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- W2893370992 endingPage "139" @default.
- W2893370992 startingPage "125" @default.
- W2893370992 abstract "Abstract Xeroderma pigmentosum group D helicase (XPD/ERCC2) is a member of the Rad3/XPD subfamily of ATP-dependent DNA helicases. It is an integral component of TFIIH, playing an essential role in transcription and nucleotide excision repair (NER). This chapter will primarily focus on studies showing that XPD associates with a functionally diverse class of proteins, including key factors involved in iron–sulfur (Fe-S) cluster assembly, cell-cycle regulation, chromosome segregation and mitochondrial function. The Fe-S cluster is crucial for XPD function. Our published data in 2012 and 2015, provide mechanistic insight into the pathways and factors required for the assembly of an Fe-S cluster on XPD. The importance of XPD’s Fe-S cluster in the context of NER and damage recognition will be discussed. Understanding different aspects of XPD biology in relation to the regulation of NER will be an essential aspect of cancer therapy as chemotherapy-resistant cells utilize their capacity to remove drug-induced DNA lesions." @default.
- W2893370992 created "2018-10-05" @default.
- W2893370992 creator A5005240902 @default.
- W2893370992 creator A5006474948 @default.
- W2893370992 date "2019-01-01" @default.
- W2893370992 modified "2023-09-25" @default.
- W2893370992 title "Role of Human Xeroderma Pigmentosum Group D (XPD) Helicase in Various Cellular Pathways" @default.
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- W2893370992 doi "https://doi.org/10.1016/b978-0-12-814685-9.00008-7" @default.