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verified SJR 1,382 · Q1 • database Scopus / SJR & Web of Science indexed
Journal of General Physiology
United States · Rockefeller University Press
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Journal of General Physiology

Journal of General Physiology is a journal indexed in SJR in Physiology with an H index of 143. It has an SJR impact factor of 1,382 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 1,382.

Journal of General Physiology focuses its scope in these topics and keywords: ion, gating, channel, voltage, cluster, enduring, defined, domains, impulse, formation, ...

ISSN: 0022-1295
Publisher: Rockefeller University Press
Category: Physiology
Indexation: verifiedScopus / SJR verifiedWeb of Science
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SJR Impact Factor trending_up
1,382 Q1
H-index 143
Acceptance rate pie_chart
22% Selective
Source Acceptance_Rate
Time to publication hourglass_top
NPD
Field NPD
Publication cost (APC) payments
NPD Subscription
Non-OA path NPD

Metrics

Scimago and CountryOfPapers database fields

Scopus / SJR Web of Science

SJR Impact

1,382

H-index

143

Docs (year)

69

Docs 3y

322

Total refs

3560

Cites 3y

770

Citable 3y

257

Cites/Doc 2y

2.21

Ref/Doc

51.59

Immediate OA

—

Embargoed OA

NPD

Non OA / Submission

—

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Best articles by citations

Chemical Modification of Membranes

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Voltage-dependent inactivation of T-tubular skeletal calcium channels in planar lipid bilayers.

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ENaC-Membrane Interactions

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Electrophysiological properties of the membrane and acetylcholine receptor in developing rat and chick myotubes.

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Editorial

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Editorial

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Divalent cation activation and inhibition of single calcium release channels from sheep cardiac sarcoplasmic reticulum.

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Differential Effects of Tyrosine Kinase Inhibitors on Volume-sensitive Chloride Current in Human Atrial Myocytes

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Desensitization of Mouse Nicotinic Acetylcholine Receptor Channels

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Correlations between Electron Microscopic and Physiological Observations in Heart Muscle

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Correction: Table I

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Correction

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Cardiac sodium channels (hH1) are intrinsically more sensitive to block by lidocaine than are skeletal muscle (mu 1) channels.

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