Walsh J - Search Results

1

Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene.

Liu XZ, Walsh J, Tamagawa Y, Kitamura K, Nishizawa M, Steel KP, Brown SD. Liu XZ, et al. Among authors: walsh j. Nat Genet. 1997 Nov;17(3):268-9. doi: 10.1038/ng1197-268. Nat Genet. 1997. PMID: 9354784 No abstract available.

2

Mutations in the myosin VIIA gene cause non-syndromic recessive deafness.

Liu XZ, Walsh J, Mburu P, Kendrick-Jones J, Cope MJ, Steel KP, Brown SD. Liu XZ, et al. Among authors: walsh j. Nat Genet. 1997 Jun;16(2):188-90. doi: 10.1038/ng0697-188. Nat Genet. 1997. PMID: 9171832

3

A type VII myosin encoded by the mouse deafness gene shaker-1.

Gibson F, Walsh J, Mburu P, Varela A, Brown KA, Antonio M, Beisel KW, Steel KP, Brown SD. Gibson F, et al. Among authors: walsh j. Nature. 1995 Mar 2;374(6517):62-4. doi: 10.1038/374062a0. Nature. 1995. PMID: 7870172

4

Mutation analysis of the mouse myosin VIIA deafness gene.

Mburu P, Liu XZ, Walsh J, Saw D Jr, Cope MJ, Gibson F, Kendrick-Jones J, Steel KP, Brown SD. Mburu P, et al. Among authors: walsh j. Genes Funct. 1997 Jun;1(3):191-203. doi: 10.1046/j.1365-4624.1997.00020.x. Genes Funct. 1997. PMID: 9680294

5

Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome.

Liu XZ, Hope C, Walsh J, Newton V, Ke XM, Liang CY, Xu LR, Zhou JM, Trump D, Steel KP, Bundey S, Brown SD. Liu XZ, et al. Among authors: walsh j. Am J Hum Genet. 1998 Sep;63(3):909-12. doi: 10.1086/302026. Am J Hum Genet. 1998. PMID: 9718356 Free PMC article. No abstract available.

6

Effects of shaker-1 mutations on myosin-VIIa protein and mRNA expression.

Hasson T, Walsh J, Cable J, Mooseker MS, Brown SD, Steel KP. Hasson T, et al. Among authors: walsh j. Cell Motil Cytoskeleton. 1997;37(2):127-38. doi: 10.1002/(SICI)1097-0169(1997)37:2<127::AID-CM5>3.0.CO;2-5. Cell Motil Cytoskeleton. 1997. PMID: 9186010

7

Sensorineural hearing impairment non-syndromic, dominant DFNA11.

Tamagawa Y, Kitamura K, Ishida T, Nishizawa M, Liu XZ, Walsh J, Steel KP, Brown SD. Tamagawa Y, et al. Among authors: walsh j. Adv Otorhinolaryngol. 2000;56:103-6. doi: 10.1159/000059092. Adv Otorhinolaryngol. 2000. PMID: 10868221 No abstract available.

8

Unravelling the genetics of deafness.

Steel KP, Mburu P, Gibson F, Walsh J, Varela A, Brown K, Self T, Mahony M, Fleming J, Pearce A, Harvey D, Cable J, Brown SD. Steel KP, et al. Among authors: walsh j. Ann Otol Rhinol Laryngol Suppl. 1997 May;168:59-62. Ann Otol Rhinol Laryngol Suppl. 1997. PMID: 9153119 Review.

9

Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells.

Self T, Mahony M, Fleming J, Walsh J, Brown SD, Steel KP. Self T, et al. Among authors: walsh j. Development. 1998 Feb;125(4):557-66. doi: 10.1242/dev.125.4.557. Development. 1998. PMID: 9435277

10

Defective myosin VIIA gene responsible for Usher syndrome type 1B.

Weil D, Blanchard S, Kaplan J, Guilford P, Gibson F, Walsh J, Mburu P, Varela A, Levilliers J, Weston MD, et al. Weil D, et al. Among authors: walsh j. Nature. 1995 Mar 2;374(6517):60-1. doi: 10.1038/374060a0. Nature. 1995. PMID: 7870171

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