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Eric Schulze

Showing results (121-130 of 155) with videos related to

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Journal of Personalized Medicine|July 27, 2022
Detection of Patients with Congenital and Often Concealed Long-QT Syndrome by Novel Deep Learning ModelsFlorian Doldi, Lucas Plagwitz, Lea Philine Hoffmann, et al.
European Journal of Human Genetics : EJHG|December 17, 2015
Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunctionHideki Itoh, Myriam Berthet, Véronique Fressart, et al.
European Heart Journal|August 14, 2015
Estradiol regulates human QT-interval: acceleration of cardiac repolarization by enhanced KCNH2 membrane traffickingLars Anneken, Stefan Baumann, Patrick Vigneault, et al.
The Journal of Clinical Investigation|May 3, 2008
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndromeNaomasa Makita, Elijah Behr, Wataru Shimizu, et al.
Circulation|November 7, 2007
The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratificationLia Crotti, Carla Spazzolini, Peter J Schwartz, et al.
European Heart Journal|June 14, 2020
An autoantibody profile detects Brugada syndrome and identifies abnormally expressed myocardial proteinsDiptendu Chatterjee, Maurizio Pieroni, Meena Fatah, et al.
Nature Communications|October 13, 2016
KCNE1 induces fenestration in the Kv7.1/KCNE1 channel complex that allows for highly specific pharmacological targetingEva Wrobel, Ina Rothenberg, Christoph Krisp, et al.
Basic Research in Cardiology|May 4, 2016
Coding and non-coding variants in the SHOX2 gene in patients with early-onset atrial fibrillationSandra Hoffmann, Sebastian Clauss, Ina M Berger, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|August 5, 2021
Investigation on Sudden Unexpected Death in the Young (SUDY) in Europe: results of the European Heart Rhythm Association SurveyElijah R Behr, Chiara Scrocco, Arthur A M Wilde, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 10, 2024
KCNQ1 is an essential mediator of the sex-dependent perception of moderate cold temperaturesAytug K Kiper, Sven Wegner, Aklesso Kadala, et al.
Pageof 16

Showing results (121-130 of 155) with videos related to

Sort By:
Pageof 16
Journal of Personalized Medicine|July 27, 2022
Detection of Patients with Congenital and Often Concealed Long-QT Syndrome by Novel Deep Learning ModelsFlorian Doldi, Lucas Plagwitz, Lea Philine Hoffmann, et al.
European Journal of Human Genetics : EJHG|December 17, 2015
Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunctionHideki Itoh, Myriam Berthet, Véronique Fressart, et al.
European Heart Journal|August 14, 2015
Estradiol regulates human QT-interval: acceleration of cardiac repolarization by enhanced KCNH2 membrane traffickingLars Anneken, Stefan Baumann, Patrick Vigneault, et al.
The Journal of Clinical Investigation|May 3, 2008
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndromeNaomasa Makita, Elijah Behr, Wataru Shimizu, et al.
Circulation|November 7, 2007
The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratificationLia Crotti, Carla Spazzolini, Peter J Schwartz, et al.
European Heart Journal|June 14, 2020
An autoantibody profile detects Brugada syndrome and identifies abnormally expressed myocardial proteinsDiptendu Chatterjee, Maurizio Pieroni, Meena Fatah, et al.
Nature Communications|October 13, 2016
KCNE1 induces fenestration in the Kv7.1/KCNE1 channel complex that allows for highly specific pharmacological targetingEva Wrobel, Ina Rothenberg, Christoph Krisp, et al.
Basic Research in Cardiology|May 4, 2016
Coding and non-coding variants in the SHOX2 gene in patients with early-onset atrial fibrillationSandra Hoffmann, Sebastian Clauss, Ina M Berger, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|August 5, 2021
Investigation on Sudden Unexpected Death in the Young (SUDY) in Europe: results of the European Heart Rhythm Association SurveyElijah R Behr, Chiara Scrocco, Arthur A M Wilde, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 10, 2024
KCNQ1 is an essential mediator of the sex-dependent perception of moderate cold temperaturesAytug K Kiper, Sven Wegner, Aklesso Kadala, et al.
Pageof 16