scholarly article | Q13442814 |
P50 | author | Walter Bodmer | Q7964332 |
Carolina Bonilla | Q55174109 | ||
Jean-François Fléjou | Q72536365 | ||
P2093 | author name string | Florence Coulet | |
Florent Soubrier | |||
Yann Parc | |||
Najat Mourra | |||
Emmanuel Tiret | |||
Jérémie H Lefevre | |||
Chrystelle Colas | |||
P2860 | cites work | Human MutY homolog, a DNA glycosylase involved in base excision repair, physically and functionally interacts with mismatch repair proteins human MutS homolog 2/human MutS homolog 6 | Q24292187 |
Carcinogenesis in MYH-associated polyposis follows a distinct genetic pathway | Q28186388 | ||
BRAF mutation is frequently present in sporadic colorectal cancer with methylated hMLH1, but not in hereditary nonpolyposis colorectal cancer | Q28239788 | ||
Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma | Q29615026 | ||
Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumors and mismatch repair-defective human tumor cell lines | Q29620526 | ||
A founding locus within the RET proto-oncogene may account for a large proportion of apparently sporadic Hirschsprung disease and a subset of cases of sporadic medullary thyroid carcinoma | Q34355050 | ||
Immunohistochemistry for MSH2 and MHL1: a method for identifying mismatch repair deficient colorectal cancer | Q35399001 | ||
BRAF screening as a low-cost effective strategy for simplifying HNPCC genetic testing | Q35446668 | ||
The interacting pathways for prevention and repair of oxidative DNA damage | Q35592880 | ||
Prognostic significance of microsatellite instability determined by immunohistochemical staining of MSH2 and MLH1 in sporadic T3N0M0 colon cancer | Q35596287 | ||
The role of MYH and microsatellite instability in the development of sporadic colorectal cancer | Q36611848 | ||
Inherited variants of MYH associated with somatic G:C-->T:A mutations in colorectal tumors | Q43871566 | ||
The mammalian mismatch repair pathway removes DNA 8-oxodGMP incorporated from the oxidized dNTP pool | Q44025676 | ||
Hypermethylation of the hMLH1 promoter in colon cancer with microsatellite instability | Q47704165 | ||
Gene conversion is a frequent mechanism of inactivation of the wild-type allele in cancers from MLH1/MSH2 deletion carriers. | Q53350238 | ||
Implication of MYH in colorectal polyposis. | Q54451550 | ||
Aberrant splicing in MLH1 and MSH2 due to exonic and intronic variants. | Q54627316 | ||
No evidence for dual role of loss of heterozygosity in hereditary non-polyposis colorectal cancer | Q57567633 | ||
Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancer | Q57568035 | ||
Efficiency of the revised Bethesda guidelines (2003) for the detection of mutations in mismatch repair genes in Austrian HNPCC patients | Q81312576 | ||
Deletions account for 17% of pathogenic germline alterations in MLH1 and MSH2 in hereditary nonpolyposis colorectal cancer (HNPCC) families | Q81826211 | ||
P433 | issue | 4 | |
P921 | main subject | colorectal cancer | Q188874 |
P304 | page(s) | 589-594 | |
P577 | publication date | 2010-12-01 | |
P1433 | published in | Familial Cancer | Q15761917 |
P1476 | title | MYH biallelic mutation can inactivate the two genetic pathways of colorectal cancer by APC or MLH1 transversions. | |
P478 | volume | 9 |