Human Genome Epidemiology Literature Finder
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Records 1 - 7 (of 7 Records) |
| Query Trace: Disease and CIC[original query] |
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| Polymorphisms of CD16A and CD32 Fc? receptors and circulating immune complexes in Ménière's disease: a case-control study. BMC medical genetics 2011 12 2. Lopez-Escamez José A, Saenz-Lopez Pablo, Gazquez Irene, Moreno Antonia, Gonzalez-Oller Carlos, Soto-Varela Andrés, Santos Sofía, Aran Ismael, Perez-Garrigues Herminio, Ibañez Agueda, Lopez-Nevot Miguel |
| The genomic landscape of the Ewing Sarcoma family of tumors reveals recurrent STAG2 mutation. PLoS genetics 2014 Jul 10 (7): e1004475. Brohl Andrew S, Solomon David A, Chang Wendy, Wang Jianjun, Song Young, Sindiri Sivasish, Patidar Rajesh, Hurd Laura, Chen Li, Shern Jack F, Liao Hongling, Wen Xinyu, Gerard Julia, Kim Jung-Sik, Lopez Guerrero Jose Antonio, Machado Isidro, Wai Daniel H, Picci Piero, Triche Timothy, Horvai Andrew E, Miettinen Markku, Wei Jun S, Catchpool Daniel, Llombart-Bosch Antonio, Waldman Todd, Khan Jav |
| The clinical and laboratory features of Chinese Han anti-factor H autoantibody-associated hemolytic uremic syndrome. Pediatric nephrology (Berlin, Germany) 2016 12 32 (5): 811-822. Song Di, Liu Xiao-Rong, Chen Zhi, Xiao Hui-Jie, Ding Jie, Sun Shu-Zhen, Liu Hong-Yan, Guo Wei-Yi, Wang Su-Xia, Yu Feng, Zhao Ming-Hui, |
| Recurrent CIC Gene Abnormalities in Angiosarcomas: A Molecular Study of 120 Cases With Concurrent Investigation of PLCG1, KDR, MYC, and FLT4 Gene Alterations. The American journal of surgical pathology 2016 Jan . Huang Shih-Chiang, Zhang Lei, Sung Yun-Shao, Chen Chun-Liang, Kao Yu-Chien, Agaram Narasimhan P, Singer Samuel, Tap William D, D'Angelo Sandra, Antonescu Cristina |
| 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 |
| Landscape of driver mutations and their clinical impacts in pediatric B-cell precursor acute lymphoblastic leukemia. Blood advances 2020 Oct 4 (20): 5165-5173. Ueno Hiroo, Yoshida Kenichi, Shiozawa Yusuke, Nannya Yasuhito, Iijima-Yamashita Yuka, Kiyokawa Nobutaka, Shiraishi Yuichi, Chiba Kenichi, Tanaka Hiroko, Isobe Tomoya, Seki Masafumi, Kimura Shunsuke, Makishima Hideki, Nakagawa Masahiro M, Kakiuchi Nobuyuki, Kataoka Keisuke, Yoshizato Tetsuichi, Nishijima Dai, Deguchi Takao, Ohki Kentaro, Sato Atsushi, Takahashi Hiroyuki, Hashii Yoshiko, Tokimasa Sadao, Hara Junichi, Kosaka Yoshiyuki, Kato Koji, Inukai Takeshi, Takita Junko, Imamura Toshihiko, Miyano Satoru, Manabe Atsushi, Horibe Keizo, Ogawa Seishi, Sanada Masas |
| Whole-Exome Sequencing Among Chinese Patients With Hereditary Diffuse Gastric Cancer. JAMA network open 2022 Dec 5 (12): e2245836. Liu Ze-Xian, Zhang Xiao-Long, Zhao Qi, Chen Yungchang, Sheng Hui, He Cai-Yun, Sun Yu-Ting, Lai Ming-Yu, Wu Min-Qing, Zuo Zhi-Xiang, Wang Wei, Zhou Zhi-Wei, Wang Feng-Hua, Li Yu-Hong, Xu Rui-Hua, Qiu Miao-Zh |
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