المؤلفون: Newton Bishop, J., Gruis, N., Genetics Consortium, Melanoma

المصدر: European Journal of Cancer Supplements ; volume 5, issue 4, page 40 ; ISSN 1359-6349

مصطلحات موضوعية: Cancer Research, Oncology

الإتاحة: https://doi.org/10.1016/s1359-6349Test(07)70259-8
https://api.elsevier.com/content/article/PII:S1359634907702598?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S1359634907702598?httpAccept=text/plainTest

المؤلفون: Ioannidis, J. P., Gwinn, M., Little, J., Higgins, J. P., Bernstein, J. L., Boffetta, P., Bondy, M., Bray, M. S., Brenchley, P. E., Buffler, P. A., Casas, J. P., Chokkalingam, A., Danesh, J., Smith, G. D., Dolan, S., Duncan, R., Gruis, N. A., Hartge, P., Hashibe, M., Hunter, D. J., Jarvelin, M. R., Malmer, B., Maraganore, D. M., Newton-Bishop, J. A., O'Brien, T. R., Petersen, G., Riboli, E., Salanti, G., Seminara, D., Smeeth, L., Taioli, E., Timpson, N., Uitterlinden, A. G., Vineis, P., Wareham, N., Winn, D. M., Zimmern, R., Khoury, M. J.

مصطلحات موضوعية: Databases, Factual, Epidemiologic Methods, Genetic Predisposition to Disease, Genome, Human, Human Genome Project, Humans, Medline, Research Design

العلاقة: http://olympias.lib.uoi.gr/jspui/handle/123456789/24222Test

الإتاحة: http://olympias.lib.uoi.gr/jspui/handle/123456789/24222Test

المؤلفون: Ioannidis, J. P. A., Gwinn, M., Little, J., Higgins, J. P. T., Bernstein, J. L., Boffetta, P., Bondy, M., Bray, M. S., Brenchley, P. E., Buffler, P. A., Casas, J. P., Chokkalingam, A., Danesh, J., Smith, G. D., Dolan, S., Duncan, R., Gruis, N. A., Hartge, P., Hashibe, M., Hunter, D. J., Jarvelin, M. -R., Malmer, B., Maraganore, D. M., Newton-Bishop, J. A., O'Brien, T. R., Petersen, G., Riboli, E., Salanti, G., Seminara, D., Smeeth, L., Taioli, E., Timpson, N., Uitterlinden, A. G., Vineis, P., Wareham, N., Winn, D. M., Zimmern, R., Khoury, M. J.

المساهمون: Ioannidis, J.P.A., Gwinn, M., Little, J., Higgins, J.P.T., Bernstein, J.L., Boffetta, P., Bondy, M., Bray, M.S., Brenchley, P.E., Buffler, P.A., Casas, J.P., Chokkalingam, A., Danesh, J., Smith, G.D., Dolan, S., Duncan, R., Gruis, N.A., Hartge, P., Hashibe, M., Hunter, D.J., Jarvelin, M.-R., Malmer, B., Maraganore, D.M., Newton-Bishop, J.A., O'Brien, T.R., Petersen, G., Riboli, E., Salanti, G., Seminara, D., Smeeth, L., Taioli, E., Timpson, N., Uitterlinden, A.G., Vineis, P., Wareham, N., Winn, D.M., Zimmern, R., Khoury, M.J.

مصطلحات موضوعية: Human genome

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000234227200002; volume:38; issue:1; firstpage:3; lastpage:5; numberofpages:3; journal:NATURE GENETICS; http://hdl.handle.net/11585/669438Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-29444443206; https://www.scopus.com/inward/record.uri?eid=2-s2.0-29444443206&doi=10.1038%2fng0106-3&partnerID=40&md5=4fc5647703f3540c65e1ffa60384a7daTest

الإتاحة: https://doi.org/10.1038/ng0106-3Test
http://hdl.handle.net/11585/669438Test

المؤلفون: Goldstein, A. M, Chan, M., Harland, M., Hayward, N. K, Demenais, F., Timothy Bishop, D, Azizi, E., Bergman, W., Bianchi-Scarra, G., Bruno, W., Calista, D., Cannon Albright, L. A, Chaudru, V., Chompret, A., Cuellar, F., Elder, D. E, Ghiorzo, P., Gillanders, E. M, Gruis, N. A, Hansson, J., Hogg, D., Holland, E. A, Kanetsky, P. A, Kefford, R. F, Teresa Landi, M., Lang, J., Leachman, S. A, Mackie, R. M, Magnusson, V., Mann, G. J, Newton Bishop, J., Palmer, J. M, Puig, S., Puig-Butille, J. A, Stark, M., Tsao, H., Tucker, M. A, Whitaker, L., Yakobson, E.

العلاقة: Goldstein, A. M. et al. (2006) Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents. Journal of Medical Genetics , 44(2), pp. 99-106. (doi:10.1136/jmg.2006.043802 )

الإتاحة: https://doi.org/10.1136/jmg.2006.043802Test
http://eprints.gla.ac.uk/40893Test/

المؤلفون: Harland, M, Goldstein, Am, Kukalizch, K, Taylor, C, Hogg, D, Puig, S, Badenas, C, Gruis, N, TER HUURNE, J, Bergman, W, Hayward, Nk, Stark, M, Tsao, H, Tucker, Ma, Landi, Mt, Bianchi, Giovanna, Ghiorzo, Paola, Kanetsky, Pa, Elder, D, Mann, Gj, Holland, Ea, Bishop, Dt, NEWTON BISHOP, J, Malvehy, J., Badenas, C., Cervera, R., Francisco, Cuellar, Rosa, Marti, JOAN BRUNET VIDAL, Guang, Yang, Nicholas, Martin, David, Whiteman, Adele, Green, Joanne, Aitken, Paola, Minghetti, Michela, Mantelli, Pastorino, Lorenza, Nasti, Sabina, Gargiulo, Sara, Sara, Gliori, Sushila, Mistry, JULIETTE RERSON MOOR, Wilma, Bergman, TER HUURNE, JEANET A. C., CLASINE VAN DER DRIFT, LENY VAN MOURIK, COBY OUT LUITING, FRANS VAN NIEUWPOORT, Valerie, Chaudru, Agnes, Chompret, Caroline, Kanengiesser, Michel, J. L., Grange, F., Sassolas, B., Limacher, J. M., Couillet, D., Truchetet, F., Cesarini, J. P., Boitier, F., CHEVRANT BRETON, J., Lasset, C., Longy, M., Joly, P., BASSET SEGUIN, N., Lesimple, T., Dugast, C., Michael, Ming, PATRICIA VAN BELLE, Anton, Platz, Suzanne, Egyhazi, Rainer, Tuominen, Diana, Linden, Helen, Schmid, Alon, Scope, Felix, Pavlotsky, Eitan, Friedman, Mark, Eliason

مصطلحات موضوعية: Genetics, Cancer Research, Polymorphism, Genetic, Skin Neoplasms, Genes, p16, Melanoma, Cancer, Biology, medicine.disease, Article, Denaturing high performance liquid chromatography, Germline mutation, Oncology, CDKN2A, Genotype, medicine, Humans, Genetic Predisposition to Disease, Genetic variability, Gene, Chromatography, High Pressure Liquid, Germ-Line Mutation

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e469e193a66e631a943aac0b0395b78Test
http://hdl.handle.net/11567/273207Test

المؤلفون: 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.

مصطلحات موضوعية: MAPK pathway, Uveal melanoma, BRAF, RAS, Mutation, 1306 Cancer Research, 2730 Oncology

العلاقة: orcid:0000-0002-4510-2161; orcid:0000-0003-4519-5932

الإتاحة: https://doi.org/10.1038/sj.bjc.6602598Test
https://espace.library.uq.edu.au/view/UQ:164052Test

المؤلفون: van der Velden, P. A., Zuidervaart, W., Hurks, M. H., Pavey, S., Ksander, B. R., Krijgsman, E., Frants, R. R., Tensen, C. P., Willemze, R., Jager, M. J., Gruis, N. A.

العلاقة: orcid:0000-0003-4519-5932

الإتاحة: https://doi.org/10.1002/ijc.20479Test
https://espace.library.uq.edu.au/view/UQ:236502Test

المؤلفون: Goldstein, A. M., Chan, M., Harland, M., Hayward, N. K., Demenais, F., Bishop, D. T., Azizi, E., Bergman, W., Bianchi, Giovanna, Bruno, William, Calista, D., CANNON ALBRIGHT, L. A., Chaudru, V., Chompret, A., Cuellar, F., Elder, D. E., Ghiorzo, Paola, Gillanders, E. M., Gruis, N. A., Jhansson, Dhogg, Holland, E. A., Kanetsky, PETER A., Kefford, R. F., Landi, Mt, Lang, Ju, Leachman, S. A., Mackie, R. M., Magnusson, V., Mann, G. J., NEWTON BISHOP, J., Palmer, J. M., Spuig, PUIG BUTILLE, J. A., Stark, M., Tsao, H., Tucker, M. A., Whitaker, L., Yakobson, E., Malvehy, J., Badenas, C., Cervera, R., Francisco, Cuellar, Rosa, Marti´, JOAN BRUNET VIDAL, Guang, Yang, Nicholas, Martin, David, Whiteman, Adele, Green, Joanne, Aitken, Paola, Minghetti, Mantelli, Michela, Pastorino, Lorenza, Nasti, Sabina, Gargiulo, Sara, Sara, Gliori, Sushila, Mistry, JULIETTE RANDERSON MOOR, Wilma, Bergman, TER HUURNE, JEANET A. C., CLASINE VAN DER DRIFT, LENY VAN MOURIK, COBY OUT LUITING, FRANS VAN NIEUWPOORT, Valerie, Chaudru, Agnes, Chompret, Caroline, Kanengiesser, Michel, J. L., Grange, F., Sassolas, B., Limacher, J. M., Couillet, D., Truchetet, F., Cesarini, J. P., Boitier, F., CHEVRANT BRETON, J., Lasset, C., Longy, M., Joly, P., BASSET SEGUIN, N., Lesimple, T., Dugast, C., Arupa, Ganguly, Michael, Ming, PATRICIA VAN BELLE, Anton, Platz, Suzanne, Egyhazi, Rainer, Tuominen, Diana, Linden, Helen, Schmid, Alon, Scope, Felix, Pavlotsky, Eitan, Friedman, Mark, Eliason

مصطلحات موضوعية: Male, medicine.medical_specialty, Skin Neoplasms, Biology, medicine.disease_cause, Germline mutation, CDKN2A, Genetic variation, Genetics, medicine, Humans, Hereditary Melanoma, neoplasms, Melanoma, Genetics (clinical), Cyclin-Dependent Kinase Inhibitor p16, Germ-Line Mutation, Mutation, Incidence (epidemiology), Incidence, Australia, Genetic Variation, medicine.disease, Europe, North America, Medical genetics, Original Article, Female, Demography

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f91cfc5ee3b3040ec3c1722872069b35Test
https://europepmc.org/articles/PMC2598064Test/

المؤلفون: Velden, P. A., Nieuwpoort, F. A., Out-Luiting, C., Smit, N. P., Pavel, S., Snoo, F. A., Bergman, W., Tensen, C. P., Frants, R. R., Willemze, R., Gruis, N. A.

المصدر: Pigment Cell Research ; volume 16, issue 5, page 579-579 ; ISSN 0893-5785 1600-0749

الإتاحة: https://doi.org/10.1034/j.1600-0749.2003.08328.xTest

المؤلفون: Brookes, S, Rowe, J, Ruas, M, Llanos, S, Clark, PA, Lomax, M, James, MC, Vatcheva, R, Bates, S, Vousden, KH, Parry, D, Gruis, N, Smit, N, Bergman, W, Peters, G

العلاقة: Brookes, S. et al. (2002) INK4a-deficient human diploid fibroblasts are resistant to RAS-induced senescence. EMBO Journal , 21(12), pp. 2936-2945. (doi:10.1093/emboj/cdf289 )

الإتاحة: https://doi.org/10.1093/emboj/cdf289Test
http://eprints.gla.ac.uk/23858Test/