检索结果 - Gruis, N A

Dinucleotide repeat polymorphism at the D17S513 locus 由 Oliphant, A.R., Wright, E.C., Swensen, J., Gruis, N.A., Goldgar, D., Skolnick, M.H.

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Dinucleotide repeat polymorphism at the D17S514 locus 由 Oliphant, A.R., Wright, E.C., Swensen, J., Gruis, N.A., Goldgar, D., Skolnick, M.H.

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PCR-based microsatellite polymorphisms in the detection of loss of heterozygosity in fresh and archival tumour tissue. 由 Gruis, N. A., Abeln, E. C., Bardoel, A. F., Devilee, P., Frants, R. R., Cornelisse, C. J.

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Localization of a putative tumor suppressor gene by using homozygous deletions in melanomas. 由 Weaver-Feldhaus, J, Gruis, N A, Neuhausen, S, Le Paslier, D, Stockert, E, Skolnick, M H, Kamb, A

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Infrequent CDKN2 (MTS1/p16) gene alterations in human primary breast cancer. 由 Berns, E. M., Klijn, J. G., Smid, M., van Staveren, I. L., Gruis, N. A., Foekens, J. A.

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Episodic Src activation in uveal melanoma revealed by kinase activity profiling 由 Maat, W, Filali, M el, Mulder, A Dirks-, Luyten, G P M, Gruis, N A, Desjardins, L, Boender, P, Jager, M J, van der Velden, P A

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Activation of the MAPK pathway is a common event in uveal melanomas although it rarely occurs through mutation of BRAF or RAS 由 Zuidervaart, W, van Nieuwpoort, F, Stark, M, Dijkman, R, Packer, L, Borgstein, A-M, Pavey, S, van der Velden, P, Out, C, Jager, M J, Hayward, N K, Gruis, N A

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Gene expression profiling identifies tumour markers potentially playing a role in uveal melanoma development 由 Zuidervaart, W, van der Velden, P A, Hurks, M H, van Nieuwpoort, F A, Out-Luiting, C J J, Singh, A D, Frants, R R, Jager, M J, Gruis, N A

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GNAQ and GNA11 mutations and downstream YAP activation in choroidal nevi 由 Vader, M J C, Madigan, M C, Versluis, M, Suleiman, H M, Gezgin, G, Gruis, N A, Out-Luiting, J J, Bergman, W, Verdijk, R M, Jager, M J, van der Velden, P A

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MC1R gene variants and non-melanoma skin cancer: a pooled-analysis from the M-SKIP project 由 Tagliabue, E, Fargnoli, M C, Gandini, S, Maisonneuve, P, Liu, F, Kayser, M, Nijsten, T, Han, J, Kumar, R, Gruis, N A, Ferrucci, L, Branicki, W, Dwyer, T, Blizzard, L, Helsing, P, Autier, P, García-Borrón, J C, Kanetsky, P A, Landi, M T, Little, J, Newton-Bishop, J, Sera, F, Raimondi, S

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MC1R variants in relation to naevi in melanoma cases and controls: a pooled-analysis from the M-SKIP project 由 Stefanaki, I., Stratigos, AJ., Kypreou, K.P., Evangelou, E., Gandini, S., Maisonneuve, P., Polsky, D., Lazovich, D., Newton-Bishop, J., Kanetsky, P.A., Puig, S., Gruis, N.A., Ghiorzo, P., Pellegrini, C., De Nicolo, A., Ribas, G., Guida, G., Garcia-Borron, J.C., Fargnoli, M.C., Nan, H., Landi, M.T., Little, J., Sera, F., Raimondi, S.

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Germline ATM variants predispose to melanoma: a joint analysis across the GenoMEL and MelaNostrum consortia 由 Dalmasso, B., Pastorino, L., Nathan, V., Shah, N. N., Palmer, J. M., Howlie, M., Johansson, P. A., Freedman, N. D., Carter, B. D., Beane-Freeman, L., Hicks, B., Molven, A., Helgadottir, H., Sankar, A., Tsao, H., Stratigos, A. J., Helsing, P., Van Doorn, R., Gruis, N. A., Visser, M., Wadt, K. A. W., Mann, G., Holland, E. A., Nagore, E., Potrony, M., Puig, S., Menin, C., Peris, K., Fargnoli, M. C., Calista, D., Soufir, N., Harland, M., Bishop, T., Kanetsky, P. A., Elder, D. E., Andreotti, V., Vanni, I., Bruno, W., Höiom, V., Tucker, M. A., Yang, X. R., Andresen, P. A., Adams, D. J., Landi, M. T., Hayward, N. K., Goldstein, A. M., Ghiorzo, P.

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