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期刊名:Journal of general physiology

缩写:J GEN PHYSIOL

ISSN:0022-1295

e-ISSN:1540-7748

IF/分区:2.9/Q2

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共收录本刊相关文章索引1923
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
Adam Feher,Geraldo Jorge Domingos,Martina Piga et al. Adam Feher et al.
A recent publication by our research team has introduced a novel group of hHv1 inhibitors, the 5-phenyl-2-aminoimidazoles. To guide rational drug design of selective derivatives, our goal was to map the molecular mechanism of compound 13 (i...
Yenisleidy Lorenzo-Ceballos,Pedro L Martinez-Espinosa,Xiao-Ming Xia et al. Yenisleidy Lorenzo-Ceballos et al.
A-isoforms of cytosolic growth factor homologous factors (FGF11-14) mediate long-term inactivation (LTI) of voltage-dependent sodium (NaV) channels. LTI is a rapid onset process that is competitive with the fast inactivation (IF) intrinsic ...
Varun Verma,Ethan S Lindgren,Marc H Levin et al. Varun Verma et al.
The composition and volume of tear fluid lining the ocular surface are governed by the rates of lacrimal gland secretion, tear film evaporation, nasolacrimal drainage, and epithelial ion and water transport. Tear fluid hyperosmolality and r...
Rosa Scala,Yuezhou Chen,Berk Mizrak et al. Rosa Scala et al.
ATP-sensitive potassium (KATP) channels are among the most expressed ion channels in skeletal muscle sarcolemma. While all KATP subunits can be detected in skeletal muscles, transcripts are enriched for KCNJ11 and ABCC9, suggesting that non...
Magalí Colomer-Molera,Daniel Sastre,Antonio Felipe Magalí Colomer-Molera
Kv1.3 channels participate in the activation and proliferation of leukocytes. The KCNE4 regulatory subunit associates with the channel and functions as a negative regulator. KCNE4, via its transmembrane and C-terminal domains, interacts wit...
Valeriy Lukyanenko,Joaquin Muriel,Kassidy K Banford et al. Valeriy Lukyanenko et al.
Dysferlin is required for the health of skeletal muscle, where it mediates at least two seemingly distinct processes, repair of the sarcolemmal membrane and stabilization of Ca2+ release after injury. Dysferlin is a ∼230-kDa protein compri...
Jörg Striessnig Jörg Striessnig
Calmodulin (CaM) serves as one of the key cellular Ca2+ sensors with >300 targets and a highly conserved structure since its appearance in early eukaryogenesis. Three distinct CaM genes (CALM1, CALM2, and CALM3) encode one identical CaM pro...
Yichen Liu,Cesar A Amaya-Rodriguez,Victoria Collio et al. Yichen Liu et al.
Voltage-gated sodium (Nav) channels enable the rapid influx of sodium ions that are essential to generating the rising phase of the action potential. As originally described by Hodgkin and Huxley, once the Nav channel is activated, it switc...
Amin Akhshi,Myriah Haggard,Mariana M Marquez et al. Amin Akhshi et al.
Heterogeneity in spiking activity is ubiquitous among neurons even within a given cell type. To date, the relative contributions of extrinsic mechanisms (e.g., synaptic bombardment), intrinsic mechanisms (e.g., conductances), and cell morph...
John W Hussey,Emily DeMarco,Deborah DiSilvestre et al. John W Hussey et al.
Calmodulinopathies are caused by mutations in calmodulin (CaM) and result in debilitating cardiac arrythmias such as long-QT syndrome (LQTS) and catecholaminergic polymorphic ventricular tachycardia (CPVT). In addition, many patients exhibi...