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PRDM16 co-operates with LHX2 to shape the human brain

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.08.12.553065Source: DataRank Database

PRDM16 co-operates with LHX2 to shape the human brain is a research paper published in bioRxiv (Cold Spring Harbor Laboratory) (2023). On theSindex it has a DataRank of 0. It has been cited 4 times.

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Open Access4 citations

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (5 grants)OA: greenTopics (41)IDs (PubMed, OpenAlex)SDGs (1)

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Findable (1/2)

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Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (14)

Bidisha Bhattacharya ORCID,Rami Yair Tshuva ORCID,Miri Danan-Gotthold ORCID,Tsviya Olender ORCID,Mahima Bose ORCID

Live enrichment

PubMed:37609127 OpenAlex:https://openalex.org/W4385793660

National Institutes of Health

Grant: 5R01NS102228-03

Epigenetic Regulation of Cortical Neuronal Lineage Progression

National Institutes of Health

Grant: 1R21NS127983-01A1

Modeling NDE1 function in dysregulated brain development using a microfluidic CNS model

Canadian Institutes of Health Research

Grant: unidentified

unidentified

National Institutes of Health

Grant: 5R00NS112604-05

Role for ion conducting proteins in cortical malformation diseases

NINDS NIH HHS

Grant: R21 NS127983

greenLicense: CC BY

repositoryhttps://www.biorxiv.org/content/biorxiv/early/2023/08/12/2023.08.12.553065.full.pdf

publisherhttps://syndication.highwire.org/content/doi/10.1101/2023.08.12.553065

repositoryhttps://doi.org/10.1101/2023.08.12.553065

repositoryhttps://pubmed.ncbi.nlm.nih.gov/37609127

Fields of Study

RNA Research and SplicingRNA modifications and cancerEpigenetics and DNA Methylation03 medical and health sciences0303 health sciences

Keywords

BiologyNeural stem cellCorticogenesisCell biologyStem cellPRDM16LissencephalyWnt signaling pathwayGeneticsProgenitor cellGeneGene expression1.1 Normal biological development and functioningBioinformatics and Computational Biologybrain developmentRegenerative Medicine1p36 deletion syndromeRare DiseasesStem Cell Research - Nonembryonic - Human2.1 Biological and endogenous factorsStem Cell Research - Embryonic - HumanPediatricBiomedical and Clinical SciencesStem Cell Research - Induced Pluripotent Stem Cell - HumanStem Cell Research - Induced Pluripotent Stem CellHuman GenomeNeurosciencesLHX2Biological SciencesStem Cell Researchhuman disease modelNeurologicalcerebral organoidsCongenital Structural AnomaliesStem Cell Research - Nonembryonic - Non-HumanResearch Article

Sustainable Development Goals

SDG 0: Partnerships for the goals