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Effects of therapeutically approved individual bile acids on the development of metabolic dysfunction-associated steatohepatitis a low bile acid mouse model

Toxicological Sciences(2024)10.1093/toxsci/kfae110Source: DataRank Database

Effects of therapeutically approved individual bile acids on the development of metabolic dysfunction-associated steatohepatitis a low bile acid mouse model is a research paper published in Toxicological Sciences (2024). On theSindex it has a DataRank of 0. It has been cited 7 times.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access7 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (18 grants)Impact (FWCI 2.00)OA: greenTopics (61)IDs (PubMed, PMC, OpenAlex)

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 (18)

Veronia Basaly ORCID,Bo Kong ORCID,Ill Yang ORCID,Anita Brinker ORCID,Gina E Capece ORCID

Live enrichment

PubMed:39302723 PMC:PMC12104526 OpenAlex:https://openalex.org/W4402665902

New Jersey Space Grant Consortium

Grant: T32 ES007148

New Jersey Space Grant Consortium

Grant: GM135258

New Jersey Space Grant Consortium

Grant: ES029258

New Jersey Space Grant Consortium

Grant: DK122725

New Jersey Space Grant Consortium

Grant: BX002741

ASPET Summer Intern Program

Grant: ES020721

ASPET Summer Intern Program

Grant: ES005022

NIEHS NIH HHS

Grant: P30 ES005022

NIEHS NIH HHS

Grant: R25 ES020721

NIGMS NIH HHS

Grant: R01 GM135258

NIEHS NIH HHS

Grant: R21 ES029258

BLRD VA

Grant: I01 BX002741

NIDDK NIH HHS

Grant: F31 DK122725

NIH

BMS

Rutgers University COVID-19 Dissertation Completion Fellowship

BMS

Rutgers University COVID-19 Dissertation Completion Fellowship

FWCI

2.00

Citation Percentile

0.9%

Citation Trend

2025

2026

greenLicense: public-domain

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC12104526/pdf/kfae110.pdf

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC12104526/pdf/kfae110.pdf

publisherhttps://academic.oup.com/toxsci/advance-article-pdf/doi/10.1093/toxsci/kfae110/59355188/kfae110.pdf

publisherhttps://academic.oup.com/toxsci/article-pdf/202/2/179/60807975/kfae110.pdf

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/12104526

Fields of Study

Liver Disease Diagnosis and TreatmentDrug Transport and Resistance MechanismsLiver Diseases and ImmunityAnimalsMice, KnockoutDisease Models, AnimalBile Acids and SaltsMice, Inbred C57BLReceptors, Cytoplasmic and NuclearMaleMiceLiverCholesterol 7-alpha-HydroxylaseFatty LiverCholic AcidLipid MetabolismUrsodeoxycholic AcidDeoxycholic AcidCholestanetriol 26-MonooxygenaseNon-alcoholic Fatty Liver DiseaseReceptor, Farnesoid X-Activated

MeSH Terms

Receptor, Farnesoid X-ActivatedAnimalsBile Acids and SaltsCholesterol 7-alpha-HydroxylaseDeoxycholic AcidDisease Models, AnimalFatty LiverLiverMaleMice, Inbred C57BLUrsodeoxycholic AcidReceptors, Cytoplasmic and NuclearMice, KnockoutCholic AcidLipid MetabolismMiceCholestanetriol 26-MonooxygenaseNon-alcoholic Fatty Liver Disease

Keywords

Farnesoid X receptorCholesterol 7 alpha-hydroxylaseBile acidUrsodeoxycholic acidSteatohepatitisDeoxycholic acidG protein-coupled bile acid receptorLipid metabolismEndocrinologyCholic acidInternal medicineCYP27A1HepatoprotectionInflammationFatty liverBiologyBiochemistryNuclear receptorMedicineBile acidsNuclear ReceptorsFxr