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Volumn 64, Issue 3, 2000, Pages 189-196

2E4/Kaptin (KPTN) - A candidate gene for the hearing loss locus, DFNA4

Author keywords

[No Author keywords available]

Indexed keywords

ACTIN BINDING PROTEIN; COMPLEMENTARY DNA; KAPTIN; POLYCLONAL ANTIBODY; UNCLASSIFIED DRUG;

EID: 0033811290     PISSN: 00034800     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0003480000008071     Document Type: Article
Times cited : (18)

References (20)
  • 1
    • 0026572374 scopus 로고
    • An actin-associated protein present in the microtubule organizing center and the growth cones of PC-12 cells
    • (1992) J. Neurosci. , vol.12 , Issue.3 , pp. 750-761
    • Bearer, E.L.1
  • 4
    • 0033023110 scopus 로고    scopus 로고
    • 2E4: A novel actin-associated protein from human blood platelets found in lamellipodia and the tips of the stereocilia of the inner ear
    • (1999) Euro. J. Cell Biol. , vol.78 , pp. 117-126
    • Bearer, E.L.1    Abraham, M.2
  • 5
    • 0029031729 scopus 로고
    • Linkage of a gene for dominant non-syndromic deafness to chromosome 19
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 1073-1076
    • Chen, A.H.1
  • 6
    • 0028231090 scopus 로고
    • The 1993-1994 Genethon human genetic linkage map
    • (1994) Nat. Genet. , vol.7 , Issue.2 Spec No , pp. 246-339
    • Gyapay, G.1
  • 9
    • 0026713921 scopus 로고
    • Construction and characterization of radiation hybrids for chromosome 9, and their use in mapping cosmid probes on the chromosome
    • (1992) Som. Cell Molec. Gen. , vol.18 , pp. 285-301
    • Jackson, C.L.1
  • 11
    • 0030707797 scopus 로고    scopus 로고
    • Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous
    • (1997) Science , vol.278 , Issue.5341 , pp. 1315-1318
    • Lynch, E.D.1
  • 15
    • 0029898545 scopus 로고    scopus 로고
    • A gene for a dominant form of non-syndromic sensorineural deafness (DFNA11) maps within the region containing the DFNB2 recessive deafness gene
    • (1996) Hum. Mol. Genet. , vol.5 , Issue.6 , pp. 849-852
    • Tamagawa, Y.1
  • 16
    • 0024251007 scopus 로고
    • Actin filaments, stereocilia, and hair cells of the bird cochlea V. How the staircase pattern of stereociliary length is generated
    • (1988) J. Cell Biol. , vol.107 , pp. 2563-2574
    • Tilney, L.G.1
  • 20
    • 0030951102 scopus 로고    scopus 로고
    • The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene
    • (1997) Nat. Genet. , vol.16 , pp. 191-193
    • Weil, D.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.