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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | EMBO J |
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| Κύριοι συγγραφείς: | , , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Nature Publishing Group
1994
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| Θέματα: | |
| Διαθέσιμο Online: | 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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