Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 하헌주 | * |
dc.date.accessioned | 2017-02-15T08:02:34Z | - |
dc.date.available | 2017-02-15T08:02:34Z | - |
dc.date.issued | 2007 | * |
dc.identifier.issn | 0085-2538 | * |
dc.identifier.other | OAK-4171 | * |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/234417 | - |
dc.description.abstract | Histone deacetylase (HDAC) inhibitors are currently being tested as anticancer agents in clinical trials. Chromatin remodeling, such as through histone acetylation, is a fundamental phenomenon in eukaryotic cell biology, bearing implications to numerous physiological and pathological phenomena. Here, we discuss recent data from our own laboratory and those of others demonstrating antifibrotic and renoprotective effect of HDAC inhibitors in diabetic kidneys, and the possible mechanisms including the role of reactive oxygen species. HDAC inhibitors may prove to be a novel class of multitarget agents in the treatment of diabetic nephropathy. © 2007 International Society of Nephrology. | * |
dc.language | English | * |
dc.title | Histone deacetylase inhibitors: A novel class of therapeutic agents in diabetic nephropathy | * |
dc.type | Conference Paper | * |
dc.relation.issue | SUPPL. 106 | * |
dc.relation.volume | 72 | * |
dc.relation.index | SCI | * |
dc.relation.index | SCIE | * |
dc.relation.index | SCOPUS | * |
dc.relation.startpage | S61 | * |
dc.relation.lastpage | S66 | * |
dc.relation.journaltitle | Kidney International | * |
dc.identifier.doi | 10.1038/sj.ki.5002388 | * |
dc.identifier.wosid | WOS:000248506300010 | * |
dc.identifier.scopusid | 2-s2.0-34547431097 | * |
dc.author.google | Lee H.B. | * |
dc.author.google | Noh H. | * |
dc.author.google | Seo J.Y. | * |
dc.author.google | Yu M.R. | * |
dc.author.google | Ha H. | * |
dc.contributor.scopusid | 하헌주(7202277106) | * |
dc.date.modifydate | 20240422113229 | * |