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Craig T Basson

Showing results (11-20 of 41) with videos related to

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Circulation. Cardiovascular Genetics|October 27, 2012
TGFβRIIb mutations trigger aortic aneurysm pathogenesis by altering transforming growth factor β2 signal transductionKatharine J Bee, David C Wilkes, Richard B Devereux, et al.
Journal of Cardiovascular Electrophysiology|April 29, 2003
Molecular genetic analysis of PRKAG2 in sporadic Wolff-Parkinson-White syndromeCarl J Vaughan, Yolanda Hom, Daniel A Okin, et al.
Annals of the New York Academy of Sciences|December 22, 2006
Structural and functional genetic disorders of the great vessels and outflow tractsKatharine J Bee, David Wilkes, Richard B Devereux, et al.
Molecular Endocrinology (Baltimore, Md.)|May 27, 2006
Haploinsufficiency at the protein kinase A RI alpha gene locus leads to fertility defects in male mice and menKimberly A Burton, Deborah A McDermott, David Wilkes, et al.
Physiological Genomics|May 13, 2004
A role for Tbx5 in proepicardial cell migration during cardiogenesisCathy J Hatcher, Nata Y S-G Diman, Min-Su Kim, et al.
Physiological Genomics|March 21, 2013
Keratin gene expression profiles after digit amputation in C57BL/6 vs. regenerative MRL mice imply an early regenerative keratinocyte activated-like stateChia-Ho Cheng, John Leferovich, Xiang-Ming Zhang, et al.
Circulation Research|September 24, 2014
Tbx5 is required for avian and Mammalian epicardial formation and coronary vasculogenesisNata Y S-G Diman, Gabriel Brooks, Boudewijn P T Kruithof, et al.
Diabetes, Obesity & Metabolism|July 15, 2021
Licogliflozin versus placebo in women with polycystic ovary syndrome: A randomized, double-blind, phase 2 trialSusanne Tan, Stanislav Ignatenko, Frank Wagner, et al.
Circulation|May 24, 2007
Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of PediatricsMary Ella Pierpont, Craig T Basson, D Woodrow Benson, et al.
Cardiovascular Research|November 17, 2007
A KCNE2 mutation in a patient with cardiac arrhythmia induced by auditory stimuli and serum electrolyte imbalanceEarl Gordon, Gianina Panaghie, Liyong Deng, et al.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
Circulation. Cardiovascular Genetics|October 27, 2012
TGFβRIIb mutations trigger aortic aneurysm pathogenesis by altering transforming growth factor β2 signal transductionKatharine J Bee, David C Wilkes, Richard B Devereux, et al.
Journal of Cardiovascular Electrophysiology|April 29, 2003
Molecular genetic analysis of PRKAG2 in sporadic Wolff-Parkinson-White syndromeCarl J Vaughan, Yolanda Hom, Daniel A Okin, et al.
Annals of the New York Academy of Sciences|December 22, 2006
Structural and functional genetic disorders of the great vessels and outflow tractsKatharine J Bee, David Wilkes, Richard B Devereux, et al.
Molecular Endocrinology (Baltimore, Md.)|May 27, 2006
Haploinsufficiency at the protein kinase A RI alpha gene locus leads to fertility defects in male mice and menKimberly A Burton, Deborah A McDermott, David Wilkes, et al.
Physiological Genomics|May 13, 2004
A role for Tbx5 in proepicardial cell migration during cardiogenesisCathy J Hatcher, Nata Y S-G Diman, Min-Su Kim, et al.
Physiological Genomics|March 21, 2013
Keratin gene expression profiles after digit amputation in C57BL/6 vs. regenerative MRL mice imply an early regenerative keratinocyte activated-like stateChia-Ho Cheng, John Leferovich, Xiang-Ming Zhang, et al.
Circulation Research|September 24, 2014
Tbx5 is required for avian and Mammalian epicardial formation and coronary vasculogenesisNata Y S-G Diman, Gabriel Brooks, Boudewijn P T Kruithof, et al.
Diabetes, Obesity & Metabolism|July 15, 2021
Licogliflozin versus placebo in women with polycystic ovary syndrome: A randomized, double-blind, phase 2 trialSusanne Tan, Stanislav Ignatenko, Frank Wagner, et al.
Circulation|May 24, 2007
Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of PediatricsMary Ella Pierpont, Craig T Basson, D Woodrow Benson, et al.
Cardiovascular Research|November 17, 2007
A KCNE2 mutation in a patient with cardiac arrhythmia induced by auditory stimuli and serum electrolyte imbalanceEarl Gordon, Gianina Panaghie, Liyong Deng, et al.
Pageof 5