Evidence map›Paper›PMID 21787867›Full record

ArticleNeuroImage2011

Distribution of M-channel subunits KCNQ2 and KCNQ3 in rat hippocampus.

Felicia Klinger, Georgianna Gould, Stefan Boehm, Mark S Shapiro

Open access · greenAbstract read
In one paragraph

Article in NeuroImage, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
1.3field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 57 citations in OpenAlex.

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  3. Cytoskeletal scaffolding of NaCurrent opinion in cell biology · 2025
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  7. Plural molecular and cellular mechanisms of pore domainbioRxiv : the preprint server for biology · 2024
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  10. KCNQ5 Potassium Channel Activation Underlies Vasodilation by Tea.Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 2021
    Article
  11. Article
  12. Article
  13. Article
  14. Kv7 Channels and Excitability Disorders.Handbook of experimental pharmacology · 2021
    Article
  15. Article
  16. Article
  17. The Role of KFrontiers in physiology · 2020
    Review
  18. Review
  19. Article
  20. Cilantro leaf harbors a potent potassium channel-activating anticonvulsant.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 2 countries.

Felicia KlingerDepartment of Physiology, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.
Georgianna Gould
Stefan Boehm
Mark S Shapiro
Medical University of Vienna · ATThe University of Texas Health Science Center at San Antonio · US

Funding

Modulation of Neuronal Ion Channels by 2nd MessengersR01NS043394 · NINDS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI SHAPIRO, MARK S · 2002 to 2014
$4.5M
Mechanism and functional role of AKAP79/150 in M current control and excitabilityR01NS065138 · NINDS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI SHAPIRO, MARK S · 2009 to 2010
$788k
NINDS NIH HHS R01 NS043394NINDS NIH HHS R01 NS065138
6 · The paper itself

Abstract

Neuronal M-channels are low threshold, slowly activating and non-inactivating, voltage dependent K(+) channels that play a crucial role in controlling neuronal excitability. The native M-channel is composed of heteromeric or homomeric assemblies of subunits belonging to the Kv7/KCNQ family, with KCNQ2/3 heteromers being the most abundant form. KCNQ2 and KCNQ3 subunits have been found to be expressed in various neurons in the central and peripheral nervous system of rodents and humans. Previous evidence shows preferential localization of both subunits to axon initial segments, somata and nodes of Ranvier. In this work, we show the distribution and co-localization of KCNQ2 and KCNQ3 subunits throughout the hippocampal formation, via immunostaining experiments on unfixed rat brain slices and confocal microscopy. We find intense localization and colocalization to the axonal initial segment in several regions of the hippocampus, as well as staining for non-neuronal cells in the area of the lateral ventricle. We did not observe colocalization of KCNQ2 or KCNQ3 with the presynaptic protein, synaptophysin.

Indexed as

Brain ChemistryAnimalsHippocampusImmunohistochemistryKCNQ2 Potassium ChannelKCNQ3 Potassium ChannelMicroscopy, ConfocalProtein SubunitsRatsRats, Sprague-DawleyKCNQ2 Potassium ChannelKcnq2 protein, ratKCNQ3 Potassium ChannelKcnq3 protein, ratProtein Subunits

Identifiers

PMID21787867
PMCPMC3166433
OpenAlexW1988598597

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.