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Volumn 11, Issue 1, 2001, Pages 41-49

Evaluation of the dystrophin-glycoprotein complex, α-actinin, dysferlin and calpain 3 in an autosomal recessive muscular dystrophy in Labrador retrievers

Author keywords

Autosomal recessive muscular dystrophy in Labrador retrievers; Calpain 3; Congenital muscular dystrophy; Dysferlin; Limb girdle muscular dystrophy; Merosin; Sarcoglycan

Indexed keywords

ALPHA ACTININ; CALPAIN; CALPAIN 3; CREATINE KINASE; DYSFERLIN; DYSTROPHIN; GLYCOPROTEIN; MEROSIN; PROTEIN; PROTEINASE; SARCOGLYCAN; UNCLASSIFIED DRUG;

EID: 0035144734     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-8966(00)00166-8     Document Type: Article
Times cited : (12)

References (47)
  • 10
    • 0028914964 scopus 로고
    • Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage
    • (1995) Cell , vol.80 , pp. 675-679
    • Campbell, K.P.1
  • 13
    • 0032231939 scopus 로고    scopus 로고
    • A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus
    • (1998) Am J Hum Genet , vol.63 , pp. 140-147
    • Weiler, T.1    Greenberg, C.R.2    Zelinski, T.3
  • 14
    • 0028905205 scopus 로고
    • A novel mechanism leading to muscular dystrophy: mutations in calpain 3 cause limb-girdle muscular dystrophy type 2A
    • (1995) Cell , vol.81 , pp. 27-40
    • Richard, I.1    Broux, O.2    Allamand, V.3
  • 25
    • 17344365600 scopus 로고    scopus 로고
    • Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
    • (1998) Nat Genet , vol.20 , pp. 31-36
    • Liu, J.1    Aoki, M.2    Illa, I.3
  • 33
    • 0030220198 scopus 로고    scopus 로고
    • Deficiency of a skeletal muscle isoform of alpha-actinin (alpha-actinin-3) in merosin positive congenital muscular dystrophy
    • (1996) Neuromusc Disord , vol.6 , pp. 229-235
    • North, K.N.1    Beggs, A.H.2
  • 34
    • 0030951089 scopus 로고    scopus 로고
    • Primary adhalinopathy (α-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy
    • (1997) Neurology , vol.48 , pp. 1227-1234
    • Eymard, B.1    Romero, N.B.2    Leturcq, F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.