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Volumn 79, Issue 2, 2002, Pages 146-149

The muscular dystrophy with myositis (mdm) mouse mutation disrupts a skeletal muscle-specific domain of titin

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; CALPAIN; CALPAIN 3; CONNECTIN; UNCLASSIFIED DRUG;

EID: 0035707910     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.2002.6685     Document Type: Article
Times cited : (118)

References (17)
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  • 8
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    • Sorimachi, H.1
  • 10
    • 0028905205 scopus 로고
    • Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A
    • (1995) Cell , vol.81 , pp. 27-40
    • Richard, I.1
  • 12
    • 0034739841 scopus 로고    scopus 로고
    • Loss of calpain 3 proteolytic activity, leads to muscular dystrophy and to apoptosis-associated IκBα/nuclear factor κB pathway perturbation in mice
    • (2000) J. Cell Biol. , vol.151 , pp. 1583-1590
    • Richard, I.1
  • 13
    • 0001634301 scopus 로고    scopus 로고
    • Myopathy phenotype of transgenic mice expressing active site-mutated inactive p94 skeletal muscle-specific calpain, the gene product responsible for limb girdle muscular dystrophy type 2A
    • (2000) Hum. Mol. Genet. , vol.9 , pp. 1393-1402
    • Tagawa, K.1
  • 15
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    • (1997) Cell , vol.91 , pp. 139-148
    • Cox, G.A.1
  • 17
    • 0027186053 scopus 로고
    • Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity
    • (1993) Nature , vol.364 , pp. 725-729
    • Cox, G.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.