A Central Role for Troponin C Amino-Terminal α-Helix in Vertebrate Thin Filament Ca<sup>2+</sup>-Activation
Summary
working-paper
A Central Role for Troponin C Amino-Terminal α-Helix in Vertebrate Thin Filament Ca<sup>2+</sup>-Activation
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Physchem
Summary
journal-article
A Central Role for Troponin C Amino-Terminal α-Helix in Vertebrate Thin Filament Ca<sup>2+</sup>-Activation
Summary
preprint
A Central Role for Troponin C Amino-Terminal α-Helix in Vertebrate Thin Filament Ca2+-Activation
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Physchem
Summary
journal-article
Guidelines on antibody use in physiology research
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American Journal of Physiology-Renal Physiology
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Evaluating the Sex Dependent Influence of Sarcospan on Cardiometabolic Disease Traits in Mice
Summary
preprint
Sarcospan Deficiency Increases Oxidative Stress and Arrhythmias in Hearts after Acute Ischemia-Reperfusion Injury
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International Journal of Molecular Sciences
Summary
journal-article
Sarcospan Deficiency Increases Oxidative Stress and Arrhythmias in Hearts after Acute Ischemia-Reperfusion Injury
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International Journal of Molecular Sciences
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Editorial: Skeletal muscle in age-related diseases: From molecular pathogenesis to potential interventions.
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Frontiers in physiology
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Autoimmunity as a sequela to obesity and systemic inflammation.
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Frontiers in physiology
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On 'The content of troponin, tropomyosin, actin, and myosin in rabbit skeletal muscle myofibrils' by James D. Potter.
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Archives of biochemistry and biophysics
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A comprehensive guide to genetic variants and post-translational modifications of cardiac troponin C
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Post-translational modification patterns on β-myosin heavy chain are altered in ischemic and non-ischemic human hearts
Summary
other
Cardiovascular Injury Due to SARS-CoV-2
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Current Clinical Microbiology Reports
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Anomalous structural dynamics of minimally frustrated residues in cardiac troponin C triggers hypertrophic cardiomyopathy.
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Chemical science
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Sexual dimorphism in cardiac transcriptome associated with a troponin C murine model of hypertrophic cardiomyopathy.
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Physiological reports
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Essential roles of the dystrophin-glycoprotein complex in different cardiac pathologies.
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Advances in medical sciences
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Meta-analysis of cardiomyopathy-associated variants in troponin genes identifies loci and intragenic hotspots that are associated with worse clinical outcomes.
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Journal of Molecular and Cellular Cardiology
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Sexual dimorphism in cardiac transcriptome associated with a troponin C murine model of hypertrophic cardiomyopathy
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Physiological Reports
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The missing links within troponin
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Archives of Biochemistry and Biophysics
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Stabilization of the cardiac sarcolemma by sarcospan rescues DMD-associated cardiomyopathy
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JCI Insight
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Hypertrophic cardiomyopathy cardiac troponin C mutations differentially affect slow skeletal and cardiac muscle regulation
In Vivo Analysis of Troponin C Knock-In (A8V) Mice: Evidence that TNNC1 Is a Hypertrophic Cardiomyopathy Susceptibility Gene
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Circulation: Cardiovascular Genetics
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Pathogenesis associated with a restrictive cardiomyopathy mutant in cardiac troponin T is due to reduced protein stability and greatly increased myofilament Ca<sup>2+</sup> sensitivity
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Biochimica et Biophysica Acta - General Subjects
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Structural considerations for chromatin state models with transcription as a functional readout
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FEBS Letters
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A mutation in TNNC1-encoded cardiac troponin C, TNNC1-A31S, predisposes to hypertrophic cardiomyopathy and ventricular fibrillation
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Journal of Biological Chemistry
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Quantitative analysis of chromatin proteomes in disease.
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Journal of visualized experiments : JoVE
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other
The functional properties of human slow skeletal troponin T isoforms in cardiac muscle regulation
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Journal of Biological Chemistry
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Functional characterization of TNNC1 rare variants identified in dilated cardiomyopathy
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Journal of Biological Chemistry
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Fetal cardiac troponin isoforms rescue the increased Ca<sup>2+</sup> sensitivity produced by a novel double deletion in cardiac troponin T linked to restrictive cardiomyopathy: A clinical, genetic, and functional approach
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Journal of Biological Chemistry
Summary
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Strong cross-bridges potentiate the Ca<sup>2+</sup> affinity changes produced by hypertrophic cardiomyopathy cardiac troponin C mutants in myofilaments: A fast kinetic approach
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Journal of Biological Chemistry
Summary
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Mutations in Troponin that cause HCM, DCM AND RCM: What can we learn about thin filament function?
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Journal of Molecular and Cellular Cardiology
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Cardiac troponin mutations and restrictive cardiomyopathy
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Journal of Biomedicine and Biotechnology
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Predicting cardiomyopathic phenotypes by altering Ca<sup>2+</sup> affinity of cardiac troponin C
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Journal of Biological Chemistry
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A functional and structural study of tropon in C mutations related to hypertrophic cardiomyopathy
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Journal of Biological Chemistry
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Clinical and functional Characterization of TNNT2 mutations identified in patients with dilated cardiomyopathy
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Circulation: Cardiovascular Genetics
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Troponin and cardiomyopathy
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Biochemical and Biophysical Research Communications
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A troponin T mutation that causes infantile restrictive cardiomyopathy increases Ca<sup>2+</sup> sensitivity of force development and impairs the inhibitory properties of troponin
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Journal of Biological Chemistry
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Molecular and functional characterization of novel hypertrophic cardiomyopathy susceptibility mutations in TNNC1-encoded troponin C
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Journal of Molecular and Cellular Cardiology
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Transgenic mice expressing Na<sup>+</sup>-K<sup>+</sup>-ATPase in smooth muscle decreases blood pressure
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American Journal of Physiology - Heart and Circulatory Physiology
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Global analysis of cellular factors and responses involved in Pseudomonas aeruginosa resistance to arsenite
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Journal of Bacteriology
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Na<sup>+</sup> pump α<inf>2</inf>-isoform specifically couples to contractility in vascular smooth muscle: Evidence from gene-targeted neonatal mice