Steel KP - Search Results

1

Myosin VIIA gene: heterogeneity of the mutations responsible for Usher syndrome type IB.

Lévy G, Levi-Acobas F, Blanchard S, Gerber S, Larget-Piet D, Chenal V, Liu XZ, Newton V, Steel KP, Brown SD, Munnich A, Kaplan J, Petit C, Weil D. Lévy G, et al. Among authors: steel kp. Hum Mol Genet. 1997 Jan;6(1):111-6. doi: 10.1093/hmg/6.1.111. Hum Mol Genet. 1997. PMID: 9002678

2

Close linkage of the olfactory marker protein gene to the mouse deafness mutation shaker-1.

Brown KA, Sutcliffe MJ, Steel KP, Brown SD. Brown KA, et al. Among authors: steel kp. Genomics. 1992 May;13(1):189-93. doi: 10.1016/0888-7543(92)90219-i. Genomics. 1992. PMID: 1349573

3

Gene linkage and genetic deafness.

Cremers CW, Brown SD, Steel KP, Brunner HG, Read AP, Kimberling WJ. Cremers CW, et al. Among authors: steel kp. Int J Pediatr Otorhinolaryngol. 1995 Jun;32 Suppl:S167-74. doi: 10.1016/0165-5876(94)01154-p. Int J Pediatr Otorhinolaryngol. 1995. PMID: 7665287 No abstract available.

4

Genetic deafness--progress with mouse models.

Brown SD, Steel KP. Brown SD, et al. Among authors: steel kp. Hum Mol Genet. 1994;3 Spec No:1453-6. doi: 10.1093/hmg/3.suppl_1.1453. Hum Mol Genet. 1994. PMID: 7849737 Review.

5

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: steel kp. Nature. 1995 Mar 2;374(6517):62-4. doi: 10.1038/374062a0. Nature. 1995. PMID: 7870172

6

Genes and deafness.

Steel KP, Brown SD. Steel KP, et al. Trends Genet. 1994 Dec;10(12):428-35. doi: 10.1016/0168-9525(94)90113-9. Trends Genet. 1994. PMID: 7871592 Review.

7

Linkage analysis of the whirler deafness gene on mouse chromosome 4.

Fleming J, Rogers MJ, Brown SD, Steel KP. Fleming J, et al. Among authors: steel kp. Genomics. 1994 May 1;21(1):42-8. doi: 10.1006/geno.1994.1222. Genomics. 1994. PMID: 8088814

8

Sequencing of the olfactory marker protein gene in normal and shaker-1 mutant mice.

Brown KA, Sutcliffe MJ, Steel KP, Brown SD. Brown KA, et al. Among authors: steel kp. Mamm Genome. 1994 Jan;5(1):11-4. doi: 10.1007/BF00360561. Mamm Genome. 1994. PMID: 8111122

9

Human olfactory marker protein maps close to tyrosinase and is a candidate gene for Usher syndrome type I.

Evans KL, Fantes J, Simpson C, Arveiler B, Muir W, Fletcher J, van Heyningen V, Steel KP, Brown KA, Brown SD, et al. Evans KL, et al. Among authors: steel kp. Hum Mol Genet. 1993 Feb;2(2):115-8. doi: 10.1093/hmg/2.2.115. Hum Mol Genet. 1993. PMID: 8499899

10

The Sp4H deletion may contain a new locus essential for postimplantation development.

Fleming J, Pearce A, Brown SD, Steel KP. Fleming J, et al. Among authors: steel kp. Genomics. 1996 Jun 1;34(2):205-12. doi: 10.1006/geno.1996.0267. Genomics. 1996. PMID: 8661050

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