Journal of General Physiology

Papers
(The TQCC of Journal of General Physiology is 9. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2022-06-01 to 2026-06-01.)
ArticleCitations
Interrogating the gating motions of the NaK channel58
Kv1.1 channels help set the pace51
Anionic omega currents from single countercharge mutants in the voltage-sensing domain of Ci-VSP46
Investigating the role of the I–II linker in Nav1.5 channel function44
Mutations in proteins involved in E-C coupling and SOCE and congenital myopathies39
Voltage-sensor gating charge interactions bimodally regulate voltage dependence and kinetics of calcium channel activation34
Machine learning meets Monte Carlo methods for models of muscle’s molecular machinery to classify mutations32
NALCN/Cch1 channelosome subunits originated in early eukaryotes29
Differential state-dependent Nav1.8 inhibition by suzetrigine, LTGO-33, and A-88782628
Stochastic force generation in an isometric binary mechanical system27
Reconstituting depolarization-induced calcium release27
Distinct properties and activation of hexameric and heptameric Pannexin 1 channel concatemers26
The relationship between apparent potentiation and the magnitude of the control response26
Variants of the myosin interacting-heads motif25
The funny current If is essential for the fight-or-flight response in cardiac pacemaker cells25
Superfast excitation–contraction coupling in adult zebrafish skeletal muscle fibers24
Regulation of NMDAR activation efficiency by environmental factors and subunit composition22
Beat-locked ATP microdomains in the sinoatrial node map a Ca2+-timed energetic hierarchy and regional pacemaker roles22
Light induces a rapid increase in cAMP and activates PKA in rod outer segments of the frog retina22
Niclosamide potentiates TMEM16A and induces vasoconstriction21
Altered NaV1.9 channel activity in two Tyr66Ser variant carriers with small fiber dysfunction20
Coincidence detection supported by electrical synapses is shaped by the D-type K+ current19
About hysteresis in Shaker: Response to note by Villalba-Galea19
Mechanism of external K+ sensitivity of KCNQ1 channels19
Orai1 as a potential “fits-all approach” therapeutic target for the treatment of DMD19
ANO1, CaV1.2, and IP3R form a localized unit of EC-coupling in mouse pulmonary arterial smooth muscle19
Connecting the dots on connexin function19
Nerve-dependent distribution of subsynaptic type 1 inositol 1,4,5-trisphosphate receptor at the neuromuscular junction18
Piezo2 interacts with E-cadherin in specialized gastrointestinal epithelial mechanoreceptors18
Mechanism of hydrophobic gating in the acetylcholine receptor channel pore18
Blood flow-bearing physical forces, endothelial glycocalyx, and liver enzyme mobilization: A hypothesis18
Myosin-binding protein-H: Not just filler18
A complete set of rate constants for a transporter’s catalytic cycle17
Mitochondrial morphology governs ATP production rate17
Segregation of Ca2+ signaling in olfactory signal transduction17
Examination of conformational dynamics of AdiC transporter with fluorescence-polarization microscopy17
Mechanistic understanding of KCNQ1 activating polyunsaturated fatty acid analogs16
EAAT5 glutamate transporter rapidly binds glutamate with micromolar affinity in mouse rods16
A primer on the methods of skeletal and cardiac muscle mechanics using permeabilized preparations16
Myosin’s powerstroke transitions define atomic scale movement of cardiac thin filament tropomyosin16
Molecular mechanism of claudin-15 strand flexibility: A computational study16
Null method to estimate the maximal PA at subsaturating concentrations of agonist16
BK channels of five different subunit combinations underlie the de novo KCNMA1 G375R channelopathy15
Acid-sensing ion channel 1a activates IKCa/SKCa channels and contributes to endothelium-dependent dilation15
Expression of ENaC subunits in epithelia15
Blockade of TRPV channels by intracellular spermine15
Allosteric modulation of GluN1/GluN3 NMDA receptors by GluN1-selective competitive antagonists15
Na+/Ca2+ exchange in enamel cells is dominated by the K+-dependent NCKX exchanger14
Myosin-binding protein H-like nonsense variants exhibit impaired sarcomere incorporation and alter contractility14
How a tyrosine primes the pump14
Diminished gap junction coupling under diabetogenic conditions does not drive loss of functional β-cell subpopulations14
A novel method for determining murine skeletal muscle fiber type using autofluorescence lifetimes14
A sodium channel mutant removes fast inactivation with the inactivation particle bound14
Sodium channel subpopulations with distinct biophysical properties and subcellular localization enhance cardiac conduction13
Variability in reported midpoints of (in)activation of cardiac INa13
Dependence of myosin filament structure on intracellular calcium concentration in skeletal muscle13
GRIN2B disease-associated mutations disrupt the function of BK channels and NMDA receptor signaling nanodomains13
A high-throughput electrophysiology assay to study the response of PIEZO1 to mechanical stimulation13
Asymmetric contribution of a selectivity filter gate in triggering inactivation of CaV1.3 channels13
Subunit composition of the KATP channels that modulate contractility of skeletal muscle during fatigue12
Directing two-way traffic in the kidney: A tale of two ions12
Multiscale molecular dynamics simulations predict arachidonic acid binding sites in human ASIC1a and ASIC3 transmembrane domains12
Blue flash sheds light on the roles of individual phosphoserines in CFTR channel activation12
Fifty years of gating currents and channel gating12
Screening for bilayer-active and likely cytotoxic molecules reveals bilayer-mediated regulation of cell function12
Mechanisms of dihydropyridine agonists and antagonists in view of cryo-EM structures of calcium and sodium channels12
Molecular dynamics analyses of CLDN15 pore size and charge selectivity12
Trouble in store for muscle fibers12
Probenecid affects muscle Ca2+ homeostasis and contraction independently from pannexin channel block11
Differential regulation of cardiac sodium channels by intracellular fibroblast growth factors11
Fusion pore flux controls the rise-times of quantal synaptic responses11
Evaluating sequential and allosteric activation models in IKs channels with mutated voltage sensors11
Subtype-selective targeting of NMDA receptors—A potent new compound emerges11
Mechanisms underlying dilated cardiomyopathy associated with FKBP12 deficiency11
Phosphorylation of RyR2 simultaneously expands the dyad and rearranges the tetramers11
The S1 helix is a VIP in VSP11
Glycerol storage increases passive stiffness of muscle fibers through effects on titin extensibility10
Brain voltage-gated Ca2+ channels and calmodulin: Teaming up in calmodulinopathies?10
Mind the midpoints: Rethinking variability in cardiac INa10
Regulation of voltage-sensing structures of CaV1.2 calcium channel by the auxiliary β3-subunit10
Examining the calcium sensitivity of skeletal muscle thick filaments10
The Cranefield Awards 202210
Mechanistic insights on KATP channel regulation from cryo-EM structures10
Distinctive mechanical response characteristics of the guinea pig apical cochlear organ of Corti and basilar membrane10
The physical basis of osmosis10
Nociceptor sodium channels shape subthreshold phase, upstroke, and shoulder of action potentials10
Manganese and intracellular Ca2+ handling9
ON and OFF starburst amacrine cells are controlled by distinct cholinergic pathways9
Titin’s P-zone domains A164–167 are essential for thick filament structural arrangement9
Structural basis for severe pain caused by mutations in the voltage sensors of sodium channel NaV1.79
TMEM120A/TACAN inhibits mechanically activated PIEZO2 channels9
Exploring voltage-gated sodium channel conformations and protein–protein interactions using AlphaFold29
Physical activity impacts resting skeletal muscle myosin conformation and lowers its ATP consumption9
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