PT Bradford, AM Goldstein, D Tamura… - Journal of medical …, 2011 - jmg.bmj.com Results In the 65 per cent (n=69) of patients with skin cancer, non-melanoma skin cancer (NMSC) was increased 10 000-fold and melanoma was increased 2000-fold in patients under age 20. The 9 year median age at diagnosis of first non-melanoma skin cancer (NMSC) ... Cited by 4 - Related articles - All 4 versions
P Hentosh, T Benjamin, L Hall, S Leap… - Experimental and …, 2011 - ncbi.nlm.nih.gov Deficiencies of DNA polymerase eta-an enzyme mediating replication past UV-induced DNA damage-predispose individuals to xeroderma pigmentosum variant (XPV) and result in a high incidence of skin cancers. We designed, developed and assessed several ...
M Saijo, A Takedachi… - Journal of Biological Chemistry, 2011 - ASBMB The xeroderma pigmentosum group A protein (XPA) is a core component of nucleotide excision repair (NER). To coordinate early stage NER, XPA interacts with various proteins, including replication protein A (RPA), ERCC1, DDB2, and TFIIH, in addition to UV-damaged or chemical ... Related articles - All 4 versions
AM Alfawaz… - Ophthalmic Plastic & …, 2011 - journals.lww.com Wolters Kluwer Health may email you for journal alerts and information, but is committed to maintaining your privacy and will not share your personal information without your express consent. For more information, please refer to our Privacy Policy. ... Skip Navigation Links Home > ... Related articles - All 4 versions
HL Ramkumar, BP Brooks, X Cao, D Tamura… - Survey of …, 2011 - Elsevier Xeroderma pigmentosum is a rare, autosomal recessive disease caused by a defect in DNA repair. Patients with xeroderma pigmentosum often have cutaneous and ocular sun sensitivity, freckle-like skin pigmentation, multiple skin and eye cancers, and, in some ... Related articles - All 3 versions