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D Woodrow

Showing results (121-130 of 177) with videos related to

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Human Genetics|January 5, 2007
Evidence in favor of linkage to human chromosomal regions 18q, 5q and 13q for bicuspid aortic valve and associated cardiovascular malformationsLisa J Martin, Vijaya Ramachandran, Linda H Cripe, et al.
Pediatric Research|March 7, 2003
Clinical, genetic, and biophysical characterization of a homozygous HERG mutation causing severe neonatal long QT syndromeWalter H Johnson, Ping Yang, Tao Yang, et al.
Circulation. Arrhythmia and Electrophysiology|August 1, 2015
Mouse Model of Human Congenital Heart Disease: Progressive Atrioventricular Block Induced by a Heterozygous Nkx2-5 Homeodomain Missense MutationRajib Chowdhury, Hassan Ashraf, Michelle Melanson, et al.
The American Journal of Cardiology|January 21, 2011
Spontaneous rupture of atrioventricular valve tensor apparatus as late manifestation of anti-Ro/SSA antibody-mediated cardiac diseaseBettina F Cuneo, Deborah Fruitman, D Woodrow Benson, et al.
The Journal of Clinical Investigation|October 3, 2003
Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)D Woodrow Benson, Dao W Wang, Macaira Dyment, et al.
Journal of Medicinal Chemistry|December 6, 2011
Fragment-based discovery of bromodomain inhibitors part 2: optimization of phenylisoxazole sulfonamidesPaul Bamborough, Hawa Diallo, Jonathan D Goodacre, et al.
Circulation. Cardiovascular Genetics|August 3, 2014
Whole exome sequencing for familial bicuspid aortic valve identifies putative variantsLisa J Martin, Valentina Pilipenko, Kenneth M Kaufman, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|July 11, 2006
Abnormalities of diastolic function precede dilated cardiomyopathy associated with Duchenne muscular dystrophyLarry W Markham, Erik C Michelfelder, William L Border, et al.
Heart Rhythm|November 9, 2011
Developmentally regulated SCN5A splice variant potentiates dysfunction of a novel mutation associated with severe fetal arrhythmiaLisa L Murphy, Anita J Moon-Grady, Bettina F Cuneo, et al.
Human Molecular Genetics|November 28, 2009
Deletion of ETS-1, a gene in the Jacobsen syndrome critical region, causes ventricular septal defects and abnormal ventricular morphology in miceMaoqing Ye, Chris Coldren, Xingqun Liang, et al.
Pageof 18

Showing results (121-130 of 177) with videos related to

Sort By:
Pageof 18
Human Genetics|January 5, 2007
Evidence in favor of linkage to human chromosomal regions 18q, 5q and 13q for bicuspid aortic valve and associated cardiovascular malformationsLisa J Martin, Vijaya Ramachandran, Linda H Cripe, et al.
Pediatric Research|March 7, 2003
Clinical, genetic, and biophysical characterization of a homozygous HERG mutation causing severe neonatal long QT syndromeWalter H Johnson, Ping Yang, Tao Yang, et al.
Circulation. Arrhythmia and Electrophysiology|August 1, 2015
Mouse Model of Human Congenital Heart Disease: Progressive Atrioventricular Block Induced by a Heterozygous Nkx2-5 Homeodomain Missense MutationRajib Chowdhury, Hassan Ashraf, Michelle Melanson, et al.
The American Journal of Cardiology|January 21, 2011
Spontaneous rupture of atrioventricular valve tensor apparatus as late manifestation of anti-Ro/SSA antibody-mediated cardiac diseaseBettina F Cuneo, Deborah Fruitman, D Woodrow Benson, et al.
The Journal of Clinical Investigation|October 3, 2003
Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)D Woodrow Benson, Dao W Wang, Macaira Dyment, et al.
Journal of Medicinal Chemistry|December 6, 2011
Fragment-based discovery of bromodomain inhibitors part 2: optimization of phenylisoxazole sulfonamidesPaul Bamborough, Hawa Diallo, Jonathan D Goodacre, et al.
Circulation. Cardiovascular Genetics|August 3, 2014
Whole exome sequencing for familial bicuspid aortic valve identifies putative variantsLisa J Martin, Valentina Pilipenko, Kenneth M Kaufman, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|July 11, 2006
Abnormalities of diastolic function precede dilated cardiomyopathy associated with Duchenne muscular dystrophyLarry W Markham, Erik C Michelfelder, William L Border, et al.
Heart Rhythm|November 9, 2011
Developmentally regulated SCN5A splice variant potentiates dysfunction of a novel mutation associated with severe fetal arrhythmiaLisa L Murphy, Anita J Moon-Grady, Bettina F Cuneo, et al.
Human Molecular Genetics|November 28, 2009
Deletion of ETS-1, a gene in the Jacobsen syndrome critical region, causes ventricular septal defects and abnormal ventricular morphology in miceMaoqing Ye, Chris Coldren, Xingqun Liang, et al.
Pageof 18