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Mark T Keating

Showing results (31-40 of 43) with videos related to

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Development (Cambridge, England)|December 6, 2002
A critical role for elastin signaling in vascular morphogenesis and diseaseSatyajit K Karnik, Benjamin S Brooke, Antonio Bayes-Genis, et al.
Cardiovascular Research|June 15, 2007
Impaired interaction between the slide helix and the C-terminus of Kir2.1: a novel mechanism of Andersen syndromeNiels Decher, Vijay Renigunta, Marylou Zuzarte, et al.
Molecular Cell|December 22, 2004
The SRF target gene Fhl2 antagonizes RhoA/MAL-dependent activation of SRFUlrike Philippar, Gerhard Schratt, Christoph Dieterich, et al.
Science (New York, N.Y.)|August 24, 2002
Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmiaIgor Splawski, Katherine W Timothy, Michihiro Tateyama, et al.
Journal of the American College of Cardiology|September 15, 2004
An intronic mutation causes long QT syndromeLi Zhang, G Michael Vincent, Marco Baralle, et al.
Nature Chemical Biology|March 28, 2006
Chemical modulation of receptor signaling inhibits regenerative angiogenesis in adult zebrafishPeter E Bayliss, Kimberly L Bellavance, Geoffrey G Whitehead, et al.
Biomaterials|December 5, 2016
Recapitulating the human tumor microenvironment: Colon tumor-derived extracellular matrix promotes angiogenesis and tumor cell growthMónica Romero-López, Andrew L Trinh, Agua Sobrino, et al.
Cell|September 30, 2004
Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autismIgor Splawski, Katherine W Timothy, Leah M Sharpe, et al.
Heart Rhythm|April 27, 2005
Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testingMichael J Ackerman, Igor Splawski, Jonathan C Makielski, et al.
American Journal of Medical Genetics. Part A|October 14, 2003
GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome regionColleen A Morris, Carolyn B Mervis, Holly H Hobart, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Development (Cambridge, England)|December 6, 2002
A critical role for elastin signaling in vascular morphogenesis and diseaseSatyajit K Karnik, Benjamin S Brooke, Antonio Bayes-Genis, et al.
Cardiovascular Research|June 15, 2007
Impaired interaction between the slide helix and the C-terminus of Kir2.1: a novel mechanism of Andersen syndromeNiels Decher, Vijay Renigunta, Marylou Zuzarte, et al.
Molecular Cell|December 22, 2004
The SRF target gene Fhl2 antagonizes RhoA/MAL-dependent activation of SRFUlrike Philippar, Gerhard Schratt, Christoph Dieterich, et al.
Science (New York, N.Y.)|August 24, 2002
Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmiaIgor Splawski, Katherine W Timothy, Michihiro Tateyama, et al.
Journal of the American College of Cardiology|September 15, 2004
An intronic mutation causes long QT syndromeLi Zhang, G Michael Vincent, Marco Baralle, et al.
Nature Chemical Biology|March 28, 2006
Chemical modulation of receptor signaling inhibits regenerative angiogenesis in adult zebrafishPeter E Bayliss, Kimberly L Bellavance, Geoffrey G Whitehead, et al.
Biomaterials|December 5, 2016
Recapitulating the human tumor microenvironment: Colon tumor-derived extracellular matrix promotes angiogenesis and tumor cell growthMónica Romero-López, Andrew L Trinh, Agua Sobrino, et al.
Cell|September 30, 2004
Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autismIgor Splawski, Katherine W Timothy, Leah M Sharpe, et al.
Heart Rhythm|April 27, 2005
Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testingMichael J Ackerman, Igor Splawski, Jonathan C Makielski, et al.
American Journal of Medical Genetics. Part A|October 14, 2003
GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome regionColleen A Morris, Carolyn B Mervis, Holly H Hobart, et al.
Pageof 5