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Volumn 9, Issue 6-7, 1999, Pages 421-422

Immunomarkers for molecular mass

Author keywords

Monoclonal antibodies; Muscular dystrophy; Western blotting

Indexed keywords

CALPAIN; DYSTROPHIN; LAMININ; MEROSIN; MUSCLE PROTEIN; MYOSIN HEAVY CHAIN; SARCOGLYCAN;

EID: 0032832801     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-8966(99)00043-7     Document Type: Article
Times cited : (1)

References (5)
  • 1
    • 0032929386 scopus 로고    scopus 로고
    • A multiplex western blotting system for the analysis of muscular dystrophy proteins
    • Anderson L.V.B., Davison K. A multiplex western blotting system for the analysis of muscular dystrophy proteins. Am J Pathol. 154:1999;1017-1022.
    • (1999) Am J Pathol , vol.154 , pp. 1017-1022
    • Anderson, L.V.B.1    Davison, K.2
  • 2
    • 0026658952 scopus 로고
    • Dystrophin or a 'related protein' in Duchenne muscular dystrophy?
    • Nicholson L.V.B., Johnson M.A., Davison K., et al. Dystrophin or a 'related protein' in Duchenne muscular dystrophy? Acta Neurol Scand. 86:1992;8-14.
    • (1992) Acta Neurol Scand , vol.86 , pp. 8-14
    • Nicholson, L.V.B.1    Johnson, M.A.2    Davison, K.3
  • 3
    • 0032955751 scopus 로고    scopus 로고
    • Dysferlin is a plasma membrane protein and is expressed early in human development
    • Anderson L.V.B., Davison K., Moss J.A., et al. Dysferlin is a plasma membrane protein and is expressed early in human development. Hum Mol Genet. 8:1999;855-861.
    • (1999) Hum Mol Genet , vol.8 , pp. 855-861
    • Anderson, L.V.B.1    Davison, K.2    Moss, J.A.3
  • 4
    • 0031662389 scopus 로고    scopus 로고
    • Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2A
    • Anderson L.V.B., Davison K., Moss J.A., et al. Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2A. Am J Pathol. 153:1998;1169-1179.
    • (1998) Am J Pathol , vol.153 , pp. 1169-1179
    • Anderson, L.V.B.1    Davison, K.2    Moss, J.A.3
  • 5
    • 0029319426 scopus 로고
    • Primary adhalinopathy: A common cause of autosomal recessive muscular dystrophy of variable severity
    • Piccolo F., Roberds S.L., Jeanpierre M., et al. Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity. Nature Genet. 10:1995;243-245.
    • (1995) Nature Genet , vol.10 , pp. 243-245
    • Piccolo, F.1    Roberds, S.L.2    Jeanpierre, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.