Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Aneuploidy and CDKN2A[original query] |
---|
NSAIDs modulate CDKN2A, TP53, and DNA content risk for progression to esophageal adenocarcinoma. PLoS medicine 2007 Feb 4 (2): e67. Galipeau Patricia C, Li Xiaohong, Blount Patricia L, Maley Carlo C, Sanchez Carissa A, Odze Robert D, Ayub Kamran, Rabinovitch Peter S, Vaughan Thomas L, Reid Brian |
MLPA and DNA index improve the molecular diagnosis of childhood B-cell acute lymphoblastic leukemia. Scientific reports 2020 Jul 10 (1): 11501. Yu Chih-Hsiang, Lin Tze-Kang, Jou Shiann-Tarng, Lin Chien-Yu, Lin Kai-Hsin, Lu Meng-Yao, Chen Shu-Huey, Cheng Chao-Neng, Wu Kang-Hsi, Wang Shih-Chung, Chang Hsiu-Hao, Li Meng-Ju, Ni Yu-Ling, Su Yi-Ning, Lin Dong-Tsamn, Chen Hsuan-Yu, Harrison Christine J, Hung Chia-Cheng, Lin Shu-Wha, Yang Yung- |
Genetic alterations associated with F-fluorodeoxyglucose positron emission tomography/computed tomography in head and neck squamous cell carcinoma. Translational oncology 2020 12 14 (2): 100988. Han Sangwon, Oh Jungsu S, Lee Hyo Sang, Kim Jae Seu |
CDKN2C-Null Leiomyosarcoma: A Novel, Genomically Distinct Class of TP53/RB1-Wild-Type Tumor With Frequent CIC Genomic Alterations and 1p/19q-Codeletion. JCO precision oncology 2020 10 4 . Williams Erik A, Sharaf Radwa, Decker Brennan, Werth Adrienne J, Toma Helen, Montesion Meagan, Sokol Ethan S, Pavlick Dean C, Shah Nikunj, Williams Kevin Jon, Venstrom Jeffrey M, Alexander Brian M, Ross Jeffrey S, Albacker Lee A, Lin Douglas I, Ramkissoon Shakti H, Elvin Julia |
Co-occurrence of CDKN2A/B and IFN-I homozygous deletions correlates with an immunosuppressive phenotype and poor prognosis in lung adenocarcinoma. Molecular oncology 2022 3 16 (8): 1746-1760. Peng Yuan, Chen Yonghong, Song Mengmeng, Zhang Xiaoyue, Li Pansong, Yu Xian, Huang Yusheng, Zhang Ni, Ji Liyan, Xia Lei, Xia Xuefeng, Yi Xin, Tan Benxu, Yang Zhenzh |
High-grade glioma with pleomorphic and pseudopapillary features (HPAP): a proposed type of circumscribed glioma in adults harboring frequent TP53 mutations and recurrent monosomy 13. Acta neuropathologica 2022 2 143 (3): 403-414. Pratt Drew, Abdullaev Zied, Papanicolau-Sengos Antonios, Ketchum Courtney, Panneer Selvam Pavalan, Chung Hye-Jung, Lee Ina, Raffeld Mark, Gilbert Mark R, Armstrong Terri S, Pytel Peter, Borys Ewa, Klonoski Joshua M, McCord Matthew, Horbinski Craig, Brat Daniel, Perry Arie, Solomon David, Eberhart Charles, Giannini Caterina, Quezado Martha, Aldape Kenne |
- Page last reviewed:Feb 1, 2024
- Content source: