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期刊名:Journal of molecular and cellular cardiology plus

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ISSN:N/A

e-ISSN:2772-9761

IF/分区:2.2/Q2

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共收录本刊相关文章索引167
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Jessica Joshua,Jeff L Caswell,Josep M Monné Rodriguez et al. Jessica Joshua et al.
Hypertrophic cardiomyopathy (HCM) is a common heart disease in humans and cats, nonetheless, the disease pathogenesis is still poorly understood. MicroRNAs are suspected to be involved in the disease process but the myocardial microRNA expr...
Garrett Jensen,Xinjie Wang,Jacob Kuempel et al. Garrett Jensen et al.
Immune checkpoint inhibitor-associated myocarditis is the most lethal side effect of immune checkpoint blockade. Myocarditis leads to persistently increased mortality and lacks effective treatments. The development of patient-relevant disea...
Jules C Hancox,Yibo Wang,Caroline S Copeland et al. Jules C Hancox et al.
The growing use of nitazene synthetic opioids heralds a new phase of the opioid crisis. However, limited information exists on the toxic effects of these drugs, aside from a propensity for respiratory depression. With restricted research av...
Yangpeng Li,Zhu Liu,Christopher O&#x;Shea et al. Yangpeng Li et al.
Abnormal regional variations in electrical and calcium homeostasis properties have been implicated in catecholaminergic polymorphic ventricular tachycardias (CPVT) attributable to abnormal RyR2-mediated store Ca2+ release, but their underly...
Arpita Deb,Brian D Tow,Jie Hao et al. Arpita Deb et al.
Background: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a genetic arrhythmic syndrome caused by mutations in the calcium (Ca2+) release channel ryanodine receptor (RyR2) and its accessory proteins. The...
Allison C Wexler,Holly Dooge,Sarah El-Meanawy et al. Allison C Wexler et al.
The small splice variant of the sulfonylurea receptor protein isoform 2 A (SUR2A-55) targets mitochondria and enhances mitoKATP activity. In male mice the overexpression of this protein promotes cardioprotection, reducing myocardial injury ...
Arpana Vaniya,Anja Karlstaedt,Damla Gulkok et al. Arpana Vaniya et al.
Introduction: Hypertrophic cardiomyopathy (HCM) results from pathogenic variants in sarcomeric protein genes that increase myocyte energy demand and lead to cardiac hypertrophy. However, it is unknown whether a common met...
Jessa L Aldridge,Emily Davis Alexander,Allison A Franklin et al. Jessa L Aldridge et al.
Dravet Syndrome (DS) is a pediatric-onset epilepsy with an elevated risk of Sudden Unexpected Death in Epilepsy (SUDEP). Most individuals with DS possess mutations in the voltage-gated sodium channel gene Scn1a, expressed in both the brain ...
Natalie N Khalil,Megan L Rexius-Hall,Sean Escopete et al. Natalie N Khalil et al.
Myocardial infarction (MI) causes hypoxic injury to downstream myocardial tissue, which initiates a wound healing response that replaces injured myocardial tissue with a scar. Wound healing is a complex process that consists of multiple pha...
Amanda Davenport,Chase W Kessinger,Ryan D Pfeiffer et al. Amanda Davenport et al.
We have previously shown that the Myh6 promoter drives Cre expression in a subset of male germ line cells in three independent Myh6-Cre mouse lines, including two transgenic lines and one knock-in allele. In this study, we further compared ...