Listar por Materia MUTACIÓN
Mostrando resultados 1 a 5 de 5
| Fecha de publicación | Título | Autor(es) |
| 2022 | Information theory approaches to improve glioma diagnostic workflows in surgical neuropathology | Cevik, Lokman; Vázquez Landrove, Marilyn; Aslan, Mehmet Tahir; Khammad, Vasilii; Garagorry Guerra, Francisco José; Cabello Izquierdo, Yolanda; Wang, Wesley; Zhao, Jing; Becker, Aline Paixao; Czeisler, Catherine; Rendeiro, Anne Costa; Véras, Lucas Luis Sousa; Zanon, Maicon Fernando; Reis, Rui Manuel; Matsushita, Marcus de Medeiros; Ozduman, Koray; Pamir, M. Necmettin; Ersen Danyeli, Ayca; Pearce, Thomas; Felicella, Michelle; Eschbacher, Jennifer; Arakaki, Naomi; Martinetto, Horacio; Parwani, Anil; Thomas, Diana L.; Otero, José Javier |
| 2023 | Multiple oxidative post-translational modifications of human glutamine synthetase mediate peroxynitrite-dependent enzyme inactivation and aggregation | Campolo, Nicolás; Mastrogiovanni, Mauricio; Mariotti, Michele; Issoglio, Fernando M.; Estrin, Darío; Hägglund, Per; Grune, Tilman; Davies, Michael J.; Bartesaghi, Silvina; Radi, Rafael |
| 2022 | Novel frameshift mutation in LIS1 gene is a probable cause of lissencephaly: a case report | Simoes, Camila; Graña, Martín; Rodríguez, Soledad; Baltar Yanes, Federico; Tapié, Alejandra; Dell’Oca, Nicolás; Naya, Hugo; Raggio, Víctor; Spangenberg, Lucía |
| 2022 | STK11 and KEAP1 mutations in non-small cell lung cancer patients: Descriptive analysis and prognostic value among Hispanics (STRIKE registry-CLICaP) | Cordeiro de Lima, Vladimir C.; Corassa, Marcelo; Saldanha, Erick; Freitas, Helano; Arrieta, Oscar; Raez, Luis; Samtani, Suraj; Ramos, Maritza; Rojas, Carlos; Burotto, Mauricio; Chamorro, Diego F.; Recondo, Gonzalo; Ruiz-Patiño, Alejandro; Más, Luis; Zataraín-Barrón, Zyanya Lucía; Mejía, Sergio; Minata, José Nicolás; Martín, Claudio; Blaquier, Juan Bautista; Motta Guerrero, Rodrigo; Aliaga-Macha, Carlos; Carracedo, Carlos; Ordóñez- Reyes, Camila; Garcia-Robledo, Juan Esteban; Corrales, Luis; Sotelo, Carolina; Ricaurte, Luisa; Santoyo, Nicolás; Cuello, Mauricio; Jaller, Elvira; Rodríguez, July; Archila, Pilar; Bermudez, Maritza; Gamez, Tatiana; Russo, Alessandro; Viola, Lucía; Malapelle, Umberto; de Miguel Pérez, Diego; Rolfo, Christian; Rosell, Rafael; Cardona, Andrés F. |
| 2022 | Two mutations in the SBDS gene reveal a diagnosis of Shwachman-Diamond syndrome in a patient with atypical symptoms | Spangenberg, María Noel; Grille, Sofía; Simoes, Camila; Dell’Oca, Nicolás; Boada, Matilde; Guillermo, Cecilia; Raggio, Víctor; Spangenberg, Lucía |
