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1 |
Material Type: Artigo
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Average Risks of Breast and Ovarian Cancer Associated with BRCA1 or BRCA2 Mutations Detected in Case Series Unselected for Family History: A Combined Analysis of 22 StudiesAntoniou, A. ; Pharoah, P.D.P. ; Narod, S. ; Risch, H.A. ; Eyfjord, J.E. ; Hopper, J.L. ; Loman, N. ; Olsson, H. ; Johannsson, O. ; Borg, Å. ; Pasini, B. ; Radice, P. ; Manoukian, S. ; Eccles, D.M. ; Tang, N. ; Olah, E. ; Anton-Culver, H. ; Warner, E. ; Lubinski, J. ; Gronwald, J. ; Gorski, B. ; Tulinius, H. ; Thorlacius, S. ; Eerola, H. ; Nevanlinna, H. ; Syrjäkoski, K. ; Kallioniemi, O.-P. ; Thompson, D. ; Evans, C. ; Peto, J. ; Lalloo, F. ; Evans, D.G. ; Easton, D.F.American journal of human genetics, 2003-05, Vol.72 (5), p.1117-1130 [Periódico revisado por pares]Chicago, IL: Elsevier IncTexto completo disponível |
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2 |
Material Type: Livro
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Race, Science and Medicine, 1700–1960Ernst, Waltraud ; Harris, Bernard Harris, Bernard ; Ernst, WaltraudLondon: Routledge 1999Sem texto completo |
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3 |
Material Type: Artigo
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HRPT2 , encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndromeCarpten, J.D ; Larsson, C ; Robbins, C.M ; Villablanca, A ; Forsberg, L ; Presciuttini, S ; Bailey-Wilson, J ; Simonds, W.F ; Gillanders, E.M ; Kennedy, A.M ; Chen, J.D ; Agarwal, S.K ; Sood, R ; Jones, M.P ; Moses, T.Y ; Haven, C ; Petillo, D ; Leotlela, P.D ; Harding, B ; Cameron, D ; Pannett, A.A ; Höög, A ; Heath, H ; James-Newton, L.A ; Robinson, B ; Zarbo, R.J ; Cavaco, B.M ; Wassif, W ; Perrier, N.D ; Rosen, I.B ; Kristoffersson, U ; Turnpenny, P.D ; Farnebo, L.-O ; Besser, G.M ; Jackson, C.E ; Morreau, H ; Trent, J.M ; Thakker, R.V ; Marx, S.J ; Teh, B.T ; Hobbs, M.RNature genetics, 2002-12, Vol.32 (4), p.676-680 [Periódico revisado por pares]London: Nature Publishing GroupTexto completo disponível |
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4 |
Material Type: Artigo
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Telomere Dysfunction Triggers Extensive DNA Fragmentation and Evolution of Complex Chromosome Abnormalities in Human Malignant TumorsGisselsson, David ; Jonson, Tord ; Petersén, Åsa ; Strömbeck, Bodil ; Cin, Paola Dal ; Höglund, Mattias ; Mitelman, Felix ; Mertens, Fredrik ; Mandahl, NilsProceedings of the National Academy of Sciences - PNAS, 2001-10, Vol.98 (22), p.12683-12688 [Periódico revisado por pares]United States: National Academy of SciencesTexto completo disponível |
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Material Type: Artigo
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DNA methylation patterns in hereditary human cancers mimic sporadic tumorigenesisEsteller, M ; Fraga, M F ; Guo, M ; Garcia-Foncillas, J ; Hedenfalk, I ; Godwin, A K ; Trojan, J ; Vaurs-Barrière, C ; Bignon, Y J ; Ramus, S ; Benitez, J ; Caldes, T ; Akiyama, Y ; Yuasa, Y ; Launonen, V ; Canal, M J ; Rodriguez, R ; Capella, G ; Peinado, M A ; Borg, A ; Aaltonen, L A ; Ponder, B A ; Baylin, S B ; Herman, J GHuman molecular genetics, 2001-12, Vol.10 (26), p.3001-3007 [Periódico revisado por pares]England: Oxford Publishing Limited (England)Texto completo disponível |
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6 |
Material Type: Livro
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Responsible Genetics: The Moral Responsibility of Geneticists for the Consequences of Human Genetics ResearchNordgren, AndersDordrecht: Springer Netherlands 2001Texto completo disponível |
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7 |
Material Type: Livro
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THE FUTURE OF HUMAN NATUREHabermas, Jurgen2003Sem texto completo |
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8 |
Material Type: Artigo
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Gene expression profile in multiple sclerosis patients and healthy controls: identifying pathways relevant to diseaseBomprezzi, Roberto ; Ringnér, Markus ; Kim, Seungchan ; Bittner, Michael L. ; Khan, Javed ; Chen, Yidong ; Elkahloun, Abdel ; Yu, Aimee ; Bielekova, Bibiana ; Meltzer, Paul S. ; Martin, Roland ; McFarland, Henry F. ; Trent, Jeffrey M.Human molecular genetics, 2003-09, Vol.12 (17), p.2191-2199 [Periódico revisado por pares]Oxford: Oxford University PressTexto completo disponível |
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9 |
Material Type: Artigo
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Chromosomal Breakage-Fusion-Bridge Events Cause Genetic Intratumor HeterogeneityGisselsson, David ; Pettersson, Louise ; Hoglund, Mattias ; Heidenblad, Markus ; Gorunova, Ludmila ; Wiegant, Joop ; Mertens, Fredrik ; Cin, Paola Dal ; Mitelman, Felix ; Mandahl, NilsProceedings of the National Academy of Sciences - PNAS, 2000-05, Vol.97 (10), p.5357-5362 [Periódico revisado por pares]United States: National Academy of Sciences of the United States of AmericaTexto completo disponível |
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10 |
Material Type: Artigo
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Impaired dopamine storage resulting from α-synuclein mutations may contribute to the pathogenesis of Parkinson's diseaseLotharius, Julie ; Brundin, PatrikHuman molecular genetics, 2002-10, Vol.11 (20), p.2395-2407 [Periódico revisado por pares]Oxford: Oxford University PressTexto completo disponível |