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 |