A Manually Curated Knowledgebase of Aging across a variety of Species

Details


Name SIRT1
Type gene
Species Homo sapiens
Tissue U-2 OS
Experiment Method PCR,Western Blot,other
Up/Down Up
Pro/Anti Anti
Funtion Description Mutations in genes for WRN and BLM RecQ family helicases cause cancer prone syndromes. Werner syndrome, resulting from WRN mutation, is a segmental progeria. Endogenous WRN and BLM proteins localize in nucleoli and in nuclear PML bodies defined by isoform
Regulation Gene NA
Year 2007
Pubmed ID 17996922
Title Expression and localization of Werner syndrome protein is modulated by SIRT1 and PML.
Drug NA
Disease NA
Environment Factors NA
Circulating NA
Variant NA
High-throughput NA