Two deaf mice, two deaf mice ...

被引：7

作者：

Heller, S ^{[1
]}

Hudspeth, AJ

机构：

[1] Rockefeller Univ, Howard Hughes Med Inst, New York, NY 10021 USA

[2] Rockefeller Univ, Lab Sensory Neurosci, New York, NY 10021 USA

来源：

NATURE MEDICINE | 1998年 / 4卷 / 05期

关键词：

D O I：

10.1038/nm0598-560

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

Murine candidate genes pinpoint the genetic bases of nonsyndromic hearing loss in humans.

引用

页码：560 / 561

页数：2

共 8 条

[1] Role of transcription factors Brn-3.1 and Brn-3.2 in auditory and visual system development [J].

Erkman, L ;

McEvilly, RJ ;

Luo, L ;

Ryan, AK ;

Hooshmand, F ;

OConnell, SM ;

Keithley, EM ;

Rapaport, DH ;

Ryan, AF ;

Rosenfeld, MG .

NATURE, 1996, 381 (6583) :603-606

[2]

LUYNCH ED, 1997, SCIENCE, V278, P1315

[3] Genetic analysis of vertebrate sensory hair cell mechanosensation:: the zebrafish circler mutants [J].

Nicolson, T ;

Rüsch, A ;

Friedrich, RW ;

Granato, M ;

Ruppersberg, JP ;

Nüsslein-Volhard, C .

NEURON, 1998, 20 (02) :271-283

[4]

Steel KP, 1995, ANNU REV GENET, V29, P675

[5] Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans [J].

Vahava, O ;

Morell, R ;

Lynch, ED ;

Weiss, S ;

Kagan, ME ;

Ahituv, N ;

Morrow, JE ;

Lee, MK ;

Skvorak, AB ;

Morton, CC ;

Blumenfeld, A ;

Frydman, M ;

Friedman, TB ;

King, MC ;

Avraham, KB .

SCIENCE, 1998, 279 (5358) :1950-1954

[6]

VANCAMP C, 1998, HEREDITARY HEARING L

[7]

VanCamp G, 1997, AM J HUM GENET, V60, P758

[8] Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment [J].

Verhoeven, K ;

Van Laer, L ;

Kirschhofer, K ;

Legan, PK ;

Hughes, DC ;

Schatteman, I ;

Verstreken, M ;

Van Hauwe, P ;

Coucke, P ;

Chen, A ;

Smith, RJH ;

Somers, T ;

Offeciers, FE ;

Van de Heyning, P ;

Richardson, GP ;

Wachtler, F ;

Kimberling, WT ;

Willems, PJ ;

Govaerts, PJ ;

Van Camp, G .

NATURE GENETICS, 1998, 19 (01) :60-62

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