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Cold Spring Harbor Perspectives in Medicine
|
October 3, 2014
Insights into the genetic structure of congenital heart disease from human and murine studies on monogenic disorders
Terence Prendiville, Patrick Y Jay, William T Pu
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
February 8, 2008
HIV protease inhibitors that block GLUT4 precipitate acute, decompensated heart failure in a mouse model of dilated cardiomyopathy
Paul W Hruz, Qingyun Yan, Heidi Struthers, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
April 7, 2017
The Complex Genetic Basis of Congenital Heart Defects
Ehiole Akhirome, Nephi A Walton, Julie M Nogee, et al.
Cardiovascular Research
|
November 1, 2011
Enhanced cardiac PI3Kα signalling mitigates arrhythmogenic electrical remodelling in pathological hypertrophy and heart failure
Kai-Chien Yang, Patrick Y Jay, Julie R McMullen, et al.
Journal of Cardiovascular Electrophysiology
|
January 28, 2005
Absence of Msx2 does not affect cardiac conduction or rescue conduction defects associated with Nkx2-5 mutation
Patrick Y Jay, Colin T Maguire, Hiroko Wakimoto, et al.
Physiological Genomics
|
November 22, 2012
Association of genes with physiological functions by comparative analysis of pooled expression microarray data
Iuan-bor D Chen, Vinay K Rathi, Diana S DeAndrade, et al.
Physiological Reports
|
April 29, 2014
Ex vivo, microelectrode analysis of conduction through the AV node of wild-type and Nkx2-5 mutant mouse hearts as guided by a Cx40-eGFP transgenic reporter
Avihu Z Gazit, Alex Li, Jacob S Choi, et al.
Development, Growth & Differentiation
|
April 16, 2009
Activation of Tolloid-like 1 gene expression by the cardiac specific homeobox gene Nkx2-5
Inna Sabirzhanova, Boris Sabirzhanov, Joy Bjordahl, et al.
Novartis Foundation Symposium
|
September 6, 2003
Cardiac conduction and arrhythmia: insights from Nkx2.5 mutations in mouse and humans
Patrick Y Jay, Charles I Berul, Makoto Tanaka, et al.
Advances in Experimental Medicine and Biology
|
June 17, 2024
Molecular Pathways and Animal Models of Atrial Septal Defect
Rachel A Magnan, Lillian Kang, Karl R Degenhardt, et al.
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of 7
Search research articles
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Showing results (11-20 of 69) with videos related to
Sort By:
Page
of 7
Cold Spring Harbor Perspectives in Medicine
|
October 3, 2014
Insights into the genetic structure of congenital heart disease from human and murine studies on monogenic disorders
Terence Prendiville, Patrick Y Jay, William T Pu
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
February 8, 2008
HIV protease inhibitors that block GLUT4 precipitate acute, decompensated heart failure in a mouse model of dilated cardiomyopathy
Paul W Hruz, Qingyun Yan, Heidi Struthers, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
April 7, 2017
The Complex Genetic Basis of Congenital Heart Defects
Ehiole Akhirome, Nephi A Walton, Julie M Nogee, et al.
Cardiovascular Research
|
November 1, 2011
Enhanced cardiac PI3Kα signalling mitigates arrhythmogenic electrical remodelling in pathological hypertrophy and heart failure
Kai-Chien Yang, Patrick Y Jay, Julie R McMullen, et al.
Journal of Cardiovascular Electrophysiology
|
January 28, 2005
Absence of Msx2 does not affect cardiac conduction or rescue conduction defects associated with Nkx2-5 mutation
Patrick Y Jay, Colin T Maguire, Hiroko Wakimoto, et al.
Physiological Genomics
|
November 22, 2012
Association of genes with physiological functions by comparative analysis of pooled expression microarray data
Iuan-bor D Chen, Vinay K Rathi, Diana S DeAndrade, et al.
Physiological Reports
|
April 29, 2014
Ex vivo, microelectrode analysis of conduction through the AV node of wild-type and Nkx2-5 mutant mouse hearts as guided by a Cx40-eGFP transgenic reporter
Avihu Z Gazit, Alex Li, Jacob S Choi, et al.
Development, Growth & Differentiation
|
April 16, 2009
Activation of Tolloid-like 1 gene expression by the cardiac specific homeobox gene Nkx2-5
Inna Sabirzhanova, Boris Sabirzhanov, Joy Bjordahl, et al.
Novartis Foundation Symposium
|
September 6, 2003
Cardiac conduction and arrhythmia: insights from Nkx2.5 mutations in mouse and humans
Patrick Y Jay, Charles I Berul, Makoto Tanaka, et al.
Advances in Experimental Medicine and Biology
|
June 17, 2024
Molecular Pathways and Animal Models of Atrial Septal Defect
Rachel A Magnan, Lillian Kang, Karl R Degenhardt, et al.
Page
of 7