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T Keating

Showing results (151-160 of 213) with videos related to

Pageof 22
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Human Molecular Genetics|July 1, 1997
Elastin point mutations cause an obstructive vascular disease, supravalvular aortic stenosisD Y Li, A E Toland, B B Boak, et al.
Biological Psychology|August 19, 2021
Measuring interoception: The phase adjustment taskD Plans, S Ponzo, D Morelli, et al.
Journal of Medical Genetics|May 4, 2004
The common SCN5A mutation R1193Q causes LQTS-type electrophysiological alterations of the cardiac sodium channelQ Wang, S Chen, Q Chen, et al.
Cell|April 29, 1999
MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmiaG W Abbott, F Sesti, I Splawski, et al.
Nature|June 2, 1998
Elastin is an essential determinant of arterial morphogenesisD Y Li, B Brooke, E C Davis, et al.
Cell|March 10, 1995
SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndromeQ Wang, J Shen, I Splawski, et al.
Genes & Development|May 5, 2005
p38 MAP kinase inhibition enables proliferation of adult mammalian cardiomyocytesFelix B Engel, Michael Schebesta, Mychelle T Duong, et al.
Cardiovascular Research|May 24, 2019
Aldosterone induces trained immunity: the role of fatty acid synthesisCharlotte D C C van der Heijden, Samuel T Keating, Laszlo Groh, et al.
Nature Genetics|September 1, 1993
Hemizygosity at the elastin locus in a developmental disorder, Williams syndromeA K Ewart, C A Morris, D Atkinson, et al.
Journal of Inflammation (London, England)|September 22, 2007
Host predisposition by endogenous Transforming Growth Factor-beta1 overexpression promotes pulmonary fibrosis following bleomycin injuryYussef Haider, Andrea P Malizia, Dominic T Keating, et al.
Pageof 22

Showing results (151-160 of 213) with videos related to

Sort By:
Pageof 22
Human Molecular Genetics|July 1, 1997
Elastin point mutations cause an obstructive vascular disease, supravalvular aortic stenosisD Y Li, A E Toland, B B Boak, et al.
Biological Psychology|August 19, 2021
Measuring interoception: The phase adjustment taskD Plans, S Ponzo, D Morelli, et al.
Journal of Medical Genetics|May 4, 2004
The common SCN5A mutation R1193Q causes LQTS-type electrophysiological alterations of the cardiac sodium channelQ Wang, S Chen, Q Chen, et al.
Cell|April 29, 1999
MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmiaG W Abbott, F Sesti, I Splawski, et al.
Nature|June 2, 1998
Elastin is an essential determinant of arterial morphogenesisD Y Li, B Brooke, E C Davis, et al.
Cell|March 10, 1995
SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndromeQ Wang, J Shen, I Splawski, et al.
Genes & Development|May 5, 2005
p38 MAP kinase inhibition enables proliferation of adult mammalian cardiomyocytesFelix B Engel, Michael Schebesta, Mychelle T Duong, et al.
Cardiovascular Research|May 24, 2019
Aldosterone induces trained immunity: the role of fatty acid synthesisCharlotte D C C van der Heijden, Samuel T Keating, Laszlo Groh, et al.
Nature Genetics|September 1, 1993
Hemizygosity at the elastin locus in a developmental disorder, Williams syndromeA K Ewart, C A Morris, D Atkinson, et al.
Journal of Inflammation (London, England)|September 22, 2007
Host predisposition by endogenous Transforming Growth Factor-beta1 overexpression promotes pulmonary fibrosis following bleomycin injuryYussef Haider, Andrea P Malizia, Dominic T Keating, et al.
Pageof 22