Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Ependymoma and TP53[original query] |
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Complex cytogenetic abnormalities including telomeric associations and MEN1 mutation in a pediatric ependymoma. Cancer genetics and cytogenetics 2002 12 138 (2): 107-10. Urioste M, Martínez-Ramírez A, Cigudosa J C, Colmenero I, Madero L, Robledo M, Martínez-Delgado B, Benítez |
The TP53 p.R337H mutation is uncommon in a Brazilian cohort of pediatric patients diagnosed with ependymoma. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2019 Nov . de Almeida Magalhães Taciani, Borges Kleiton Silva, de Sousa Graziella Ribeiro, Brandalise Silvia Regina, Seidinger Ana Luiza, Scrideli Carlos Alberto, Oba-Shinjo Sueli Mieko, Yunes José Andrés, Tone Luiz Gonza |
Mutation Profiling of Intracranial Myxopapillary Ependymoma by Next Generation DNA Sequencing. The Gulf journal of oncology 2022 2 1 (37): 7-16. Taher Mohiuddin M, Alhussini Abdulaziz Abdulnasser, Saeed Muhammad, Athar Mohammad, Bantan Najwa Abdalkabeer A, Jastania Raid A, Balkhoyour Kamal Bakour, Nageeti Tahani |
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 |
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