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M Moorman

Showing results (231-240 of 248) with videos related to

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Circulation Research|December 9, 2008
A caudal proliferating growth center contributes to both poles of the forming heart tubeGert van den Berg, Radwan Abu-Issa, Bouke A de Boer, et al.
Circulation Research|January 20, 2007
Molecular pathway for the localized formation of the sinoatrial nodeMathilda T M Mommersteeg, Willem M H Hoogaars, Owen W J Prall, et al.
Cellular and Molecular Life Sciences : CMLS|December 2, 2011
Tbx2 and Tbx3 induce atrioventricular myocardial development and endocardial cushion formationReena Singh, Willem M Hoogaars, Phil Barnett, et al.
Plos One|August 10, 2011
The BMP antagonist follistatin-like 1 is required for skeletal and lung organogenesisMarc Sylva, Vivian S W Li, Anita A A Buffing, et al.
Science (New York, N.Y.)|November 26, 2016
An interactive three-dimensional digital atlas and quantitative database of human developmentBernadette S de Bakker, Kees H de Jong, Jaco Hagoort, et al.
Cardiovascular Research|August 29, 2006
Temporal patterns of electrical remodeling in canine ventricular hypertrophy: focus on IKs downregulation and blunted beta-adrenergic activationMilan Stengl, Christian Ramakers, Dirk W Donker, et al.
Genes & Development|May 3, 2007
Tbx3 controls the sinoatrial node gene program and imposes pacemaker function on the atriaWillem M H Hoogaars, Angela Engel, Janynke F Brons, et al.
Circulation. Cardiovascular Genetics|December 4, 2010
Mutations in the sarcomere gene MYH7 in Ebstein anomalyAlex V Postma, Klaartje van Engelen, Judith van de Meerakker, et al.
European Journal of Human Genetics : EJHG|March 10, 2011
A novel autosomal dominant condition consisting of congenital heart defects and low atrial rhythm maps to chromosome 9qJudith B A van de Meerakker, Klaartje van Engelen, Inge B Mathijssen, et al.
Journal of Medical Genetics|November 21, 2013
Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canalA V Postma, M Alders, M Sylva, et al.
Pageof 25

Showing results (231-240 of 248) with videos related to

Sort By:
Pageof 25
Circulation Research|December 9, 2008
A caudal proliferating growth center contributes to both poles of the forming heart tubeGert van den Berg, Radwan Abu-Issa, Bouke A de Boer, et al.
Circulation Research|January 20, 2007
Molecular pathway for the localized formation of the sinoatrial nodeMathilda T M Mommersteeg, Willem M H Hoogaars, Owen W J Prall, et al.
Cellular and Molecular Life Sciences : CMLS|December 2, 2011
Tbx2 and Tbx3 induce atrioventricular myocardial development and endocardial cushion formationReena Singh, Willem M Hoogaars, Phil Barnett, et al.
Plos One|August 10, 2011
The BMP antagonist follistatin-like 1 is required for skeletal and lung organogenesisMarc Sylva, Vivian S W Li, Anita A A Buffing, et al.
Science (New York, N.Y.)|November 26, 2016
An interactive three-dimensional digital atlas and quantitative database of human developmentBernadette S de Bakker, Kees H de Jong, Jaco Hagoort, et al.
Cardiovascular Research|August 29, 2006
Temporal patterns of electrical remodeling in canine ventricular hypertrophy: focus on IKs downregulation and blunted beta-adrenergic activationMilan Stengl, Christian Ramakers, Dirk W Donker, et al.
Genes & Development|May 3, 2007
Tbx3 controls the sinoatrial node gene program and imposes pacemaker function on the atriaWillem M H Hoogaars, Angela Engel, Janynke F Brons, et al.
Circulation. Cardiovascular Genetics|December 4, 2010
Mutations in the sarcomere gene MYH7 in Ebstein anomalyAlex V Postma, Klaartje van Engelen, Judith van de Meerakker, et al.
European Journal of Human Genetics : EJHG|March 10, 2011
A novel autosomal dominant condition consisting of congenital heart defects and low atrial rhythm maps to chromosome 9qJudith B A van de Meerakker, Klaartje van Engelen, Inge B Mathijssen, et al.
Journal of Medical Genetics|November 21, 2013
Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canalA V Postma, M Alders, M Sylva, et al.
Pageof 25