MYH, OGG1, MTH1, and APC alterations involved in the colorectal tumorigenesis of Korean patients with multiple adenomas. (Q54447917)

29 May 2018

title

MYH, OGG1, MTH1, and APC alterations involved in the colorectal tumorigenesis of Korean patients with multiple adenomas. (English)

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29 May 2018

author name string

Jin C Kim

1

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29 May 2018

In H Ka

2

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29 May 2018

Yoo M Lee

3

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29 May 2018

Kum H Koo

4

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29 May 2018

Hee C Kim

5

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29 May 2018

Chang S Yu

6

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29 May 2018

Se J Jang

7

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29 May 2018

Yong S Kim

8

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29 May 2018

Han I Lee

9

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29 May 2018

Kang H Lee

10

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29 May 2018

publication date

25 January 2007

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29 May 2018

published in

Virchows Archiv

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29 May 2018

volume

450

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29 May 2018

issue

3

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29 May 2018

page(s)

311-319

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29 May 2018

https://scigraph.springernature.com/pub.10.1007/s00428-006-0363-6

exact match

0 references

cites work

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Colorectal cancer risk in individuals with biallelic or monoallelic mutations of MYH

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MYH mutations in patients with attenuated and classic polyposis and with young-onset colorectal cancer without polyps

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Autosomal recessive colorectal adenomatous polyposis due to inherited mutations of MYH

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Mutational analysis of OGG1, MYH, MTH1 in FAP, HNPCC and sporadic colorectal cancer patients: R154H OGG1 polymorphism is associated with sporadic colorectal cancer patients.

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Comprehensive analysis of the contribution of germline MYH variation to early-onset colorectal cancer

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Definition of candidate low risk APC alleles in a Swedish population

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The APC tumour suppressor has a nuclear export function.

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Nuclear accumulation of full-length and truncated adenomatous polyposis coli protein in tumor cells depends on proliferation

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Targeted expression of oncogenic K-ras in intestinal epithelium causes spontaneous tumorigenesis in mice

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Biallelic germline mutations in MYH predispose to multiple colorectal adenoma and somatic G:C-->T:A mutations

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Mutations of the APC (adenomatous polyposis coli) gene

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Colorectal cancer with and without microsatellite instability involves different genes

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High frequency of MYH gene mutations in a subset of patients with familial adenomatous polyposis

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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

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Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH

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Germline APC variants in patients with multiple colorectal adenomas, with evidence for the particular importance of E1317Q

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Clinical diagnosis and management of hereditary colorectal cancer syndromes

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10.1007/S00428-006-0363-6

Identifiers

DOI

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29 May 2018

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29 May 2018