Kết quả tìm kiếm - Diaz-Navarro, Ander

PanCancer analysis of somatic mutations in repetitive regions reveals recurrent mutations in snRNA U2 Bằng Bousquets-Muñoz, Pablo, Díaz-Navarro, Ander, Nadeu, Ferran, Sánchez-Pitiot, Ana, López-Tamargo, Sara, Shuai, Shimin, Balbín, Milagros, Tubio, Jose M. C., Beà, Sílvia, Martin-Subero, Jose I., Gutiérrez-Fernández, Ana, Stein, Lincoln D., Campo, Elías, Puente, Xose S.

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Circulating tumour DNA from the cerebrospinal fluid allows the characterisation and monitoring of medulloblastoma Bằng Escudero, Laura, Llort, Anna, Arias, Alexandra, Diaz-Navarro, Ander, Martínez-Ricarte, Francisco, Rubio-Perez, Carlota, Mayor, Regina, Caratù, Ginevra, Martínez-Sáez, Elena, Vázquez-Méndez, Élida, Lesende-Rodríguez, Iván, Hladun, Raquel, Gros, Luis, Ramón y Cajal, Santiago, Poca, Maria A., Puente, Xose S., Sahuquillo, Juan, Gallego, Soledad, Seoane, Joan

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Tumor xenograft modeling identifies an association between TCF4 loss and breast cancer chemoresistance Bằng Ruiz de Garibay, Gorka, Mateo, Francesca, Stradella, Agostina, Valdés-Mas, Rafael, Palomero, Luis, Serra-Musach, Jordi, Puente, Diana A., Díaz-Navarro, Ander, Vargas-Parra, Gardenia, Tornero, Eva, Morilla, Idoia, Farré, Lourdes, Martinez-Iniesta, María, Herranz, Carmen, McCormack, Emmet, Vidal, August, Petit, Anna, Soler, Teresa, Lázaro, Conxi, Puente, Xose S., Villanueva, Alberto, Pujana, Miguel Angel

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Chromosome 12p amplification in triple-negative/BRCA1-mutated breast cancer associates with emergence of docetaxel resistance and carboplatin sensitivity Bằng Gómez-Miragaya, Jorge, Díaz-Navarro, Ander, Tonda, Raul, Beltran, Sergi, Palomero, Luis, Palafox, Marta, Dobrolecki, Lacey E., Huang, Chen, Vasaikar, Suhas, Zhang, Bing, Wulf, Gerburg M., Collado-Sole, Alejandro, Trinidad, Eva M, Muñoz, Purificación, Paré, Laia, Prat, Aleix, Bruna, Alejandra, Caldas, Carlos, Arribas, Joaquín, Soler-Monso, María Teresa, Petit, Anna, Balmaña, Judith, Cruz, Cristina, Serra, Violeta, Pujana, Miguel Angel, Lewis, Michael T., Puente, Xose S., González-Suárez, Eva

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Genomic and epigenomic insights into the origin, pathogenesis, and clinical behavior of mantle cell lymphoma subtypes Bằng Nadeu, Ferran, Martin-Garcia, David, Clot, Guillem, Díaz-Navarro, Ander, Duran-Ferrer, Martí, Navarro, Alba, Vilarrasa-Blasi, Roser, Kulis, Marta, Royo, Romina, Gutiérrez-Abril, Jesús, Valdés-Mas, Rafael, López, Cristina, Chapaprieta, Vicente, Puiggros, Montserrat, Castellano, Giancarlo, Costa, Dolors, Aymerich, Marta, Jares, Pedro, Espinet, Blanca, Muntañola, Ana, Ribera-Cortada, Inmaculada, Siebert, Reiner, Colomer, Dolors, Torrents, David, Gine, Eva, López-Guillermo, Armando, Küppers, Ralf, Martin-Subero, Jose I., Puente, Xose S., Beà, Sílvia, Campo, Elias

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Recurrent non-coding U1-snRNA mutations drive cryptic splicing in Shh medulloblastoma Bằng Suzuki, Hiromichi, Kumar, Sachin A., Shuai, Shimin, Diaz-Navarro, Ander, Gutierrez-Fernandez, Ana, De Antonellis, Pasqualino, Cavalli, Florence M. G., Juraschka, Kyle, Farooq, Hamza, Shibahara, Ichiyo, Vladoiu, Maria C., Zhang, Jiao, Abeysundara, Namal, Przelicki, David, Skowron, Patryk, Gauer, Nicole, Luu, Betty, Daniels, Craig, Wu, Xiaochong, Forget, Antoine, Momin, Ali, Wang, Jun, Dong, Weifan, Kim, Seung-Ki, Grajkowska, Wieslawa A., Jouvet, Anne, Fèvre-Montange, Michelle, Garrè, Maria Luisa, Nageswara Rao, Amulya A., Giannini, Caterina, Kros, Johan M., French, Pim J., Jabado, Nada, Ng, Ho-Keung, Poon, Wai Sang, Eberhart, Charles G., Pollack, Ian F., Olson, James M., Weiss, William A., Kumabe, Toshihiro, López-Aguilar, Enrique, Lach, Boleslaw, Massimino, Maura, Van Meir, Erwin G., Rubin, Joshua B., Vibhakar, Rajeev, Chambless, Lola B., Kijima, Noriyuki, Klekner, Almos, Bognár, László, Chan, Jennifer A., Faria, Claudia C., Ragoussis, Jiannis, Pfister, Stefan M., Goldenberg, Anna, Wechsler-Reya, Robert J., Bailey, Swneke D., Garzia, Livia, Morrissy, A. Sorana, Marra, Marco A., Huang, Xi, Malkin, David, Ayrault, Olivier, Ramaswamy, Vijay, Puente, Xose S., Calarco, John A., Stein, Lincoln, Taylor, Michael D.

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