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Daniel C Bartos

Showing results (11-20 of 16) with videos related to

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American Journal of Physiology. Cell Physiology|July 19, 2013
Pharmacological correction of long QT-linked mutations in KCNH2 (hERG) increases the trafficking of Kv11.1 channels stored in the transitional endoplasmic reticulumJennifer L Smith, Allison R Reloj, Parvathi S Nataraj, et al.
Heart Rhythm|September 21, 2010
R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillationDaniel C Bartos, Sabine Duchatelet, Don E Burgess, et al.
Journal of Cardiovascular Electrophysiology|January 29, 2013
A KCNQ1 mutation causes a high penetrance for familial atrial fibrillationDaniel C Bartos, Jeffrey B Anderson, Rachel Bastiaenen, et al.
The Journal of Physiology|November 19, 2016
Potassium channels in the heart: structure, function and regulationEleonora Grandi, Michael C Sanguinetti, Daniel C Bartos, et al.
Biochemistry|October 25, 2012
High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K(+) permeationDon E Burgess, Daniel C Bartos, Allison R Reloj, et al.
JAMA|April 11, 2013
Long QT syndrome-associated mutations in intrauterine fetal deathLia Crotti, David J Tester, Wendy M White, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
American Journal of Physiology. Cell Physiology|July 19, 2013
Pharmacological correction of long QT-linked mutations in KCNH2 (hERG) increases the trafficking of Kv11.1 channels stored in the transitional endoplasmic reticulumJennifer L Smith, Allison R Reloj, Parvathi S Nataraj, et al.
Heart Rhythm|September 21, 2010
R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillationDaniel C Bartos, Sabine Duchatelet, Don E Burgess, et al.
Journal of Cardiovascular Electrophysiology|January 29, 2013
A KCNQ1 mutation causes a high penetrance for familial atrial fibrillationDaniel C Bartos, Jeffrey B Anderson, Rachel Bastiaenen, et al.
The Journal of Physiology|November 19, 2016
Potassium channels in the heart: structure, function and regulationEleonora Grandi, Michael C Sanguinetti, Daniel C Bartos, et al.
Biochemistry|October 25, 2012
High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K(+) permeationDon E Burgess, Daniel C Bartos, Allison R Reloj, et al.
JAMA|April 11, 2013
Long QT syndrome-associated mutations in intrauterine fetal deathLia Crotti, David J Tester, Wendy M White, et al.
Pageof 2