A murine model for the development of melanocytic nevi and their progression to melanoma

Author:

Nasti Tahseen H.1,Cochran J. Barry1,Tsuruta Yuko12,Yusuf Nabiha123,McKay Kristopher M.1,Athar Mohammad12,Timares Laura123,Elmets Craig A.123

Affiliation:

1. The Department of Dermatology; The University of Alabama at Birmingham School of Medicine; Birmingham Alabama

2. The Skin Diseases Research Center; and The University of Alabama at Birmingham School of Medicine; Birmingham Alabama

3. The Birmingham VA Medical Center; Birmingham Alabama

Funder

UAB Skin Diseases Research Center Core

National Institutes of Health

Heflin Center Genomic Core and Cancer Center Core

UAB Comprehensive Flow Cytometry Core of the Rheumatic Diseases Core Center

Publisher

Wiley

Subject

Cancer Research,Molecular Biology

Reference58 articles.

1. Nevus size and number are associated with telomere length and represent potential markers of a decreased senescence in vivo;Bataille;Cancer Epidemiol Biomarkers Prev,2007

2. The genetics of melanoma: The UK experience;Newton;Clin Exp Dermatol,1998

3. Acquired melanocytic nevi as risk factor for melanoma development. A comprehensive review of epidemiological data;Bauer;Pigment Cell Res,2003

4. Examination of DNA-ploidy in melanocytic nevi cells using video-imaging cytometry;Skowronek;Pol J Pathol,1997

5. BRAFE600-associated senescence-like cell cycle arrest of human naevi;Michaloglou;Nature,2005

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