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Paper · 41003497

Modification of Closed-State Inactivation in Voltage-Gated Sodium Channel Nav1.7 by Two Novel Arachnid Toxins.

Johnson JW and 2 others. Toxins (Basel), 2025. Cited by 0 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Modification of Closed-State Inactivation in Voltage-Gated Sodium Channel Nav1.7 by Two Novel Arachnid Toxins. Papers, record 41003497. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/41003497

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title
Modification of Closed-State Inactivation in Voltage-Gated Sodium Channel Nav1.7 by Two Novel Arachnid Toxins.
PubMed
Journal
Toxins (Basel)
PubMed
Year
2025
PubMed
Publication types
Journal Article
PubMed
Citations, by iCite
0
iCite
Revised in PubMed
2025-09-28
PubMed

Authors3

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

OrderAuthorForenameKindORCID iD
1Johnson JWJohn W
2Rikli HGHillary G
3Johnson SRStephen Rhttps://orcid.org/0000-0002-7025-4933

Source PubMed

Topics6

NLM's MeSH indexing of the paper, its major topics first.

MeSH termMajor
NAV1.7 Voltage-Gated Sodium ChannelMajor topic
Spider VenomsMajor topic
Arthropod VenomsMajor topic
Animals
Humans
Xenopus laevis

Source PubMed

Grants0

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

None in this release.

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References68

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

OrderPMIDTitleJournalYearIn PapersSource
115,683,238A spider toxin that induces a typical effect of scorpion alpha-toxins but competes with beta-toxins on binding to insect sodium channels.Biochemistry2005https://conductscience.org/library/papers/15683238PubMed
222,160,714Structural basis for gating charge movement in the voltage sensor of a sodium channel.Proc Natl Acad Sci U S A2012https://conductscience.org/library/papers/22160714PubMed
323,055,474The Hodgkin-Huxley heritage: from channels to circuits.J Neurosci2012https://conductscience.org/library/papers/23055474PubMed
426,921,461Isolation, chemical and functional characterization of several new K(+)-channel blocking peptides from the venom of the scorpion Centruroides tecomanus.Toxicon2016https://conductscience.org/library/papers/26921461PubMed
512,843,211Distinct repriming and closed-state inactivation kinetics of Nav1.6 and Nav1.7 sodium channels in mouse spinal sensory neurons.J Physiol2003https://conductscience.org/library/papers/12843211PubMed
625,088,688From foe to friend: using animal toxins to investigate ion channel function.J Mol Biol2015https://conductscience.org/library/papers/25088688PubMed
720,585,544Fast- or slow-inactivated state preference of Na+ channel inhibitors: a simulation and experimental study.PLoS Comput Biol2010https://conductscience.org/library/papers/20585544PubMed
86,327,148Inactivation of open and closed sodium channels determined separately.Cold Spring Harb Symp Quant Biol1983https://conductscience.org/library/papers/6327148PubMed
92,427,018Molecular properties of voltage-sensitive sodium channels.Annu Rev Biochem1986https://conductscience.org/library/papers/2427018PubMed
1010,798,388From ionic currents to molecular mechanisms: the structure and function of voltage-gated sodium channels.Neuron2000https://conductscience.org/library/papers/10798388PubMed

Cited by0

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 0 citations.

None in this release.

Genes5

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

GeneNCBI Gene IDLinked byIn GenesSource
MAPT4,137PubTator's text mininghttps://conductscience.org/library/genes/4137NCBI Gene
SCN10A6,336PubTator's text mininghttps://conductscience.org/library/genes/6336NCBI Gene
SCN4A6,329PubTator's text mininghttps://conductscience.org/library/genes/6329NCBI Gene
SCN5A6,331PubTator's text mininghttps://conductscience.org/library/genes/6331NCBI Gene
SCN9A6,335PubTator's text mininghttps://conductscience.org/library/genes/6335NCBI Gene

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed
2026-11-06
PubMed
iCite
2026-11-05
iCite
PMC's ID file
2026-11-05
PMC's ID file
NIH RePORTER's grant and paper links
2026-11-01
NIH RePORTER's grant and paper links
Trials
2026-11-12
Gene search
2026-11-11
Pipelines
2026-09-18

Sources 11

  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • HGNCCC0
  • iCiteCC BY 4.0
  • NCBI GenePublic domain (US government)
  • NIH RePORTER's grant and paper linksPublic domain
  • Open TargetsCC0 1.0
  • PMC's ID filePublic domain (US government)
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • HGNCCC0: https://www.genenames.org/about/license/
  • iCiteCC BY 4.0
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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