DNA Methylation Identifies Loci Distinguishing Hereditary Nonpolyposis Colorectal Cancer Without Germ-Line MLH1/MSH2 Mutation from Sporadic Colorectal Cancer

OBJECTIVES: Roughly half of hereditary nonpolyposis colorectal cancer (HNPCC) cases are Lynch syndrome and exhibit germ-line mutations in DNA mismatch repair (MMR) genes; the other half are familial colorectal cancer (CRC) type X (FCCTX) and are MMR proficient. About 70% of Lynch syndrome tumors hav...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Chung-Hsing, Sheng Jiang, Shih, Hsieh, Ling-Ling, Tang, Reiping, Hsiung, Chao A, Tsai, Hui-Ju, Chang, I-Shou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Original Contributions
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288582/
https://www.ncbi.nlm.nih.gov/pubmed/27977020
http://dx.doi.org/10.1038/ctg.2016.59

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288582/
https://www.ncbi.nlm.nih.gov/pubmed/27977020
http://dx.doi.org/10.1038/ctg.2016.59

Ejemplares similares