Evidence map›Paper›PMID 33201382›Full record

ReviewMolecular and cellular biochemistry2021

Role of Genetic Mutations of the Na

Larry Fliegel

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular and cellular biochemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Ion channel trafficking implications in heart failure.Frontiers in cardiovascular medicine · 2024
    Review
  7. NaInternational journal of molecular sciences · 2023
    Review
  8. Stress-induced reduction of NaScience advances · 2022
    Article
  9. The Remaining Conundrum of the Role of the NaReviews in cardiovascular medicine · 2022
    Review
  10. NaPharmaceuticals (Basel, Switzerland) · 2022
    Review
  11. Review
  12. Review
  13. 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

1 author at 1 institution in 1 country.

Larry FliegelDepartment of Biochemistry, University Alberta, 347 Medical Sciences Building, Edmonton, AB, T6G 2H7, Canada. lfliegel@ualberta.ca.ORCID http://orcid.org/0000-0002-8946-4850
University of Alberta · CA

Funding

NSERC RGPIN-2020-03932
6 · The paper itself

Abstract

The mammalian Na

Indexed as

MutationAmino Acid SequenceAnimalsFaciesFibrous Dysplasia of BoneHumansImmunologic Deficiency SyndromesNeurodegenerative DiseasesNeutropeniaProtein TransportProteolysisSodium-Hydrogen Exchanger 1SLC9A1 protein, humanSlc9a1 protein, mouseSodium-Hydrogen Exchanger 1Cerebellar ataxiaLichtenstein-Knorr syndromeNa+/H+ exchangerNHE1Protein degradationProtein mistargetingSLC9A1Stop codon polymorphism

Identifiers

PMID33201382
OpenAlexW3099270868

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.