Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Genomic Instability and CCND1[original query] |
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An Old Story Retold: Loss of G1 Control Defines A Distinct Genomic Subtype of Esophageal Squamous Cell Carcinoma. Genomics, proteomics & bioinformatics 2015 Sep . Wang Qiyan, Bai Jian, Abliz Amir, Liu Ying, Gong Kenan, Li Jingjing, Shi Wenjie, Pan Yaqi, Liu Fangfang, Lai Shujuan, Yang Haijun, Lu Changdong, Zhang Lixin, Chen Wei, Xu Ruiping, Cai Hong, Ke Yang, Zeng Changqi |
The significant association of CCND1 genotypes with colorectal cancer in Taiwan. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2015 Aug 36 (8): 6533-40. Huang Chung-Yu, Tsai Chia-Wen, Hsu Chin-Mu, Chang Wen-Shin, Shui Hao-Ai, Bau Da-Ti |
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 |
Association of FOSL1 copy number alteration and triple negative breast tumors. Genetics and molecular biology 2019 Feb . Serino Leandro Tamião Rodrigues, Jucoski Tayana Schultz, Morais Stephanie Bath de, Fernandes Cíntia Callegari Coêlho, Lima Rubens Silveira de, Urban Cícero Andrade, Cavalli Luciane Regina, Cavalli Iglenir João, Ribeiro Enilze Maria de Souza Fonse |
Aggressive morphologic variants of mantle cell lymphoma characterized with high genomic instability showing frequent chromothripsis, CDKN2A/B loss, and TP53 mutations: A multi-institutional study. Genes, chromosomes & cancer 2020 4 59 (8): 484-494. Streich Lukas, Sukhanova Madina, Lu Xinyan, Chen Yi-Hua, Venkataraman Girish, Mathews Stephanie, Zhang Shanxiang, Kelemen Katalin, Segal Jeremy, Gao Juehua, Gordon Leo, Chen Qing, Behdad Am |
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 25, 2023
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