Evidence map›Paper›PMID 41601423›Full record

ReviewBrain and behavior2026

Neurogenesis and the Epigenetic Landscape: Role of Histone Modifications and Chromatin Remodeling.

Degisew Yinur Mengistu, Biniam Moges Eskeziyaw

Abstract readReview
In one paragraph

Review in Brain and behavior, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. 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

2 authors.

Degisew Yinur MengistuDepartment of Biology and Biotechnology "Charles Darwin", Sapienza University, Rome, Italy.
Biniam Moges EskeziyawDepartment of Biotechnology, Debre Berhan University, Debre Berhan, Ethiopia.

Funding

European Union-Next Generation EU 2022M75NN8European Union-Next Generation EU B53D23008270006European Union-Next Generation EU B53D23008280006
6 · The paper itself

Abstract

aimsThe purpose of this review is to examine how epigenetic regulation particularly chromatin modification and histone methylation controls gene expression during embryonic neurogenesis. It aims to highlight the role of these mechanisms in neural stem cell (NSC) fate specification and their implications in neurological and neurodevelopmental disorders.

methodsThrough reviewing recent research findings, this study synthesizes current literature on epigenetic mechanisms involved in embryonic brain development, with a focus on histone modifications, chromatin remodeling, and chromatin compartmentalization. The review also evaluates existing in vivo research while noting the technical challenges of tracking adult neurons and isolating NSCs.

findingsThe review identifies that epigenetic mechanisms, including histone methylation (notably H3K9 as a repressive mark), histone deacetylases, and chromatin remodeling complexes, play essential roles in regulating gene expression required for neurogenesis and neuroplasticity. Alterations in these epigenetic processes significantly affect neural development and contribute to a range of neurological and neurodevelopmental disorders.

conclusionsUnderstanding the epigenetic regulation of neurogenesis particularly through chromatin modification and structural chromatin dynamics provides valuable insight into cell fate determination during embryonic brain development. These insights may guide the development of novel therapeutic strategies for neurological and neurodevelopmental disorders.

Indexed as

Chromatin Assembly and DisassemblyEpigenesis, GeneticHistone CodeNeurogenesisAnimalsBrainHistonesHumansNeural Stem CellsNeurodevelopmentHistonesChromatin remodelinghistone deacetylaseshistone methylationneural stem cellproliferationsymmetric division

Identifiers

PMID41601423
PMCPMC12848536

What OpenQuestion holds

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Registered trials

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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.