Evidence map›Paper›PMID 30811176›Full record

ArticleBiochemistry2019

Na/K Pump Mutations Associated with Primary Hyperaldosteronism Cause Loss of Function.

Dylan J Meyer, Craig Gatto, Pablo Artigas

Abstract read
In one paragraph

Article in Biochemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Mechanism of Rescue of NaInternational journal of molecular sciences · 2026
    Article
  2. Article
  3. Association of the RecurrentNeurology. Genetics · 2025
    Article
  4. ATP1A1-linked diseases require a malfunctioning protein product from one allele.Biochimica et biophysica acta. Molecular cell research · 2024
    Article
  5. The NaeLife · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Diseases caused by mutations in the NaAmerican journal of physiology. Cell physiology · 2021
    Review
  10. Article
  11. Prevalence of Somatic Mutations in Aldosterone-Producing Adenomas in Japanese Patients.The Journal of clinical endocrinology and metabolism · 2020
    Article
  12. Review
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 2 institutions in 1 country.

Dylan J MeyerDepartment of Cell Physiology and Molecular Biophysics, Center for Membrane Protein Research , Texas Tech University Health Sciences Center , Lubbock , Texas 79430 , United States.
Craig GattoSchool of Biological Sciences , Illinois State University , Normal , Illinois 61790 , United States.
Pablo ArtigasDepartment of Cell Physiology and Molecular Biophysics, Center for Membrane Protein Research , Texas Tech University Health Sciences Center , Lubbock , Texas 79430 , United States.ORCID 0000-0002-6893-9765
Texas Tech University · USIllinois State University · US

Funding

STRUCTURE OF THE SODIUM PUMP NUCLEOTIDE BINDING DOMAINR15GM061583 · NIGMS · ILLINOIS STATE UNIVERSITY · PI GATTO, CRAIG · 2000 to 2015
$1.0M
NIGMS NIH HHS R15 GM061583
6 · The paper itself

Abstract

Primary hyperaldosteronism (Conn's syndrome), a common cause of secondary hypertension, is frequently produced by unilateral aldosterone-producing adenomas that carry mutations in ion-transporting genes, including ATP1A1, encoding the Na/K pump's α1 subunit. Whether Na/K pump mutant-mediated inward currents are required to depolarize the cell and increase aldosterone production remains unclear, as such currents were observed in four out of five mutants described so far. Here, we use electrophysiology and uptake of the K

Indexed as

Loss of Function MutationAnimalsHumansHyperaldosteronismModels, MolecularPotassiumSequence DeletionSodiumSodium-Potassium-Exchanging ATPaseXenopusATP1A1 protein, humanPotassiumSodiumSodium-Potassium-Exchanging ATPase

Identifiers

PMID30811176
PMCPMC6779590
OpenAlexW2917534477

What OpenQuestion holds

Textmetadata
LicenceTDM
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.