XPC and human homologs of RAD23: intracellular localization and relationship to other nucleotide excision repair complexes.

The xeroderma pigmentosum syndrome complementation group C (XP-C) is due to a defect in the global genome repair subpathway of nucleotide excision repair (NER). The XPC protein is complexed with HHR23B, one of the two human homologs of the yeast NER protein, RAD23 (Masutani at al. (1994) EMBO J. 8,...

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Detalhes bibliográficos

Publicado no:	Nucleic Acids Res
Principais autores:	van der Spek, P J, Eker, A, Rademakers, S, Visser, C, Sugasawa, K, Masutani, C, Hanaoka, F, Bootsma, D, Hoeijmakers, J H
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Oxford University Press 1996
Assuntos:	Research Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC145966/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8692695/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/24.13.2551
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