Código QR (código de barras bidimensional)

Structure and function of the human Werner syndrome gene promoter: evidence for transcriptional modulation.

The Werner syndrome (WS) is an autosomal recessive segmental progeroid syndrome caused by mutations in a novel member ( WRN ) of the RecQ family of helicases. Somatic WS cells are hypermutable and have elongated S phases, suggesting possible defects in DNA replication and/or repair. As an initial ap...

Fuld beskrivelse

Na minha lista:
Udgivet i:Nucleic Acids Res
Principais autores: Wang, L, Hunt, K E, Martin, G M, Oshima, J
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 1998
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC147734/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9671808/
https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/26.15.3480
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker