Keats BJ - Search Results

1

Genetic variation of recent Alu insertions in human populations.

Batzer MA, Arcot SS, Phinney JW, Alegria-Hartman M, Kass DH, Milligan SM, Kimpton C, Gill P, Hochmeister M, Ioannou PA, Herrera RJ, Boudreau DA, Scheer WD, Keats BJ, Deininger PL, Stoneking M. Batzer MA, et al. Among authors: keats bj. J Mol Evol. 1996 Jan;42(1):22-9. doi: 10.1007/BF00163207. J Mol Evol. 1996. PMID: 8576959

2

Phylogenetic analysis of the Friedreich ataxia GAA trinucleotide repeat.

Justice CM, Den Z, Nguyen SV, Stoneking M, Deininger PL, Batzer MA, Keats BJ. Justice CM, et al. Among authors: keats bj. J Mol Evol. 2001 Mar;52(3):232-8. doi: 10.1007/s002390010151. J Mol Evol. 2001. PMID: 11428460

3

Analysis of CAG repeat of the Machado-Joseph gene in human, chimpanzee and monkey populations: a variant nucleotide is associated with the number of CAG repeats.

Limprasert P, Nouri N, Heyman RA, Nopparatana C, Kamonsilp M, Deininger PL, Keats BJ. Limprasert P, et al. Among authors: keats bj. Hum Mol Genet. 1996 Feb;5(2):207-13. doi: 10.1093/hmg/5.2.207. Hum Mol Genet. 1996. PMID: 8824876

4

Structure, diversity, and evolution of the 45-bp VNTR in intron 5 of the USH1C gene.

Savas S, Frischhertz B, Batzer MA, Deininger PL, Keats BJ. Savas S, et al. Among authors: keats bj. Genomics. 2004 Mar;83(3):439-44. doi: 10.1016/j.ygeno.2003.09.006. Genomics. 2004. PMID: 14962669

5

Comparative studies of the CAG repeats in the spinocerebellar ataxia type 1 (SCA1) gene.

Limprasert P, Nouri N, Nopparatana C, Deininger PL, Keats BJ. Limprasert P, et al. Among authors: keats bj. Am J Med Genet. 1997 Sep 19;74(5):488-93. doi: 10.1002/(sici)1096-8628(19970919)74:5<488::aid-ajmg6>3.0.co;2-k. Am J Med Genet. 1997. PMID: 9342197

6

Assembly of a high-resolution map of the Acadian Usher syndrome region and localization of the nuclear EF-hand acidic gene.

DeAngelis MM, Doucet JP, Drury S, Sherry ST, Robichaux MB, Den Z, Pelias MZ, Ditta GM, Keats BJ, Deininger PL, Batzer MA. DeAngelis MM, et al. Among authors: keats bj. Biochim Biophys Acta. 1998 Jul 1;1407(1):84-91. doi: 10.1016/s0925-4439(98)00025-8. Biochim Biophys Acta. 1998. PMID: 9639681 Free article.

7

The mouse deafness locus (dn) is associated with an inversion on chromosome 19.

Viñas AM, Drury SS, DeAngelis MM, Den Z, Huang JM, Berlin CI, Hunt JD, Batzer MA, Deininger PL, Keats BJ. Viñas AM, et al. Among authors: keats bj. Biochim Biophys Acta. 1998 Sep 30;1407(3):257-62. doi: 10.1016/s0925-4439(98)00050-7. Biochim Biophys Acta. 1998. PMID: 9748617 Free article.

8

Tightly linked flanking microsatellite markers for the Usher syndrome type I locus on the short arm of chromosome 11.

Keats BJ, Nouri N, Pelias MZ, Deininger PL, Litt M. Keats BJ, et al. Am J Hum Genet. 1994 Apr;54(4):681-6. Am J Hum Genet. 1994. PMID: 8128966 Free PMC article.

9

Identification and mutation analysis of a cochlear-expressed, zinc finger protein gene at the DFNB7/11 and dn hearing-loss loci on human chromosome 9q and mouse chromosome 19.

Scott DA, Greinwald JH Jr, Marietta JR, Drury S, Swiderski RE, Viñas A, DeAngelis MM, Carmi R, Ramesh A, Kraft ML, Elbedour K, Skworak AB, Friedman RA, Srikumari Srisailapathy CR, Verhoeven K, Van Gamp G, Lovett M, Deininger PL, Batzer MA, Morton CC, Keats BJ, Smith RJ, Sheffield VC. Scott DA, et al. Among authors: keats bj. Gene. 1998 Jul 30;215(2):461-9. doi: 10.1016/s0378-1119(98)00316-3. Gene. 1998. PMID: 9758550

10

The USH1C 216G-->A splice-site mutation results in a 35-base-pair deletion.

Lentz J, Savas S, Ng SS, Athas G, Deininger P, Keats B. Lentz J, et al. Hum Genet. 2005 Feb;116(3):225-7. doi: 10.1007/s00439-004-1217-4. Epub 2004 Dec 1. Hum Genet. 2005. PMID: 15578223

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