Timothy KW - Search Results

1

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: timothy kw. 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.

2

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. Among authors: timothy kw. N Engl J Med. 1992 Sep 17;327(12):846-52. doi: 10.1056/NEJM199209173271204. N Engl J Med. 1992. PMID: 1508244 Free article.

3

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

4

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.

5

Effects of exercise on heart rate, QT, QTc and QT/QS2 in the Romano-Ward inherited long QT syndrome.

Vincent GM, Jaiswal D, Timothy KW. Vincent GM, et al. Among authors: timothy kw. Am J Cardiol. 1991 Aug 15;68(5):498-503. doi: 10.1016/0002-9149(91)90785-j. Am J Cardiol. 1991. PMID: 1872278

6

Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity.

Jiang C, Atkinson D, Towbin JA, Splawski I, Lehmann MH, Li H, Timothy K, Taggart RT, Schwartz PJ, Vincent GM, et al. Jiang C, et al. Nat Genet. 1994 Oct;8(2):141-7. doi: 10.1038/ng1094-141. Nat Genet. 1994. PMID: 7842012

7

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: timothy kw. Cell. 1995 Mar 10;80(5):795-803. doi: 10.1016/0092-8674(95)90358-5. Cell. 1995. PMID: 7889573 Free article.

8

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.

9

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: timothy kw. Nat Genet. 1996 Jan;12(1):17-23. doi: 10.1038/ng0196-17. Nat Genet. 1996. PMID: 8528244

10

Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.

Wang Q, Shen J, Li Z, Timothy K, Vincent GM, Priori SG, Schwartz PJ, Keating MT. Wang Q, et al. Hum Mol Genet. 1995 Sep;4(9):1603-7. doi: 10.1093/hmg/4.9.1603. Hum Mol Genet. 1995. PMID: 8541846

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