檢索結果 - Juan Pablo Trujillo‐Quintero
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Targeted gene therapy and cell reprogramming in <scp>F</scp>anconi anemia 由 Paula Rı́o, Rocío Baños, Angelo Lombardo, Oscar Quintana‐Bustamante, Lara Álvarez, Zita Garate, Pietro Genovese, Elena Almarza, Antonio Valeri, Begoña Díez, Susana Navarro, Yaima Torres, Juan Pablo Trujillo‐Quintero, Rodolfo Murillas, José C. Segovia, Enrique Samper, Jordi Surrallés, Philip D. Gregory, Michael C. Holmes, Luigi Naldini, Juan A. Bueren
出版 2014Artigo -
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Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia 由 Massimo Bogliolo, Beatrice Schuster, Chantal Stoepker, Burak Derkunt, Yan Su, Anja Raams, Juan Pablo Trujillo‐Quintero, Jordi Minguillón, Marı́a José Ramı́rez, Roser Pujol, José Antonio Casado, Rocío Baños, Paula Rı́o, Kerstin Knies, S. Zúñiga, Javier Benı́tez, Juan A. Bueren, Nicolaas G.J. Jaspers, Orlando D. Schärer, Johan P. de Winter, Detlev Schindler, Jordi Surrallés
出版 2013Artigo -
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Origin, functional role, and clinical impact of Fanconi anemia FANCA mutations 由 María Castellà, Roser Pujol, Elsa Callén, Juan Pablo Trujillo‐Quintero, José Antonio Casado, Gilles Thomas, Francis P. Lach, Arleen D. Auerbach, Detlev Schindler, Javier Benı́tez, Beatriz Porto, Teresa Ferró, A. de Arriba Muñoz, Julián Sevilla, Luís Madero, Elena Cela, Cristina Beléndez, Cristina Díaz de Heredia, Teresa Olivé, Joan Sánchez-de-Toledo, Isabel Badell, Montserrat Torrent, Jesús Estella, Ángeles Dasí, Antonia Rodríguez-Villa, Pedro Gómez, José Barbot, Maria C. Tapia, Antonio Molinés, Á Figuera, Juan A. Bueren, Jordi Surrallés
出版 2011Artigo -
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Modelling Fanconi anemia pathogenesis and therapeutics using integration-free patient-derived iPSCs 由 Guang Hui Liu, Keiichiro Suzuki, Mo Li, Jing Qu, Núria Montserrat, Carolina Tarantino, Ying Gu, Fei Yi, Xiuling Xu, Weiqi Zhang, Sergio Ruiz, Nongluk Plongthongkum, Kun Zhang, Shigeo Masuda, Emmanuel Nivet, Yuji Tsunekawa, Rupa Devi Soligalla, April Goebl, Emi Aizawa, Na Young Kim, Jessica Kim, Ilir Dubova, Ying Li, Ruotong Ren, Christopher Benner, Antonio del Sol, Juan A. Bueren, Juan Pablo Trujillo‐Quintero, Jordi Surrallés, Enrico Cappelli, Carlo Dufour, Concepción Rodrı́guez Esteban, Juan Carlos Izpisúa Belmonte
出版 2014Artigo -
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Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies 由 Martín Ortiz-Genga, Sofía Cuenca, Matteo Dal Ferro, Esther Zorio, Ricardo Salgado‐Aranda, Vicente Climent, Laura Padrón-Barthe, Iria Duro-Aguado, Juan Jiménez‐Jáimez, Víctor M. Hidalgo-Olivares, Enrique García‐Campo, Chiara Lanzillo, M. Paz Suárez-Mier, Hagith Yonath, Sonia Marcos‐Alonso, Juan Pablo Ochoa, José L. Santomé, Diego García-Giustiniani, Jorge Rodríguez-Garrido, Fernándo Domínguez, Marco Merlo, Julián Palomino, María Luisa Peña Peña, Juan Pablo Trujillo‐Quintero, Alicia Martín-Vila, Davide Stolfo, Pilar Molina, Enrique Lara‐Pezzi, Francisco Calvo, Eyal Nof, Leonardo Calò, Roberto Barriales‐Villa, Juan R. Gimeno, Michael Arad, Pablo García‐Pavía, Lorenzo Monserrat
出版 2016Artigo -
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Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy 由 Juan Pablo Ochoa, María Sabater‐Molina, José Manuel García‐Pinilla, Jens Mogensen, Maria Alejandra Restrepo‐Córdoba, Julián Palomino-Doza, Eduardo Villacorta, Marina Martínez Moreno, Javier Ramos‐Maqueda, Esther Zorio, María Luisa Peña‐Peña, Pablo Elpidio García-Granja, José F. Rodríguez‐Palomares, Ivonne J. Cárdenas-Reyes, Maria M. de la Torre‐Carpente, A Bautista-Paves, Mohammed Akhtar, Marcos Cicerchia, Raquel Bilbao-Quesada, María Victoria Mogollón‐Jiménez, Joel Salazar‐Mendiguchía, José M. Mesa Latorre, Blanca Arnáez, Ivan Olavarri-Miguel, María Eugenia Fuentes‐Cañamero, Arsonval Lamounier, José María Pérez Ruiz, Vicente Climent, Inmaculada Pérez-Sánchez, Juan Pablo Trujillo‐Quintero, Luís R. Lopes, Alfredo Repáraz-Andrade, Rosario Marín-Iglesias, Alejandro Rodríguez-Vilela, María Sandín‐Fuentes, José Antonio Garrote, Alejandro Cortel-Fuster, Miguel A. López-Garrido, Ana Fontalba-Romero, Tomás Ripoll‐Vera, Isabel Llano‐Rivas, Xusto Fernández, María Isidoro‐García, Diego García-Giustiniani, Roberto Barriales‐Villa, Martín Ortiz-Genga, Pablo García‐Pavía, Perry Elliott, Juan R. Gimeno, Lorenzo Monserrat
出版 2018Artigo
相關主題
Biology
Genetics
Gene
DNA repair
Fanconi anemia
Medicine
Cancer research
FANCA
Haematopoiesis
Mutation
Stem cell
Bone marrow failure
Cardiology
Cardiomyopathy
DNA
Heart failure
Internal medicine
Phenotype
Proband
Cell biology
Complementation
DNA damage
Dilated cardiomyopathy
Embryonic stem cell
Endonuclease
Environmental health
FANCD2
Genetic enhancement
Genome instability
Heart disease