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Circulation. Cardiovascular genetics

Showing results (51-60 of 961) with videos related to

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Circulation. Cardiovascular Genetics|September 16, 2015
Quantitative Proteome Analysis Reveals Increased Content of Basement Membrane Proteins in Arteries From Patients With Type 2 Diabetes Mellitus and Lower Levels Among Metformin UsersSimone A R Preil, Lars P Kristensen, Hans C Beck, et al.
Circulation. Cardiovascular Genetics|September 17, 2015
Characterization of Autosomal Dominant Hypercholesterolemia Caused by PCSK9 Gain of Function Mutations and Its Specific Treatment With Alirocumab, a PCSK9 Monoclonal AntibodyPaul N Hopkins, Joep Defesche, Sigrid W Fouchier, et al.
Circulation. Cardiovascular Genetics|September 17, 2015
Synthesis of an Endogenous Steroidal Na Pump Inhibitor Marinobufagenin, Implicated in Human Cardiovascular Diseases, Is Initiated by CYP27A1 via Bile Acid PathwayOlga V Fedorova, Valentina I Zernetkina, Victoria Y Shilova, et al.
Circulation. Cardiovascular Genetics|November 1, 2015
Functional Genomics Analysis of Big Data Identifies Novel Peroxisome Proliferator-Activated Receptor γ Target Single Nucleotide Polymorphisms Showing Association With Cardiometabolic OutcomesKris Richardson, Gavin R Schnitzler, Chao-Qiang Lai, et al.
Circulation. Cardiovascular Genetics|October 27, 2015
Eya4 Induces Hypertrophy via Regulation of p27kip1Tatjana Williams, Moritz Hundertmark, Peter Nordbeck, et al.
Circulation. Cardiovascular Genetics|December 4, 2014
Genetic evidence for PLASMINOGEN as a shared genetic risk factor of coronary artery disease and periodontitisArne S Schaefer, Gregor Bochenek, Arne Jochens, et al.
Circulation. Cardiovascular Genetics|May 10, 2011
Proteomic analysis yields an unexpected trans-acting point in control of the human sympathochromaffin phenotypeStéphane Chiron, Zhiyun Wei, Yuqing Chen, et al.
Circulation. Cardiovascular Genetics|May 10, 2011
Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotypeSusanne Probst, Erwin Oechslin, Pia Schuler, et al.
Circulation. Cardiovascular Genetics|April 20, 2010
A common variant at chromosome 9P21.3 is associated with age of onset of coronary disease but not subsequent mortalityKatrina L Ellis, Anna P Pilbrow, Chris M Frampton, et al.
Circulation. Cardiovascular Genetics|April 22, 2010
Letter by yilmaz et Al regarding article, "analysis of dystrophin deletion mutations predicts age of cardiomyopathy onset in becker muscular dystrophy"Ali Yilmaz, Joseph Suttie, Steffen E Petersen
Pageof 97

Showing results (51-60 of 961) with videos related to

Sort By:
Pageof 97
Circulation. Cardiovascular Genetics|September 16, 2015
Quantitative Proteome Analysis Reveals Increased Content of Basement Membrane Proteins in Arteries From Patients With Type 2 Diabetes Mellitus and Lower Levels Among Metformin UsersSimone A R Preil, Lars P Kristensen, Hans C Beck, et al.
Circulation. Cardiovascular Genetics|September 17, 2015
Characterization of Autosomal Dominant Hypercholesterolemia Caused by PCSK9 Gain of Function Mutations and Its Specific Treatment With Alirocumab, a PCSK9 Monoclonal AntibodyPaul N Hopkins, Joep Defesche, Sigrid W Fouchier, et al.
Circulation. Cardiovascular Genetics|September 17, 2015
Synthesis of an Endogenous Steroidal Na Pump Inhibitor Marinobufagenin, Implicated in Human Cardiovascular Diseases, Is Initiated by CYP27A1 via Bile Acid PathwayOlga V Fedorova, Valentina I Zernetkina, Victoria Y Shilova, et al.
Circulation. Cardiovascular Genetics|November 1, 2015
Functional Genomics Analysis of Big Data Identifies Novel Peroxisome Proliferator-Activated Receptor γ Target Single Nucleotide Polymorphisms Showing Association With Cardiometabolic OutcomesKris Richardson, Gavin R Schnitzler, Chao-Qiang Lai, et al.
Circulation. Cardiovascular Genetics|October 27, 2015
Eya4 Induces Hypertrophy via Regulation of p27kip1Tatjana Williams, Moritz Hundertmark, Peter Nordbeck, et al.
Circulation. Cardiovascular Genetics|December 4, 2014
Genetic evidence for PLASMINOGEN as a shared genetic risk factor of coronary artery disease and periodontitisArne S Schaefer, Gregor Bochenek, Arne Jochens, et al.
Circulation. Cardiovascular Genetics|May 10, 2011
Proteomic analysis yields an unexpected trans-acting point in control of the human sympathochromaffin phenotypeStéphane Chiron, Zhiyun Wei, Yuqing Chen, et al.
Circulation. Cardiovascular Genetics|May 10, 2011
Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotypeSusanne Probst, Erwin Oechslin, Pia Schuler, et al.
Circulation. Cardiovascular Genetics|April 20, 2010
A common variant at chromosome 9P21.3 is associated with age of onset of coronary disease but not subsequent mortalityKatrina L Ellis, Anna P Pilbrow, Chris M Frampton, et al.
Circulation. Cardiovascular Genetics|April 22, 2010
Letter by yilmaz et Al regarding article, "analysis of dystrophin deletion mutations predicts age of cardiomyopathy onset in becker muscular dystrophy"Ali Yilmaz, Joseph Suttie, Steffen E Petersen
Pageof 97