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...

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Vydáno v:EMBO J
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: Nature Publishing Group 1994
Témata:
Research Article
On-line přístup: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
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