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Novel Grm6 Variant in a no b-wave (nob) Mouse Model: Phenotype Characterization and Gene Therapy

Investigative Ophthalmology & Visual Science(2025)10.1167/iovs.66.12.20Source: DataRank Database

Novel Grm6 Variant in a no b-wave (nob) Mouse Model: Phenotype Characterization and Gene Therapy is a research paper published in Investigative Ophthalmology & Visual Science (2025). On theSindex it has a DataRank of 0.

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (12 grants)Impact (FWCI 0.00)OA: goldTopics (43)IDs (PubMed, PMC, OpenAlex)Annotations (2)

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 (16)

Eugene Yu‐Chuan Kang ORCID,Neoklis Makrides,Winston Lee ORCID,Yun-Ju Tseng,Peiliang Wu ORCID

Live enrichment

PubMed:40923695 PMC:PMC12425143 OpenAlex:https://openalex.org/W4414081270

NEI NIH HHS

Grant: R01 EY018868

NIH HHS

Grant: S10 OD028637

NEI NIH HHS

Grant: P30 EY001319

NEI NIH HHS

Grant: P30 EY019007

NEI NIH HHS

Grant: R01 EY031354

NCI NIH HHS

Grant: P30 CA013696

NIH HHS

Grant: S10 OD030401

NEI NIH HHS

Grant: R01 EY031210

NEI NIH HHS

Grant: R01 EY012951

NEI NIH HHS

Grant: R01 EY017061

NEI NIH HHS

Grant: R21 EY037007

NEI NIH HHS

Grant: R01 EY025933

FWCI

0.00

Citation Percentile

0.1%

goldLicense: cc-by-nc-nd

journalhttps://doi.org/10.1167/iovs.66.12.20

publisherhttps://doi.org/10.1167/iovs.66.12.20

publisherhttps://iovs.arvojournals.org/article.aspx?articleid=2810799

repositoryhttps://pubmed.ncbi.nlm.nih.gov/40923695

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC12425143/

Fields of Study

Retinal Development and DisordersPhotochromic and Fluorescence ChemistryPhotoreceptor and optogenetics researchAnimalsGenetic TherapyMiceElectroretinographyDisease Models, AnimalMyopiaPhenotypeEye Diseases, HereditaryReceptors, Metabotropic GlutamateTomography, Optical CoherenceNight BlindnessGenetic Diseases, X-LinkedDependovirusRetinal Bipolar CellsMice, Inbred C57BLMaleFemaleNight blindness, congenital stationary

MeSH Terms

DependovirusAnimalsDisease Models, AnimalElectroretinographyFemaleMaleMice, Inbred C57BLMyopiaNight BlindnessPhenotypeGenetic TherapyEye Diseases, HereditaryReceptors, Metabotropic GlutamateGenetic Diseases, X-LinkedTomography, Optical CoherenceRetinal Bipolar CellsMice

Keywords

PhenotypeGenetic enhancementTransduction (biophysics)GeneClinical phenotype

Novel Grm6 Variant in a no b-wave (nob) Mouse Model: Phenotype Characterization and Gene Therapy

FAIR Checklist

Authors (16)

Funding (12 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)