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Xeroderma Pigmentosum and other Diseases of Human Premature Aging and DNA Repair: Molecules to Patients

Tuesday, September 05, 2006
National Conference Center, Lansdowne, VA

This meeting was a follow-up of one held in 2004. The purpose of this workshop was to gather leading scientists and clinicians in this very active area of research. The clinical and mechanistic aspects of Cowden's syndrome (CS) and related DNA repair/transcription defective disorders such as xeroderma pigmentosum (XP) and trichothiodystrophy (TTD) were explored. Our goals were to develop new multidisciplinary collaborations, interactions, and relationships that can lead to a greater understanding of the pathophysiological mechanisms involved in these disorders and to conceive new therapeutic strategies for their treatment.

Dr. Vilhelm A. Bohr (301) 558-8223

Co-funding Institute(s):
National Institute on Aging

From the National Center for Advancing Translational Sciences

From the National Institutes of Health

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