Recherche
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Mutation in exon 7 of PTCH deregulates SHH/PTCH/SMO signaling: Possible linkage to WNT
(International Journal of Molecular Medicine, 2006-05-01)Article de revue -
Etude clinique de mutations germinales du gène PTCH dans une série de 22 malades atteints du Syndrome de Gorlin
(Annales de Dermatologie et de Vénéréologie. vol. 133, n° 2, 2006)Article de revue -
Spectrum of PTCH1 Mutations in French Patients with Gorlin Syndrome
(Journal of Investigative Dermatology. vol. 121, n° 3, pp. 478-481, 2003-09)Article de revue -
The contribution of large genomic deletions at the CDKN2A locus to the burden of familial melanoma
(British Journal of Cancer. vol. 99, n° 2, pp. 364-370, 2008-07)Article de revue -
Heterozygous mutations in the tumor suppressor gene PATCHED provoke basal cell carcinoma-like features in human organotypic skin cultures
(Oncogene. vol. 27, n° 51, pp. 6601-6606, 2008-10)Article de revue -
Ultraviolet responses of Gorlin syndrome primary skin cells
(British Journal of Dermatology. vol. 159, n° 2, pp. 445-452, 2008-08)Article de revue -
Familial melanoma: Clinical factors associated with germline CDKN2A mutations according to the number of patients affected by melanoma in a family
(Journal of The American Academy of Dermatology. vol. 67, n° 6, pp. 1257-1264.e2, 2012-12)Article de revue