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Plos One
|
December 19, 2013
The disease-specific phenotype in cardiomyocytes derived from induced pluripotent stem cells of two long QT syndrome type 3 patients
Azra Fatima, Shao Kaifeng, Sven Dittmann, et al.
International Journal of Cardiology
|
December 29, 2020
Functional characterization of novel alpha-helical rod domain desmin (DES) pathogenic variants associated with dilated cardiomyopathy, atrioventricular block and a risk for sudden cardiac death
Björn Fischer, Sven Dittmann, Andreas Brodehl, et al.
International Journal of Molecular Sciences
|
November 26, 2022
Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene <i>CACNA1D</i> Associated with Familial Sinus Node Dysfunction and Focal Idiopathic Epilepsy
Susanne Rinné, Birgit Stallmeyer, Alexandra Pinggera, et al.
Journal of Molecular and Cellular Cardiology
|
February 7, 2015
TASK-1 and TASK-3 may form heterodimers in human atrial cardiomyocytes
Susanne Rinné, Aytug K Kiper, Günter Schlichthörl, et al.
Journal of the American Heart Association
|
July 26, 2017
Switch From Fetal to Adult <i>SCN5A</i> Isoform in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Unmasks the Cellular Phenotype of a Conduction Disease-Causing Mutation
Christiaan C Veerman, Isabella Mengarelli, Elisabeth M Lodder, et al.
Journal of Personalized Medicine
|
July 27, 2022
Detection of Patients with Congenital and Often Concealed Long-QT Syndrome by Novel Deep Learning Models
Florian Doldi, Lucas Plagwitz, Lea Philine Hoffmann, et al.
European Heart Journal
|
June 14, 2020
An autoantibody profile detects Brugada syndrome and identifies abnormally expressed myocardial proteins
Diptendu Chatterjee, Maurizio Pieroni, Meena Fatah, et al.
Circulation. Genomic and Precision Medicine
|
August 21, 2019
Cardiac α-Actin (ACTC1) Gene Mutation Causes Atrial-Septal Defects Associated With Late-Onset Dilated Cardiomyopathy
Derk Frank, Ashraf Yusuf Rangrez, Corinna Friedrich, et al.
Journal of Molecular and Cellular Cardiology
|
June 15, 2020
POPDC2 a novel susceptibility gene for conduction disorders
Susanne Rinné, Beatriz Ortiz-Bonnin, Birgit Stallmeyer, et al.
Heart Rhythm
|
February 22, 2023
Genetic analysis identifies the SLC4A3 anion exchanger as a major gene for short QT syndrome
Morten Krogh Christiansen, Kasper Kjær-Sørensen, Natacha C Clavsen, et al.
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Search research articles
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Showing results (21-30 of 39) with videos related to
Sort By:
Page
of 4
Plos One
|
December 19, 2013
The disease-specific phenotype in cardiomyocytes derived from induced pluripotent stem cells of two long QT syndrome type 3 patients
Azra Fatima, Shao Kaifeng, Sven Dittmann, et al.
International Journal of Cardiology
|
December 29, 2020
Functional characterization of novel alpha-helical rod domain desmin (DES) pathogenic variants associated with dilated cardiomyopathy, atrioventricular block and a risk for sudden cardiac death
Björn Fischer, Sven Dittmann, Andreas Brodehl, et al.
International Journal of Molecular Sciences
|
November 26, 2022
Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene <i>CACNA1D</i> Associated with Familial Sinus Node Dysfunction and Focal Idiopathic Epilepsy
Susanne Rinné, Birgit Stallmeyer, Alexandra Pinggera, et al.
Journal of Molecular and Cellular Cardiology
|
February 7, 2015
TASK-1 and TASK-3 may form heterodimers in human atrial cardiomyocytes
Susanne Rinné, Aytug K Kiper, Günter Schlichthörl, et al.
Journal of the American Heart Association
|
July 26, 2017
Switch From Fetal to Adult <i>SCN5A</i> Isoform in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Unmasks the Cellular Phenotype of a Conduction Disease-Causing Mutation
Christiaan C Veerman, Isabella Mengarelli, Elisabeth M Lodder, et al.
Journal of Personalized Medicine
|
July 27, 2022
Detection of Patients with Congenital and Often Concealed Long-QT Syndrome by Novel Deep Learning Models
Florian Doldi, Lucas Plagwitz, Lea Philine Hoffmann, et al.
European Heart Journal
|
June 14, 2020
An autoantibody profile detects Brugada syndrome and identifies abnormally expressed myocardial proteins
Diptendu Chatterjee, Maurizio Pieroni, Meena Fatah, et al.
Circulation. Genomic and Precision Medicine
|
August 21, 2019
Cardiac α-Actin (ACTC1) Gene Mutation Causes Atrial-Septal Defects Associated With Late-Onset Dilated Cardiomyopathy
Derk Frank, Ashraf Yusuf Rangrez, Corinna Friedrich, et al.
Journal of Molecular and Cellular Cardiology
|
June 15, 2020
POPDC2 a novel susceptibility gene for conduction disorders
Susanne Rinné, Beatriz Ortiz-Bonnin, Birgit Stallmeyer, et al.
Heart Rhythm
|
February 22, 2023
Genetic analysis identifies the SLC4A3 anion exchanger as a major gene for short QT syndrome
Morten Krogh Christiansen, Kasper Kjær-Sørensen, Natacha C Clavsen, et al.
Page
of 4