Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: PRKD2[original query] |
---|
A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia.
Nature genetics 2008 Oct 40 (10): 1204-10. Di Bernardo Maria Chiara, Crowther-Swanepoel Dalemari, Broderick Peter, Webb Emily, Sellick Gabrielle, Wild Ruth, Sullivan Kate, Vijayakrishnan Jayaram, Wang Yufei, Pittman Alan M, Sunter Nicola J, Hall Andrew G, Dyer Martin J S, Matutes Estella, Dearden Claire, Mainou-Fowler Tryfonia, Jackson Graham H, Summerfield Geoffrey, Harris Robert J, Pettitt Andrew R, Hillmen Peter, Allsup David J, Bailey James R, Pratt Guy, Pepper Chris, Fegan Chris, Allan James M, Catovsky Daniel, Houlston Richard |
Whole-exome sequencing and neurite outgrowth analysis in autism spectrum disorder. Journal of human genetics 2015 Nov . Hashimoto Ryota, Nakazawa Takanobu, Tsurusaki Yoshinori, Yasuda Yuka, Nagayasu Kazuki, Matsumura Kensuke, Kawashima Hitoshi, Yamamori Hidenaga, Fujimoto Michiko, Ohi Kazutaka, Umeda-Yano Satomi, Fukunaga Masaki, Fujino Haruo, Kasai Atsushi, Hayata-Takano Atsuko, Shintani Norihito, Takeda Masatoshi, Matsumoto Naomichi, Hashimoto Hitos |
Identification of novel mutational drivers reveals oncogene dependencies in multiple myeloma. Blood 2018 6 132 (6): 587-597. Walker Brian A, Mavrommatis Konstantinos, Wardell Christopher P, Ashby T Cody, Bauer Michael, Davies Faith E, Rosenthal Adam, Wang Hongwei, Qu Pingping, Hoering Antje, Samur Mehmet, Towfic Fadi, Ortiz Maria, Flynt Erin, Yu Zhinuan, Yang Zhihong, Rozelle Dan, Obenauer John, Trotter Matthew, Auclair Daniel, Keats Jonathan, Bolli Niccolo, Fulciniti Mariateresa, Szalat Raphael, Moreau Philippe, Durie Brian, Stewart A Keith, Goldschmidt Hartmut, Raab Marc S, Einsele Hermann, Sonneveld Pieter, San Miguel Jesus, Lonial Sagar, Jackson Graham H, Anderson Kenneth C, Avet-Loiseau Herve, Munshi Nikhil, Thakurta Anjan, Morgan Gareth |
Histologic spectrum of polymorphous adenocarcinoma of the salivary gland harbor genetic alterations affecting PRKD genes. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2019 Sep . Sebastiao Ana Paula Martins, Xu Bin, Lozada John R, Pareja Fresia, Geyer Felipe C, Da Cruz Paula Arnaud, da Silva Edaise M, Ghossein Ronald A, Weinreb Ilan, de Noronha Lucia, Weigelt Britta, Reis-Filho Jorge S, Katabi No |
Frequent activating PIK3CA mutations in sporadic angiolipoma. Journal of cutaneous pathology 2020 7 48 (2): 211-216. Saggini Andrea, Santonja Carlos, Nájera Laura, Palmedo Gabriele, Kutzner Hei |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: