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John C Shryock

Showing results (41-50 of 52) with videos related to

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Circulation|April 13, 2011
Late sodium current contributes to the reverse rate-dependent effect of IKr inhibition on ventricular repolarizationLin Wu, Jihua Ma, Hong Li, et al.
Journal of Cardiovascular Pharmacology and Therapeutics|March 31, 2009
Ranolazine as an adjunct to cardioplegia: a potential new therapeutic applicationHyosook Hwang, Joseph M Arcidi, Sharon L Hale, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|February 21, 2007
Characterization of the potency, selectivity, and pharmacokinetic profile for six adenosine A2A receptor antagonistsMing Yang, Daniel Soohoo, Sandriyana Soelaiman, et al.
Experimental Physiology|February 3, 2015
Protein kinase C and Ca(2+) -calmodulin-dependent protein kinase II mediate the enlarged reverse INCX induced by ouabain-increased late sodium current in rabbit ventricular myocytesYing Wu, Leilei Wang, Jihua Ma, et al.
Journal of Cardiovascular Pharmacology|June 3, 2011
Antiadrenergic and hemodynamic effects of ranolazine in conscious dogsGong Zhao, Erin Walsh, John C Shryock, et al.
American Journal of Physiology. Cell Physiology|June 17, 2011
Nav1.5-dependent persistent Na+ influx activates CaMKII in rat ventricular myocytes and N1325S miceLina Yao, Peidong Fan, Zhan Jiang, et al.
Journal of Molecular and Cellular Cardiology|September 25, 2014
Intracellular Na+ overload causes oxidation of CaMKII and leads to Ca2+ mishandling in isolated ventricular myocytesSerge Viatchenko-Karpinski, Dmytro Kornyeyev, Nesrine El-Bizri, et al.
Journal of Medicinal Chemistry|February 21, 2003
Synthesis and biological effects of novel 2-amino-3-naphthoylthiophenes as allosteric enhancers of the A1 adenosine receptorPier Giovanni Baraldi, Romeo Romagnoli, Maria Giovanna Pavani, et al.
Journal of Medicinal Chemistry|August 30, 2008
Synthesis and biological evaluation of 2-amino-3-(4-chlorobenzoyl)-4-[N-(substituted) piperazin-1-yl]thiophenes as potent allosteric enhancers of the A1 adenosine receptorRomeo Romagnoli, Pier Giovanni Baraldi, Maria Dora Carrion, et al.
Bioorganic & Medicinal Chemistry|December 21, 2011
Structure-activity relationships of 2-amino-3-aroyl-4-[(4-arylpiperazin-1-yl)methyl]thiophenes. Part 2: Probing the influence of diverse substituents at the phenyl of the arylpiperazine moiety on allosteric enhancer activity at the A₁ adenosine receptorRomeo Romagnoli, Pier Giovanni Baraldi, Maria Dora Carrion, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Circulation|April 13, 2011
Late sodium current contributes to the reverse rate-dependent effect of IKr inhibition on ventricular repolarizationLin Wu, Jihua Ma, Hong Li, et al.
Journal of Cardiovascular Pharmacology and Therapeutics|March 31, 2009
Ranolazine as an adjunct to cardioplegia: a potential new therapeutic applicationHyosook Hwang, Joseph M Arcidi, Sharon L Hale, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|February 21, 2007
Characterization of the potency, selectivity, and pharmacokinetic profile for six adenosine A2A receptor antagonistsMing Yang, Daniel Soohoo, Sandriyana Soelaiman, et al.
Experimental Physiology|February 3, 2015
Protein kinase C and Ca(2+) -calmodulin-dependent protein kinase II mediate the enlarged reverse INCX induced by ouabain-increased late sodium current in rabbit ventricular myocytesYing Wu, Leilei Wang, Jihua Ma, et al.
Journal of Cardiovascular Pharmacology|June 3, 2011
Antiadrenergic and hemodynamic effects of ranolazine in conscious dogsGong Zhao, Erin Walsh, John C Shryock, et al.
American Journal of Physiology. Cell Physiology|June 17, 2011
Nav1.5-dependent persistent Na+ influx activates CaMKII in rat ventricular myocytes and N1325S miceLina Yao, Peidong Fan, Zhan Jiang, et al.
Journal of Molecular and Cellular Cardiology|September 25, 2014
Intracellular Na+ overload causes oxidation of CaMKII and leads to Ca2+ mishandling in isolated ventricular myocytesSerge Viatchenko-Karpinski, Dmytro Kornyeyev, Nesrine El-Bizri, et al.
Journal of Medicinal Chemistry|February 21, 2003
Synthesis and biological effects of novel 2-amino-3-naphthoylthiophenes as allosteric enhancers of the A1 adenosine receptorPier Giovanni Baraldi, Romeo Romagnoli, Maria Giovanna Pavani, et al.
Journal of Medicinal Chemistry|August 30, 2008
Synthesis and biological evaluation of 2-amino-3-(4-chlorobenzoyl)-4-[N-(substituted) piperazin-1-yl]thiophenes as potent allosteric enhancers of the A1 adenosine receptorRomeo Romagnoli, Pier Giovanni Baraldi, Maria Dora Carrion, et al.
Bioorganic & Medicinal Chemistry|December 21, 2011
Structure-activity relationships of 2-amino-3-aroyl-4-[(4-arylpiperazin-1-yl)methyl]thiophenes. Part 2: Probing the influence of diverse substituents at the phenyl of the arylpiperazine moiety on allosteric enhancer activity at the A₁ adenosine receptorRomeo Romagnoli, Pier Giovanni Baraldi, Maria Dora Carrion, et al.
Pageof 6