Differences in Clinical Phenotype among Patients with XP Complementation Group D: 3D Structure and ATP-Docking of XPD In Silico
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Dermatology,Molecular Biology,Biochemistry
Reference12 articles.
1. Persistence of repair proteins at unrepaired DNA damage distinguishes diseases with ERCC2 (XPD) mutations: cancer-prone xeroderma pigmentosum vs. non-cancer-prone trichothiodystrophy;Boyle;Hum Mutat,2008
2. Shining a light on xeroderma pigmentosum;DiGiovanna;J Invest Dermatol,2012
3. Strict sun protection results in minimal skin changes in a patient with xeroderma pigmentosum and a novel c.2009delG mutation in XPD (ERCC2);Emmert;Exp Dermatol,2009
4. A novel XPD mutation in a compound heterozygote; the mutation in the second allele is present in three homozygous patients with mild sun sensitivity;Falik-Zaccai;Environ Mol Mutagen,2012
5. XPD helicase structures and activities: insights into the cancer and aging phenotypes from XPD mutations;Fan;Cell,2008
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