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Quantitative RT-PCR luminometric hybridization assay with an RNA internal standard for cytokeratin-19 mRNA in peripheral blood of patients with breast cancer

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dc.contributor.author Stathopoulou, A en
dc.contributor.author Angelopoulou, K en
dc.contributor.author Perraki, M en
dc.contributor.author Georgoulias, V en
dc.contributor.author Malamos, N en
dc.contributor.author Lianidou, E en
dc.date.accessioned 2014-03-01T01:50:54Z
dc.date.available 2014-03-01T01:50:54Z
dc.date.issued 2001 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/26168
dc.subject Alkaline Phosphatase en
dc.subject Healthy Volunteer en
dc.subject Internal Standard en
dc.subject Large Scale en
dc.subject Minimal Residual Disease en
dc.subject Peripheral Blood en
dc.subject Peripheral Blood Mononuclear Cell en
dc.subject quantitative rt-pcr en
dc.subject Rna Isolation en
dc.subject Sensitivity and Specificity en
dc.subject Breast Cancer en
dc.subject Healthy Control en
dc.title Quantitative RT-PCR luminometric hybridization assay with an RNA internal standard for cytokeratin-19 mRNA in peripheral blood of patients with breast cancer en
heal.type journalArticle en
heal.identifier.primary 10.1016/S0009-9120(01)00276-4 en
heal.identifier.secondary http://dx.doi.org/10.1016/S0009-9120(01)00276-4 en
heal.publicationDate 2001 en
heal.abstract Objectives: To develop a highly sensitive quantitative RT-PCR hybridization assay for the determination of CK-19 mRNA in peripheral blood of patients with breast cancer.Patients and methods: Quantification of CK-19 mRNA was based on the coamplification of CK-19 mRNA with a recombinant CK-19 RNA internal standard (CK-19 RNA-IS) through RT-PCR. The biotinylated amplification products were immobilized on steptavidin coated wells, hybridized en
heal.journalName Clinical Biochemistry en
dc.identifier.doi 10.1016/S0009-9120(01)00276-4 en


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