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Mesenchyme-specific loss of Dot1L histone methyltransferase leads to skeletal dysplasia phenotype in mice

Bone(2020)10.1016/j.bone.2020.115677Source: DataRank Database

Mesenchyme-specific loss of Dot1L histone methyltransferase leads to skeletal dysplasia phenotype in mice is a research paper published in Bone (2020). On theSindex it has a DataRank of 0. It has been cited 13 times.

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Open Access13 citations

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Enrichment:Funding (4 grants)OA: bronzeTopics (23)IDs (PubMed, PMC)Annotations (1)

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Authors (9)

Sangita Karki,Ilan Crawley,Vijender Singh ORCID,Kathrin M. Bernt ORCID,David W. Rowe ORCID

Live enrichment

PubMed:33022452 PMC:PMC7744341

NICHD NIH HHS

Grant: R01 HD098636

NICHD NIH HHS

Grant: R03 HD097426

National Institutes of Health

Grant: 1R03HD097426-01A1

Understanding how Dot1L activity in the growth plate regulates skeletal growth

National Institutes of Health

bronzeLicense: Elsevier TDM

publisherhttps://api.elsevier.com/content/article/PII:S8756328220304579?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S8756328220304579?httpAccept=text/plain

https://doi.org/10.1016/j.bone.2020.115677

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7744341

https://pubmed.ncbi.nlm.nih.gov/33022452

Fields of Study

0301 basic medicine0303 health sciences03 medical and health sciences

MeSH Terms

ChondrocytesMesodermAnimalsMiceHistone-Lysine N-MethyltransferasePhenotypeX-Ray MicrotomographyHistone Methyltransferases

Keywords

Cartilagegrowth plateSkeletal DysplasiaDot1lMesodermMiceChondrocytesPhenotypeHistone MethyltransferasesAnimalsHistone-Lysine N-MethyltransferaseX-Ray Microtomography

Mesenchyme-specific loss of Dot1L histone methyltransferase leads to skeletal dysplasia phenotype in mice

FAIR Checklist

Authors (9)

Funding (4 grants)

Open Access

Topics

Annotations (Europe PMC)