Evidence map›Paper›PMID 28613263›Full record

ReviewMolecules (Basel, Switzerland)2017

Protein Interaction and Na/K-ATPase-Mediated Signal Transduction.

Xiaoyu Cui, Zijian Xie

Open access · goldAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 94 papers.

0numbers the graph read from it
0cells of the map it votes in
94citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

94 citing papers in PubMed, 157 citations in OpenAlex.

  1. Trial
  2. Oral digoxin effects on exercise performance, KThe Journal of physiology · 2022
    Trial
  3. Article
  4. NabioRxiv : the preprint server for biology · 2026
    Article
  5. Article
  6. Article
  7. Steroid hormone ouabain cooperates with NaActa pharmaceutica Sinica. B · 2026
    Article
  8. Exploring the Mechanism of NabioRxiv : the preprint server for biology · 2026
    Article
  9. Review
  10. Article
  11. Review
  12. NaFrontiers in chemistry · 2026
    Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article

34 more citing papers are in PubMed but not listed here.

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

2 authors at 1 institution in 1 country.

Xiaoyu CuiMarshall Institute for Interdisciplinary Research, Marshall University, Huntington, WV 25703, USA. cuix@marshall.edu.
Zijian XieMarshall Institute for Interdisciplinary Research, Marshall University, Huntington, WV 25703, USA. xiez@marshall.edu.
Marshall University · US

Funding

Receptor Na/K-ATPase Antagonists As Novel Therapeutics For Renal/Cardiac DiseasesR01HL109015 · NHLBI · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI SHAPIRO, JOSEPH ISAAC, XIE, ZIJIAN · 2011 to 2014
$2.2M
NHLBI NIH HHS R01 HL109015
6 · The paper itself

Abstract

The Na/K-ATPase (NKA), or Na pump, is a member of the P-type ATPase superfamily. In addition to pumping ions across cell membrane, it is engaged in assembly of multiple protein complexes in the plasma membrane. This assembly allows NKA to perform many non-pumping functions including signal transduction that are important for animal physiology and disease progression. This article will focus on the role of protein interaction in NKA-mediated signal transduction, and its potential utility as target for developing new therapeutics.

Indexed as

AnimalsCell MembraneMultiprotein ComplexesProtein Interaction MapsSignal TransductionSodium-Potassium-Exchanging ATPaseMultiprotein ComplexesSodium-Potassium-Exchanging ATPasecardiotonic steroidsdrug targetNa/K-ATPasesignal transductionSrc

Identifiers

PMID28613263
PMCPMC6152704
OpenAlexW2626722091

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.