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M T Keating

Showing results (51-60 of 76) with videos related to

Pageof 8
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Science (New York, N.Y.)|May 23, 1998
Actin mutations in dilated cardiomyopathy, a heritable form of heart failureT M Olson, V V Michels, S N Thibodeau, et al.
Developmental Biology|June 6, 2000
Roles for Fgf signaling during zebrafish fin regenerationK D Poss, J Shen, A Nechiporuk, et al.
Genomics|August 7, 1998
Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1I Splawski, J Shen, K W Timothy, et al.
Cell|March 10, 1995
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndromeM E Curran, I Splawski, K W Timothy, et al.
The American Journal of Physiology|November 24, 1999
Relation between outer and luminal diameter in cannulated arteriesG Faury, G M Maher, D Y Li, et al.
Cell|April 9, 1993
The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosisM E Curran, D L Atkinson, A K Ewart, et al.
Nature|November 7, 1996
Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channelM C Sanguinetti, M E Curran, A Zou, et al.
Circulation Research|May 1, 1996
Multiple mechanisms of Na+ channel--linked long-QT syndromeR Dumaine, Q Wang, M T Keating, et al.
Human Molecular Genetics|September 1, 1995
Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmiaQ Wang, J Shen, Z Li, et al.
Human Genetics|December 22, 1998
Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genesX Meng, X Lu, Z Li, et al.
Pageof 8

Showing results (51-60 of 76) with videos related to

Sort By:
Pageof 8
Science (New York, N.Y.)|May 23, 1998
Actin mutations in dilated cardiomyopathy, a heritable form of heart failureT M Olson, V V Michels, S N Thibodeau, et al.
Developmental Biology|June 6, 2000
Roles for Fgf signaling during zebrafish fin regenerationK D Poss, J Shen, A Nechiporuk, et al.
Genomics|August 7, 1998
Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1I Splawski, J Shen, K W Timothy, et al.
Cell|March 10, 1995
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndromeM E Curran, I Splawski, K W Timothy, et al.
The American Journal of Physiology|November 24, 1999
Relation between outer and luminal diameter in cannulated arteriesG Faury, G M Maher, D Y Li, et al.
Cell|April 9, 1993
The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosisM E Curran, D L Atkinson, A K Ewart, et al.
Nature|November 7, 1996
Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channelM C Sanguinetti, M E Curran, A Zou, et al.
Circulation Research|May 1, 1996
Multiple mechanisms of Na+ channel--linked long-QT syndromeR Dumaine, Q Wang, M T Keating, et al.
Human Molecular Genetics|September 1, 1995
Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmiaQ Wang, J Shen, Z Li, et al.
Human Genetics|December 22, 1998
Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genesX Meng, X Lu, Z Li, et al.
Pageof 8