메뉴 건너뛰기




Volumn 3, Issue 6, 1997, Pages 608-609

Motors, channels and the sounds of silence

Author keywords

[No Author keywords available]

Indexed keywords

GAP JUNCTION PROTEIN; GENE PRODUCT; MYOSIN;

EID: 0030953144     PISSN: 10788956     EISSN: None     Source Type: Journal    
DOI: 10.1038/nm0697-608     Document Type: Short Survey
Times cited : (3)

References (11)
  • 1
    • 0031007349 scopus 로고    scopus 로고
    • Connexin 26 mutations in hereditary non-syndromic sensorineural deafness (DFNA3 and DFNB1)
    • Kelsell, D. P. et al. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness (DFNA3 and DFNB1). Nature 387, 80-83 (1997).
    • (1997) Nature , vol.387 , pp. 80-83
    • Kelsell, D.P.1
  • 2
    • 0030960855 scopus 로고    scopus 로고
    • Mutations in the myosin VIIA gene cause non-syndromic recessive deafness
    • Liu, X.-Z. et al. Mutations in the myosin VIIA gene cause non-syndromic recessive deafness. Nature Genet. 16, 188-190 (1997).
    • (1997) Nature Genet. , vol.16 , pp. 188-190
    • Liu, X.-Z.1
  • 3
    • 0030951102 scopus 로고    scopus 로고
    • The autosomal recessive isolated deafness, DFNB2, and the Usher IB syndrome are allelic defects of the myosin VIIA gene
    • Weil, D. et al. The autosomal recessive isolated deafness, DFNB2, and the Usher IB syndrome are allelic defects of the myosin VIIA gene. Nature Cenet. 16, 191-193 (1997).
    • (1997) Nature Cenet. , vol.16 , pp. 191-193
    • Weil, D.1
  • 4
    • 0026409026 scopus 로고
    • Genetics of hearing impairment
    • Waelsch, S. G. Genetics of hearing impairment. Ann. NY Acad. Sci. 630, 3-5 (1991).
    • (1991) Ann. NY Acad. Sci. , vol.630 , pp. 3-5
    • Waelsch, S.G.1
  • 5
    • 0026410464 scopus 로고
    • Genetic epidemiology of hearing impairment
    • Morton, N. E. Genetic epidemiology of hearing impairment. Ann. NY Acad. Sci. 630, 16-31 (1991).
    • (1991) Ann. NY Acad. Sci. , vol.630 , pp. 16-31
    • Morton, N.E.1
  • 6
    • 0028860302 scopus 로고
    • A type VII myosin encoded by the mouse deafness gene shaker-1
    • Gibson, F. et al. A type VII myosin encoded by the mouse deafness gene shaker-1. Nature 374, 62-64 (1995).
    • (1995) Nature , vol.374 , pp. 62-64
    • Gibson, F.1
  • 7
    • 0028803112 scopus 로고
    • The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for the structural integrity of inner ear hair cells
    • Avraham, K. B. et al. The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for the structural integrity of inner ear hair cells. Nature Cenet. 11, 369-375 (1995).
    • (1995) Nature Cenet. , vol.11 , pp. 369-375
    • Avraham, K.B.1
  • 8
    • 0028815440 scopus 로고
    • Defective myosin VIIA gene responsible for Usher syndrome type 1B
    • Weil, D. et al. Defective myosin VIIA gene responsible for Usher syndrome type 1B. Nature 374, 60-61 (1995).
    • (1995) Nature , vol.374 , pp. 60-61
    • Weil, D.1
  • 9
    • 0030973305 scopus 로고    scopus 로고
    • Unconventional myosins in inner ear sensory epithelia
    • in press
    • Hasson, T. et al. Unconventional myosins in inner ear sensory epithelia. J. Cell Biol. (1997) in press.
    • (1997) J. Cell Biol.
    • Hasson, T.1
  • 10
    • 0028843286 scopus 로고
    • Gap junctions in the rat cochlea: Immuno-histochemical and ultrastructural analysis
    • Kikuchi, T., Kimura, R. S., Paul, D. L. & Adams, J. C. Gap junctions in the rat cochlea: immuno-histochemical and ultrastructural analysis. Anat. Embryol. 191, 101-118 (1995).
    • (1995) Anat. Embryol. , vol.191 , pp. 101-118
    • Kikuchi, T.1    Kimura, R.S.2    Paul, D.L.3    Adams, J.C.4
  • 11
    • 16944366498 scopus 로고
    • Deaf is beautiful
    • August 28, section 6
    • Solomon, A. Deaf is beautiful. N.Y. Times Magazine. August 28, section 6(1994).
    • (1994) N.Y. Times Magazine
    • Solomon, A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.