Projects per year
Personal profile
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
Education/Academic qualification
Ph. D., Universitat Autònoma de Barcelona (UAB)
Award Date: 1 Dec 2015
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Collaborations and top research areas from the last five years
Projects
- 5 Finished
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Reparación del DNA y anemia de Fanconi: investigación genética y aplicaciones terapéuticas
Surralles Calonge, J. (Principal Investigator), Umbert Maestre, M. G. (Collaborator), Bogliolo , M. (Investigator), Castells Roca, L. (Investigator), Pujol Calvet, M. R. (Investigator) & Ramirez de Haro, M. J. (Investigator)
Spanish Ministry of Economy and Competitiveness (MINECO)
1/01/16 → 31/12/18
Project: Research Projects and Other Grants
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ANEMIA DE FANCONI: INVESTIGACION GENETICA Y APLICACIONES TERAPEUTICAS
Surralles Calonge, J. (Principal Investigator), Mina Ibarra, L. B. (Scholar), Trujillo Quintero, J. P. (Scholar), Bogliolo , M. (Investigator), Pujol Calvet, R. (Investigator), Ramírez De Haro, M. J. (Investigator) & Umbert Maestre, M. G. (Investigator)
Spanish Ministry of Economy and Competitiveness (MINECO)
1/01/13 → 31/12/15
Project: Research Projects and Other Grants
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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. (Principal Investigator), Bogliolo , M. (Investigator), Estella Aguado, J. (Investigator), Pujol Calvet, M. R. (Investigator) & Ramirez de Haro, M. J. (Investigator)
1/01/13 → 30/06/16
Project: Research Projects and Other Grants
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Genética Funcional y Biología Molecular del Síndrome de Predisposición al Cáncer Anemia de Fanconi
Surralles Calonge, J. (Principal Investigator), Villa Fontes, J. (Scholar), Bogliolo , M. (Investigator), Cabré Fabré, O. (Investigator), Castella Castella, M. (Investigator), Castillo Bosch, P. (Investigator), Minguillon Pedreño, J. (Investigator), Pujol Calvet, M. R. (Investigator), Ramirez de Haro, M. J. (Investigator) & Umbert Maestre, M. G. (Investigator)
Spanish Ministry of Science and Innovation
1/01/10 → 31/12/12
Project: Research Projects and Other Grants
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Mechanisms of formation of ionizing radiation-induced chromosomal aberrations: Impact of repair pathways and nuclear architecture
Surralles Calonge, J. (Principal Investigator) & Bogliolo , M. (Scholar)
1/02/02 → 31/01/04
Project: International research project
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A self-repair history: compensatory effect of a de novo variant on the FANCA c.2778+83C>G splicing mutation.
Persico, I., Fontana, G., Faleschini, M., Zanchetta, M. E., Ammeti, D., Cappelli, E., Corsolini, F., Mosa, C., Guarina, A., Bogliolo, M., Surrallés, J., Dufour, C., Farruggia, P., Savoia, A. & Bottega, R., 2023, In: Frontiers in Genetics. 14, 10 p., 1209138.Research output: Contribution to journal › Article › Research › peer-review
1 Citation (Scopus) -
CDK5RAP3, a New BRCA2 Partner That Regulates DNA Repair, Is Associated with Breast Cancer Survival
Minguillón Pedreño, J., Bogliolo, M., Surrallés i Calonge, J., Rovirosa Mulet, L., Bustamante-Madrid, P., Camps-Fajol, C., de Garibay, G. R., Shimelis, H., Montanuy Escribano, H., Pujol, R., Hernandez, G., Castillo, P., Soucy, P., Martrat, G., Gómez Moruno, A., Cuadras, D., García, M. J., Gayarre, J., Lázaro Garcia, C. & Benitez, J. & 2 others, , 2022, In: Cancers. 14, 2Research output: Contribution to journal › Article › Research › peer-review
Open Access -
Clinical consequences of BRCA2 hypomorphism
Castells-Roca, L., Gutiérrez-Enríquez, S., Bonache, S., Bogliolo, M., Carrasco, E., Aza-Carmona, M., Montalban, G., Muñoz-Subirana, N., Pujol, R., Cruz Zambrano, C., Llop-Guevara, A., Ramírez de Haro, M. J., Saura, C., Lasa, A., Serra, V., Diez, O., Balmaña Gelpí, J. & Surrallés i Calonge, J., 2021, In: npj Breast Cancer. 7, 1Research output: Contribution to journal › Article › Research › peer-review
Open Access3 Citations (Scopus) -
FANCA Gene Mutations in North African Fanconi Anemia Patients
Ben, H. A. A., Messaoud, O., Elouej, S., Talmoudi, F., Ayed, W., Mellouli, F., Ouederni, M., Hadiji, S., De, S.-G. A., Delague, V., Lévy, N., Bogliolo, M., Surralles Calonge, J., Abdelhak, S. & Amouri, A., Feb 2021, In: Frontiers in Genetics. 12, 12 p., 610050.Research output: Contribution to journal › Article › Research › peer-review
Open Access5 Citations (Scopus) -
Hematopoietic Stem Cell Collection for the Gene Therapy of Fanconi Anemia Patients
Navarro, S., Sevilla, J., Rio, P., Sanchez, R., Zubicaray, J., Galvez, E., Merino, E., Sebastian, E., Azqueta, C., Casado, J. A., Segovia, J. C., Alberquilla, O., Bogliolo, M., Roman-Rodriguez, F. J., Gimenez, Y., Larcher, L., Salgado, R., Pujol, R. M., Haldun, R. & Castillo, A. & 10 others, , 27 Apr 2021, In: Molecular Therapy. 29, 4, p. 342-342 1 p.Research output: Contribution to journal › Article › Research › peer-review
Thesis
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Secuenciación del exoma en anemia de Fanconi: del diagnostico al descubrimiento de un nuevo gen
Bogliolo , M. (Author), Surrallés Calonge, J. (Director), 1 Dec 2015Student thesis: Doctoral thesis