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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
February 24, 2004
High-throughput analysis of genome-wide receptor tyrosine kinase expression in human cancers identifies potential novel drug targets
Carsten Müller-Tidow, Joachim Schwäble, Björn Steffen, et al.
Human Molecular Genetics
|
August 23, 2006
C-terminal HERG (LQT2) mutations disrupt IKr channel regulation through 14-3-3epsilon
Chi-un Choe, Eric Schulze-Bahr, Axel Neu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 3, 2014
Recessive cardiac phenotypes in induced pluripotent stem cell models of Jervell and Lange-Nielsen syndrome: disease mechanisms and pharmacological rescue
Miao Zhang, Cristina D'Aniello, Arie O Verkerk, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
July 5, 2013
Coxsackievirus B3 modulates cardiac ion channels
Katja Steinke, Frank Sachse, Nicole Ettischer, et al.
Circulation. Heart Failure
|
November 27, 2014
First report on an inotropic peptide activating tetrodotoxin-sensitive, "neuronal" sodium currents in the heart
Paulus Kirchhof, Tzachy Tal, Larissa Fabritz, et al.
EMBO Molecular Medicine
|
March 1, 2017
Sodium permeable and "hypersensitive" TREK-1 channels cause ventricular tachycardia
Niels Decher, Beatriz Ortiz-Bonnin, Corinna Friedrich, et al.
The New England Journal of Medicine
|
December 29, 2006
Female predominance and transmission distortion in the long-QT syndrome
Medea Imboden, Heikki Swan, Isabelle Denjoy, et al.
International Journal of Molecular Sciences
|
November 18, 2020
New Cav1.2 Channelopathy with High-Functioning Autism, Affective Disorder, Severe Dental Enamel Defects, a Short QT Interval, and a Novel <i>CACNA1C</i> Loss-Of-Function Mutation
Dominique Endres, Niels Decher, Isabell Röhr, et al.
Molecular Genetics and Metabolism Reports
|
August 11, 2017
Limitations of galactose therapy in phosphoglucomutase 1 deficiency
Kristine Nolting, Julien H Park, Laura C Tegtmeyer, et al.
Cardiovascular Research
|
July 27, 2005
Role of sequence variations in the human ether-a-go-go-related gene (HERG, KCNH2) in the Brugada syndrome
Arie O Verkerk, Ronald Wilders, Eric Schulze-Bahr, et al.
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Search research articles
Search
Showing results (111-120 of 155) with videos related to
Sort By:
Page
of 16
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
February 24, 2004
High-throughput analysis of genome-wide receptor tyrosine kinase expression in human cancers identifies potential novel drug targets
Carsten Müller-Tidow, Joachim Schwäble, Björn Steffen, et al.
Human Molecular Genetics
|
August 23, 2006
C-terminal HERG (LQT2) mutations disrupt IKr channel regulation through 14-3-3epsilon
Chi-un Choe, Eric Schulze-Bahr, Axel Neu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 3, 2014
Recessive cardiac phenotypes in induced pluripotent stem cell models of Jervell and Lange-Nielsen syndrome: disease mechanisms and pharmacological rescue
Miao Zhang, Cristina D'Aniello, Arie O Verkerk, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
July 5, 2013
Coxsackievirus B3 modulates cardiac ion channels
Katja Steinke, Frank Sachse, Nicole Ettischer, et al.
Circulation. Heart Failure
|
November 27, 2014
First report on an inotropic peptide activating tetrodotoxin-sensitive, "neuronal" sodium currents in the heart
Paulus Kirchhof, Tzachy Tal, Larissa Fabritz, et al.
EMBO Molecular Medicine
|
March 1, 2017
Sodium permeable and "hypersensitive" TREK-1 channels cause ventricular tachycardia
Niels Decher, Beatriz Ortiz-Bonnin, Corinna Friedrich, et al.
The New England Journal of Medicine
|
December 29, 2006
Female predominance and transmission distortion in the long-QT syndrome
Medea Imboden, Heikki Swan, Isabelle Denjoy, et al.
International Journal of Molecular Sciences
|
November 18, 2020
New Cav1.2 Channelopathy with High-Functioning Autism, Affective Disorder, Severe Dental Enamel Defects, a Short QT Interval, and a Novel <i>CACNA1C</i> Loss-Of-Function Mutation
Dominique Endres, Niels Decher, Isabell Röhr, et al.
Molecular Genetics and Metabolism Reports
|
August 11, 2017
Limitations of galactose therapy in phosphoglucomutase 1 deficiency
Kristine Nolting, Julien H Park, Laura C Tegtmeyer, et al.
Cardiovascular Research
|
July 27, 2005
Role of sequence variations in the human ether-a-go-go-related gene (HERG, KCNH2) in the Brugada syndrome
Arie O Verkerk, Ronald Wilders, Eric Schulze-Bahr, et al.
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of 16