Keating MT - Search Results

1

Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.

Splawski I, Shen J, Timothy KW, Vincent GM, Lehmann MH, Keating MT. Splawski I, et al. Among authors: keating mt. Genomics. 1998 Jul 1;51(1):86-97. doi: 10.1006/geno.1998.5361. Genomics. 1998. PMID: 9693036

2

Compound mutations: a common cause of severe long-QT syndrome.

Westenskow P, Splawski I, Timothy KW, Keating MT, Sanguinetti MC. Westenskow P, et al. Among authors: keating mt. Circulation. 2004 Apr 20;109(15):1834-41. doi: 10.1161/01.CIR.0000125524.34234.13. Epub 2004 Mar 29. Circulation. 2004. PMID: 15051636

3

An intronic mutation causes long QT syndrome.

Zhang L, Vincent GM, Baralle M, Baralle FE, Anson BD, Benson DW, Whiting B, Timothy KW, Carlquist J, January CT, Keating MT, Splawski I. Zhang L, et al. Among authors: keating mt. J Am Coll Cardiol. 2004 Sep 15;44(6):1283-91. doi: 10.1016/j.jacc.2004.06.045. J Am Coll Cardiol. 2004. PMID: 15364333 Free article.

4

The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome.

Vincent GM, Timothy KW, Leppert M, Keating M. Vincent GM, et al. N Engl J Med. 1992 Sep 17;327(12):846-52. doi: 10.1056/NEJM199209173271204. N Engl J Med. 1992. PMID: 1508244 Free article.

5

Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene.

Keating M, Atkinson D, Dunn C, Timothy K, Vincent GM, Leppert M. Keating M, et al. Science. 1991 May 3;252(5006):704-6. doi: 10.1126/science.1673802. Science. 1991. PMID: 1673802

6

Consistent linkage of the long-QT syndrome to the Harvey ras-1 locus on chromosome 11.

Keating M, Dunn C, Atkinson D, Timothy K, Vincent GM, Leppert M. Keating M, et al. Am J Hum Genet. 1991 Dec;49(6):1335-9. Am J Hum Genet. 1991. PMID: 1746560 Free PMC article.

7

Locus heterogeneity of autosomal dominant long QT syndrome.

Curran M, Atkinson D, Timothy K, Vincent GM, Moss AJ, Leppert M, Keating M. Curran M, et al. J Clin Invest. 1993 Aug;92(2):799-803. doi: 10.1172/JCI116653. J Clin Invest. 1993. PMID: 8102381 Free PMC article.

8

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome.

Curran ME, Splawski I, Timothy KW, Vincent GM, Green ED, Keating MT. Curran ME, et al. Among authors: keating mt. Cell. 1995 Mar 10;80(5):795-803. doi: 10.1016/0092-8674(95)90358-5. Cell. 1995. PMID: 7889573 Free article.

9

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome.

Wang Q, Shen J, Splawski I, Atkinson D, Li Z, Robinson JL, Moss AJ, Towbin JA, Keating MT. Wang Q, et al. Among authors: keating mt. Cell. 1995 Mar 10;80(5):805-11. doi: 10.1016/0092-8674(95)90359-3. Cell. 1995. PMID: 7889574 Free article.

10

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias.

Wang Q, Curran ME, Splawski I, Burn TC, Millholland JM, VanRaay TJ, Shen J, Timothy KW, Vincent GM, de Jager T, Schwartz PJ, Toubin JA, Moss AJ, Atkinson DL, Landes GM, Connors TD, Keating MT. Wang Q, et al. Among authors: keating mt. Nat Genet. 1996 Jan;12(1):17-23. doi: 10.1038/ng0196-17. Nat Genet. 1996. PMID: 8528244

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