Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Lymphoma and PRF1[original query] |
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| Germline mutations of the perforin gene are a frequent occurrence in childhood anaplastic large cell lymphoma. Cancer 2007 Jun 109 (12): 2566-71. Cannella Sonia, Santoro Alessandra, Bruno Giuseppa, Pillon Marta, Mussolin Lara, Mangili Giovanna, Rosolen Angelo, Aricò Mauriz |
| Analysis of the -398C/T polymorphism in the perforin gene in oncohematological patients. Revista brasileira de hematologia e hemoterapia 2012 10 33 (4): 274-6. Garcia Fernanda Bernadelli, Dos Reis Rafaella Kizzy Inácio, da Silva Lucas Emanuel Pinheiro, Moraes-Souza Hel |
| Human perforin mutations and susceptibility to multiple primary cancers. Oncoimmunology 2013 Apr 2 (4): e24185. Trapani Joseph A, Thia Kevin Y T, Andrews Miles, Davis Ian D, Gedye Craig, Parente Philip, Svobodova Suzanne, Chia Jenny, Browne Kylie, Campbell Ian G, Phillips Wayne A, Voskoboinik Ilia, Cebon Jonathan |
| Monoallelic mutations of the perforin gene may represent a predisposing factor to childhood anaplastic large cell lymphoma. Journal of pediatric hematology/oncology 2014 Aug 36 (6): e359-65. Ciambotti Benedetta, Mussolin Lara, d'Amore Emanuele S G, Pillon Marta, Sieni Elena, Coniglio Maria L, Ros Martina D, Cetica Valentina, Aricò Maurizio, Rosolen Ange |
| Familial hematological malignancies: ASXL1 gene investigation. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 2015 Aug . Hamadou W S, Abed R E, Besbes S, Bourdon V, Fabre A, Youssef Y B, Laatiri M A, Eisinger F, Mari V, Gesta P, Dreyfus H, Bonadona V, Dugast C, Zattara H, Faivre L, Jemni S Y, Noguchi T, Khélif A, Sobol H, Soua |
| Germline cytotoxic lymphocytes defective mutations in Chinese patients with lymphoma. Oncology letters 2017 Nov 14 (5): 5249-5256. Chen Xue, Zhang Yang, Wang Fang, Wang Mangju, Teng Wen, Lin Yuehui, Han Xiangping, Jin Fangyuan, Xu Yuanli, Cao Panxiang, Fang Jiancheng, Zhu Ping, Tong Chunrong, Liu Hongxi |
| Inherited Genetic Susceptibility to Nonimmunosuppressed Epstein-Barr Virus-associated T/NK-cell Lymphoproliferative Diseases in Chinese Patients. Current medical science 2021 6 41 (3): 482-490. Guan Yu-Qi, Shen Ke-Feng, Yang Li, Cai Hao-Dong, Zhang Mei-Lan, Wang Jia-Chen, Long Xiao-Lu, Xiong Jie, Gu Jia, Zhang Pei-Ling, Xiao Min, Zhang Wei, Zhou Jian-Fe |
| Hemophagocytic Lymphohistiocytosis Gene Mutations in Adult Patients Presenting With CLIPPERS-Like Syndrome. Neurology(R) neuroimmunology & neuroinflammation 2021 05 8 (3): . Taieb Guillaume, Kaphan Elsa, Duflos Claire, Lebrun-Frénay Christine, Rigau Valérie, Thouvenot Eric, Duhin-Gand Emeline, Lefaucheur Romain, Hoang-Xuan Khe, Coulette Sarah, Ouallet Jean Christophe, Menjot de Champfleur Nicolas, Tranchant Christine, Picard Capucine, Fusaro Mathieu, Sepulveda Fernando E, Labauge Pierre, de Saint Basile Geneviè |
| [Gene Polymorphisms of Patients with Lymphoma-Associated Hemophagocytic Syndrome in Longyan area, Fujian Province]. Zhongguo shi yan xue ye xue za zhi 2023 2 31 (1): 104-108. Wu Wei-Hao, Chen Cong-Jie, Yu Lian, Ma Xiao-Mei, Huang Jian-Qing, Chen Long-Ti |
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