Evidence map›Paper›PMID 37040696›Full record

ArticleDevelopmental cell2023

Deregulation of ER-mitochondria contact formation and mitochondrial calcium homeostasis mediated by VDAC in fragile X syndrome.

Ji Geng, Tejinder Pal Khaket, Jie Pan, Wen Li, Yan Zhang, Yong Ping, Maria Inmaculada Cobos Sillero, Bingwei Lu

Open access · greenAbstract read
In one paragraph

Article in Developmental cell, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
11.0field-weighted citation impact, top 1% 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

28 citing papers in PubMed, 35 citations in OpenAlex.

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  8. Signaling architecture of the glucagon-like peptide-1 receptor.The Journal of clinical investigation · 2026
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  14. taVNS alleviates preeclampsia-induced vascular endothelial dysfunction via α7nAChR- IP3R1/GRP75/VDAC1 signal pathway.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    Article
  15. Biomolecules · 2025
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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 2 countries.

Ji GengDepartment of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Tejinder Pal KhaketDepartment of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Jie PanDepartment of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Wen LiDepartment of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Yan ZhangBio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders, Ministry of Education, Shanghai Jiao Tong University, Shanghai 200240, China; Shanghai Key Laboratory of Psychotic Disorders (No. 13dz2260500), Shanghai Mental Health Center, School of Medicine, Shanghai Jiao Tong University, Shanghai 200030, China.
Yong PingBio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders, Ministry of Education, Shanghai Jiao Tong University, Shanghai 200240, China; Shanghai Key Laboratory of Psychotic Disorders (No. 13dz2260500), Shanghai Mental Health Center, School of Medicine, Shanghai Jiao Tong University, Shanghai 200030, China.
Maria Inmaculada Cobos SilleroDepartment of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Bingwei LuDepartment of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA. Electronic address: bingwei@stanford.edu.
Stanford University · USShanghai Jiao Tong University · CNStanford Medicine · US

Funding

Molecular Genetic Analysis of TORC1 and TORC2 Signaling in Neuronal MaintenanceR01NS084412 · NINDS · STANFORD UNIVERSITY · PI Bingwei Lu · 2014 to 2026
$4.9M
Genetic Control of Neural Stem Cell HomeostasisR01NS083417 · NINDS · STANFORD UNIVERSITY · PI LU, BINGWEI · 2013 to 2022
$3.5M
Mitochondrial inner membrane architecture in skeletal muscle pathophysiologyR01AR074875 · NIAMS · STANFORD UNIVERSITY · PI LU, BINGWEI · 2019 to 2023
$2.0M
Linking the Mitochondrial and Epigenetic Pathways of Life Span ExtensionR21AG045753 · NIA · STANFORD UNIVERSITY · PI LU, BINGWEI · 2014 to 2015
$434k
A Novel Role of Fragile-X Mental Retardation Protein in Mitochondrial Calcium HomeostasisR21MH127340 · NIMH · STANFORD UNIVERSITY · PI LU, BINGWEI · 2022 to 2023
$433k
NIAMS NIH HHS R01 AR074875NIA NIH HHS R21 AG045753NIMH NIH HHS R21 MH127340NINDS NIH HHS R01 NS083417NINDS NIH HHS R01 NS084412
6 · The paper itself

Abstract

Loss of fragile X messenger ribonucleoprotein (FMRP) causes fragile X syndrome (FXS), the most prevalent form of inherited intellectual disability. Here, we show that FMRP interacts with the voltage-dependent anion channel (VDAC) to regulate the formation and function of endoplasmic reticulum (ER)-mitochondria contact sites (ERMCSs), structures that are critical for mitochondrial calcium (mito-Ca

Indexed as

Drosophila ProteinsFragile X SyndromeAnimalsCalciumDrosophilaEndoplasmic ReticulumFragile X Messenger Ribonucleoprotein 1HomeostasisMiceMice, KnockoutMitochondriaVoltage-Dependent Anion ChannelsCalciumDrosophila ProteinsFMR1 protein, DrosophilaFmr1 protein, mouseFragile X Messenger Ribonucleoprotein 1Voltage-Dependent Anion ChannelsERMCSER-mitochondria contact siteFMRPfragile X messenger ribonucleoproteinfragile X syndromeFXSmito-Ca(2+) homeostasismitochondrial calcium homeostasisVDACvoltage-dependent anion channel

Identifiers

PMID37040696
PMCPMC10113018
OpenAlexW4363676331

What Socratic 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 Socratic graph.