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Volumn 77, Issue 3-4, 1997, Pages 259-260

Assignment of the human nebulin gene (NEB) to chromosome band 2q24.2 and the α1 (III) collagen gene (COL3A1) to chromosome band 2q32.2 by in situ hybridization; The FRA2G common fragile site lies between the two genes in the 2q31 band

Author keywords

[No Author keywords available]

Indexed keywords

COLLAGEN TYPE 3; NEBULIN;

EID: 0030757679     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (5)

References (14)
  • 2
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    • Human α1(III) and α2(V) procollagen genes are located on the long arm of chromosome 2
    • USA
    • Emanuel BS, Cannizzaro LA, Seyer JM, Myers JC: Human α1(III) and α2(V) procollagen genes are located on the long arm of chromosome 2. Proc natl Acad Sci, USA 82:3385-3389 (1985).
    • (1985) Proc Natl Acad Sci , vol.82 , pp. 3385-3389
    • Emanuel, B.S.1    Cannizzaro, L.A.2    Seyer, J.M.3    Myers, J.C.4
  • 3
    • 0021278143 scopus 로고
    • DNA polymerase a inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes
    • Glover TW, Berger C, Coyle J, Echo B: DNA polymerase a inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes. Hum Genet 67:136-142 (1984).
    • (1984) Hum Genet , vol.67 , pp. 136-142
    • Glover, T.W.1    Berger, C.2    Coyle, J.3    Echo, B.4
  • 5
    • 0029037896 scopus 로고
    • The complete primary structure of human nebulin and its correlation to muscle structure
    • Labeit S, Kolmerer B: The complete primary structure of human nebulin and its correlation to muscle structure. J Mol Biol 248:308-315 (1995).
    • (1995) J Mol Biol , vol.248 , pp. 308-315
    • Labeit, S.1    Kolmerer, B.2
  • 7
    • 0027936493 scopus 로고
    • A family with Ehlers-Danlos syndrome type III/articular hypermobility syndrome has a glycine 637 to serine substitution in type III collagen
    • Narcisi P, Richards AJ, Ferguson SD, Pope FM: A family with Ehlers-Danlos syndrome type III/articular hypermobility syndrome has a glycine 637 to serine substitution in type III collagen. Hum mol Genet 3:1617-1620 (1994).
    • (1994) Hum Mol Genet , vol.3 , pp. 1617-1620
    • Narcisi, P.1    Richards, A.J.2    Ferguson, S.D.3    Pope, F.M.4
  • 8
    • 0022483455 scopus 로고
    • DAPI-inducible common fragile sites
    • Pelliccia F, Rocchi A: DAPI-inducible common fragile sites. Cytogenet Cell Genet 42:174-176 (1986).
    • (1986) Cytogenet Cell Genet , vol.42 , pp. 174-176
    • Pelliccia, F.1    Rocchi, A.2
  • 9
    • 0023781608 scopus 로고
    • Synergistic effect of DAPI and thymidylate stress conditions on the induction of common fragile sites
    • Rocchi A, Pelliccia F: Synergistic effect of DAPI and thymidylate stress conditions on the induction of common fragile sites. Cytogenet Cell Genet 48:51-54 (1988).
    • (1988) Cytogenet Cell Genet , vol.48 , pp. 51-54
    • Rocchi, A.1    Pelliccia, F.2
  • 13
    • 0030060945 scopus 로고    scopus 로고
    • FRA3B extends over a broad region and contains a spontaneous HPV16 integration site: Direct evidence for the coincidence of viral integration sites and fragile sites
    • Wilke CM, Hall BK, Hoge A, Paradee W, Smith DI, Glover TW: FRA3B extends over a broad region and contains a spontaneous HPV16 integration site: direct evidence for the coincidence of viral integration sites and fragile sites. Hum mol Genet 5:187-195 (1996).
    • (1996) Hum Mol Genet , vol.5 , pp. 187-195
    • Wilke, C.M.1    Hall, B.K.2    Hoge, A.3    Paradee, W.4    Smith, D.I.5    Glover, T.W.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.