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Volumn 62, Issue 2, 1999, Pages 172-176

Human connexin 30 (GJB6), a candidate gene for nonsyndromic hearing loss: Molecular cloning, tissue-specific expression, and assignment to chromosome 13q12

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26; CONNEXIN 30; GAP JUNCTION PROTEIN; UNCLASSIFIED DRUG;

EID: 0033393433     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1999.6002     Document Type: Article
Times cited : (45)

References (20)
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    • (1996) J. Biol. Chem. , vol.271 , pp. 17903-17910
    • Dahl, E.1    Manthey, D.2    Chen, Y.3    Schwarz, H.J.4    Chang, Y.S.5    Lalley, P.A.6    Nicholson, B.J.7    Willecke, K.8
  • 6
    • 0016937549 scopus 로고
    • Development of absolute auditory thresholds in the house mouse (Mus musculus)
    • Ehret G. Development of absolute auditory thresholds in the house mouse (Mus musculus). J. Am. Audiol. Soc. 1:1976;179-184.
    • (1976) J. Am. Audiol. Soc. , vol.1 , pp. 179-184
    • Ehret, G.1
  • 9
    • 0032530408 scopus 로고    scopus 로고
    • Molecular markers for cell types of the inner ear and candidate genes for hearing disorders
    • Heller S., Sheane C. A., Javed Z., Hudspeth A. J. Molecular markers for cell types of the inner ear and candidate genes for hearing disorders. Proc. Natl. Acad. Sci. USA. 95:1998;11400-11405.
    • (1998) Proc. Natl. Acad. Sci. USA , vol.95 , pp. 11400-11405
    • Heller, S.1    Sheane, C.A.2    Javed, Z.3    Hudspeth, A.J.4
  • 12
    • 0028843286 scopus 로고
    • Gap junctions in the rat cochlea: Immunohistochemical and ultrastructural analysis
    • Kikuchi T., Kimura R. S., Paul D. L., Adams J. C. Gap junctions in the rat cochlea: Immunohistochemical and ultrastructural analysis. Anat. Embryol. 191:1995;101-118.
    • (1995) Anat. Embryol. , vol.191 , pp. 101-118
    • Kikuchi, T.1    Kimura, R.S.2    Paul, D.L.3    Adams, J.C.4
  • 15
    • 0029985259 scopus 로고    scopus 로고
    • Assignment of connexin 26 (GJB2) and 46 (GJA3) genes to human chromosome 13q11 → q12 and mouse chromosome 14D1-E1 by in situ hybridization
    • Mignon C., Fromaget C., Mattei M. G., Gros D., Yamasaki H., Mesnil M. Assignment of connexin 26 (GJB2) and 46 (GJA3) genes to human chromosome 13q11 → q12 and mouse chromosome 14D1-E1 by in situ hybridization. Cytogenet. Cell Genet. 72:1996;185-186.
    • (1996) Cytogenet. Cell Genet. , vol.72 , pp. 185-186
    • Mignon, C.1    Fromaget, C.2    Mattei, M.G.3    Gros, D.4    Yamasaki, H.5    Mesnil, M.6
  • 17
    • 0031722150 scopus 로고    scopus 로고
    • Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma
    • Richard G., White T. W., Smith L. E., Bailey R. A., Compton J. G., Paul D. L., Bale S. J. Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma. Hum. Genet. 103:1998;393-399.
    • (1998) Hum. Genet. , vol.103 , pp. 393-399
    • Richard, G.1    White, T.W.2    Smith, L.E.3    Bailey, R.A.4    Compton, J.G.5    Paul, D.L.6    Bale, S.J.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.