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Volumn 180, Issue 1, 1996, Pages 57-63

Quantitative estimation of dystrophin protein: A sensitive and convenient "two-antibody sandwich" ELISA

Author keywords

Becker muscular dystrophy; Duchenne muscular dystrophy; Dystrophin; ELISA

Indexed keywords

DYSTROPHIN; MONOCLONAL ANTIBODY;

EID: 0030226133     PISSN: 00408727     EISSN: None     Source Type: Journal    
DOI: 10.1620/tjem.180.57     Document Type: Article
Times cited : (6)

References (15)
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  • 4
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  • 5
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    • Normal dystrophin transcripts detected in Duchenne muscular dystrophy patients after myoblast transplantation
    • Gussoni, E., Pavlath, G.K., Lanctot, A.M., Sharma, K.R., Miller, R.G., Steinman, L. & Blau, H.M. (1992) Normal dystrophin transcripts detected in Duchenne muscular dystrophy patients after myoblast transplantation. Nature, 356, 435-438
    • (1992) Nature , vol.356 , pp. 435-438
    • Gussoni, E.1    Pavlath, G.K.2    Lanctot, A.M.3    Sharma, K.R.4    Miller, R.G.5    Steinman, L.6    Blau, H.M.7
  • 6
    • 0023614188 scopus 로고
    • Dystrophin: The protein products of the Duchenne muscular dystrophy locus
    • Hoffman, E.P., Brown, R.H., Jr. & Kunkel, L.M. (1987) Dystrophin: The protein products of the Duchenne muscular dystrophy locus. Cell, 51, 919-928.
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    • Hoffman, E.P.1    Brown Jr., R.H.2    Kunkel, L.M.3
  • 9
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    • Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
    • Koenig, M., Hoffman, E.P., Bertelson, C.J., Monaco, A.P., Feener, C. & Kunkel, L.M. (1987) Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell, 50, 509-517.
    • (1987) Cell , vol.50 , pp. 509-517
    • Koenig, M.1    Hoffman, E.P.2    Bertelson, C.J.3    Monaco, A.P.4    Feener, C.5    Kunkel, L.M.6
  • 11
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    • A two-step procedure for efficient electrotransfer of both high-molecular-weight (>400,000) and low-molecular-weight (<20,000) proteins
    • Otter, T., King, S.M. & Witman, G.B. (1987) A two-step procedure for efficient electrotransfer of both high-molecular-weight (>400,000) and low-molecular-weight (<20,000) proteins. Anal. Biochem., 162, 370-377.
    • (1987) Anal. Biochem. , vol.162 , pp. 370-377
    • Otter, T.1    King, S.M.2    Witman, G.B.3
  • 13
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    • Amino-terminal deletion of 53% of dystrophin results in an intermediate Duchenne-Becker muscular dystrophy phenotype
    • Takeshima, Y., Nishio, H., Narita, N., Wada, H., Ishikawa, Y., Ishikawa, Y., Minami, R., Nakamura, H. & Matsuo, M. (1994) Amino-terminal deletion of 53% of dystrophin results in an intermediate Duchenne-Becker muscular dystrophy phenotype. Neurology, 44, 1648-1651.
    • (1994) Neurology , vol.44 , pp. 1648-1651
    • Takeshima, Y.1    Nishio, H.2    Narita, N.3    Wada, H.4    Ishikawa, Y.5    Ishikawa, Y.6    Minami, R.7    Nakamura, H.8    Matsuo, M.9
  • 14
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    • Is the maintainance of the C-terminus domain of dystrophin enough to ensure a milder Becker muscular dystrophy phenotype?
    • Vainzof, M., Takata, R.I., Passos-Bueno, M.R., Pavanello, R.C.M. & Zatz, M. (1993) Is the maintainance of the C-terminus domain of dystrophin enough to ensure a milder Becker muscular dystrophy phenotype? Hum. Mol. Genet., 2, 39-42.
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  • 15
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    • Wells, D.J., Wells, K.E., Asante, E.A., Turner, G., Sunada, Y., Campbell, K.P., Walsh, F.S. &. Dickson, G. (1995) Expression of human full-length and minidystrophin in transgenic mdx mice: Implications for gene therapy of Duchenne muscular dystrophy. Hum. Mol. Genet., 4, 1245-1250.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.