Evidence map›Paper›PMID 33880623›Full record

ArticleHandbook of experimental pharmacology2021

The Pharmacology of Two-Pore Domain Potassium Channels.

Jordie M Kamuene, Yu Xu, Leigh D Plant

Abstract read
PubMed Publisher
In one paragraph

Article in Handbook of experimental pharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
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  5. Review
  6. The effects of doxapram and its potential interactions with K2P channels in experimental model preparations.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2024
    Article
  7. Article
  8. Review
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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

3 authors at 1 institution in 1 country.

Jordie M KamueneDepartment of Pharmaceutical Sciences, Northeastern University, Boston, MA, USA.ORCID https://orcid.org/0000-0002-2759-3251
Yu XuDepartment of Pharmaceutical Sciences, Northeastern University, Boston, MA, USA.ORCID https://orcid.org/0000-0002-2428-0428
Leigh D PlantDepartment of Pharmaceutical Sciences, Northeastern University, Boston, MA, USA. l.plant@northeastern.edu.ORCID https://orcid.org/0000-0002-1622-1655
Northeastern University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Two-pore domain potassium channels are formed by subunits that each contain two pore-loops moieties. Whether the channels are expressed in yeast or the human central nervous system, two subunits come together to form a single potassium selective pore. TOK1, the first two-domain channel was cloned from Saccharomyces cerevisiae in 1995 and soon thereafter, 15 distinct K

Indexed as

Potassium Channels, Tandem Pore DomainHumansPotassium Channels, Tandem Pore DomainBackground currentK2P channelKCNKTALKTASKTHIKTRAAKTREKTRESKTWIK

Identifiers

PMID33880623
OpenAlexW3156046902

What OpenQuestion holds

Textmetadata
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.