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Quoted phrase not found in phrase index: "Genetic mechanisms in the hereditary predisposition to colorectal cancer"
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[Genetic mechanisms in the hereditary predisposition to colorectal cancer].
Alonso A, Moreno S, Valiente A, Artigas M, Pérez-Juana A, Ramos Arroyo MA. Alonso A, et al. An Sist Sanit Navar. 2006 Jan-Apr;29(1):59-76. doi: 10.4321/s1137-66272006000100006. An Sist Sanit Navar. 2006. PMID: 16670730 Free article. Review. Spanish.
A proportion of colorectal cancers shows some type of genetic predisposition that can be recognised in clinical practice. From the classical dominant inheritance pattern of familial adenomatous polyposis or hereditary non-polyposis colorectal …
A proportion of colorectal cancers shows some type of genetic predisposition that can be recognised in clinical practic …
Primary constitutional MLH1 epimutations: a focal epigenetic event.
Dámaso E, Castillejo A, Arias MDM, Canet-Hermida J, Navarro M, Del Valle J, Campos O, Fernández A, Marín F, Turchetti D, García-Díaz JD, Lázaro C, Genuardi M, Rueda D, Alonso Á, Soto JL, Hitchins M, Pineda M, Capellá G. Dámaso E, et al. Br J Cancer. 2018 Oct;119(8):978-987. doi: 10.1038/s41416-018-0019-8. Epub 2018 Oct 4. Br J Cancer. 2018. PMID: 30283143 Free PMC article.
BACKGROUND: Constitutional MLH1 epimutations are characterised by monoallelic methylation of the MLH1 promoter throughout normal tissues, accompanied by allele-specific silencing. The mechanism underlying primary MLH1 epimutations is currently unknown. ...CONCLUSION: Prima …
BACKGROUND: Constitutional MLH1 epimutations are characterised by monoallelic methylation of the MLH1 promoter throughout normal tissues, ac …
NTHL1 biallelic mutations seldom cause colorectal cancer, serrated polyposis or a multi-tumor phenotype, in absence of colorectal adenomas.
Belhadj S, Quintana I, Mur P, Munoz-Torres PM, Alonso MH, Navarro M, Terradas M, Piñol V, Brunet J, Moreno V, Lázaro C, Capellá G, Valle L. Belhadj S, et al. Sci Rep. 2019 Jun 21;9(1):9020. doi: 10.1038/s41598-019-45281-1. Sci Rep. 2019. PMID: 31227763 Free PMC article.
The cancer-predisposing syndrome caused by biallelic mutations in NTHL1 may not be a solely colorectal cancer (CRC) and polyposis syndrome but rather a multi-tumor recessive disease. ...NTHL1 mutational screening was performed in 312 cancer pati …
The cancer-predisposing syndrome caused by biallelic mutations in NTHL1 may not be a solely colorectal cancer (CRC) and …