Title
[Molecular research methods in the detection of germinal mutations in hereditary colorectal cancer]
Other title
Metodos de investigacion molecular en la deteccion de mutaciones germinativas en cancer colorrectal hereditario
Date Issued
01 January 2009
Access level
metadata only access
Resource Type
review
Author(s)
Bastos E.P.
Silva S.D.
Rossi B.M.
Hospital A.C. Camargo
Abstract
Colorectal cancer (CRC) is one of the main causes of death in South American countries. The hereditary forms of CRC are, familial adenomatous (FAP) and hereditary nonpolyposis colorectal cancer (HNPCC) or Lynch Syndrome (LS), which is the most common form. The detection of mutations in the DNA repair genes (MMR) and in the APC genes enables the development of prevention strategies. Some of these methods for molecular diagnosis are applied in research and the detection of mutations of these genes, such as the partial thromboplastin time test (PTT), the single strand conformational polymorphism test (SSCP), the Denaturing High Performance Liquid Chromatography test (DHPLC) and the Polymerase Chain Reaction (PCR) in real time (qPCR).
Start page
247
End page
253
Volume
29
Issue
3
Language
Spanish
OCDE Knowledge area
Gastroenterología, Hepatología Oncología
Scopus EID
2-s2.0-79958100764
PubMed ID
Source
Revista de gastroenterología del Perú : órgano oficial de la Sociedad de Gastroenterología del Perú
ISSN of the container
10225129
Sources of information: Directorio de Producción Científica Scopus