Search for germline alterations in CDKN2A/ARF and CDK4 of 42 Jewish melanoma families with or without neural system tumours

por Marian, C, Scope, A, Laud, K, Friedman, E, Pavlotsky, F, Yakobson, E, Bressac-de Paillerets, B, Azizi, E
Publicado 2005

Absence of somatic alterations of the EB1 gene adenomatous polyposis coli-associated protein in human sporadic colorectal cancers.

por Jaïs, P., Sabourin, J. C., Bombled, J., Rougier, P., Lasser, P., Duvillard, P., Bénard, J., Bressac-de Paillerets, B.
Publicado 1998

Individuals with presumably hereditary uveal melanoma do not harbour germline mutations in the coding regions of either the P16(INK4A), P14(ARF) or cdk4 genes

por Soufir, N, Bressac-de Paillerets, B, Desjardins, L, Lévy, C, Bombled, J, Gorin, I, Schlienger, P, Stoppa-Lyonnet, D
Publicado 2000

Breast cancer risk in ataxia telangiectasia (AT) heterozygotes: haplotype study in French AT families

por Janin, N, Andrieu, N, Ossian, K, Laugé, A, Croquette, M-F, Griscelli, C, Debré, M, Bressac-de-Paillerets, B, Aurias, A, Stoppa-Lyonnet, D
Publicado 1999

The contribution of large genomic deletions at the CDKN2A locus to the burden of familial melanoma

por Lesueur, F, de Lichy, M, Barrois, M, Durand, G, Bombled, J, Avril, M-F, Chompret, A, Boitier, F, Lenoir, G M, Bressac-de Paillerets, B
Publicado 2008

Therapeutic activity of CPT-11, a DNA-topoisomerase I inhibitor, against peripheral primitive neuroectodermal tumour and neuroblastoma xenografts.

por Vassal, G., Terrier-Lacombe, M. J., Bissery, M. C., Vénuat, A. M., Gyergyay, F., Bénard, J., Morizet, J., Boland, I., Ardouin, P., Bressac-de-Paillerets, B., Gouyette, A.
Publicado 1996

Extensive molecular screening for hereditary non-polyposis colorectal cancer

por Dieumegard, B, Grandjouan, S, Sabourin, J-C, Bihan, M-L Le, Lefrère, I, Bellefqih, Pignon, J-P, Rougier, P, Lasser, P, Bénard, J, Couturier, D, Bressac-de Paillerets, B
Publicado 2000

Mutations in BHD and TP53 genes, but not in HNF1β gene, in a large series of sporadic chromophobe renal cell carcinoma

por Gad, S, Lefèvre, S H, Khoo, S K, Giraud, S, Vieillefond, A, Vasiliu, V, Ferlicot, S, Molinié, V, Denoux, Y, Thiounn, N, Chrétien, Y, Méjean, A, Zerbib, M, Benoît, G, Hervé, J M, Allègre, G, Bressac-de Paillerets, B, Teh, B T, Richard, S
Publicado 2007

Mutations in BHD and TP53 genes, but not in HNF1β gene, in a large series of sporadic chromophobe renal cell carcinoma

por Gad, S, Lefèvre, S H, Khoo, S K, Giraud, S, Vieillefond, A, Vasiliu, V, Ferlicot, S, Molinié, V, Denoux, Y, Thiounn, N, Chrétien, Y, Méjean, A, Zerbib, M, Benoît, G, Hervé, J M, Allègre, G, Bressac-de Paillerets, B, Teh, B T, Richard, S
Publicado 2007

Association of MC1R Variants and Host Phenotypes With Melanoma Risk in CDKN2A Mutation Carriers: A GenoMEL Study

por Demenais, F., Mohamdi, H., Chaudru, V., Goldstein, A. M., Newton Bishop, J. A., Bishop, D. T., Kanetsky, P. A., Hayward, N. K., Gillanders, E., Elder, D. E., Avril, M. F., Azizi, E., van Belle, P., Bergman, W., Bianchi-Scarrà, G., Bressac-de Paillerets, B., Calista, D., Carrera, C., Hansson, J., Harland, M., Hogg, D., Höiom, V., Holland, E. A., Ingvar, C., Landi, M. T., Lang, J. M., Mackie, R. M., Mann, G. J., Ming, M. E., Njauw, C. J., Olsson, H., Palmer, J., Pastorino, L., Puig, S., Randerson-Moor, J., Stark, M., Tsao, H., Tucker, M. A., van der Velden, P., Yang, X. R., Gruis, N.
Publicado 2010