Characteristics of Xeroderma Pigmentosum in Japan: Lessons From Two Clinical Surveys and Measures for Patient Care

Author:

Nishigori Chikako1,Nakano Eiji1,Masaki Taro1,Ono Ryusuke1,Takeuchi Seiji1,Tsujimoto Mariko1,Ueda Takehiro2

Affiliation:

1. Department of Dermatology; Graduate School of Medicine; Kobe University; Kobe Hyogo Japan

2. Division of Neurology; Graduate School of Medicine; Kobe University; Kobe Hyogo Japan

Funder

Ministry of Health, Labour and Welfare

Publisher

Wiley

Subject

Physical and Theoretical Chemistry,General Medicine,Biochemistry

Reference57 articles.

1. Defective repair replication of DNA in xeroderma pigmentosum;Cleaver;Nature,1968

2. The human DNA repair gene, ERCC2 (XPD), corrects ultraviolet hypersensitivity and ultraviolet hypermutability of a shuttle vector replicated in xeroderma pigmentosum group D cells;Gözükara;Cancer Res.,1994

3. UV-induced ubiquitylation of XPC protein mediated by UV-DDB-ubiquitin ligase complex;Sugasawa;Cell,2005

4. The xeroderma pigmentosum group C protein complex XPC-HR23B plays an important role in the recruitment of transcription factor IIH to damaged DNA;Yokoi;J. Biol. Chem.,2000

5. Mechanism of open complex and dual incision formation by human nucleotide excision repair factors;Evans;EMBO J.,1997

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