Evidence map›Paper›PMID 38222853›Full record

ArticleDisease markers2024

Examining the Association of Rare Allelic Variants in Urate Transporters

Jiří Vávra, Kateřina Pavelcová, Jana Mašínová, Lenka Hasíková, Eliška Bubeníková, Aneta Urbanová, Andrea Mančíková, Blanka Stibůrková

Open access · hybridAbstract read
In one paragraph

Article in Disease markers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
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  6. 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

8 authors at 3 institutions in 1 country.

Jiří VávraDepartment of Cell Biology, Faculty of Science, Charles University, Prague, Czech Republic.ORCID https://orcid.org/0000-0001-6547-7625
Kateřina PavelcováInstitute of Rheumatology, Prague, Czech Republic.ORCID https://orcid.org/0000-0002-5379-7282
Jana MašínováInstitute of Rheumatology, Prague, Czech Republic.ORCID https://orcid.org/0000-0002-7446-1542
Lenka HasíkováInstitute of Rheumatology, Prague, Czech Republic.ORCID https://orcid.org/0000-0002-4794-2252
Eliška BubeníkováInstitute of Rheumatology, Prague, Czech Republic.
Aneta Urbanová1st Department of Medicine, Department of Hematology; First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
Andrea MančíkováDepartment of Staphylococcal and Food-Borne Bacterial Infections, The National Institute of Public Health, Prague, Czech Republic.ORCID https://orcid.org/0000-0003-4487-1943
Blanka StibůrkováInstitute of Rheumatology, Prague, Czech Republic.ORCID https://orcid.org/0000-0003-2465-1476
Charles University · CZInstitute of Rheumatology · CZNational Institute of Public Health · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic variations in urate transporters play a significant role in determining human urate levels and have been implicated in developing hyperuricemia or gout. Polymorphism in the key urate transporters, such as ABCG2, URAT1, or GLUT9 was well-documented in the literature. Therefore in this study, our objective was to determine the frequency and effect of rare nonsynonymous allelic variants of

Indexed as

GoutHyperuricemiaOrganic Anion TransportersOrganic Anion Transporters, Sodium-IndependentSodium-Phosphate Cotransporter Proteins, Type IHumansUric AcidOrganic Anion TransportersOrganic Anion Transporters, Sodium-IndependentSLC17A1 protein, humanSLC22A11 protein, humanSLC22A13 protein, humanSodium-Phosphate Cotransporter Proteins, Type Iurate transporterUric Acid

Identifiers

PMID38222853
PMCPMC10787658
OpenAlexW4390640192

What OpenQuestion 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 OpenQuestion graph.