Carlos Mario Muñetón-Peña
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Carlos Mario Muñetón-Peña has a total of 8 co-authors. Here are the top co-authors by number of shared publications:
E. Ahumada-Rodríguez
Departamento de Patología, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia
1 shared publicationGabriel Bedoya B
Universidad de Antioquía, Medellín, Colombia
1 shared publicationH. Ceballos-García
1 shared publicationJosé Luis Ramírez-Castro
Universidad de Antioquía, Medellín, Colombia
1 shared publicationK.A. Palacio-Rúa
Unidad de Genética Médica, Departamento de Pediatría, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia
1 shared publicationL.F. Isaza-Jiménez
Departamento de Cirugía, Facultad de Medicina, Universidad de Antioquia, Hospital San Vicente de Paúl, Medellín, Colombia
1 shared publication
Latest Publications
- Open Access
- 1 April 2014
- Published by Elsevier in Revista de Gastroenterología de México
- Vol. 79 (2) , 79-89
Análisis genético en APC, KRAS y TP53 en pacientes con cáncer de estómago y colon
- 1 April 2014
- Published by Elsevier in Revista de Gastroenterología de México
- Vol. 79 (2) , 79-89
Open AccessAnálisis genético en APC, KRAS y TP53 en pacientes con cáncer de estómago y colon
- Open Access
- 1 October 2006
- Published by SciELO Agencia Nacional de Investigacion y Desarrollo (ANID) in Revista médica de Chile
- Vol. 134 (10) , 1221-1229
Análisis genético en pacientes con cáncer colorrectal
In patients with colorectal carcinoma, insertions or deletions of short sequences of DNA, a phenomenon called microsatellite instability, are observed. To look for microsatellite instability and mutations of MLH1 and MSH2 gene mutations in patients with colorectal carcinoma. Ten patients with sporadic colorectal carcinoma and 31 patients fulfilling criteria for hereditary nonpolyposis colon cancer (HNPCC), aged 9 to 70 years, were studied. Microsatellite instability was studied in samples of tumor and peripheral blood mononuclear cell DNA. Six markers were amplified by polymerase chain reaction and capillary electrophoresis. In samples with microsatellite instability, mutations of MLH1 and MSH2 genes were studied by direct sequencing. Thirty four percent of patients had microsatellite instability and among these, 76% had a high degree of instability. BAT40 marker had the higher frequency of instability. No mutations for MLH1 and MSH2 genes were observed. However a new polymorphism, C399T, was identified in exon 3 of MSH2 gene. This polymorphism was observed both in patients with sporadic colorectal carcinoma and patients with HNPCC. There is a high frequency of microsatellite instability among patients with colorectal cancer. A new polymorphism, not previously reported, was identified in MSH2 gene.
- 1 October 2006
- Published by SciELO Agencia Nacional de Investigacion y Desarrollo (ANID) in Revista médica de Chile
- Vol. 134 (10) , 1221-1229
Open AccessAnálisis genético en pacientes con cáncer colorrectal
In patients with colorectal carcinoma, insertions or deletions of short sequences of DNA, a phenomenon called microsatellite instability, are observed. To look for microsatellite instability and mutations of MLH1 and MSH2 gene mutations in patients with colorectal carcinoma. Ten patients with sporadic colorectal carcinoma and 31 patients fulfilling criteria for hereditary nonpolyposis colon cancer (HNPCC), aged 9 to 70 years, were studied. Microsatellite instability was studied in samples of tumor and peripheral blood mononuclear cell DNA. Six markers were amplified by polymerase chain reaction and capillary electrophoresis. In samples with microsatellite instability, mutations of MLH1 and MSH2 genes were studied by direct sequencing. Thirty four percent of patients had microsatellite instability and among these, 76% had a high degree of instability. BAT40 marker had the higher frequency of instability. No mutations for MLH1 and MSH2 genes were observed. However a new polymorphism, C399T, was identified in exon 3 of MSH2 gene. This polymorphism was observed both in patients with sporadic colorectal carcinoma and patients with HNPCC. There is a high frequency of microsatellite instability among patients with colorectal cancer. A new polymorphism, not previously reported, was identified in MSH2 gene.