메뉴 건너뛰기




Volumn 942, Issue , 2001, Pages 493-496

Hereditary familial vestibular degenerative diseases

Author keywords

[No Author keywords available]

Indexed keywords

CONFERENCE PAPER; CONTROLLED STUDY; FAMILIAL DISEASE; GENETIC DISORDER; HAIR CELL; HUMAN; MOUSE; NONHUMAN; USHER SYNDROME; VESTIBULAR DISORDER; VESTIBULAR FUNCTION; VESTIBULAR NERVE;

EID: 0034751578     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.2001.tb03779.x     Document Type: Conference Paper
Times cited : (3)

References (30)
  • 1
    • 0030960855 scopus 로고    scopus 로고
    • Mutations in the myosin VIIA gene cause non-syndromic recessive deafness
    • (1997) Nat. Genet. , vol.16 , pp. 188-190
    • Liu, X.Z.1
  • 2
    • 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
  • 3
    • 17644442703 scopus 로고    scopus 로고
    • Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene
    • (1998) Science , vol.280 , pp. 1444-1447
    • Probst, F.J.1
  • 4
    • 0031007349 scopus 로고    scopus 로고
    • Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
    • (1997) Nature , vol.387 , pp. 80-83
    • Kelsell, D.P.1
  • 5
    • 17344373747 scopus 로고    scopus 로고
    • Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment
    • (1998) Nat. Genet. , vol.20 , pp. 370-373
    • Xia, J.H.1
  • 6
    • 0028988233 scopus 로고
    • Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4
    • (1995) Science , vol.267 , pp. 685-688
    • De Kok, Y.J.1
  • 7
    • 7144257859 scopus 로고    scopus 로고
    • Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans
    • (1998) Science , vol.279 , pp. 1950-1954
    • Vahava, O.1
  • 8
    • 17344364928 scopus 로고    scopus 로고
    • Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment
    • (1998) Nat. Genet. , vol.19 , pp. 60-62
    • Verhoeven, K.1
  • 9
    • 0032977996 scopus 로고    scopus 로고
    • An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21
    • (1999) Hum. Mol. Genet. , vol.8 , pp. 409-412
    • Mustapha, M.1
  • 10
    • 17344363707 scopus 로고    scopus 로고
    • Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction
    • (1998) Nat. Genet. , vol.20 , pp. 299-303
    • Robertson, N.G.1
  • 11
    • 0032011145 scopus 로고    scopus 로고
    • A mutation in PDS causes non-syndromic recessive deafness
    • (1998) Nat. Genet. , vol.18 , pp. 215-217
    • Li, X.C.1
  • 12
    • 0027226069 scopus 로고
    • Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness
    • (1993) Nat. Genet. , vol.4 , pp. 289-294
    • Prezant, T.R.1
  • 13
    • 0028815440 scopus 로고
    • Defective myosin VIIA gene responsible for Usher syndrome type 1B
    • (1995) Nature , vol.374 , pp. 60-61
    • Weil, D.1
  • 15
    • 0028860302 scopus 로고
    • A type VII myosin encoded by the mouse deafness gene shaker-1
    • (1995) Nature , vol.374 , pp. 62-64
    • Gibson, F.1
  • 16
    • 7944229728 scopus 로고
    • Retinitis pigmentosa combined with congenital deafness; with vestibulo-cerebellar ataxia and mental abnormality in a proportion of cases: A clinical and genetic statistic study
    • (1959) Acta Psychiatr. Scand. , vol.34 , pp. 5-101
    • Hallgren, B.1
  • 22
    • 0000870234 scopus 로고
    • The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse
    • (1956) Proc. R. Soc. Lond. B , vol.145 , pp. 206-213
    • Deol, M.S.1
  • 24
    • 0030973305 scopus 로고    scopus 로고
    • Unconventional myosins in inner-ear sensory epithelia
    • (1997) J. Cell Biol. , vol.137 , pp. 1287-1307
    • Hasson, T.1
  • 26
    • 0031865677 scopus 로고    scopus 로고
    • Oculomotor testing in the differential diagnosis of degenerative ataxic disorders
    • (1998) Arch. Neurol. , vol.55 , pp. 949-956
    • Wessel, K.1
  • 27
    • 0028256473 scopus 로고
    • Oculomotor abnormalities and MRI findings in idiopathic cerebellar ataxia
    • (1994) J. Neurol. , vol.241 , pp. 234-241
    • Fetter, M.1
  • 28
    • 0031151943 scopus 로고    scopus 로고
    • Gain adaptation and phase dynamics of compensatory eye movements in mice
    • (1997) Genes Funct. , vol.1 , pp. 175-190
    • Koekkoek, S.K.1
  • 29
    • 0028784445 scopus 로고
    • Phase relations of Purkinje cells in the rabbit flocculus during compensatory eye movements
    • (1995) J. Neurophysiol. , vol.74 , pp. 2051-2064
    • De Zeeuw, C.I.1
  • 30
    • 0030057741 scopus 로고    scopus 로고
    • Pattern of selected calcium-binding proteins in the vestibular nuclear complex of two rodent species
    • (1996) J. Comp. Neurol. , vol.365 , pp. 575-584
    • Kevetter, G.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.