Kimberling WJ - Search Results

1

Isolation of a novel human homologue of the gene coding for echinoderm microtubule-associated protein (EMAP) from the Usher syndrome type 1a locus at 14q32.

Eudy JD, Ma-Edmonds M, Yao SF, Talmadge CB, Kelley PM, Weston MD, Kimberling WJ, Sumegi J. Eudy JD, et al. Among authors: kimberling wj. Genomics. 1997 Jul 1;43(1):104-6. doi: 10.1006/geno.1997.4779. Genomics. 1997. PMID: 9226380

2

Identification of the mouse and rat orthologs of the gene mutated in Usher syndrome type IIA and the cellular source of USH2A mRNA in retina, a target tissue of the disease.

Huang D, Eudy JD, Uzvolgyi E, Davis JR, Talmadge CB, Pretto D, Weston MD, Lehman JE, Zhou M, Seemayer TA, Ahmad I, Kimberling WJ, Sumegi J. Huang D, et al. Among authors: kimberling wj. Genomics. 2002 Aug;80(2):195-203. doi: 10.1006/geno.2002.6823. Genomics. 2002. PMID: 12160733

3

Narrowing the genetic interval and yeast artificial chromosome map in the branchio-oto-renal region on chromosome 8q.

Kumar S, Kimberling WJ, Lanyi A, Sumegi J, Pinnt J, Ing P, Tinley S, Marres HA, Cremers CW. Kumar S, et al. Among authors: kimberling wj. Genomics. 1996 Jan 1;31(1):71-9. doi: 10.1006/geno.1996.0011. Genomics. 1996. PMID: 8808282 Free article.

4

Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients.

Weston MD, Kelley PM, Overbeck LD, Wagenaar M, Orten DJ, Hasson T, Chen ZY, Corey D, Mooseker M, Sumegi J, Cremers C, Moller C, Jacobson SG, Gorin MB, Kimberling WJ. Weston MD, et al. Among authors: kimberling wj. Am J Hum Genet. 1996 Nov;59(5):1074-83. Am J Hum Genet. 1996. PMID: 8900236 Free PMC article.

5

The genomic structure of the gene defective in Usher syndrome type Ib (MYO7A).

Kelley PM, Weston MD, Chen ZY, Orten DJ, Hasson T, Overbeck LD, Pinnt J, Talmadge CB, Ing P, Mooseker MS, Corey D, Sumegi J, Kimberling WJ. Kelley PM, et al. Among authors: kimberling wj. Genomics. 1997 Feb 15;40(1):73-9. doi: 10.1006/geno.1996.4545. Genomics. 1997. PMID: 9070921 Free article.

6

Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.

Eudy JD, Weston MD, Yao S, Hoover DM, Rehm HL, Ma-Edmonds M, Yan D, Ahmad I, Cheng JJ, Ayuso C, Cremers C, Davenport S, Moller C, Talmadge CB, Beisel KW, Tamayo M, Morton CC, Swaroop A, Kimberling WJ, Sumegi J. Eudy JD, et al. Among authors: kimberling wj. Science. 1998 Jun 12;280(5370):1753-7. doi: 10.1126/science.280.5370.1753. Science. 1998. PMID: 9624053

7

Isolation of a gene encoding a novel member of the nuclear receptor superfamily from the critical region of Usher syndrome type IIa at 1q41.

Eudy JD, Yao S, Weston MD, Ma-Edmonds M, Talmadge CB, Cheng JJ, Kimberling WJ, Sumegi J. Eudy JD, et al. Among authors: kimberling wj. Genomics. 1998 Jun 15;50(3):382-4. doi: 10.1006/geno.1998.5345. Genomics. 1998. PMID: 9676434 No abstract available.

8

Human connexin 30 (GJB6), a candidate gene for nonsyndromic hearing loss: molecular cloning, tissue-specific expression, and assignment to chromosome 13q12.

Kelley PM, Abe S, Askew JW, Smith SD, Usami Si, Kimberling WJ. Kelley PM, et al. Among authors: kimberling wj. Genomics. 1999 Dec 1;62(2):172-6. doi: 10.1006/geno.1999.6002. Genomics. 1999. PMID: 10610709

9

Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11.

Kimberling WJ, Möller CG, Davenport S, Priluck IA, Beighton PH, Greenberg J, Reardon W, Weston MD, Kenyon JB, Grunkemeyer JA, et al. Kimberling WJ, et al. Genomics. 1992 Dec;14(4):988-94. doi: 10.1016/s0888-7543(05)80121-1. Genomics. 1992. PMID: 1478677

10

Localization of Usher syndrome type II to chromosome 1q.

Kimberling WJ, Weston MD, Möller C, Davenport SL, Shugart YY, Priluck IA, Martini A, Milani M, Smith RJ. Kimberling WJ, et al. Genomics. 1990 Jun;7(2):245-9. doi: 10.1016/0888-7543(90)90546-7. Genomics. 1990. PMID: 2347588

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