Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Balmaña Gelpí, Judith"'
Autor:
Balmaña Gelpí, Judith
Publikováno v:
TDX (Tesis Doctorals en Xarxa).
Externí odkaz:
http://hdl.handle.net/10803/4562
Autor:
Gomez-Puerto, Diego, Llop Guevara, Alba, Cruellas Lapeña, Mara, Torres Esquius, Sara, De la Torre Fdez de Vega, Fco Javier, Peg Camara, Vicente, Balmaña Gelpí, Judith, Pimentel, Isabel
Publikováno v:
Scientia
HRD-biomarkers; Pathological complete response; Triple-negative breast cancer Biomarcadores HRD; Respuesta patológica completa; Cáncer de mama triple negativo Biomarcadors HRD; Resposta patològica completa; Càncer de mama triple negatiu Triple-ne
Autor:
Balaguer, Francesc, Balmaña Gelpí, Judith, Bellosillo, Beatriu, Brunet, Joan, Lazaro Garcia, Conxi, Montoro Gómez, Mª Julia, Puig-Butille, Joan Anton, Salvador, Hector, Tuset, E.
Publikováno v:
Scientia
Càncer en l’adult i pediatria; Síndromes hereditàries; Perfil genètic; Precisió Cáncer en el adulto y pediatría; Síndromes hereditarios; Perfil genético; Precisión Cancer in adults and pediatrics; Hereditary syndromes; Genetic profile; Ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::72e4a1a4273eb1c6c13b0740b78110d7
https://hdl.handle.net/11351/8438.2
https://hdl.handle.net/11351/8438.2
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Shah, Jennifer B., Pueschl, Dana, Wubbenhorst, Bradley, Fan, Mengyao, Pluta, John, D'Andrea, Kurt, Hubert, Anna P., Shilan, Jake S., Zhou, Wenting, Kraya, Adam A., Llop Guevara, Alba, Ruan, Catherine, Serra, Violeta, Balmaña Gelpí, Judith, Feldman, Michael, Morin, Pat J., Nayak, Anupma, Maxwell, Kara N., Domchek, Susan M., Nathanson, Katherine L., Universitat Autònoma de Barcelona
Publikováno v:
Scientia
Breast cancer; Cancer genetics; RNA sequencing Cáncer de mama; Genética del cáncer; Secuenciación de ARN Càncer de mama; Genètica del càncer; Seqüenciació d'ARN Recurrence is a major cause of death among BRCA1/2 mutation carriers with breast
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a3769f8ba0b3578a17a61ac489246a2
https://ddd.uab.cat/record/269572
https://ddd.uab.cat/record/269572
Autor:
Castells-Roca, Laia, Gutiérrez-Enríquez, Sara, Bonache, Sandra, Bogliolo, Massimo, Carrasco, E., Aza-Carmona, Miriam, Montalban, G., Muñoz-Subirana, N., Pujol, Roser, Cruz Zambrano, Cristina, Llop-Guevara, A., Ramírez de Haro, Ma. José, Saura, Cristina, Lasa, Adriana, Serra, V., Diez, Orland, Balmaña Gelpí, Judith, Surrallés i Calonge, Jordi, Universitat Autònoma de Barcelona
Publikováno v:
Scientia
npj Breast Cancer, Vol 7, Iss 1, Pp 1-9 (2021)
NPJ Breast Cancer
npj Breast Cancer
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
npj Breast Cancer, Vol 7, Iss 1, Pp 1-9 (2021)
NPJ Breast Cancer
npj Breast Cancer
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
The tumor suppressor FANCD1/BRCA2 is crucial for DNA homologous recombination repair (HRR). BRCA2 biallelic pathogenic variants result in a severe form of Fanconi anemia (FA) syndrome, whereas monoallelic pathogenic variants cause mainly hereditary b
Autor:
Rofes, Paula, Del Valle, Jesús, Torres Esquius, Sara, Feliubadaló, Lídia, Stradella, Agostina, Moreno-Cabrera, José Marcos, López-Doriga, Adriana, Munté, Elisabet, de Cid, R., Campos, Olga, Cuesta, Raquel, Teulé, Álex, Grau, Èlia, Sanz, Judit, Capellá, G. (Gabriel), Diez, Orland, Brunet, Joan, Balmaña Gelpí, Judith, Lázaro, Conxi, Universitat Autònoma de Barcelona
Publikováno v:
Genes
Volume 12
Issue 2
Scientia
Genes, Vol 12, Iss 150, p 150 (2021)
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Dipòsit Digital de la UB
Universidad de Barcelona
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
Volume 12
Issue 2
Scientia
Genes, Vol 12, Iss 150, p 150 (2021)
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Dipòsit Digital de la UB
Universidad de Barcelona
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
Only a small fraction of hereditary breast and/or ovarian cancer (HBOC) cases are caused by germline variants in the high-penetrance breast cancer 1 and 2 genes (BRCA1 and BRCA2). BRCA1-associated ring domain 1 (BARD1), nuclear partner of BRCA1, has
Autor:
Singer, Christian.F., Balmaña Gelpí, Judith, Bürki, Nicole., Delaloge, S., Filieri, M.E., Gerdes, A.M., Grindedal, E.M., Han, Suzette., Johansson, Oskar., Kaufman, Bella., Krajc, Mateja., Loman, Niklas., Olah, Edith., Paluch-Shimon, Shani., Plavetic, Natalija Dedic, Pohlodek, Kamil., Rhiem, Kerstin., Teixeira, Manuel., Evans, D.Gareth., Universitat Autònoma de Barcelona
Publikováno v:
Singer, C F, Balmaña, J, Bürki, N, Delaloge, S, Filieri, M E, Gerdes, A, Grindedal, E M, Han, S, Johansson, O, Kaufman, B, Krajc, M, Loman, N, Olah, E, Paluch-shimon, S, Plavetic, N D, Pohlodek, K, Rhiem, K, Teixeira, M & Evans, D G 2019, ' Genetic counselling and testing of susceptibility genes for therapeutic decision-making in breast cancer—an European consensus statement and expert recommendations ', European Journal of Cancer, vol. 106, pp. 54-60 . https://doi.org/10.1016/j.ejca.2018.10.007
Singer, C F, Balmaña, J, Bürki, N, Delaloge, S, Filieri, M E, Gerdes, A-M, Grindedal, E M, Han, S, Johansson, O, Kaufman, B, Krajc, M, Loman, N, Olah, E, Paluch-Shimon, S, Plavetic, N D, Pohlodek, K, Rhiem, K, Teixeira, M & Evans, D G 2019, ' Genetic counselling and testing of susceptibility genes for therapeutic decision-making in breast cancer-an European consensus statement and expert recommendations ', European Journal of Cancer, vol. 106, pp. 54-60 . https://doi.org/10.1016/j.ejca.2018.10.007
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Singer, C F, Balmaña, J, Bürki, N, Delaloge, S, Filieri, M E, Gerdes, A-M, Grindedal, E M, Han, S, Johansson, O, Kaufman, B, Krajc, M, Loman, N, Olah, E, Paluch-Shimon, S, Plavetic, N D, Pohlodek, K, Rhiem, K, Teixeira, M & Evans, D G 2019, ' Genetic counselling and testing of susceptibility genes for therapeutic decision-making in breast cancer-an European consensus statement and expert recommendations ', European Journal of Cancer, vol. 106, pp. 54-60 . https://doi.org/10.1016/j.ejca.2018.10.007
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Travel expenses for (some) participants were sponsored by an unrestricted grant from AstraZeneca (AZ). AZ had no role in the organization of the meeting, in the invitation of panel members, and in the selection of questions. Participants were solely
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75253c7bf6f2079c7e463abd5dcf4bd7
https://www.research.manchester.ac.uk/portal/en/publications/genetic-counselling-and-testing-of-susceptibility-genes-for-therapeutic-decisionmaking-in-breast-canceran-european-consensus-statement-and-expert-recommendations(605a9391-1994-4561-8be4-d6c3e7a39306).html
https://www.research.manchester.ac.uk/portal/en/publications/genetic-counselling-and-testing-of-susceptibility-genes-for-therapeutic-decisionmaking-in-breast-canceran-european-consensus-statement-and-expert-recommendations(605a9391-1994-4561-8be4-d6c3e7a39306).html
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.