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483 results

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Page 1
EDNRB gene variants and melanoma risk in two southern European populations.
Spica T, Fargnoli MC, Hetet G, Bertrand G, Formicone F, Descamps V, Wolkenstein P, Dupin N, Lebbe C, Basset-Seguin N, Saiag P, Cambien F, Grandchamp B, Peris K, Soufir N. Spica T, et al. Among authors: dupin n. Clin Exp Dermatol. 2011 Oct;36(7):782-7. doi: 10.1111/j.1365-2230.2011.04062.x. Epub 2011 Apr 20. Clin Exp Dermatol. 2011. PMID: 21507037
The A148T variant of the CDKN2A gene is not associated with melanoma risk in the French and Italian populations.
Spica T, Portela M, Gérard B, Formicone F, Descamps V, Crickx B, Ollivaud L, Archimbaud A, Dupin N, Wolkenstein P, Vitoux D, Lebbe C, Saiag P, Basset-Seguin N, Fargnoli MC, Grandchamp B, Peris K, Soufir N; MELAN-COHORT. Spica T, et al. Among authors: dupin n. J Invest Dermatol. 2006 Jul;126(7):1657-60. doi: 10.1038/sj.jid.5700293. Epub 2006 Apr 13. J Invest Dermatol. 2006. PMID: 16614725 Free article. No abstract available.
MC1R and PTCH gene polymorphism in French patients with basal cell carcinomas.
Liboutet M, Portela M, Delestaing G, Vilmer C, Dupin N, Gorin I, Saiag P, Lebbé C, Kerob D, Dubertret L, Grandchamp B, Basset-Seguin N, Soufir N. Liboutet M, et al. Among authors: dupin n. J Invest Dermatol. 2006 Jul;126(7):1510-7. doi: 10.1038/sj.jid.5700263. Epub 2006 Apr 27. J Invest Dermatol. 2006. PMID: 16645598 Free article.
PTCH mutations and deletions in patients with typical nevoid basal cell carcinoma syndrome and in patients with a suspected genetic predisposition to basal cell carcinoma: a French study.
Soufir N, Gerard B, Portela M, Brice A, Liboutet M, Saiag P, Descamps V, Kerob D, Wolkenstein P, Gorin I, Lebbe C, Dupin N, Crickx B, Basset-Seguin N, Grandchamp B. Soufir N, et al. Among authors: dupin n. Br J Cancer. 2006 Aug 21;95(4):548-53. doi: 10.1038/sj.bjc.6603303. Br J Cancer. 2006. PMID: 16909134 Free PMC article.
Melanoma susceptibility and progression: Association study between polymorphisms of the chemokine (CCL2) and chemokine receptors (CX3CR1, CCR5).
Rodero M, Rodero P, Descamps V, Lebbe C, Wolkenstein P, Aegerter P, Vitoux D, Basset-Seguin N, Dupin N, Grandchamp B, Soufir N, Combadière C, Saiag P; Melan-cohort investigators. Rodero M, et al. Among authors: dupin n. J Dermatol Sci. 2007 Apr;46(1):72-6. doi: 10.1016/j.jdermsci.2006.11.007. Epub 2006 Dec 13. J Dermatol Sci. 2007. PMID: 17169533 No abstract available.
A French CDK4-positive melanoma family with a co-inherited EDNRB mutation.
Soufir N, Ollivaud L, Bertrand G, Lacapère JJ, Descamps V, Vitoux D, Lebbe C, Wolkenstein P, Dupin N, Saiag P, Basset-Seguin N, Grandchamp B; MELAN-COHORT. Soufir N, et al. Among authors: dupin n. J Dermatol Sci. 2007 Apr;46(1):61-4. doi: 10.1016/j.jdermsci.2006.11.016. Epub 2007 Jan 12. J Dermatol Sci. 2007. PMID: 17223014 No abstract available.
Variants of the MATP/SLC45A2 gene are protective for melanoma in the French population.
Guedj M, Bourillon A, Combadières C, Rodero M, Dieudé P, Descamps V, Dupin N, Wolkenstein P, Aegerter P, Lebbe C, Basset-Seguin N, Prum B, Saiag P, Grandchamp B, Soufir N; MelanCohort Investigators. Guedj M, et al. Among authors: dupin n. Hum Mutat. 2008 Sep;29(9):1154-60. doi: 10.1002/humu.20823. Hum Mutat. 2008. PMID: 18683857
Variants of the xeroderma pigmentosum variant gene (POLH) are associated with melanoma risk.
Di Lucca J, Guedj M, Lacapère JJ, Fargnoli MC, Bourillon A, Dieudé P, Dupin N, Wolkenstein P, Aegerter P, Saiag P, Descamps V, Lebbe C, Basset-Seguin N, Peris K, Grandchamp B, Soufir N. Di Lucca J, et al. Among authors: dupin n. Eur J Cancer. 2009 Dec;45(18):3228-36. doi: 10.1016/j.ejca.2009.04.034. Epub 2009 May 26. Eur J Cancer. 2009. PMID: 19477635
483 results