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Article: Kidney Fibrosis: Lock out SIRT4

TitleKidney Fibrosis: Lock out SIRT4
Authors
KeywordsCCN2
cell biology
kidney fibrosis
mouse
nuclear translocation
sirtuin 4
splicing
TGF-β1
Issue Date13-Sep-2024
PublishereLife Sciences Publications
Citation
eLife, 2024, v. 13 How to Cite?
AbstractThe accumulation of SIRT4 in the nuclei of kidney cells drives kidney fibrosis, so blocking the movement of this protein could be a potential therapeutic strategy against fibrosis.
Persistent Identifierhttp://hdl.handle.net/10722/354530
ISSN
2023 Impact Factor: 6.4
2023 SCImago Journal Rankings: 3.932
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorZhao, Kaiqiang-
dc.contributor.authorZhou, Zhongjun-
dc.date.accessioned2025-02-12T00:35:17Z-
dc.date.available2025-02-12T00:35:17Z-
dc.date.issued2024-09-13-
dc.identifier.citationeLife, 2024, v. 13-
dc.identifier.issn2050-084X-
dc.identifier.urihttp://hdl.handle.net/10722/354530-
dc.description.abstractThe accumulation of SIRT4 in the nuclei of kidney cells drives kidney fibrosis, so blocking the movement of this protein could be a potential therapeutic strategy against fibrosis.-
dc.languageeng-
dc.publishereLife Sciences Publications-
dc.relation.ispartofeLife-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectCCN2-
dc.subjectcell biology-
dc.subjectkidney fibrosis-
dc.subjectmouse-
dc.subjectnuclear translocation-
dc.subjectsirtuin 4-
dc.subjectsplicing-
dc.subjectTGF-β1-
dc.titleKidney Fibrosis: Lock out SIRT4-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.7554/eLife.102355-
dc.identifier.pmid39269433-
dc.identifier.scopuseid_2-s2.0-85204167393-
dc.identifier.volume13-
dc.identifier.isiWOS:001312079100001-
dc.identifier.issnl2050-084X-

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