Evidence map›Paper›PMID 35095417›Full record

ArticleFrontiers in molecular neuroscience2021

HDAC1 Regulates Neuronal Differentiation.

Vanesa Nieto-Estevez, Gopakumar Changarathil, Adebayo Olukayode Adeyeye, Marissa Olga Coppin, Rawan Serena Kassim, Jingfei Zhu, Jenny Hsieh

Open access · goldAbstract read
In one paragraph

Article in Frontiers in molecular neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Cellular senescence and aging: molecular mechanisms and convergent pathways.Cellular and molecular life sciences : CMLS · 2026
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  5. DifferentialProceedings of the National Academy of Sciences of the United States of America · 2026
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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

7 authors at 2 institutions in 1 country.

Vanesa Nieto-EstevezDepartment of Neuroscience, Developmental and Regenerative Biology, The University of Texas at San Antonio, San Antonio, TX, United States.
Gopakumar ChangarathilDepartment of Neuroscience, Developmental and Regenerative Biology, The University of Texas at San Antonio, San Antonio, TX, United States.
Adebayo Olukayode AdeyeyeDepartment of Neuroscience, Developmental and Regenerative Biology, The University of Texas at San Antonio, San Antonio, TX, United States.
Marissa Olga CoppinDepartment of Neuroscience, Developmental and Regenerative Biology, The University of Texas at San Antonio, San Antonio, TX, United States.
Rawan Serena KassimDepartment of Neuroscience, Developmental and Regenerative Biology, The University of Texas at San Antonio, San Antonio, TX, United States.
Jingfei ZhuDepartment of Molecular Biology, UT Southwestern Medical Center, Dallas, TX, United States.
Jenny HsiehDepartment of Neuroscience, Developmental and Regenerative Biology, The University of Texas at San Antonio, San Antonio, TX, United States.
The University of Texas at San Antonio · USSouthwestern Medical Center · US

Funding

Precision models of ARX-associated neurodevelopmental disordersR01NS113516 · NINDS · UNIVERSITY OF TEXAS SAN ANTONIO · PI GOLDEN, JEFFREY A, HSIEH, JENNY · 2019 to 2023
$2.6M
Circuitry mechanisms underlying new neuron development in adult and epileptic brainR01NS089770 · NINDS · STATE UNIVERSITY NEW YORK STONY BROOK · PI GE, SHAOYU, HSIEH, JENNY · 2015 to 2019
$1.8M
Targeting aberrant neurogenesis to prevent epilepsy and associated cognitive declineR01NS093992 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI HSIEH, JENNY · 2016 to 2020
$1.7M
ApoE4 in human cortical interneuron degeneration and network activityR21AG066496 · NIA · UNIVERSITY OF TEXAS SAN ANTONIO · PI HSIEH, JENNY · 2020 to 2020
$412k
NIA NIH HHS R21 AG066496NINDS NIH HHS R01 NS089770NINDS NIH HHS R01 NS093992NINDS NIH HHS R01 NS113516
6 · The paper itself

Abstract

In adult hippocampal neurogenesis, chromatin modification plays an important role in neural stem cell self-renewal and differentiation by regulating the expression of multiple genes. Histone deacetylases (HDACs), which remove acetyl groups from histones, create a non-permissive chromatin that prevents transcription of genes involved in adult neurogenesis. HDAC inhibitors have been shown to promote adult neurogenesis and have also been used to treat nervous system disorders, such as epilepsy. However, most HDAC inhibitors are not specific and may have other targets. Therefore, it is important to decipher the role of individual HDACs in adult hippocampal neurogenesis. HDACs 1, 2, and 3 have been found expressed at different cellular stages during neurogenesis. Conditional deletion of HDAC2 in neural stem cells impairs neuronal differentiation in adult hippocampus. HDAC3 supports proliferation of adult hippocampal neural stem/progenitor cells. The role of HDAC1 in adult neurogenesis remains still open. Here, we used a conditional knock-out mouse to block HDAC1 expression in neural stem cells (Nestin

Indexed as

HDAC1hippocampal neurogenesisneural stem cellsneuronal differentiationvalproic acid

Identifiers

PMID35095417
PMCPMC8789757
OpenAlexW4205330451

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.