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期刊名:Function

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e-ISSN:2633-8823

IF/分区:5.0/Q1

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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
Katherine E Shipman,Ora A Weisz Katherine E Shipman
Dent disease (DD) is a rare kidney disorder caused by mutations in the Cl-/H+ exchanger ClC-5. Extensive physiologic characterization of the transporter has begun to illuminate its role in endosomal ion homeostasis. Nevertheless, we have ye...
Conor McClenaghan,Yan Huang,Scot J Matkovich et al. Conor McClenaghan et al.
Dramatic cardiomegaly arising from gain-of-function (GoF) mutations in the ATP-sensitive potassium (KATP) channels genes, ABCC9 and KCNJ8, is a characteristic feature of Cantú syndrome (CS). How potassium channel over-activity results in c...
Kevin A Murach,Ivan J Vechetti Jr,Douglas W Van Pelt et al. Kevin A Murach et al.
The "canonical" function of Pax7+ muscle stem cells (satellite cells) during hypertrophic growth of adult muscle fibers is myonuclear donation via fusion to support increased transcriptional output. In recent years, however, emerging eviden...
Hypertension is a major risk factor of cardiovascular disease affecting nearly half of adult population, but only 25% patients have their blood pressure under control. Hypertension is associated with mitochondrial dysfunction; however, its ...