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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

D. Perucca-Lostanlen


Faculté de Médecine

Avenue de Valombrose

06107 Nice Cedex 02



Name/email consistency: high



  • UMR 6549 CNRS/UNSA, Faculté de Médecine, Avenue de Valombrose, 06107 Nice Cedex 02, France. 2002 - 2004
  • Laboratoire de Neurobiologie Cellulaire, UMR CNRS 6549 and Biostatistics and Medical Informatics Department, Faculté de Médecine, Avenue de Valombrose, France. 2000
  • Instabilité et Altérations des Génomes, CNRS/UNSA UMR 6549, France. 1997


  1. Distinct MDM2 and P14ARF expression and centrosome amplification in well-differentiated liposarcomas. Perucca-Lostanlen, D., Rostagno, P., Grosgeorge, J., Marcié, S., Gaudray, P., Turc-Carel, C. Genes. Chromosomes. Cancer (2004) [Pubmed]
  2. Molecular and functional effects of the T14709C point mutation in the mitochondrial DNA of a patient with maternally inherited diabetes and deafness. Perucca-Lostanlen, D., Taylor, R.W., Narbonne, H., Mousson de Camaret, B., Hayes, C.M., Saunieres, A., Paquis-Flucklinger, V., Turnbull, D.M., Vialettes, B., Desnuelle, C. Biochim. Biophys. Acta (2002) [Pubmed]
  3. Mitochondrial DNA variations in patients with maternally inherited diabetes and deafness syndrome. Perucca-Lostanlen, D., Narbonne, H., Hernandez, J.B., Staccini, P., Saunieres, A., Paquis-Flucklinger, V., Vialettes, B., Desnuelle, C. Biochem. Biophys. Res. Commun. (2000) [Pubmed]
  4. Mapping FRA11A, a folate-sensitive fragile site in human chromosome band 11q13.3. Perucca-Lostanlen, D., Hecht, B.K., Courseaux, A., Grosgeorge, J., Hecht, F., Gaudray, P. Cytogenet. Cell Genet. (1997) [Pubmed]
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