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Cardiovascular Research
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July 19, 2002
A novel SCN5A arrhythmia mutation, M1766L, with expression defect rescued by mexiletine
Carmen R Valdivia, Michael J Ackerman, David J Tester, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
February 5, 2013
Digenic inheritance novel mutations in SCN5a and SNTA1 increase late I(Na) contributing to LQT syndrome
Rou-Mu Hu, Bi-Hua Tan, Kate M Orland, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 20, 2001
Disruption of Sur2-containing K(ATP) channels enhances insulin-stimulated glucose uptake in skeletal muscle
W A Chutkow, V Samuel, P A Hansen, et al.
Circulation Research
|
September 23, 2003
A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channels
Jonathan C Makielski, Bin Ye, Carmen R Valdivia, et al.
Neurosurgery
|
October 1, 1985
Aneurysm clip motion during magnetic resonance imaging: in vivo experimental study with metallurgical factor analysis
M Dujovny, N Kossovsky, R Kossowsky, et al.
Cardiovascular Research
|
January 1, 2010
Loss-of-function mutation of the SCN3B-encoded sodium channel {beta}3 subunit associated with a case of idiopathic ventricular fibrillation
Carmen R Valdivia, Argelia Medeiros-Domingo, Bin Ye, et al.
Circulation
|
October 31, 2007
Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome
David W Van Norstrand, Carmen R Valdivia, David J Tester, et al.
JAMA
|
November 17, 2001
Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome
M J Ackerman, B L Siu, W Q Sturner, et al.
Multiple Sclerosis and Related Disorders
|
July 7, 2024
Corrigendum to "Validation of the Brief International Cognitive Assessment for Multiple Sclerosis (BICAMS) in individuals with multiple sclerosis from Mexico" [Multiple Sclerosis and Related Disorders, Volume 83, March 2024, 105451]
Edgar R Valdivia-Tangarife, Alejandra Morlett-Paredes, Teresita Villaseñor-Cabrera, et al.
The Journal of Physiology
|
October 22, 2021
The V2475F CPVT1 mutation yields distinct RyR2 channel populations that differ in their responses to cytosolic Ca<sup>2+</sup> and Mg<sup>2</sup>
Abigail D Wilson, Jianshu Hu, Charalampos Sigalas, et al.
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of 8
Search research articles
Search
Showing results (31-40 of 78) with videos related to
Sort By:
Page
of 8
Cardiovascular Research
|
July 19, 2002
A novel SCN5A arrhythmia mutation, M1766L, with expression defect rescued by mexiletine
Carmen R Valdivia, Michael J Ackerman, David J Tester, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
February 5, 2013
Digenic inheritance novel mutations in SCN5a and SNTA1 increase late I(Na) contributing to LQT syndrome
Rou-Mu Hu, Bi-Hua Tan, Kate M Orland, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 20, 2001
Disruption of Sur2-containing K(ATP) channels enhances insulin-stimulated glucose uptake in skeletal muscle
W A Chutkow, V Samuel, P A Hansen, et al.
Circulation Research
|
September 23, 2003
A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channels
Jonathan C Makielski, Bin Ye, Carmen R Valdivia, et al.
Neurosurgery
|
October 1, 1985
Aneurysm clip motion during magnetic resonance imaging: in vivo experimental study with metallurgical factor analysis
M Dujovny, N Kossovsky, R Kossowsky, et al.
Cardiovascular Research
|
January 1, 2010
Loss-of-function mutation of the SCN3B-encoded sodium channel {beta}3 subunit associated with a case of idiopathic ventricular fibrillation
Carmen R Valdivia, Argelia Medeiros-Domingo, Bin Ye, et al.
Circulation
|
October 31, 2007
Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome
David W Van Norstrand, Carmen R Valdivia, David J Tester, et al.
JAMA
|
November 17, 2001
Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome
M J Ackerman, B L Siu, W Q Sturner, et al.
Multiple Sclerosis and Related Disorders
|
July 7, 2024
Corrigendum to "Validation of the Brief International Cognitive Assessment for Multiple Sclerosis (BICAMS) in individuals with multiple sclerosis from Mexico" [Multiple Sclerosis and Related Disorders, Volume 83, March 2024, 105451]
Edgar R Valdivia-Tangarife, Alejandra Morlett-Paredes, Teresita Villaseñor-Cabrera, et al.
The Journal of Physiology
|
October 22, 2021
The V2475F CPVT1 mutation yields distinct RyR2 channel populations that differ in their responses to cytosolic Ca<sup>2+</sup> and Mg<sup>2</sup>
Abigail D Wilson, Jianshu Hu, Charalampos Sigalas, et al.
Page
of 8