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Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|August 26, 2003
The molecular genetics of arrhythmogenic right ventricular dysplasia-cardiomyopathyFerhaan Ahmad
European Heart Journal. Case Reports|August 27, 2019
Patient with a PRKAG2 mutation who developed Immunoglobulin A nephropathy: a case reportMichael C Giudici, Ferhaan Ahmad, Danniele G Holanda
Annual Review of Genomics and Human Genetics|August 30, 2005
The genetic basis for cardiac remodelingFerhaan Ahmad, J G Seidman, Christine E Seidman
Biochimica Et Biophysica Acta|December 17, 2009
Activation of cardiac hypertrophic signaling pathways in a transgenic mouse with the human PRKAG2 Thr400Asn mutationSanjay K Banerjee, Kenneth R McGaffin, Xueyin N Huang, et al.
BMC Medical Genetics|March 31, 2012
Functional effects of the TMEM43 Ser358Leu mutation in the pathogenesis of arrhythmogenic right ventricular cardiomyopathyRevathi Rajkumar, John C Sembrat, Barbara McDonough, et al.
Cardiovascular Research|June 11, 2009
SGLT1 is a novel cardiac glucose transporter that is perturbed in disease statesSanjay K Banerjee, Kenneth R McGaffin, Núria M Pastor-Soler, et al.
Western Journal of Nursing Research|December 13, 2018
Family Relationships Associated With Communication and Testing for Inherited Cardiac ConditionsLisa L Shah, Sandra Daack-Hirsch, Anne L Ersig, et al.
Biochemical and Biophysical Research Communications|June 29, 2007
A PRKAG2 mutation causes biphasic changes in myocardial AMPK activity and does not protect against ischemiaSanjay K Banerjee, Ravi Ramani, Samir Saba, et al.
American Journal of Physiology. Heart and Circulatory Physiology|January 19, 2010
Genomewide RNA expression profiling in lung identifies distinct signatures in idiopathic pulmonary arterial hypertension and secondary pulmonary hypertensionRevathi Rajkumar, Kazuhisa Konishi, Thomas J Richards, et al.
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