Literature DB >> 939913

Myodystrophy, a new myopathy on chromosome 8 of the mouse.

P W Lane, T C Beamer, D D Myers.   

Abstract

A new recessive mutation, myd, causing a diffuse and progressive myopathy in the mouse is described. Histopathological comparisons with normal littermates showed widely distributed focal lesions in all skeletal muscles of myd/myd. Body and organ weights of affected mice were considerably less than those of normal littermates and the mean lifespan of myodystrophic mice that survived weaning was 17 weeks with a range of 5 to 39 weeks. Myodystrophy is located on chromosome 8; it is linked to Os with about 6 percent and to Eso with about 37 percent recombination.

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Year:  1976        PMID: 939913     DOI: 10.1093/oxfordjournals.jhered.a108687

Source DB:  PubMed          Journal:  J Hered        ISSN: 0022-1503            Impact factor:   2.645


  16 in total

Review 1.  Mouse chromosome 8.

Authors:  J D Ceci; A J Lusis
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

2.  Congenital muscular dystrophy type 1D (MDC1D) due to a large intragenic insertion/deletion, involving intron 10 of the LARGE gene.

Authors:  Nigel F Clarke; Svetlana Maugenre; Aurélie Vandebrouck; J Andoni Urtizberea; Tobias Willer; Rachel A Peat; Françoise Gray; Céline Bouchet; Hiroshi Manya; Sandrine Vuillaumier-Barrot; Tamao Endo; Eliane Chouery; Kevin P Campbell; André Mégarbané; Pascale Guicheney
Journal:  Eur J Hum Genet       Date:  2011-01-19       Impact factor: 4.246

Review 3.  Laminin-211 in skeletal muscle function.

Authors:  Johan Holmberg; Madeleine Durbeej
Journal:  Cell Adh Migr       Date:  2012-11-15       Impact factor: 3.405

Review 4.  What do mouse models of muscular dystrophy tell us about the DAPC and its components?

Authors:  Charlotte Whitmore; Jennifer Morgan
Journal:  Int J Exp Pathol       Date:  2014-09-30       Impact factor: 1.925

5.  A syntrophin gene maps to mouse chromosome 8 and is not the myodystrophy gene.

Authors:  K A Mills; Y Sunada; K P Campbell; K D Mathews
Journal:  Mamm Genome       Date:  1995-09       Impact factor: 2.957

6.  The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8.

Authors:  P K Grewal; J C van Deutekom; K A Mills; R J Lemmers; K D Mathews; R R Frants; J E Hewitt
Journal:  Mamm Genome       Date:  1997-06       Impact factor: 2.957

7.  Genetic mapping near the myd locus on mouse chromosome 8.

Authors:  K A Mills; K D Mathews; T Scherpbier-Heddema; R L Schelper; R Schmalzel; H L Bailey; J H Nadeau; K H Buetow; J C Murray
Journal:  Mamm Genome       Date:  1995-04       Impact factor: 2.957

Review 8.  Mouse forward genetics in the study of the peripheral nervous system and human peripheral neuropathy.

Authors:  Darlene S Douglas; Brian Popko
Journal:  Neurochem Res       Date:  2008-05-15       Impact factor: 3.996

9.  A laminin-2, dystroglycan, utrophin axis is required for compartmentalization and elongation of myelin segments.

Authors:  Felipe A Court; Jane E Hewitt; Kay Davies; Bruce L Patton; Antonino Uncini; Lawrence Wrabetz; M Laura Feltri
Journal:  J Neurosci       Date:  2009-03-25       Impact factor: 6.167

10.  Central nervous system involvement in the animal model of myodystrophy.

Authors:  Clarissa M Comim; Bruna P Mendonça; Diogo Dominguini; Andreza L Cipriano; Amanda V Steckert; Giselli Scaini; Mariz Vainzof; Emílio L Streck; Felipe Dal-Pizzol; João Quevedo
Journal:  Mol Neurobiol       Date:  2013-03-19       Impact factor: 5.590

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