Evidence map›Paper›PMID 36594399›Full record

ArticleGlia2023

Dysregulated cholesterol metabolism, aberrant excitability and altered cell cycle of astrocytes in fragile X syndrome.

Baiyan Ren, Maria Burkovetskaya, Yoosun Jung, Lara Bergdolt, Steven Totusek, Veronica Martinez-Cerdeno, Kelly Stauch, Zeljka Korade, Anna Dunaevsky

Open access · hybridAbstract read
In one paragraph

Article in Glia, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
5.9field-weighted citation impact, top 4% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
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  10. Review
  11. Review
  12. Astrocytes in fragile X syndrome.Frontiers in cellular neuroscience · 2023
    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

9 authors at 3 institutions in 1 country.

Baiyan RenDepartment of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Maria BurkovetskayaDepartment of Neurological Sciences, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Yoosun JungDepartment of Neurological Sciences, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Lara BergdoltDepartment of Pharmacology and Experimental Neuroscience, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Steven TotusekDepartment of Neurological Sciences, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Veronica Martinez-CerdenoDepartment of Pathology and Laboratory Medicine, MIND Institute, and Institute for Pediatric Regenerative Medicine at UC Davis School of Medicine, and Shriners Hospitals for Children of Northern California, Sacramento, California, USA.ORCID 0000-0002-9613-3603
Kelly StauchDepartment of Neurological Sciences, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Zeljka KoradeDepartment of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Anna DunaevskyDepartment of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, Nebraska, USA.ORCID 0000-0002-0172-9448
University of Nebraska Medical Center · USNebraska Medical Center · USShriners Hospitals for Children - Erie · US

Funding

UNMC Structural Biology CoreP20GM103427 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Heather Colleen Jensen-Smith · 2012 to 2026
$59.2M
UNMC/EPPLEY CANCER CENTER SUPPORT GRANTP30CA036727 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI James Eudy · 1985 to 2026
$55.0M
Tracking and Evaluation CoreU54GM115458 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI ESTABROOKS, PAUL · 2016 to 2025
$42.8M
The Role of Astrocytes in the Fragile X PathogenesisR01NS109381 · NINDS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI DUNAEVSKY, ANNA · 2019 to 2023
$2.3M
Developing an Astroglial Model for Fragile X SyndromeR21NS122157 · NINDS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI DUNAEVSKY, ANNA · 2021 to 2021
$434k
NCI NIH HHS P30 CA036727NIGMS NIH HHS P20 GM103427NIGMS NIH HHS U54 GM115458NINDS NIH HHS R01 NS109381NINDS NIH HHS R21 NS122157
6 · The paper itself

Abstract

Fragile X syndrome (FXS), the most prevalent heritable form of intellectual disability, is caused by the transcriptional silencing of the FMR1 gene. While neuronal contribution to FXS has been extensively studied in both animal and human-based models of FXS, the roles of astrocytes, a type of glial cells in the brain, are largely unknown. Here, we generated a human-based FXS model via differentiation of astrocytes from human-induced pluripotent stem cells (hiPSCs) and human embryonic stem cells (hESCs) and characterized their development, function, and proteomic profiles. We identified shortened cell cycle, enhanced Ca

Indexed as

Fragile X SyndromeAnimalsAstrocytesCell CycleCholesterolFragile X Messenger Ribonucleoprotein 1HumansProteomicsCholesterolFMR1 protein, humanFragile X Messenger Ribonucleoprotein 1

Identifiers

PMID36594399
PMCPMC10023374
OpenAlexW4313454708

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.