the Drosophila fat tumor suppressor gene, maps to chromosome 8;Mammalian Genome;1997-05

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