Evidence map›Paper›PMID 33484482›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2021

Mutation of the TRPM3 cation channel underlies progressive cataract development and lens calcification associated with pro-fibrotic and immune cell responses.

Yuefang Zhou, Thomas M Bennett, Alan Shiels

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

24 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Through theGenes · 2024
    Review
  8. Article
  9. Review
  10. The odyssey of the TR(i)P journey to the cellular membrane.Frontiers in cell and developmental biology · 2024
    Review
  11. Article
  12. Article
  13. Article
  14. Charged multivesicular body protein 4b forms complexes with gap junction proteins during lens fiber cell differentiation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Connexin Mutants Cause Cataracts Through Deposition of Apatite.Frontiers in cell and developmental biology · 2022
    Article
  20. 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

3 authors at 1 institution in 1 country.

Yuefang ZhouOphthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, MO, USA.ORCID https://orcid.org/0000-0002-8517-1292
Thomas M BennettOphthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, MO, USA.
Alan ShielsOphthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, MO, USA.
Washington University in St. Louis · US

Funding

WASHINGTON UNIVERSITY CENTER VISION RESEARCHP30EY002687 · NEI · WASHINGTON UNIVERSITY · PI Philip Raymond Williams · 1985 to 2026
$18.4M
TRP-CHANNELS IN LENS DEVELOPMENT AND CATARACTR01EY028899 · NEI · WASHINGTON UNIVERSITY · PI SHIELS, ALAN · 2019 to 2023
$1.9M
NEI NIH HHS P30 EY002687NEI NIH HHS R01 EY028899
6 · The paper itself

Abstract

Transient-receptor-potential cation channel, subfamily M, member 3 (TRPM3) serves as a polymodal calcium sensor in diverse mammalian cell-types. Mutation of the human TRPM3 gene (TRPM3) has been linked with inherited forms of early-onset cataract with or without other eye abnormalities. Here, we have characterized the ocular phenotypes of germline "knock-in" mice that harbor a human cataract-associated isoleucine-to-methionine mutation (p.I65M) in TRPM3 (Trpm3-mutant) compared with germline "knock-out" mice that functionally lack TRPM3 (Trpm3-null). Despite strong expression of Trpm3 in lens epithelial cells, neither heterozygous (Trpm3

Indexed as

ActinsAnimalsCalcinosisCalciumCalpainCataractCollagenFibrosisHeterozygoteLens, CrystallineMacrophagesMiceMice, Inbred C57BLTRPM Cation ChannelsActinsCalciumCalpainCollagenTRPM3 protein, mouseTRPM Cation ChannelscalciumcataractlensmacrophagemyofibroblastTRP-channel

Identifiers

PMID33484482
PMCPMC7891105
OpenAlexW3123244655

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.