The association between genetic variants in hMLH1 and hMSH2 and the development of sporadic colorectal cancer in the Danish population (Q33343083)

26 July 2017

title

The association between genetic variants in hMLH1 and hMSH2 and the development of sporadic colorectal cancer in the Danish population (English)

1 reference

26 July 2017

0 references

1 reference

Ann-Christine Syvänen

8

Ann-Christine Syvänen

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Anne Tjønneland

6

Anne Tjønneland

1 reference

26 July 2017

Claus Lindbjerg Andersen

Claus L Andersen

9

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Carsten Wiuf

Carsten Wiuf

4

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Anja Olsen

Anja Olsen

7

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author name string

Lise Lotte Christensen

1

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26 July 2017

Bo E Madsen

2

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26 July 2017

Friedrik P Wikman

3

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26 July 2017

Karen Koed

5

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26 July 2017

Torben F Orntoft

10

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26 July 2017

publication date

11 June 2008

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26 July 2017

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26 July 2017

volume

9

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26 July 2017

page(s)

52

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Snap: an integrated SNP annotation platform

26 July 2017

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21 June 2018

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21 June 2018

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Pedigree and genetic analysis of a novel mutation carrier patient suffering from hereditary nonpolyposis colorectal cancer

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HNPCC mutation MLH1 P648S makes the functional protein unstable, and homozygosity predisposes to mild neurofibromatosis type 1.

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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Transient mismatch repair gene transfection for functional analysis of genetic hMLH1 and hMSH2 variants

21 June 2018

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Human non-synonymous SNPs: server and survey

21 June 2018

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21 June 2018

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21 June 2018

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The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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The interaction of the human MutL homologues in hereditary nonpolyposis colon cancer

21 June 2018

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Functional domains of the Saccharomyces cerevisiae Mlh1p and Pms1p DNA mismatch repair proteins and their relevance to human hereditary nonpolyposis colorectal cancer-associated mutations

21 June 2018

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21 June 2018

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Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16

21 June 2018

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Mutational analysis of the hMSH2 gene reveals a three base pair deletion in a family predisposed to colorectal cancer development

21 June 2018

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Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis

21 June 2018

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21 June 2018

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21 June 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Promoter analysis of the human mismatch repair gene hMSH2.

21 January 2018

1 reference

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Germ line mutations of mismatch repair genes in hereditary nonpolyposis colorectal cancer patients with small bowel cancer: International Society for Gastrointestinal Hereditary Tumours Collaborative Study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-9-52

Common variants in mismatch repair genes and risk of invasive ovarian cancer.

21 January 2018

1 reference

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Low allele frequency of MLH1 D132H in American colorectal and endometrial cancer patients

21 January 2018

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Mutator phenotypes of common polymorphisms and missense mutations in MSH2.

21 January 2018

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The colon cancer burden of genetically defined hereditary nonpolyposis colon cancer

21 January 2018

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https://api.crossref.org/works/10.1186%2F1471-2350-9-52

Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: a population-based study in northern Sweden.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-9-52

Novel hMLH1 and hMSH2 germline mutations in African Americans with colorectal cancer

21 January 2018

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Characterization of hereditary nonpolyposis colorectal cancer families from a population-based series of cases

21 January 2018

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DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer

21 January 2018

1 reference

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Mutational analysis of promoters of mismatch repair genes hMSH2 and hMLH1 in hereditary nonpolyposis colorectal cancer and early onset colorectal cancer patients: identification of three novel germ-line mutations in promoter of the hMSH2 gene.

21 January 2018

1 reference

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DGGE screening of mutations in mismatch repair genes (hMSH2 and hMLH1) in 34 Swedish families with colorectal cancer.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2438340

Analysis of mismatch repair genes in hereditary non–polyposis colorectal cancer patients

31 October 2018

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https://api.crossref.org/works/10.1186%2F1471-2350-9-52

Clinical Findings with Implications for Genetic Testing in Families with Clustering of Colorectal Cancer

21 January 2018

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https://api.crossref.org/works/10.1186%2F1471-2350-9-52

Mutation screening in the hMLH1 gene in Swedish hereditary nonpolyposis colon cancer families

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2438340

10 December 2018

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12 December 2020

Presymptomatic diagnosis using a deletion of a single codon in families with hereditary non-polyposis colorectal cancer

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12 December 2020

Functional Significance and Clinical Phenotype of Nontruncating Mismatch Repair Variants of MLH1

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12 December 2020

Single-nucleotide polymorphisms of mismatch repair genes in healthy Chinese individuals and sporadic colorectal cancer patients

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12 December 2020

Hereditary non-polyposis colorectal cancer (HNPCC): phenotype-genotype correlation between patients with and without identified mutation

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12 December 2020

Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability

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12 December 2020

Low frequency of hMSH2 mutations in Swedish HNPCC families

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12 December 2020

MSH2 andMLH1 mutations in sporadic replication error-positive colorectal carcinoma as assessed by two-dimensional DNA electrophoresis

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12 December 2020

MSH2 codon 322 Gly to Asp seems not to confer an increased risk for colorectal cancer susceptibility

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12 December 2020

Identifiers

DOI

10.1186/1471-2350-9-52

1 reference

Dimensions Publication ID

26 July 2017

0 references

1 reference

26 July 2017

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