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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorDe Asis Tuazon, Anna Marie
dc.contributor.authorLott, Paul
dc.contributor.authorBohórquez, Mabel
dc.contributor.authorBenavides, Jennyfer
dc.contributor.authorRamirez, Carolina
dc.contributor.authorCriollo, Angel
dc.contributor.authorDiez Gibert, Orland
dc.date.accessioned2021-09-10T10:03:41Z
dc.date.available2021-09-10T10:03:41Z
dc.date.issued2020-10-21
dc.identifier.citationDe Asis Tuazon AM, Lott P, Bohórquez M, Benavides J, Ramirez C, Criollo A, et al. Haplotype analysis of the internationally distributed BRCA1 c.3331_3334delCAAG founder mutation reveals a common ancestral origin in Iberia. Breast Cancer Res. 2020 Oct 21;22:108.
dc.identifier.issn1465-542X
dc.identifier.urihttps://hdl.handle.net/11351/6296
dc.descriptionCàncer de mama; Mutació fundadora; Haplotip
dc.description.sponsorshipAMDEA was supported with graduate Fellowships from UC Davis T32 Biotechnology Program. MB, ME, and LGC-C received funding from GSK Oncology and from “Oficina de Desarrollo a la Docencia de la Universidad del Tolima, Convocatoria 2010”. AC and AEF received funding from the Colciencias program “Becas Doctorales Nacionales, Convocatorias 528-2011 and 647-2015”. JB received funding from the Colciencias program “Formación de Capital Humano de Alto Nivel para el Departamento de Tolima- 2016, convocatoria 755”. BRCA1/2 genotyping of the Brazilian patients was performed in part with grants from CNPq (408313/2016-1), FAPERGS and Fundo de Incentivo a Pesquisa (FIPE) do Hospital de Clínicas de Porto Alegre, Brazil. AV received funding from CIBERER (grant ER17P1AC7112/2017). PC received funding from FONDEF grant #CA12I10152. CL was Supported by the Carlos III National Health Institute funded by FEDER funds—a way to build Europe—[PI19/00553; PI16/00563; PI16/01898; SAF2015-68016-R and CIBERONC]; the Government of Catalonia [Pla estratègic de recerca i innovació en salut (PERIS_MedPerCan and URDCat projects), 2017SGR1282 and 2017SGR496]. BR received funding from the National Institutes of Health (R01GM123306). The contents of this article are solely the responsibility of the authors and do not reflect the official views of the National Institutes of Health. LGC-C received from the V Foundation for Cancer Research and from The Auburn Community Cancer Endowed Chair in Basic Science.
dc.language.isoeng
dc.publisherBMC
dc.relation.ispartofseriesBreast Cancer Research;22
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectMama - Càncer
dc.subjectCàncer - Aspectes genètics
dc.subject.meshBreast Neoplasms
dc.subject.meshGenetic Predisposition to Disease
dc.titleHaplotype analysis of the internationally distributed BRCA1 c.3331_3334delCAAG founder mutation reveals a common ancestral origin in Iberia
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1186/s13058-020-01341-3
dc.subject.decsneoplasias de la mama
dc.subject.decspredisposición genética a la enfermedad
dc.relation.publishversionhttps://doi.org/10.1186/s13058-020-01341-3
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[De Asis Tuazon AM, Lott P] Genome Center, University of California Davis, Davis, CA, USA. [Bohórquez M, Benavides J, Ramirez C, Criollo A] Universidad del Tolima, Ibague, Colombia. [Diez O] Grupo de Cáncer Hereditario, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain
dc.identifier.pmid33087180
dc.identifier.wos000580569500001
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/PE2017-2020/PI19%2F00553
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/PE2013-2016/PI16%2F00563
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/PE2013-2016/PI16%2F01898
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/PE2013-2016/SAF2015-68016-R
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/PERIS2016-2020/2017SGR1282
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/PERIS2016-2020/2017SGR496
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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