Found: 21
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Novel therapeutic approaches for heart failure by normalizing calcium cycling.
- Published in:
- Nature Reviews Drug Discovery, 2004, v. 3, n. 7, p. 1, doi. 10.1038/nrd1440
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- Publication type:
- Article
PKC inhibition ameliorates the cardiac phenotype in a mouse model of myotonic dystrophy type 1.
- Published in:
- 2009
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- Publication type:
- journal article
Cardiac‐specific ablation of glutaredoxin 3 leads to cardiac hypertrophy and heart failure.
- Published in:
- Physiological Reports, 2019, v. 7, n. 8, p. N.PAG, doi. 10.14814/phy2.14071
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- Publication type:
- Article
Ranolazine prevents pressure overload‐induced cardiac hypertrophy and heart failure by restoring aberrant Na<sup>+</sup> and Ca<sup>2+</sup> handling.
- Published in:
- Journal of Cellular Physiology, 2019, v. 234, n. 7, p. 11587, doi. 10.1002/jcp.27791
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- Publication type:
- Article
Ryanodine Receptor-Targeted Anti-Arrhythmic Therapy.
- Published in:
- Annals of the New York Academy of Sciences, 2005, v. 1047, n. 1, p. 366, doi. 10.1196/annals.1341.032
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- Publication type:
- Article
Emerging roles of junctophilin-2 in the heart and implications for cardiac diseases.
- Published in:
- Cardiovascular Research, 2014, v. 103, n. 2, p. 198, doi. 10.1093/cvr/cvu151
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- Publication type:
- Article
Impaired local regulation of ryanodine receptor type 2 by protein phosphatase 1 promotes atrial fibrillation.
- Published in:
- Cardiovascular Research, 2014, v. 103, n. 1, p. 178, doi. 10.1093/cvr/cvu123
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- Publication type:
- Article
Ryanodine receptor phosphorylation by oxidized CaMKII contributes to the cardiotoxic effects of cardiac glycosides.
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- Cardiovascular Research, 2014, v. 101, n. 1, p. 165, doi. 10.1093/cvr/cvt233
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- Publication type:
- Article
Critical roles of junctophilin-2 in T-tubule and excitation–contraction coupling maturation during postnatal development.
- Published in:
- Cardiovascular Research, 2013, v. 100, n. 1, p. 54, doi. 10.1093/cvr/cvt180
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- Publication type:
- Article
Junctophilin-2 is necessary for T-tubule maturation during mouse heart development.
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- Cardiovascular Research, 2013, v. 100, n. 1, p. 44, doi. 10.1093/cvr/cvt133
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- Publication type:
- Article
The ryanodine receptor channel as a molecular motif in atrial fibrillation: pathophysiological and therapeutic implications.
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- Cardiovascular Research, 2011, v. 89, n. 4, p. 734, doi. 10.1093/cvr/cvq324
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- Publication type:
- Article
Angiogenesis-independent cardioprotection in FGF-1 transgenic mice.
- Published in:
- Cardiovascular Research, 2002, v. 55, n. 4, p. 768, doi. 10.1016/S0008-6363(02)00494-7
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- Publication type:
- Article
Mouse electrocardiography.
- Published in:
- Cardiovascular Research, 2000, v. 45, n. 1, p. 231
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- Publication type:
- Article
Novel Insights in the Congenital Long QT Syndrome.
- Published in:
- Annals of Internal Medicine, 2002, v. 137, n. 12, p. 981, doi. 10.7326/0003-4819-137-12-200212170-00012
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- Publication type:
- Article
The mitochondrial uniporter controls fight or flight heart rate increases.
- Published in:
- Nature Communications, 2015, v. 6, n. 1, p. 6081, doi. 10.1038/ncomms7081
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- Publication type:
- Article
Ca2+/calmodulin‐dependent kinase IIδC‐induced chronic heart failure does not depend on sarcoplasmic reticulum Ca2+ leak.
- Published in:
- ESC Heart Failure, 2024, v. 11, n. 4, p. 2191, doi. 10.1002/ehf2.14772
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- Publication type:
- Article
Methyl-CpG binding-protein 2 function in cholinergic neurons mediates cardiac arrhythmogenesis.
- Published in:
- Human Molecular Genetics, 2016, v. 25, n. 22, p. 4983, doi. 10.1093/hmg/ddw326
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- Publication type:
- Article
In Vivo Cardiac Electrophysiology in Mice: Determination of Atrial and Ventricular Arrhythmic Substrates.
- Published in:
- Current Protocols, 2024, v. 4, n. 2, p. 1, doi. 10.1002/cpz1.994
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- Publication type:
- Article
Heart-specific overexpression of CUGBP1 reproduces functional and molecular abnormalities of myotonic dystrophy type 1.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 6, p. 1066, doi. 10.1093/hmg/ddp570
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- Publication type:
- Article
A Novel mutation L619F in the cardiac Na<sup>+</sup> channel SCN5A associated with long-QT syndrome (LQT3): a role for the I-II linker in inactivation gating (Communicated by Mark H. Paalman) Online Citation: Human Mutation, Mutation in Brief #607(2002) online http://www.interscience.wiley.com/humanmutation/pdf/mutation/607.pdf)
- Published in:
- Human Mutation, 2003, v. 21, n. 5, p. 552, doi. 10.1002/humu.9136
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- Publication type:
- Article
A Novel mutation L619F in the cardiac Na+ channel SCN5A associated with long‐QT syndrome (LQT3): a role for the I‐II linker in inactivation gatingCommunicated by Mark H. PaalmanOnline Citation: Human Mutation, Mutation in Brief #607(2002) onlinehttp://www.interscience.wiley.com/humanmutation/pdf/mutation/607.pdf
- Published in:
- Human Mutation, 2003, v. 21, n. 5, p. 552, doi. 10.1002/humu.9136
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- Publication type:
- Article