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dc.contributor.authorAlvarez, Manuel
dc.contributor.authorCarvallo, Pilar
dc.contributor.authorCamus, Mauricio
dc.contributor.authorMunroe, David
dc.contributor.authorMaass, Alejandro
dc.contributor.authorAlvarez, Carolina
dc.contributor.authorAravena, Andres
dc.contributor.authorTapia, Teresa
dc.contributor.authorRozenblum, Ester
dc.contributor.authorSolis, Luisa
dc.contributor.authorCorvalan, Alejandro
dc.date.accessioned2021-03-05T19:54:49Z
dc.date.available2021-03-05T19:54:49Z
dc.identifier.citationAlvarez C., Aravena A., Tapia T., Rozenblum E., Solis L., Corvalan A., Camus M., Alvarez M., Munroe D., Maass A., et al., "Different Array CGH profiles within hereditary breast cancer tumors associated to BRCA1 expression and overall survival", BMC CANCER, cilt.16, 2016
dc.identifier.issn1471-2407
dc.identifier.othervv_1032021
dc.identifier.otherav_d17e784a-7e10-4d62-b3bd-ad52db529223
dc.identifier.urihttp://hdl.handle.net/20.500.12627/138468
dc.identifier.urihttps://doi.org/10.1186/s12885-016-2261-x
dc.description.abstractBackground: Array CGH analysis of breast tumors has contributed to the identification of different genomic profiles in these tumors. Loss of DNA repair by BRCA1 functional deficiency in breast cancer has been proposed as a relevant contribution to breast cancer progression for tumors with no germline mutation. Identifying the genomic alterations taking place in BRCA1 not expressing tumors will lead us to a better understanding of the cellular functions affected in this heterogeneous disease. Moreover, specific genomic alterations may contribute to the identification of potential therapeutic targets and offer a more personalized treatment to breast cancer patients.
dc.language.isoeng
dc.subjectOnkoloji
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectONKOLOJİ
dc.titleDifferent Array CGH profiles within hereditary breast cancer tumors associated to BRCA1 expression and overall survival
dc.typeMakale
dc.relation.journalBMC CANCER
dc.contributor.departmentPontificia Universidad Catolica de Chile , ,
dc.identifier.volume16
dc.contributor.firstauthorID230984


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