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Title:Rapid detection of most frequent Slovenian germ-line mutations in BRCA1 gene using real-time PCR and melting curve analysis
Authors:ID Novaković, Srdjan (Author)
ID Stegel, Vida (Author)
Files:.pdf PDF - Presentation file, download (254,79 KB)
MD5: 5F2C0C6CC3E3A191A136CD794DBDF9CE
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo OI - Institute of Oncology
Abstract:Background. Detection of inherited mutations in cancer susceptibility genes isof great importance in some types of cancers including the colorectal cancer(mutations of APC gene in familial adenomatous polyposis -FAP, mutationsin mismatch repair genes in hereditary nonpolyposis colorectal cancer- HNPCC), malignant melanoma (mutations in CDKN2A and CDK4 genes) and breast cancer (mutations in BRCA1 and BRCA2 genes). Methods. This article presents the technical data for the detection of five mutations in BRCA1 gene in breast cancer patients and their relatives. The mutations - 1806C>T, 300T>G, 300T>A, 310G>A, 5382insC -were determined by the real-time PCR and themelting curve analysis. Results and conclusion. In comparison to direct sequencing, this method proved to be sensitive and rapid enough for the routine daily determination of mutations in DNA isolated from the peripheral blood.
Publication status:Published
Publication version:Version of Record
Publication date:01.01.2005
Publisher:Association of Radiology and Oncology
Year of publishing:2005
Number of pages:str. 147-152
Numbering:Letn. 39, št. 2
Source:Ljubljana
PID:20.500.12556/DiRROS-18170 New window
UDC:618
ISSN on article:1318-2099
COBISS.SI-ID:19767769 New window
Copyright:by Authors
Note:BSDOCID115524;
Publication date in DiRROS:14.02.2024
Views:136
Downloads:39
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Record is a part of a journal

Title:Radiology and oncology
Shortened title:Radiol. oncol.
Publisher:Slovenian Medical Society - Section of Radiology, Croatian Medical Association - Croatian Society of Radiology
ISSN:1318-2099
COBISS.SI-ID:32649472 New window

Secondary language

Language:Slovenian
Title:[PCR in analiza talitvene krivulje kot metoda za odkrivanje najpogostejših dednih mutacij v BRCA1 genu pri slovenskih bolnikih]
Abstract:Odkrivanje dednih mutacij v genih, ki so povezani z nastankom raka, napove verjetnost nastanka raka pri nosilcih mutacij in pri njihovih potomcih. Najpogostejše oblike raka, ki so povezane s podedovanimi mutacijami, so črevesni rak (mutacije v APC genu pri bolnikih s familiarno adenomatozno polipozo - FAP, mutacije genov za popravljanje neujemanja pri bolnikih z dednim nepolipoznim črevesnim rakom - HNPCC), maligni melanom (mutacije v CDKN2A in CDK4 genih) in rak dojke (mutacije v BRCA1 in BRCA2 genih). V člankupodajamo osnovne metodološke podatke za odkrivanje petih različnih mutacij v BRCA1 genu pri bolnikih s karcinomom dojke in njihovih sorodnikih. Mutacije 1806C>T, 300T>G, 300T>A, 310G>A, 5382insC smo določali s pomočjo polimerazne verižne reakcije v realnem času in analizo talitvene krivulje. Primerjava z direktnim sekveniranjem je pokazala, da je uporabljena metoda dovolj občutljiva in hitra za dnevno rutinsko določanje mutacij v DNA izolirani iz periferne krvi.


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