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Volumn 7, Issue 16, 2000, Pages 1385-1391

Early adenovirus-mediated gene transfer effectively prevents muscular dystrophy in alpha-sarcoglycan-deficient mice

Author keywords

Adenovirus; Gene transfer; Limb girdle muscular dystrophy; Murine model; Sarcoglycan

Indexed keywords

SARCOGLYCAN; VIRUS VECTOR;

EID: 0033843869     PISSN: 09697128     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.gt.3301247     Document Type: Article
Times cited : (41)

References (40)
  • 2
    • 0028302369 scopus 로고
    • Dissociation of the complex of dystrophin and its associated proteins into several unique groups by n-octyl, β-D-glucoside
    • (1994) Eur J Biochem , vol.222 , pp. 1055-1061
    • Yoshida, M.1
  • 3
    • 0031451562 scopus 로고    scopus 로고
    • Sarcospan: The 25 kDa transmembrane component of the dystrophin-glycoprotein complex
    • (1997) J Biol Chem , vol.272 , pp. 31221-31224
    • Crosbie, R.H.1
  • 4
    • 0033526085 scopus 로고    scopus 로고
    • Membrane targeting and stabilization of sarcospan is mediated by the sarcoglycan complex
    • (1999) J Cell Biol , vol.145 , pp. 153-165
    • Crosbie, R.H.1
  • 6
    • 0025272250 scopus 로고
    • Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle
    • (1990) Nature , vol.345 , pp. 315-319
    • Ervasti, J.M.1
  • 9
    • 0028146869 scopus 로고
    • Missense mutations in the Adhalin gene linked to autosomal recessive muscular dystrophy
    • (1994) Cell , vol.78 , pp. 625-633
    • Roberds, S.L.1
  • 10
    • 0028971219 scopus 로고
    • β-sarcoglycan mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex
    • (1995) Nat Genet , vol.11 , pp. 266-272
    • Bonneman, C.G.1
  • 11
    • 0028971221 scopus 로고
    • β-Sarcoglycan: Characterization and role in limb-girdle muscular dystrophy linked to 4q12
    • (1995) Nat Genet , vol.11 , pp. 257-265
    • Lim, L.E.1
  • 12
    • 0028883973 scopus 로고
    • Mutations in the dystrophin-associated protein γ-sarcoglycan in chromosome 13 muscular dystrophy
    • (1995) Science , vol.270 , pp. 819-822
    • Noguchi, S.1
  • 13
    • 10344249872 scopus 로고    scopus 로고
    • Mutations that disrupt the carboxyl-terminus of γ-sarcoglycan cause muscular dystrophy
    • (1996) Hum Mol Genet , vol.5 , pp. 1841-1847
    • McNally, E.M.1
  • 14
    • 10144247267 scopus 로고    scopus 로고
    • Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein
    • (1996) Hum Mol Genet , vol.5 , pp. 1179-1186
    • Nigro, V.1
  • 15
    • 0029816797 scopus 로고    scopus 로고
    • Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ-sarcoglycan gene
    • (1996) Nat Genet , vol.14 , pp. 195-198
    • Nigro, V.1
  • 16
    • 0032882445 scopus 로고    scopus 로고
    • The limb-girdle muscular dystrophies-multiple genes, multiple mechanisms
    • (1999) Hum Mol Genet , vol.8 , pp. 1875-1882
    • Bushby, K.M.D.1
  • 18
    • 0029319426 scopus 로고
    • Primary adhalinopathy: A common cause of autosomal recessive muscular dystrophy of variable severity
    • (1995) Nat Genet , vol.10 , pp. 243-245
    • Piccolo, F.1
  • 19
    • 16944365227 scopus 로고    scopus 로고
    • Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)
    • (1997) J Med Genet , vol.34 , pp. 470-475
    • Carrie, A.1
  • 21
    • 0032062510 scopus 로고    scopus 로고
    • Functional rescue of the sarcoglycan complex in the BIO 14.6 hamster using δ-sarcoglycan gene transfer
    • (1998) Mol Cell , vol.1 , pp. 841-848
    • Holt, K.H.1
  • 22
    • 0032907636 scopus 로고    scopus 로고
    • Stable restoration of the sarcoglycan complex in dystrophic muscle perfused with histamine and a recombinant adeno-associated viral vector
    • (1999) Nature Med , vol.5 , pp. 439-443
    • Greelish, J.P.1
  • 23
    • 0032924996 scopus 로고    scopus 로고
    • rAAV vector-mediated sarcoglycan gene transfer in a hamster model for limb girdle muscular dystrophy
    • (1999) Gene Therapy , vol.6 , pp. 74-82
    • Li, J.1
  • 24
    • 19244372467 scopus 로고    scopus 로고
    • Progressive muscular dystrophy in alpha-sarcoglycan-deficient mice
    • (1998) J Cell Biol , vol.142 , pp. 1461-1471
    • Duclos, F.1
  • 27
    • 0028328261 scopus 로고
    • Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 4407-4411
    • Yang, Y.1
  • 28
    • 0028934815 scopus 로고
    • Cellular and humoral immune responses to adenoviral vectors containing factor IX gene: Tolerization of factor IX and vector antigens allows for long-term expression
    • (1995) Proc Natl Acad Sci USA , vol.92 , pp. 1401-1405
    • Dai, Y.1
  • 29
    • 0031923328 scopus 로고    scopus 로고
    • Cytotoxic T-lymphocyte target proteins and their major histocompatibility complex class I restriction in response to adenovirus vectors delivered to mouse liver
    • (1998) J Virol , vol.7 , pp. 2945-2954
    • Joos, K.1    Ertl, H.C.J.2    Wilson, J.M.3
  • 32
    • 0030999469 scopus 로고    scopus 로고
    • Adenovirus-mediated gene transfer: Influence of transgene, mouse strain and type of immune response on persistence of transgene expression
    • (1997) Gene Therapy , vol.4 , pp. 473-482
    • Michou, A.1
  • 35
    • 85092120406 scopus 로고    scopus 로고
    • Contrast agent-enhanced magnetic resonance imaging of skeletal muscle damage in animal models of muscular dystrophy
    • (in press)
    • Magn Reson Med
    • Straub, V.1
  • 36
    • 0032828285 scopus 로고    scopus 로고
    • Expression of Coxsackie adenovirus receptor and alpha(v)-integrin does not correlate with adenovector targeting in vivo indicating anatomical vector barriers
    • (1999) Gene Therapy , vol.6 , pp. 1520-1535
    • Fechner, H.1
  • 39
    • 0033963757 scopus 로고    scopus 로고
    • Disruption of the β-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E
    • (2000) Mol Cell , vol.5 , pp. 141-151
    • Durbeej, M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.