Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Mocci E"'
Autor:
Picciau Andrea, Sassu Alessandro, Persico Ivana, Fraumene Cristina, Cabras Valentina, Adamo Mauro, Pirastu Nicola, Fanciulli Manuela, Concas Maria P, Mocci Evelina, Prodi Dionigio A, Serra Donatella, Biino Ginevra, Pirastu Mario, Angius Andrea
Publikováno v:
BMC Medical Genetics, Vol 10, Iss 1, p 81 (2009)
Abstract Background A multiplicity of study designs such as gene candidate analysis, genome wide search (GWS) and, recently, whole genome association studies have been employed for the identification of the genetic components of essential hypertensio
Externí odkaz:
https://doaj.org/article/c7b2576ab3d84466a3aea14d38b4f883
Autor:
Herbert Yu, Gabriele Capurso, Robert N. Hoover, Beatrice Mohelnikova-Duchonova, Amanda L. Blackford, Harvey A. Risch, H. Bas Bueno-de-Mesquita, Timothy J. Key, Stephen J. Chanock, Ann L. Oberg, Federico Canzian, Lingeng Lu, Maria Gazouli, Michelle Cotterchio, Daniele Campa, John P. Neoptolemos, Claudio Pasquali, Rachel E. Neale, Rayjean J. Hung, William R. Bamlet, Raffaele Pezzilli, Stefano Landi, Juozas Kupcinskas, Joseph M. Herman, Erica J. Childs, Ivana Holcatova, Steven Gallinger, Manal M. Hassan, Ewa Małecka-Panas, Pavel Vodicka, Donghui Li, Maarten F. Bijlsma, Irene Orlow, Lenka Foretova, Robert C. Kurtz, Yogesh K. Vashist, Francesca Tavano, Evelina Mocci, Amethyst Saldia, Michael Borges, Sean P. Cleary, Gloria M. Petersen, Brian M. Wolpin, Sara H. Olson, Kari G. Chaffee, Aldo Scarpa, Vladimir Janout, Elizabeth A. Holly, Niccola Funel, Hermann Brenner, Ghislaine Scelo, Laufey T. Amundadottir, Rachael Z. Stolzenberg-Solomon, Paige M. Bracci, Charles S. Fuchs, Paul Brennan, Oliver Strobel, Michael Goggins, Giulia Martina Cavestro, Cosmeri Rizzato, Andrea Mambrini, Alison P. Klein
Publikováno v:
Nature genetics
Nature genetics, 47(8), 911-916. Nature Publishing Group
Nature Genetics, 47(8), 911. Nature Publishing Group
Nature genetics, 47(8), 911-916. Nature Publishing Group
Nature Genetics, 47(8), 911. Nature Publishing Group
Pancreatic cancer is the fourth leading cause of cancer death in the developed world. Both inherited high-penetrance mutations in BRCA2 (ref. 2), ATM, PALB2 (ref. 4), BRCA1 (ref. 5), STK11 (ref. 6), CDKN2A and mismatch-repair genes and low-penetrance