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Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms

(2023)10.7554/elife.87147.3Source: DataRank Database

Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms is a research paper (2023). On theSindex it has a DataRank of 0.

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Scored on demand from live citation data

Open Access0 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (4 grants)OA: goldTopics (15)IDs (PubMed, OpenAlex)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (5)

Chi Sun ORCID,Xiaodong Zhang ORCID,Philip A. Ruzycki ORCID,Shiming Chen ORCID,Yiqiao Zheng ORCID

Live enrichment

PubMed:21097893 OpenAlex:https://openalex.org/W4385984554

National Institute of Health

Grant: EY012543

National Institute of Health

Grant: EY032136

Research to Prevent Blindness

Grant: Stein Innovation Award

Widłak Family

Grant: CRX Research Fund

goldLicense: cc-by

https://elifesciences.org/reviewed-preprints/87147v3.pdf

publisherhttps://cdn.elifesciences.org/preprints/87147/elife-preprint-87147-v3.pdf

publisherhttps://cdn.elifesciences.org/preprints/87147/elife-preprint-87147-v3.xml

publisherhttps://elifesciences.org/reviewed-preprints/87147v3/pdf

Fields of Study

Retinal Development and DisordersDevelopmental Biology and Gene RegulationCRISPR and Genetic Engineering

Keywords

HomeoboxMissense mutationBiologyTransactivationTranscription factorEctopic expressionGeneticsGeneLoss functionMutationCell biologyPhenotype

Sustainable Development Goals

SDG 0: Good health and well-being