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Mutation in Eftud2 causes craniofacial defects in mice via mis-splicing of Mdm2 and increased P53

Human Molecular Genetics(2021)10.1093/hmg/ddab051Source: DataRank Database

Mutation in Eftud2 causes craniofacial defects in mice via mis-splicing of Mdm2 and increased P53 is a research paper published in Human Molecular Genetics (2021). On theSindex it has a DataRank of 0. It has been cited 48 times.

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Open Access48 citations

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (13 grants)OA: bronzeTopics (23)Linked Datasets (2)DataCite Reuse (2)IDs (PubMed, PMC)Annotations (2)SDGs (1)

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Context only (not used in score)

Findable (2/2)

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Accessible (1/2)

Open Access

Interoperable (2/2)

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Authors (12)

Anissa Djedid ORCID,Eric Bareke ORCID,Fjodor Merkuri ORCID,Rachel Aber,Annie Tam

Live enrichment

PubMed:33601405 PMC:PMC8161524

NIH

Grant: 2R15DE026611-02

Molecular and cellular mechanisms underlying Satb2-mediated variation in craniofacial disease

Canadian Institutes of Health Research

Grant: MOP#142452

CIHR

Grant: 142452

NIDCR NIH HHS

Grant: R15 DE026611

Canadian Institutes of Health Research

Grant: unidentified

unidentified

Genome Alberta

Genome British Columbia

Canadian Institutes of Health Research

Genome Quebec

Ontario Research Fund

FQRS

Genome Canada and the Ontario Genomics Institute

Children’s Hospital of Eastern Ontario Foundation

bronzeLicense: OUP Standard Publication Reuse

publisherhttps://academic.oup.com/hmg/article-pdf/30/9/739/38338347/ddab051.pdf

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/8161524

https://doi.org/10.1093/hmg/ddab051

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8161524

https://pubmed.ncbi.nlm.nih.gov/33601405

Fields of Study

0301 basic medicine0303 health sciences03 medical and health sciences

MeSH Terms

AnimalsHumansMiceRibonucleoprotein, U5 Small NuclearPeptide Elongation FactorsSequence DeletionHomozygoteMutationTumor Suppressor Protein p53Proto-Oncogene Proteins c-mdm2

Keywords

HomozygoteProto-Oncogene Proteins c-mdm2Peptide Elongation FactorsMiceMutationAnimalsHumansTumor Suppressor Protein p53Ribonucleoprotein, U5 Small NuclearSequence Deletion

Sustainable Development Goals

SDG 3: 3. Good health

Additional file 1 of Dual diagnosis of achondroplasia and mandibulofacial dysostosis with microcephaly

10.6084/m9.figshare.26962534.v1figshare

Additional file 1 of Dual diagnosis of achondroplasia and mandibulofacial dysostosis with microcephaly

10.6084/m9.figshare.26962534figshare

Mutation in Eftud2 causes craniofacial defects in mice via mis-splicing of Mdm2 and increased P53

FAIR Checklist

Authors (12)

Funding (13 grants)

Open Access

Topics

Linked Datasets (2)

Annotations (Europe PMC)