Vincent GM - Search Results

1

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. Among authors: vincent gm. Nat Genet. 1994 Oct;8(2):141-7. doi: 10.1038/ng1094-141. Nat Genet. 1994. PMID: 7842012

2

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

3

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. Among authors: vincent gm. J Clin Invest. 1993 Aug;92(2):799-803. doi: 10.1172/JCI116653. J Clin Invest. 1993. PMID: 8102381 Free PMC article.

4

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

5

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. Among authors: vincent gm. Hum Mol Genet. 1995 Sep;4(9):1603-7. doi: 10.1093/hmg/4.9.1603. Hum Mol Genet. 1995. PMID: 8541846

6

Molecular basis of the long-QT syndrome associated with deafness.

Splawski I, Timothy KW, Vincent GM, Atkinson DL, Keating MT. Splawski I, et al. Among authors: vincent gm. N Engl J Med. 1997 May 29;336(22):1562-7. doi: 10.1056/NEJM199705293362204. N Engl J Med. 1997. PMID: 9164812 Free article. No abstract available.

7

George M. Cober Lecturer: Mark T. Keating. Molecular basis of the long-QT syndrome associated with deafness.

Splawski I, Timothy KW, Vincent GM, Atkinson DL, Keating MT. Splawski I, et al. Among authors: vincent gm. Proc Assoc Am Physicians. 1997 Sep;109(5):504-11. Proc Assoc Am Physicians. 1997. PMID: 9285950

8

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: vincent gm. Genomics. 1998 Jul 1;51(1):86-97. doi: 10.1006/geno.1998.5361. Genomics. 1998. PMID: 9693036

9

The inherited long QT syndrome: from ion channel to bedside.

Vincent GM, Timothy K, Fox J, Zhang L. Vincent GM, et al. Cardiol Rev. 1999 Jan-Feb;7(1):44-55. Cardiol Rev. 1999. PMID: 10348966 Review.

10

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.

Splawski I, Shen J, Timothy KW, Lehmann MH, Priori S, Robinson JL, Moss AJ, Schwartz PJ, Towbin JA, Vincent GM, Keating MT. Splawski I, et al. Among authors: vincent gm. Circulation. 2000 Sep 5;102(10):1178-85. doi: 10.1161/01.cir.102.10.1178. Circulation. 2000. PMID: 10973849

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

146 results

Search Page

Filters