Fanconi anemia pathway A Rodríguez, A D’Andrea Current Biology 27 (18), R986-R988, 2017 | 132 | 2017 |
Chromosome instability in Fanconi anemia: from breaks to phenotypic consequences B García-de-Teresa, A Rodríguez, S Frias Genes 11 (12), 1528, 2020 | 64 | 2020 |
A Boolean network model of the FA/BRCA pathway A Rodriguez, D Sosa, L Torres, B Molina, S Frias, L Mendoza Bioinformatics 28 (6), 858-866, 2012 | 56 | 2012 |
A Boolean network model of human gonadal sex determination O Ríos, S Frias, A Rodríguez, S Kofman, H Merchant, L Torres, ... Theoretical Biology and Medical Modelling 12, 1-18, 2015 | 55 | 2015 |
MYC promotes bone marrow stem cell dysfunction in Fanconi anemia A Rodríguez, K Zhang, A Färkkilä, J Filiatrault, C Yang, M Velázquez, ... Cell stem cell 28 (1), 33-47. e8, 2021 | 44 | 2021 |
Increased red cell distribution width in Fanconi anemia: a novel marker of stress erythropoiesis R Sousa, C Gonçalves, IC Guerra, E Costa, A Fernandes, ... Orphanet journal of rare diseases 11, 1-10, 2016 | 30 | 2016 |
Heterogeneity and Clonal Evolution of Acquired PARP Inhibitor Resistance in TP53- and BRCA1-Deficient Cells A Färkkilä, A Rodríguez, J Oikkonen, DC Gulhan, H Nguyen, ... Cancer research 81 (10), 2774-2787, 2021 | 23 | 2021 |
Fanconi anemia cells with unrepaired DNA damage activate components of the checkpoint recovery process A Rodríguez, L Torres, U Juárez, D Sosa, E Azpeitia, BG Teresa, E Cortés, ... Theoretical Biology and Medical Modelling 12, 1-22, 2015 | 21 | 2015 |
La mitosis y su regulación AJ Rodríguez-Gómez, S Frias-Vázquez Acta pediátrica de México 35 (1), 55-68, 2014 | 18 | 2014 |
Fanconi anemia and dyskeratosis congenita/telomere biology disorders: Two inherited bone marrow failure syndromes with genomic instability MÓ Fiesco-Roa, B García-de Teresa, P Leal-Anaya, R van ‘t Hek, ... Frontiers in Oncology 12, 949435, 2022 | 15 | 2022 |
Síndromes de falla medular hereditarios: etiología, fisiopatología, diagnóstico y tratamiento M Fiesco-Roa, A Monsivais-Orozco, A Rodríguez, S Frias, ... Acta Pediátrica de México 42 (4), 192-207, 2021 | 9 | 2021 |
Inhibition of TGFβ1 and TGFβ3 promotes hematopoiesis in Fanconi anemia A Rodríguez, C Yang, E Furutani, BG de Teresa, M Velázquez, J Filiatrault, ... Experimental hematology 93, 70-84. e4, 2021 | 9 | 2021 |
FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México B García‐de Teresa, S Frias, B Molina, MT Villarreal, A Rodriguez, ... Molecular Genetics & Genomic Medicine 7 (6), e710, 2019 | 9 | 2019 |
Estilos de aprendizaje que favorecen la lectura y escritura en niños de grado transición A Rodríguez, D Mercado, J García, COL Montes Obtenido de Universidad Pontificia Bolivariana: https://repository. upb. edu …, 2018 | 9 | 2018 |
WIP1 contributes to the adaptation of fanconi anemia cells to DNA damage as determined by the regulatory network of the fanconi anemia and checkpoint recovery pathways A Rodríguez, JJ Naveja, L Torres, B García de Teresa, U Juárez-Figueroa, ... Frontiers in genetics 10, 411, 2019 | 8 | 2019 |
Large‐scale topological disruption of chromosome territories 9 and 22 is associated with nonresponse to treatment in CML E Fabian‐Morales, D Vallejo‐Escamilla, A Gudiño, A Rodríguez, ... International Journal of Cancer 150 (9), 1455-1470, 2022 | 7 | 2022 |
Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG P Reyes, B García-de Teresa, U Juárez, F Pérez-Villatoro, ... International Journal of Molecular Sciences 23 (4), 2334, 2022 | 7 | 2022 |
TGFβ pathway is required for viable gestation of Fanconi anemia embryos A Rodríguez, M Epperly, J Filiatrault, M Velázquez, C Yang, K McQueen, ... PLoS genetics 18 (11), e1010459, 2022 | 5 | 2022 |
7p15 deletion as the cause of hand-foot-genital syndrome: a case report, literature review and proposal of a minimum region for this phenotype E Yokoyama, DL Smith-Pellegrin, S Sánchez, B Molina, A Rodríguez, ... Molecular Cytogenetics 10, 1-9, 2017 | 4 | 2017 |
Estudio multidisciplinario del paciente con anemia de Fanconi B García de Teresa, A Rodríguez, S Frías Acta pediátrica de México 37 (1), 54-59, 2016 | 4 | 2016 |