Cardiac K+ Channels and Inherited Long QT Syndrome

2000 ◽  
pp. 347-362
Author(s):  
M.-D. Drici ◽  
J. Barhanin
Keyword(s):  
Long Qt Syndrome ◽  
Long Qt ◽  
K Channels ◽  
Qt Syndrome

scholarly journals The Trafficking of Mutant HERG K+ Channels Linked to Long QT Syndrome are Regulated by a Subdomain in the Endoplasmic Reticulum

2011 ◽  
Vol 100 (3) ◽  
pp. 427a
Author(s):  
Jennifer L. Smith ◽  
Parvathi Nataraj ◽  
Craig T. January ◽  
Brian P. Delisle
Keyword(s):  
Endoplasmic Reticulum ◽  
Long Qt Syndrome ◽  
Long Qt ◽  
K Channels ◽  
Qt Syndrome

scholarly journals KCNQ1/KCNE1 K+ Channels Associated with Long QT Syndrome are Expressed in Early Stage Human Embryonic Stem Cell-Derived Cardiomyocytes

2010 ◽  
Vol 98 (3) ◽  
pp. 335a
Author(s):  
Cecile Terrenoire ◽  
George K. Wang ◽  
Eric Adler ◽  
Aaron D. Kaplan ◽  
Kevin J. Sampson ◽  
...  
Keyword(s):  
Stem Cell ◽  
Embryonic Stem Cell ◽  
Long Qt Syndrome ◽  
Human Embryonic Stem Cell ◽  
Early Stage ◽  
Embryonic Stem ◽  
Long Qt ◽  
K Channels ◽  
Qt Syndrome

scholarly journals Cardiac Small Conductance Calcium-Activated K Channels Maintain Repolarization Reserve in a Pharmacological Model of Type 3 Long QT Syndrome

2016 ◽  
Vol 110 (3) ◽  
pp. 447a-448a
Author(s):  
Jum Suk Ko ◽  
Dechun Yin ◽  
Thomas H. Everett ◽  
Zhenhui Chen ◽  
Michael Rubart ◽  
...  
Keyword(s):  
Long Qt Syndrome ◽  
Long Qt ◽  
K Channels ◽  
Repolarization Reserve ◽  
Qt Syndrome ◽  
Type 3 ◽  
Pharmacological Model ◽  
Small Conductance

Characteristics of Ca2+ -activated K+ channels isolated from the left ventricle of a patient with idiopathic long QT syndrome

1993 ◽  
Vol 126 (5) ◽  
pp. 1134-1141 ◽  
Author(s):  
Philip C. Krause ◽  
David P. Rardon ◽  
William M. Miles ◽  
Lawrence S. Klein ◽  
Yousuf Mahomed ◽  
...  
Keyword(s):  
Left Ventricle ◽  
Long Qt Syndrome ◽  
Long Qt ◽  
K Channels ◽  
Qt Syndrome

The Hereditary Long QT Syndrome

2010 ◽  
Vol 43 (2) ◽  
pp. 19
Author(s):  
PETER HULICK
Keyword(s):  
Long Qt Syndrome ◽  
Long Qt ◽  
Qt Syndrome
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