P01 DC01813/DC/NIDCD NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1994	1
1996	4
1998	4
1999	4
2000	4
2001	1
2002	2
2003	1
2004	4
2005	2
2008	3
2009	1
2012	1
2024	0

1

Sensorineural hearing loss associated with the mitochondrial mutations.

Usami S, Abe S, Akita J, Shinkawa H, Kimberling WJ. Usami S, et al. Adv Otorhinolaryngol. 2000;56:203-11. doi: 10.1159/000059087. Adv Otorhinolaryngol. 2000. PMID: 10868237 Review. No abstract available.

2

Sensorineural hearing loss caused by mitochondrial DNA mutations: special reference to the A1555G mutation.

Usami S, Abe S, Shinkawa H, Kimberling WJ. Usami S, et al. J Commun Disord. 1998 Sep-Oct;31(5):423-34; quiz 434-5. doi: 10.1016/s0021-9924(98)00014-8. J Commun Disord. 1998. PMID: 9777488 Review.

3

Mutation screening of the PCDH15 gene in Spanish patients with Usher syndrome type I.

Jaijo T, Oshima A, Aller E, Carney C, Usami S, Millán JM, Kimberling WJ. Jaijo T, et al. Mol Vis. 2012;18:1719-26. Epub 2012 Jun 23. Mol Vis. 2012. PMID: 22815625 Free PMC article.

4

Variable clinical features in patients with CDH23 mutations (USH1D-DFNB12).

Pennings RJ, Topsakal V, Astuto L, de Brouwer AP, Wagenaar M, Huygen PL, Kimberling WJ, Deutman AF, Kremer H, Cremers CW. Pennings RJ, et al. Otol Neurotol. 2004 Sep;25(5):699-706. doi: 10.1097/00129492-200409000-00009. Otol Neurotol. 2004. PMID: 15353998

5

Collagen COL4A3 knockout: a mouse model for autosomal Alport syndrome.

Cosgrove D, Meehan DT, Grunkemeyer JA, Kornak JM, Sayers R, Hunter WJ, Samuelson GC. Cosgrove D, et al. Genes Dev. 1996 Dec 1;10(23):2981-92. doi: 10.1101/gad.10.23.2981. Genes Dev. 1996. PMID: 8956999 Free article.

6

Immunohistochemical localization of basement membrane collagens and associated proteins in the murine cochlea.

Cosgrove D, Samuelson G, Pinnt J. Cosgrove D, et al. Hear Res. 1996 Aug;97(1-2):54-65. Hear Res. 1996. PMID: 8844186

7

Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I.

Astuto LM, Weston MD, Carney CA, Hoover DM, Cremers CW, Wagenaar M, Moller C, Smith RJ, Pieke-Dahl S, Greenberg J, Ramesar R, Jacobson SG, Ayuso C, Heckenlively JR, Tamayo M, Gorin MB, Reardon W, Kimberling WJ. Astuto LM, et al. Am J Hum Genet. 2000 Dec;67(6):1569-74. doi: 10.1086/316889. Epub 2000 Nov 1. Am J Hum Genet. 2000. PMID: 11060213 Free PMC article.

8

Localization and expression of usherin: a novel basement membrane protein defective in people with Usher's syndrome type IIa.

Bhattacharya G, Miller C, Kimberling WJ, Jablonski MM, Cosgrove D. Bhattacharya G, et al. Hear Res. 2002 Jan;163(1-2):1-11. doi: 10.1016/s0378-5955(01)00344-6. Hear Res. 2002. PMID: 11788194

9

Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family.

Hmani-Aifa M, Benzina Z, Zulfiqar F, Dhouib H, Shahzadi A, Ghorbel A, Rebaï A, Söderkvist P, Riazuddin S, Kimberling WJ, Ayadi H. Hmani-Aifa M, et al. Eur J Hum Genet. 2009 Apr;17(4):474-82. doi: 10.1038/ejhg.2008.167. Epub 2008 Oct 15. Eur J Hum Genet. 2009. PMID: 18854872 Free PMC article.

10

Usher syndrome type III can mimic other types of Usher syndrome.

Pennings RJ, Fields RR, Huygen PL, Deutman AF, Kimberling WJ, Cremers CW. Pennings RJ, et al. Ann Otol Rhinol Laryngol. 2003 Jun;112(6):525-30. doi: 10.1177/000348940311200608. Ann Otol Rhinol Laryngol. 2003. PMID: 12834121

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