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Elife
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October 23, 2020
Allosteric mechanism for KCNE1 modulation of KCNQ1 potassium channel activation
Georg Kuenze, Carlos G Vanoye, Reshma R Desai, et al.
JCI Insight
|
May 21, 2024
Molecular and cellular context influences SCN8A variant function
Carlos G Vanoye, Tatiana V Abramova, Jean-Marc DeKeyser, et al.
Biorxiv : the Preprint Server for Biology
|
November 28, 2023
Molecular and Cellular Context Influences SCN8A Variant Function
Carlos G Vanoye, Tatiana V Abramova, Jean-Marc DeKeyser, et al.
Circulation. Arrhythmia and Electrophysiology
|
October 8, 2009
Malignant perinatal variant of long-QT syndrome caused by a profoundly dysfunctional cardiac sodium channel
Dao W Wang, Lia Crotti, Wataru Shimizu, et al.
Circulation
|
January 11, 2007
Cardiac sodium channel dysfunction in sudden infant death syndrome
Dao W Wang, Reshma R Desai, Lia Crotti, et al.
Science Advances
|
March 14, 2018
Mechanisms of KCNQ1 channel dysfunction in long QT syndrome involving voltage sensor domain mutations
Hui Huang, Georg Kuenze, Jarrod A Smith, et al.
Structure (London, England : 1993)
|
April 3, 2018
A Mechanism of Calmodulin Modulation of the Human Cardiac Sodium Channel
Christopher N Johnson, Franck Potet, Matthew K Thompson, et al.
Circulation. Genomic and Precision Medicine
|
December 21, 2018
High-Throughput Functional Evaluation of KCNQ1 Decrypts Variants of Unknown Significance
Carlos G Vanoye, Reshma R Desai, Katarina L Fabre, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 19, 2025
Integrative analysis of KCNQ1 variants reveals molecular mechanisms of type 1 long QT syndrome pathogenesis
Kathryn R Brewer, Carlos G Vanoye, Hui Huang, et al.
Clinical and Translational Science
|
April 10, 2020
Impact of CYP2C9-Interacting Drugs on Warfarin Pharmacogenomics
Saaket Agrawal, Meredith S Heiss, Remington B Fenter, et al.
Page
of 30
Search research articles
Search
Showing results (171-180 of 296) with videos related to
Sort By:
Page
of 30
Elife
|
October 23, 2020
Allosteric mechanism for KCNE1 modulation of KCNQ1 potassium channel activation
Georg Kuenze, Carlos G Vanoye, Reshma R Desai, et al.
JCI Insight
|
May 21, 2024
Molecular and cellular context influences SCN8A variant function
Carlos G Vanoye, Tatiana V Abramova, Jean-Marc DeKeyser, et al.
Biorxiv : the Preprint Server for Biology
|
November 28, 2023
Molecular and Cellular Context Influences SCN8A Variant Function
Carlos G Vanoye, Tatiana V Abramova, Jean-Marc DeKeyser, et al.
Circulation. Arrhythmia and Electrophysiology
|
October 8, 2009
Malignant perinatal variant of long-QT syndrome caused by a profoundly dysfunctional cardiac sodium channel
Dao W Wang, Lia Crotti, Wataru Shimizu, et al.
Circulation
|
January 11, 2007
Cardiac sodium channel dysfunction in sudden infant death syndrome
Dao W Wang, Reshma R Desai, Lia Crotti, et al.
Science Advances
|
March 14, 2018
Mechanisms of KCNQ1 channel dysfunction in long QT syndrome involving voltage sensor domain mutations
Hui Huang, Georg Kuenze, Jarrod A Smith, et al.
Structure (London, England : 1993)
|
April 3, 2018
A Mechanism of Calmodulin Modulation of the Human Cardiac Sodium Channel
Christopher N Johnson, Franck Potet, Matthew K Thompson, et al.
Circulation. Genomic and Precision Medicine
|
December 21, 2018
High-Throughput Functional Evaluation of KCNQ1 Decrypts Variants of Unknown Significance
Carlos G Vanoye, Reshma R Desai, Katarina L Fabre, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 19, 2025
Integrative analysis of KCNQ1 variants reveals molecular mechanisms of type 1 long QT syndrome pathogenesis
Kathryn R Brewer, Carlos G Vanoye, Hui Huang, et al.
Clinical and Translational Science
|
April 10, 2020
Impact of CYP2C9-Interacting Drugs on Warfarin Pharmacogenomics
Saaket Agrawal, Meredith S Heiss, Remington B Fenter, et al.
Page
of 30