HELLENIC ASSOCIATION DERMATOLOGY - VENEREOLOGY
A RANDOMIZED, DOUBLE BLIND, MULTI-CENTER CLINICAL STUDY TO TEST THE SAFETY AND EFFICACY OF T4N5 LIPOSOME LOTION ON PATIENTS WITH XERODERMA PIGMENTOSUM IN THE PREVENTION OF ACTINIC KERATOSES. Abnormal, error-prone bypass of photoproducts by xeroderma pigmentosum variant cell extracts results in extreme strand bias for the kinds of mutations induced by UV light. McGregor WG, Wei D, Maher VM, McCormick JJ Mol Cell Biol 1999 Jan;19(1):147-54 All you want to know about UV light Alliance of Genetic Support Groups Assessment of microsatellite instability in a cell line from a patient with xeroderma pigmentosum variant. Tien-Yi Tzung, Caroline Diem, T. M. Rünger. Archives of Dermatological Research, 290(3):109-112, 3/1998. Camp Sundown cancer in xeroderma pigmentosum with the use of oral isotretinoin Caractérisation moléculaire de la maladie Xeroderma pigmentosum variant CARCINOMA AND XERODERMA PIGMENTOSUM Full Image Clinical Trial of xeroderma pigmentosum patients using T4N5 Liposomes Lotion. Dermabrasion for Xeroderma Pigmentosum...[Letter, Feb Arch Dermatol. 1998;134:241-242] (c) AMA 1998 Dermatology Laboratory Dermatologie Online Atlas, Erlangen, Allemagne Dermatology Online Atlas (DOIA) Erlangen: Xeroderma Pigmentosum Tardivum DOIA: Xeroderma pigmentosum Doxorubicin and &ggr; rays increase the level of DNA topoisomerase IIα in nuclei of normal and xeroderma pigmentosum fibroblasts. Heinz Walter Thielmann, Odilia Popanda. Journal of Cancer Research and Clinical Oncology, 124(7):355-366, 7/1998. Doxorubicin and <Gamma> rays increase the level of DNA topoisomerase II<alpha> in nuclei of normal and xeroderma pigmentosum fibroblasts Heinz Walter Thielmann, Odilia Popanda: J Cancer Res Clin Oncol 124 (1998) 7, 355-366 Examination of Clinical and Laboratory Abnormalities in Patients with Xeroderma Pigmentosum Examination of Clinical and Laboratory Abnormalities in Patients with Defective DNA Repair: Xeroderma Pigmentosum, Cockayne Syndrome, or Trichothiodystrophy Family Village Free Web Graphics by Lauren Gene identified as cause of skin disease By Merritt McKinney Genetic clinics, centers, departments Genetic support groups-x HED Foundation - XP xeroderma pigmentosum, Heat and Sun Related Disorders Immunological studies in children with xeroderma pigmentosum,Berkel. 1974. Turk J Pediatr, Vol. 16, p. 43 Induction of sister chromatid exchanges in fibroblasts from normal donors and from patients with xeroderma pigmentosum after combined treatment with ultraviolet Laurie's Free Web Graphics Lentigo Maligna (Atypical Lentiginous Hyperplasia) Loss of the Xeroderma Pigmentosum Group A Gene (XPA) Enhances Apoptosis Lycos Directory: Health * Conditions and Diseases * Genetic Disorders Malignant melanoma in xeroderma pigmentosum patients: report of five cases Oya Kocabalkan, Figen Özgür, Yücel Erk, K. Güler Gürsu, Yücel Güngen. European Journal of Surgical Oncology. Abstract Mapping the multiple self-healing squamous epithelioma (MSSE) gene and investigation of xeroderma pigmentosum group A (XPA) and PATCHED (PTCH) as candidate genes. F. M. Richards, David R. Goudie, Wendy N. Cooper, Quitz Jene, Inês Barroso, Carol Wicking, Brandon J. Wainwright, M. A. Ferguson-Smith. Human Genetics,101(3):317-322, 12/1997. Monoclona anti-XPA Multiple melanoma in xeroderma pigmentosum Regina Fölster-Holst, Christoph Schubert, Enno Christophers. Hautklinik (Direktor: Prof. Dr. E. Christophers) der Christian-Albrechts - Universität, Kiel. Der Hautarzt, Volume 45 Issue 8 (1994) pp 554-561 Mutational Inactivation of the Xeroderma Pigmentosum Group C Gene Confers National organizations NCI/PDQ Citation: Prevention of skin cancer in xeroderma pigmentosum with the use of oral isotretinoin Nonmelanoma Skin Cancer...[Full text, Oct Arch Dermatol. 1997;133:1263-1270] (c) AMA 1997 NORD - Xeroderma Pigmentosum of Cultured Cerebellar Neurons Induced by UV but Not by Low-K+ Medium Yasushi Enokido, Naoko Inamura, Toshiyuki Araki, Takumi Satoh, Hironobu Nakane, Masafumi Yoshino, Yoshimichi Nakatsu, Kiyoji Tanaka, and Hiroshi Hatanaka Division of Protein Biosynthesis, Institute for Protein Research, and Division of Cellular Genetics, Institute for Molecular and Cellular Biology, Osaka University, Osaka, Japan J. Neurochem. 69, 246-251 (1997). p53 Mutations in Skin and Internal Tumors of Xeroderma Pigmentosum Patients Giuseppina Giglia, Nicolas Dumaz, Christiane Drougard, Marie-Françoise Avril, Leela Daya-Grosjean, and Alain Sarasin. [CANCER RESEARCH 58, 4402-4409, October 1 1998] Picture Gallery - Xeroderma pigmentosum - chest Pigmented Lesions in Actinically Damaged Skin... [Fulltext, Nov Arch Dermatol. 1996;132:1297-1302] (c) AMA 1996 Predisposition to 2-Acetylaminofluorene-induced Liver and Lung Cancer and to Spontaneous Testicular Cancer in Trp53-/- Mice1 David L. Cheo, Dennis K. Burns, Lisiane B. Meira, Jean Francois Houle, and Errol C. Friedberg. Laboratory of Molecular Pathology, Department of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas 75235. CANCER RESEARCH 59, 771-775, February 15, 1999] Prevention of skin cancer in xeroderma pigmentosum with the use of oral isotretinoin. Kraemer KH, DiGiovanna JJ, Moshell AN, et al.: New England Journal of Medicine 318(25): 1633-1637, 1988. Professional Genetics Societies Prolonged nuclear accumulation of p53 in xeroderma pigmentosum complementation group A cells after ultraviolet irradiation Shoji Kato (1), Y. Urano (1), Shiro Sasaki (1), Kamrul Ahsan, Masayuki Shono, Seiji Arase Archives of Dermatological Research Rare Diseases Reinfection in American Cutaneous Leishmaniasis: Evaluation of Clinical Outcom RETENTION AND EXON SKIPPING Sikandar G. Khan, Thomas D. Schneider, Kenneth H. Kraemer, Short description of cell lines. Pathology:trichotiodystrophy xeroderma pigmentosum Simplified Diagnosis of Xeroderma Pigmentosum "Variant" and Other Photosensitivity Disorders SPLICE MUTATIONS IN XERODERMA PIGMENTOSUM GROUP C DNA: INTRON Subnuclear distribution of DNA topoisomerase I and Bax protein in normal and xeroderma pigmentosum fibroblasts after irradiation with UV light and c rays or treatment with topotecan. Heinz Walter Thielmann, Odilia Popanda, Hans-Jürgen Staab. Journal of Cancer Research and Clinical Oncology, 125(3/4):193-208, 4/1999. The DRM WebWatcher: Xeroderma Pigmentosum The levels of repair of endonuclease III-sensitive sites, 6-4 photoproducts and cyclobutane pyrimidine dimers differ in a point mutant for RAD14, the Saccharomyces cerevisiae homologue of the human gene defective in XPA patients. .Simon H. Reed, Shirley McCready, Serge Boiteux, R. Waters. MGG Molecular & General Genetics, 250(4):515-522, 3/1996. THE XPA GENE AND NEURONAL APOPTOSIS The XPA protein restores a processive mechanism of action to a chromatin-associated protein complex from xeroderma pigmentosum complementation group A cells. Yang, L., and Lambert, M.W. Department. of Pathology, UMDNJ-New Jersey Medical School and GSBS, Newark, NJ 07103. Two children with xeroderma pigmentosum developing two different types of malignancies simultaneously. H. Masinjila, E. Arnbjörnsson. Pediatric Surgery International, 13(4):299-300, 4/1998. ultraviolet (UV) UV info sheet Websites by Patrick Mannix What is DNA repair? What is XP? Xeroderma Xeroderma Pigmentosum Xeroderma Pigmentosum Xeroderma Pigmentosum Xeroderma Pigmentosum Xeroderma pigmentosum. Dermatology Online Atlas Xeroderma Pigmentosum Xeroderma pigmentosum Xeroderma Pigmentosum XERODERMA PIGMENTOSUM Xeroderma pigmentosum, face Xeroderma Pigmentosum: Facts Sheet Xeroderma Pigmentosum XP Society, Inc. Box 4759 Poughkeepsie, NY 12601 (914) 473-4735 (voice & FAX) E-mail: email@example.com , < The XP Society, founded by Caren and Dan Mahar, is recognized as a key provider of information, support and activities for xeroderma pigmentosum patients and their families. XPS officers participate in worldwide professional conferences dealing with xp and related rare genetic disorders.> Xeroderma pigmentosum : sites francophones Xeroderma Pigmentosum 1999 Fund Raising Events and Activities XERODERMA PIGMENTOSUM by Dr. Al Gandy (MD.,Phd.,FRCP(c)) Xeroderma Pigmentosum I - from OMIM Xeroderma Pigmentosum IV - from OMIM Xeroderma Pigmentosum National Organization for Rare Disorders XERODERMA PIGMENTOSUM Pediatric Database (PEDBASE) Xeroderma Pigmentosum Registry Department of Pathology UMDNJ - New Jersey Medical School 185 South Orange Avenue Newark, NJ 07103 Contact: W. Clark Lambert, MD, Associate Professor Phone: 201-982-4405 Xeroderma Pigmentosum Registry New Jersey Medical School Dept. of Pathology, Rm. C-520 185 South Orange Avenue Newark, NJ 07103-2714 Phone: (201) 982-4405 or 201-982-7293 Xeroderma Pigmentosum Related Internet resources Xeroderma Pigmentosum Society Web Site Xeroderma Pigmentosum Society, Inc. ...is a not-for-profit organization founded by Caren and Dan Mahar, whose youngest daughter Katie suffers from xeroderma pigmentosum. These pages serve to provide a focal point for information about this rare genetic Disorder and to record the activities of the XP Society, which is dedicated to helping XP patients and their families. Xeroderma Pigmentosum Society, Inc. PO Box 4759 Poughkeepsie, NY 12601 Phone: 914-473-4735 Caren and Dan Mahar, XPS Inc. e-mail: firstname.lastname@example.org Xeroderma Pigmentosum XP Society, Inc. Box 4759 Poughkeepsie, NY 12601 Xeroderma Pigmentosum Tardivum Dermatology Internet Service, Xeroderma pigmentosum, face - photo Xeroderma pigmentosum. photo Xeroderma Pigmentosum: Facts Sheet XP article from Ped Base XP Grass Roots G. Karakatsanis, Dermatologist.