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Circulation. Cardiovascular Genetics
|
August 5, 2014
AKAP9 is a genetic modifier of congenital long-QT syndrome type 1
Carin P de Villiers, Lize van der Merwe, Lia Crotti, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 16, 2008
Divergent sodium channel defects in familial hemiplegic migraine
Kristopher M Kahlig, Thomas H Rhodes, Michael Pusch, et al.
The Journal of Clinical Psychiatry
|
June 14, 2024
Pharmacogenomic Characterization of Childbearing-Aged Individuals With Mood Disorders in a Tertiary Care Perinatal Mental Health Clinic
Jessica L W Mayer, Hannah K Betcher, Laura J Rasmussen-Torvik, et al.
American Journal of Medical Genetics. Part A
|
May 18, 2021
Mitochondrial cardiomyopathy and ventricular arrhythmias associated with biallelic variants in C1QBP
Gregory Webster, Meredith Reynolds, Nicoleta C Arva, et al.
Plos One
|
April 8, 2014
Multiscale complexity analysis of the cardiac control identifies asymptomatic and symptomatic patients in long QT syndrome type 1
Vlasta Bari, José F Valencia, Montserrat Vallverdú, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
August 17, 2006
Drug transporter and metabolizing enzyme gene variants and nonnucleoside reverse-transcriptase inhibitor hepatotoxicity
Marylyn D Ritchie, David W Haas, Alison A Motsinger, et al.
Cell Reports
|
April 28, 2024
Independent compartmentalization of functional, metabolic, and transcriptional maturation of hiPSC-derived cardiomyocytes
K Ashley Fetterman, Malorie Blancard, Davi M Lyra-Leite, et al.
Circulation. Cardiovascular Genetics
|
October 13, 2017
Predicting the Functional Impact of KCNQ1 Variants of Unknown Significance
Bian Li, Jeffrey L Mendenhall, Brett M Kroncke, et al.
Brain : a Journal of Neurology
|
June 22, 2002
Change of chloride ion channel conductance is an early event of slow-to-fast fibre type transition during unloading-induced muscle disuse
Sabata Pierno, Jean-François Desaphy, Antonella Liantonio, et al.
Elife
|
July 15, 2025
Differential roles of Na<sub>V</sub>1.2 and Na<sub>V</sub>1.6 in neocortical pyramidal cell excitability
Joshua D Garcia, Chenyu Wang, Ryan P D Alexander, et al.
Page
of 30
Search research articles
Search
Showing results (191-200 of 296) with videos related to
Sort By:
Page
of 30
Circulation. Cardiovascular Genetics
|
August 5, 2014
AKAP9 is a genetic modifier of congenital long-QT syndrome type 1
Carin P de Villiers, Lize van der Merwe, Lia Crotti, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 16, 2008
Divergent sodium channel defects in familial hemiplegic migraine
Kristopher M Kahlig, Thomas H Rhodes, Michael Pusch, et al.
The Journal of Clinical Psychiatry
|
June 14, 2024
Pharmacogenomic Characterization of Childbearing-Aged Individuals With Mood Disorders in a Tertiary Care Perinatal Mental Health Clinic
Jessica L W Mayer, Hannah K Betcher, Laura J Rasmussen-Torvik, et al.
American Journal of Medical Genetics. Part A
|
May 18, 2021
Mitochondrial cardiomyopathy and ventricular arrhythmias associated with biallelic variants in C1QBP
Gregory Webster, Meredith Reynolds, Nicoleta C Arva, et al.
Plos One
|
April 8, 2014
Multiscale complexity analysis of the cardiac control identifies asymptomatic and symptomatic patients in long QT syndrome type 1
Vlasta Bari, José F Valencia, Montserrat Vallverdú, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
August 17, 2006
Drug transporter and metabolizing enzyme gene variants and nonnucleoside reverse-transcriptase inhibitor hepatotoxicity
Marylyn D Ritchie, David W Haas, Alison A Motsinger, et al.
Cell Reports
|
April 28, 2024
Independent compartmentalization of functional, metabolic, and transcriptional maturation of hiPSC-derived cardiomyocytes
K Ashley Fetterman, Malorie Blancard, Davi M Lyra-Leite, et al.
Circulation. Cardiovascular Genetics
|
October 13, 2017
Predicting the Functional Impact of KCNQ1 Variants of Unknown Significance
Bian Li, Jeffrey L Mendenhall, Brett M Kroncke, et al.
Brain : a Journal of Neurology
|
June 22, 2002
Change of chloride ion channel conductance is an early event of slow-to-fast fibre type transition during unloading-induced muscle disuse
Sabata Pierno, Jean-François Desaphy, Antonella Liantonio, et al.
Elife
|
July 15, 2025
Differential roles of Na<sub>V</sub>1.2 and Na<sub>V</sub>1.6 in neocortical pyramidal cell excitability
Joshua D Garcia, Chenyu Wang, Ryan P D Alexander, et al.
Page
of 30