Keating MT - Search Results

1

Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia.

Sanguinetti MC, Curran ME, Spector PS, Keating MT. Sanguinetti MC, et al. Among authors: keating mt. Proc Natl Acad Sci U S A. 1996 Mar 5;93(5):2208-12. doi: 10.1073/pnas.93.5.2208. Proc Natl Acad Sci U S A. 1996. PMID: 8700910 Free PMC article.

2

Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations.

Splawski I, Timothy KW, Decher N, Kumar P, Sachse FB, Beggs AH, Sanguinetti MC, Keating MT. Splawski I, et al. Among authors: keating mt. Proc Natl Acad Sci U S A. 2005 Jun 7;102(23):8089-96; discussion 8086-8. doi: 10.1073/pnas.0502506102. Epub 2005 Apr 29. Proc Natl Acad Sci U S A. 2005. PMID: 15863612 Free PMC article.

3

A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel.

Sanguinetti MC, Jiang C, Curran ME, Keating MT. Sanguinetti MC, et al. Among authors: keating mt. Cell. 1995 Apr 21;81(2):299-307. doi: 10.1016/0092-8674(95)90340-2. Cell. 1995. PMID: 7736582 Free article.

4

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.

5

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

6

Class III antiarrhythmic drugs block HERG, a human cardiac delayed rectifier K+ channel. Open-channel block by methanesulfonanilides.

Spector PS, Curran ME, Keating MT, Sanguinetti MC. Spector PS, et al. Among authors: keating mt. Circ Res. 1996 Mar;78(3):499-503. doi: 10.1161/01.res.78.3.499. Circ Res. 1996. PMID: 8593709

7

Fast inactivation causes rectification of the IKr channel.

Spector PS, Curran ME, Zou A, Keating MT, Sanguinetti MC. Spector PS, et al. Among authors: keating mt. J Gen Physiol. 1996 May;107(5):611-9. doi: 10.1085/jgp.107.5.611. J Gen Physiol. 1996. PMID: 8740374 Free PMC article.

8

Genetically defined therapy of inherited long-QT syndrome. Correction of abnormal repolarization by potassium.

Compton SJ, Lux RL, Ramsey MR, Strelich KR, Sanguinetti MC, Green LS, Keating MT, Mason JW. Compton SJ, et al. Among authors: keating mt. Circulation. 1996 Sep 1;94(5):1018-22. doi: 10.1161/01.cir.94.5.1018. Circulation. 1996. PMID: 8790040

9

Pathophysiology of ion channel mutations.

Keating MT, Sanguinetti MC. Keating MT, et al. Curr Opin Genet Dev. 1996 Jun;6(3):326-33. doi: 10.1016/s0959-437x(96)80010-4. Curr Opin Genet Dev. 1996. PMID: 8791523 Review.

10

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel.

Sanguinetti MC, Curran ME, Zou A, Shen J, Spector PS, Atkinson DL, Keating MT. Sanguinetti MC, et al. Among authors: keating mt. Nature. 1996 Nov 7;384(6604):80-3. doi: 10.1038/384080a0. Nature. 1996. PMID: 8900283

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