Evidence map›Paper›PMID 36693102›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2023

Faulty TRPM4 channels underlie age-dependent cerebral vascular dysfunction in Gould syndrome.

Evan Yamasaki, Sher Ali, Alfredo Sanchez Solano, Pratish Thakore, Megan Smith, Xiaowei Wang, Cassandre Labelle-Dumais, Douglas B Gould, Scott Earley

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Guidelines for evaluating endothelial function in vascular tissue.American journal of physiology. Heart and circulatory physiology · 2026
    Review
  3. Review
  4. Collagen IV in Gould syndrome and Alport syndrome.Nature reviews. Nephrology · 2025
    Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Skeletal pathology in mouse models of Gould syndrome is partially alleviated by genetically reducing TGFβ signaling.Matrix biology : journal of the International Society for Matrix Biology · 2024
    Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Impaired intracellular CaScience signaling · 2023
    Article
  17. PI3K block restores age-dependent neurovascular coupling defects associated with cerebral small vessel disease.Proceedings of the National Academy of Sciences of the United States of America · 2023
    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

9 authors at 2 institutions in 1 country.

Evan YamasakiDepartment of Pharmacology, Center for Molecular and Cellular Signaling in the Cardiovascular System, University of Nevada, Reno School of Medicine, Reno, NV 89557-0318.ORCID 0000-0001-9052-039X
Sher AliDepartment of Pharmacology, Center for Molecular and Cellular Signaling in the Cardiovascular System, University of Nevada, Reno School of Medicine, Reno, NV 89557-0318.ORCID 0000-0001-8319-5648
Alfredo Sanchez SolanoDepartment of Pharmacology, Center for Molecular and Cellular Signaling in the Cardiovascular System, University of Nevada, Reno School of Medicine, Reno, NV 89557-0318.ORCID 0000-0002-8218-256X
Pratish ThakoreDepartment of Pharmacology, Center for Molecular and Cellular Signaling in the Cardiovascular System, University of Nevada, Reno School of Medicine, Reno, NV 89557-0318.
Megan SmithDepartments of Ophthalmology, Institute for Human Genetics, UCSF School of Medicine, San Francisco, CA 94158.ORCID 0000-0002-5679-9136
Xiaowei WangDepartments of Ophthalmology, Institute for Human Genetics, UCSF School of Medicine, San Francisco, CA 94158.
Cassandre Labelle-DumaisDepartments of Ophthalmology, Institute for Human Genetics, UCSF School of Medicine, San Francisco, CA 94158.ORCID 0000-0002-2134-2240
Douglas B GouldDepartments of Ophthalmology, Institute for Human Genetics, UCSF School of Medicine, San Francisco, CA 94158.ORCID 0000-0001-5127-5328
Scott EarleyDepartment of Pharmacology, Center for Molecular and Cellular Signaling in the Cardiovascular System, University of Nevada, Reno School of Medicine, Reno, NV 89557-0318.ORCID 0000-0001-9560-2941
University of Nevada, Reno · USCenter for Human Genetics · US

Funding

Transgenic Animal Genotyping and Phenotyping CoreP20GM130459 · NIGMS · UNIVERSITY OF NEVADA RENO · PI Yumei Feng Earley · 2019 to 2026
$20.3M
Rapid-Prototyping and Design CoreP30EY002162 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ULLIAN, ERIK M · 1985 to 2024
$16.8M
TRP channels as fundamental sensors of the cerebral microcirculationR35HL155008 · NHLBI · UNIVERSITY OF ROCHESTER · PI Scott Earley · 2021 to 2026
$5.5M
Genetic and Mechanistic Study of Cerebral Small Vessel DiseaseR01NS096173 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GOULD, DOUGLAS · 2017 to 2021
$3.5M
Mechanisms of Functional Vascular Impairment In Genetic Models of Cerebral Small Vessel DiseaseRF1NS110044 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI EARLEY, SCOTT, GOULD, DOUGLAS · 2018 to 2022
$3.3M
Diversity Supplement-MassoudiR33NS115132 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHAUMEIL, MYRIAM MARIANNE, EARLEY, SCOTT · 2021 to 2023
$2.6M
NEI NIH HHS P30 EY002162NHLBI NIH HHS R35 HL155008NIGMS NIH HHS P20 GM130459NINDS NIH HHS R01 NS096173NINDS NIH HHS R33 NS115132NINDS NIH HHS RF1 NS110044
6 · The paper itself

Abstract

Gould syndrome is a rare multisystem disorder resulting from autosomal dominant mutations in the collagen-encoding genes

Indexed as

Muscle, Smooth, VascularTRPM Cation ChannelsAnimalsCerebral ArteriesHumansMiceMiddle AgedPhosphatidylinositol 3-KinasesTransforming Growth Factor betaPhosphatidylinositol 3-KinasesTransforming Growth Factor betaTRPM4 protein, humanTRPM4 protein, mouseTRPM Cation Channelscerebral small vessel diseasesCOL4A1ion channelsPIP2vascular smooth muscle

Identifiers

PMID36693102
PMCPMC9945977
OpenAlexW4317851244

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.