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Gain of Function NOTCH3 Variants Cause Familial Partial Lipodystrophy Due to Activation of Senescence Pathways

Diabetes(2024)10.2337/db24-0624Source: DataRank Database

Gain of Function NOTCH3 Variants Cause Familial Partial Lipodystrophy Due to Activation of Senescence Pathways is a research paper published in Diabetes (2024). On theSindex it has a DataRank of 0. It has been cited 7 times.

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Open Access7 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (13 grants)Impact (FWCI 1.15)OA: greenTopics (43)IDs (PubMed, PMC, 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 (8)

Chao Xing ORCID,Anil K. Agarwal ORCID,Aundrea K. Westfall ORCID,Diana R. Tomchick ORCID,Xunzhi Zhang ORCID

Live enrichment

PubMed:39652711 PMC:PMC11842598 OpenAlex:https://openalex.org/W4405179724

National Institutes of Health

Grant: R01-DK105448

NIDDK NIH HHS

Grant: R01 DK105448

The University of Texas at Austin

NIDDK NIH HHS

UT Southwestern Medical Center

Structural Biology Laboratory

National Institute of Diabetes and Digestive and Kidney Diseases

Texas Advanced Computing Center

Structural Biology Laboratory

NIDDK NIH HHS

Texas Advanced Computing Center

UT Southwestern Medical Center

The University of Texas at Austin

FWCI

1.15

Citation Percentile

0.8%

Citation Trend

2025

2026

greenLicense: https://www.diabetesjournals.org/journals/pages/license

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC11842598/

publisherhttps://diabetesjournals.org/diabetes/article-pdf/74/3/427/791573/db240624.pdf

journalhttps://doi.org/10.2337/db24-0624

repositoryhttps://pubmed.ncbi.nlm.nih.gov/39652711

Fields of Study

Nuclear Structure and FunctionGenomics and Rare DiseasesRNA Research and SplicingHumansFemaleReceptor, Notch3Lipodystrophy, Familial PartialPedigreeAdultMaleGain of Function MutationCellular SenescenceMiddle AgedExome SequencingMutation, Missense

MeSH Terms

Receptor, Notch3Exome SequencingGain of Function MutationAdultFemaleFibroblastsHumansMaleMiddle AgedPedigreeCellular SenescenceMutation, MissenseLipodystrophy, Familial PartialYoung Adult

Keywords

LipodystrophyExome sequencingBiologyGeneticsSenescenceGain of functionExomeLoss functionMissense mutationBioinformaticsCancer researchMutationGenePhenotype

Sustainable Development Goals

SDG 0: Good health and well-being