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M T Keating

Showing results (41-50 of 76) with videos related to

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Circulation|August 29, 2001
Long-QT syndrome-associated missense mutations in the pore helix of the HERG potassium channelF D Huang, J Chen, M Lin, et al.
The Journal of Clinical Investigation|March 1, 1994
Supravalvular aortic stenosis associated with a deletion disrupting the elastin geneA K Ewart, W Jin, D Atkinson, et al.
Nature Genetics|November 14, 1997
Mutations in the hminK gene cause long QT syndrome and suppress IKs functionI Splawski, M Tristani-Firouzi, M H Lehmann, et al.
Proceedings of the Association of American Physicians|September 1, 1997
George M. Cober Lecturer: Mark T. Keating. Molecular basis of the long-QT syndrome associated with deafnessI Splawski, K W Timothy, G M Vincent, et al.
The Journal of General Physiology|May 1, 1996
Fast inactivation causes rectification of the IKr channelP S Spector, M E Curran, A Zou, et al.
Genomics|May 15, 1997
Genomic localization of the human gene for KCNA10, a cGMP-activated K channelM Orias, P Bray-Ward, M E Curran, et al.
The New England Journal of Medicine|May 29, 1997
Molecular basis of the long-QT syndrome associated with deafnessI Splawski, K W Timothy, G M Vincent, et al.
The Journal of Biological Chemistry|July 20, 1999
Long QT syndrome-associated mutations in the S4-S5 linker of KvLQT1 potassium channels modify gating and interaction with minK subunitsL Franqueza, M Lin, J Shen, et al.
Journal of Cardiovascular Electrophysiology|June 22, 1999
Functional effects of mutations in KvLQT1 that cause long QT syndromeZ Wang, M Tristani-Firouzi, Q Xu, et al.
American Journal of Respiratory Cell and Molecular Biology|September 6, 2000
Impaired distal airway development in mice lacking elastinD P Wendel, D G Taylor, K H Albertine, et al.
Pageof 8

Showing results (41-50 of 76) with videos related to

Sort By:
Pageof 8
Circulation|August 29, 2001
Long-QT syndrome-associated missense mutations in the pore helix of the HERG potassium channelF D Huang, J Chen, M Lin, et al.
The Journal of Clinical Investigation|March 1, 1994
Supravalvular aortic stenosis associated with a deletion disrupting the elastin geneA K Ewart, W Jin, D Atkinson, et al.
Nature Genetics|November 14, 1997
Mutations in the hminK gene cause long QT syndrome and suppress IKs functionI Splawski, M Tristani-Firouzi, M H Lehmann, et al.
Proceedings of the Association of American Physicians|September 1, 1997
George M. Cober Lecturer: Mark T. Keating. Molecular basis of the long-QT syndrome associated with deafnessI Splawski, K W Timothy, G M Vincent, et al.
The Journal of General Physiology|May 1, 1996
Fast inactivation causes rectification of the IKr channelP S Spector, M E Curran, A Zou, et al.
Genomics|May 15, 1997
Genomic localization of the human gene for KCNA10, a cGMP-activated K channelM Orias, P Bray-Ward, M E Curran, et al.
The New England Journal of Medicine|May 29, 1997
Molecular basis of the long-QT syndrome associated with deafnessI Splawski, K W Timothy, G M Vincent, et al.
The Journal of Biological Chemistry|July 20, 1999
Long QT syndrome-associated mutations in the S4-S5 linker of KvLQT1 potassium channels modify gating and interaction with minK subunitsL Franqueza, M Lin, J Shen, et al.
Journal of Cardiovascular Electrophysiology|June 22, 1999
Functional effects of mutations in KvLQT1 that cause long QT syndromeZ Wang, M Tristani-Firouzi, Q Xu, et al.
American Journal of Respiratory Cell and Molecular Biology|September 6, 2000
Impaired distal airway development in mice lacking elastinD P Wendel, D G Taylor, K H Albertine, et al.
Pageof 8