Unconventional myosins, the basis for deafness in mouse and man

被引：25

作者：

Hasson, T

机构：

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 1997年 / 61卷 / 04期

关键词：

D O I：

10.1086/514890

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：801 / 805

页数：5

共 29 条

[1] Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins [J].

Adato, A ;

Weil, D ;

Kalinski, H ;

PelOr, Y ;

Ayadi, H ;

Petit, C ;

Korostishevsky, M ;

BonneTamir, B .

AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) :813-821

[2] Characterization of unconventional MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice [J].

Avraham, KB ;

Hasson, T ;

Sobe, T ;

Balsara, B ;

Testa, JR ;

Skvorak, AB ;

Morton, CC ;

Copeland, NG ;

Jenkins, NA .

HUMAN MOLECULAR GENETICS, 1997, 6 (08) :1225-1231

[3] THE MOUSE SNELLS WALTZER DEAFNESS GENE ENCODES AN UNCONVENTIONAL MYOSIN REQUIRED FOR STRUCTURAL INTEGRITY OF INNER-EAR HAIR-CELLS [J].

AVRAHAM, KB ;

HASSON, T ;

STEEL, KP ;

KINGSLEY, DM ;

RUSSELL, LB ;

MOOSEKER, MS ;

COPELAND, NG ;

JENKINS, NA .

NATURE GENETICS, 1995, 11 (04) :369-375

[4] CLOSE LINKAGE OF THE OLFACTORY MARKER PROTEIN GENE TO THE MOUSE DEAFNESS MUTATION SHAKER-1 [J].

BROWN, KA ;

SUTCLIFFE, MJ ;

STEEL, KP ;

BROWN, SDM .

GENOMICS, 1992, 13 (01) :189-193

[5] Molecular cloning and domain structure of human myosin-VIIa. The gene product defective in usher syndrome 1B [J].

Chen, ZY ;

Hasson, T ;

Kelley, PM ;

Schwender, BJ ;

Schwartz, MF ;

Ramakrishnan, M ;

Kimberling, WJ ;

Mooseker, MS ;

Corey, DP .

GENOMICS, 1996, 36 (03) :440-448

[6] Cloning of the genes encoding two murine and human cochlear unconventional type I myosins [J].

Crozet, F ;

ElAmraoui, A ;

Blanchard, S ;

Lenoir, M ;

Ripoll, C ;

Vago, P ;

Hamel, C ;

Fizames, C ;

LeviAcobas, F ;

Depetris, D ;

Mattei, MG ;

Weil, D ;

Pujol, R ;

Petit, C .

GENOMICS, 1997, 40 (02) :332-341

[7] Human Usher 1B mouse shaker-1: The retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells [J].

ElAmraoui, A ;

Sahly, I ;

Picaud, S ;

Sahel, J ;

Abitbol, M ;

Petit, C .

HUMAN MOLECULAR GENETICS, 1996, 5 (08) :1171-1178

[8] A TYPE-VII MYOSIN ENCODED BY THE MOUSE DEAFNESS GENE SHAKER-1 [J].

GIBSON, F ;

WALSH, J ;

MBURU, P ;

VARELA, A ;

BROWN, KA ;

ANTONIO, M ;

BEISEL, KW ;

STEEL, KP ;

BROWN, SDM .

NATURE, 1995, 374 (6517) :62-64

[9]

Gillespie PG, 1996, COLD SPRING HARB SYM, V61, P309

[10] Vertebrate unconventional myosins [J].

Hasson, T ;

Mooseker, MS .

JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (28) :16431-16434

← 1 2 3 →