Codi QR

Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH).

ERCC3 was initially identified as a gene correcting the nucleotide excision repair (NER) defect of xeroderma pigmentosum complementation group B (XP-B). The recent finding that its gene product is identical to the p89 subunit of basal transcription factor BTF2(TFIIH), opened the possibility that it...

Descripció completa

Guardat en:
Publicat a:EMBO J
Autors principals: van Vuuren, A J, Vermeulen, W, Ma, L, Weeda, G, Appeldoorn, E, Jaspers, N G, van der Eb, A J, Bootsma, D, Hoeijmakers, J H, Humbert, S
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group 1994
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC394995/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8157004/
https://ncbi.nlm.nih.govhttps://doi.org/10.1002/j.1460-2075.1994.tb06428.x
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars