{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,10]],"date-time":"2026-06-10T16:00:05Z","timestamp":1781107205544,"version":"3.54.1"},"reference-count":31,"publisher":"National Academy of Sciences","issue":"51","content-domain":{"domain":["www.pnas.org"],"crossmark-restriction":true},"short-container-title":["Proc. Natl. Acad. Sci. U.S.A."],"published-print":{"date-parts":[[2004,12,21]]},"abstract":"<jats:p>\n                    UV radiation is the most common risk factor for skin cancer. Patients with the autosomal recessive DNA repair disorder xeroderma pigmentosum (XP) suffer high incidence of skin cancer after sunlight exposure. XP-mutant mice are attractive models to study this syndrome, as they, too, develop UV radiation-induced skin tumors, mimicking the human phenotype. Recombinant adenovirus carrying the human\n                    <jats:italic>XPA<\/jats:italic>\n                    gene was used for\n                    <jats:italic>in vivo<\/jats:italic>\n                    gene therapy in UVB-irradiated skin of such mice. Virus s.c. injection led to the expression of the XPA protein in basal keratinocytes and prevented deleterious effects in the skin, including late development of squamous cell carcinoma. Thus, efficient adenovirus gene delivery to the skin is a promising tool for reconstitution of specific DNA repair defects in XP patients.\n                  <\/jats:p>","DOI":"10.1073\/pnas.0406304101","type":"journal-article","created":{"date-parts":[[2004,12,14]],"date-time":"2004-12-14T21:58:07Z","timestamp":1103061487000},"page":"17759-17764","update-policy":"https:\/\/doi.org\/10.1073\/pnas.cm10313","source":"Crossref","is-referenced-by-count":36,"title":["Gene transduction in skin cells: Preventing cancer in xeroderma pigmentosum mice"],"prefix":"10.1073","volume":"101","author":[{"given":"Maria Carolina N.","family":"Marchetto","sequence":"first","affiliation":[{"name":"Department of Microbiology, Institute of Biomedical Sciences, Universidade de S\u00e3o Paulo, S\u00e3o Paulo 05508-900, SP, Brazil; Laboratory of Genetics, The Salk Institute, La Jolla, CA 92037; and Laboratory of Molecular Pathology, Department of Pathology, University of Texas Southwestern Medical Center, Dallas, TX 75235"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alysson R.","family":"Muotri","sequence":"additional","affiliation":[{"name":"Department of Microbiology, Institute of Biomedical Sciences, Universidade de S\u00e3o Paulo, S\u00e3o Paulo 05508-900, SP, Brazil; Laboratory of Genetics, The Salk Institute, La Jolla, CA 92037; and Laboratory of Molecular Pathology, Department of Pathology, University of Texas Southwestern Medical Center, Dallas, TX 75235"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dennis K.","family":"Burns","sequence":"additional","affiliation":[{"name":"Department of Microbiology, Institute of Biomedical Sciences, Universidade de S\u00e3o Paulo, S\u00e3o Paulo 05508-900, SP, Brazil; Laboratory of Genetics, The Salk Institute, La Jolla, CA 92037; and Laboratory of Molecular Pathology, Department of Pathology, University of Texas Southwestern Medical Center, Dallas, TX 75235"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Errol C.","family":"Friedberg","sequence":"additional","affiliation":[{"name":"Department of Microbiology, Institute of Biomedical Sciences, Universidade de S\u00e3o Paulo, S\u00e3o Paulo 05508-900, SP, Brazil; Laboratory of Genetics, The Salk Institute, La Jolla, CA 92037; and Laboratory of Molecular Pathology, Department of Pathology, University of Texas Southwestern Medical Center, Dallas, TX 75235"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Carlos F. 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