Projects per year
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Dive into the research topics where Massimo Bogliolo is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 1 Similar Profiles
Projects
- 3 Finished
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Reparación del DNA y anemia de Fanconi: investigación genética y aplicaciones terapéuticas
Surralles Calonge, J., Umbert Maestre, M. G., Bogliolo , M., Castells Roca, L., Pujol Calvet, M. R. & Ramirez de Haro, M. J.
1/01/16 → 31/12/18
Project
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Regenerative medicine for Fanconi anemia: generation of disease-free patient-specific iPS cells, and iPSC-derived hematopoietic progenitors and platelets.
Surralles Calonge, J., Bogliolo , M., Estella Aguado, J., Pujol Calvet, M. R. & Ramirez de Haro, M. J.
1/01/13 → 30/06/16
Project
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Genética Funcional y Biología Molecular del Síndrome de Predisposición al Cáncer Anemia de Fanconi
Surralles Calonge, J., Villa Fontes, J., Bogliolo , M., Cabré Fabré, O., Castella Castella, M., Castillo Bosch, P., Minguillon Pedreño, J., Pujol Calvet, M. R., Ramirez de Haro, M. J. & Umbert Maestre, M. G.
1/01/10 → 31/12/12
Project
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From exome analysis in idiopathic azoospermia to the identification of a high-risk subgroup for occult Fanconi anemia
Krausz, C., Riera-Escamilla, A., Chianese, C., Moreno-Mendoza, D., Ars, E., Rajmil, O., Pujol, R., Bogliolo, M., Blanco, I., Rodríguez, I., Badell, I., Ruiz-Castañé, E. & Surrallés, J., 1 Jan 2019, In: Genetics in Medicine. 21, p. 189-194Research output: Contribution to journal › Article › Research
17 Citations (Scopus) -
Functional comparison of XPF missense mutations associated to multiple DNA repair disorders.
Marín, M., Ramírez, M. J., Carmona, M. A., Jia, N., Ogi, T., Bogliolo, M. & Surrallés, J., 1 Jan 2019, In: Genes. p. -Research output: Contribution to journal › Article › Research
5 Citations (Scopus) -
Optimised molecular genetic diagnostics of Fanconi anaemia by whole exome sequencing and functional studies
Bogliolo, M., Pujol, R., Aza-Carmona, M., Muñoz-Subirana, N., Rodriguez-Santiago, B., Casado, J. A., Rio, P., Bauser, C., Reina-Castillón, J., Lopez-Sanchez, M., Gonzalez-Quereda, L., Gallano, P., Catalá, A., Ruiz-Llobet, A., Badell, I., Diaz-Heredia, C., Hladun, R., Senent, L., Argiles, B., Bergua Burgues, J. M. & 48 others, , 1 Jan 2019, In: Journal of Medical Genetics.Research output: Contribution to journal › Article › Research
11 Citations (Scopus) -
Biallelic truncating FANCM mutations cause early-onset cancer but not Fanconi anemia
Bogliolo, M., Bluteau, D., Lespinasse, J., Pujol, R., Vasquez, N., D'Enghien, C. D., Stoppa-Lyonnet, D., Leblanc, T., Soulier, J. & Surrallés, J., 1 Apr 2018, In: Genetics in Medicine. 20, 4, p. 458-463Research output: Contribution to journal › Article › Research › peer-review
34 Citations (Scopus) -
Decapping protein EDC4 regulates DNA repair and phenocopies BRCA1
Hernández, G., Ramírez, M. J., Minguillón, J., Quiles, P., Ruiz De Garibay, G., Aza-Carmona, M., Bogliolo, M., Pujol, R., Prados-Carvajal, R., Fernández, J., García, N., López, A., Gutiérrez-Enríquez, S., Diez, O., Benítez, J., Salinas, M., Teulé, A., Brunet, J., Radice, P., Peterlongo, P. & 7 others, , 1 Dec 2018, In: Nature Communications. 9, 967.Research output: Contribution to journal › Article › Research
25 Citations (Scopus)