The XPB subunit of repair/transcription factor TFIIH directly interacts with SUG1, a subunit of the 26S proteasome and putative transcription factor.

Mutations in the basal transcription initiation/DNA repair factor TFIIH are responsible for three human disorders: xeroderma pigmentosum (XP), cockayne syndrome (CS) and trichothiodystrophy (TTD). The non-repair features of CS and TTD are thought to be due to a partial inactivation of the transcript...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Weeda, G, Rossignol, M, Fraser, R A, Winkler, G S, Vermeulen, W, van 't Veer, L J, Ma, L, Hoeijmakers, J H, Egly, J M
Formato: Artigo
Idioma:Inglês
Publicado em: 1997
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC146752/
https://ncbi.nlm.nih.gov/pubmed/9173976
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados