Evidence map›Paper›PMID 31003562›Full record

ArticleCells2019

Functional Characterization of Clinically-Relevant Rare Variants in

Yu Toyoda, Andrea Mančíková, Vladimír Krylov, Keito Morimoto, Kateřina Pavelcová, Jana Bohatá, Karel Pavelka, Markéta Pavlíková, Hiroshi Suzuki, Hirotaka Matsuo and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
6.0field-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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 70 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Exome sequencing link mutation inFrontiers in oncology · 2022
    Article
  18. Article
  19. Article
  20. Multidrug efflux transporter ABCG2: expression and regulation.Cellular and molecular life sciences : CMLS · 2021
    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

12 authors at 4 institutions in 2 countries.

Yu ToyodaDepartment of Pharmacy, The University of Tokyo Hospital, Tokyo 113-8655, Japan. ytoyoda-tky@umin.ac.jp.
Andrea MančíkováDepartment of Cell Biology, Faculty of Science, Charles University, 128 00 Prague 2, Czech Republic. andrea.mancikova@email.cz.
Vladimír KrylovDepartment of Cell Biology, Faculty of Science, Charles University, 128 00 Prague 2, Czech Republic. vladimir.krylov@natur.cuni.cz.
Keito MorimotoDepartment of Pharmacy, The University of Tokyo Hospital, Tokyo 113-8655, Japan. kmorimoto-tky@umin.ac.jp.
Kateřina PavelcováInstitute of Rheumatology, 128 50 Prague 2, Czech Republic. pavelcova@revma.cz.
Jana BohatáInstitute of Rheumatology, 128 50 Prague 2, Czech Republic. bohata@revma.cz.
Karel PavelkaInstitute of Rheumatology, 128 50 Prague 2, Czech Republic. pavelka@revma.cz.
Markéta PavlíkováDepartment of Probability and Mathematical Statistics, Faculty of Mathematics and Physics, Charles University, 121 16 Prague 2, Czech Republic. pavlikova@karlin.mff.cuni.cz.
Hiroshi SuzukiDepartment of Pharmacy, The University of Tokyo Hospital, Tokyo 113-8655, Japan. suzukihi-tky@umin.ac.jp.
Hirotaka MatsuoDepartment of Integrative Physiology and Bio-Nano Medicine, National Defense Medical College, Saitama 359-8513, Japan. hmatsuo@ndmc.ac.jp.
Tappei TakadaDepartment of Pharmacy, The University of Tokyo Hospital, Tokyo 113-8655, Japan. pavlikova@karlin.mff.cuni.cz.
Blanka StiburkovaInstitute of Rheumatology, 128 50 Prague 2, Czech Republic. stiburkova@revma.cz.
Charles University · CZUniversity of Tokyo Hospital · JPInstitute of Rheumatology · CZNational Defense Medical College · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ATP-binding cassette subfamily G member 2 (ABCG2) is a physiologically important urate transporter. Accumulating evidence demonstrates that congenital dysfunction of ABCG2 is an important genetic risk factor in gout and hyperuricemia; recent studies suggest the clinical significance of both common and rare variants of ABCG2. However, the effects of rare variants of

Indexed as

AdolescentAdultAgedAged, 80 and overATP Binding Cassette Transporter, Subfamily G, Member 2Biological TransportChildChild, PreschoolCohort StudiesCzech RepublicFemaleGenetic Predisposition to DiseaseGoutHEK293 CellsHumansHyperuricemiaABCG2 protein, humanATP Binding Cassette Transporter, Subfamily G, Member 2Neoplasm ProteinsOrganic Anion Transportersurate transporterUric AcidABCG2/BCRPcommon diseaseEuropean cohortexon sequencefunctional studygout susceptibilityheritability of serum uric acidmultiple rare varianturate transporterWGA.

Identifiers

PMID31003562
PMCPMC6523779
OpenAlexW2940277434

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.