(Q33270665)

24 July 2017

Mechanisms of inactivation of MLH1 in hereditary nonpolyposis colorectal carcinoma: a novel approach (English)

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24 July 2017

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3

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24 July 2017

5

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24 July 2017

M Ollikainen

1

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24 July 2017

U Hannelius

series ordinal

2

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24 July 2017

W M Abdel-Rahman

series ordinal

4

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24 July 2017

P Peltomäki

series ordinal

6

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24 July 2017

language of work or name

English

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publication date

29 January 2007

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24 July 2017

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24 July 2017

26

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24 July 2017

31

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24 July 2017

4541-4549

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https://scigraph.springernature.com/pub.10.1038/sj.onc.1210236

24 July 2017

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cites work

Mutation cluster region, association between germline and somatic mutations and genotype-phenotype correlation in upper gastrointestinal familial adenomatous polyposis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

Genetic and epigenetic modification of MLH1 accounts for a major share of microsatellite-unstable colorectal cancers

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

A naturally occurring hPMS2 mutation can confer a dominant negative mutator phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

Mutations associated with HNPCC predisposition -- Update of ICG-HNPCC/INSiGHT mutation database

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

Mass spectrometry-based loss of heterozygosity analysis of single-nucleotide polymorphism loci in paraffin embedded tumors using the MassEXTEND assay: single-nucleotide polymorphism loss of heterozygosity analysis of the protein tyrosine phosphatase

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

The 'just-right' signaling model: APC somatic mutations are selected based on a specific level of activation of the beta-catenin signaling cascade.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Methylation-induced G2/M arrest requires a full complement of the mismatch repair protein hMLH1

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Hereditary and somatic DNA mismatch repair gene mutations in sporadic endometrial carcinoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Analysis of artificially degraded DNA using STRs and SNPs--results of a collaborative European (EDNAP) exercise.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

DNA methylation patterns in hereditary human cancers mimic sporadic tumorigenesis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

MLH1 promoter hypermethylation is associated with the microsatellite instability phenotype in sporadic endometrial carcinomas

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Reduced frequency of extracolonic cancers in hereditary nonpolyposis colorectal cancer families with monoallelic hMLH1 expression

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Mutation and cancer: statistical study of retinoblastoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Prediction of the coding sequences of unidentified human genes. XIX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Founding mutations and Alu-mediated recombination in hereditary colon cancer

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Molecular identification and characterization of a family of kinases with homology to Ca2+/calmodulin-dependent protein kinases I/IV

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Molecular Analysis of Familial Endometrial Carcinoma: A Manifestation of Hereditary Nonpolyposis Colorectal Cancer or a Separate Syndrome?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Genotype and phenotype in hereditary nonpolyposis colon cancer: a study of families with different vs. shared predisposing mutations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Causes of microsatellite instability in colorectal tumors

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Altered Expression of MLH1, MSH2, and MSH6 in Predisposition to Hereditary Nonpolyposis Colorectal Cancer

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Dual role of LOH at MMR loci in hereditary non-polyposis colorectal cancer?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Rapid identification of 14-3-3-binding proteins by protein microarray analysis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

MLH1 promoter methylation and gene silencing is the primary cause of microsatellite instability in sporadic endometrial cancers

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Stac, a novel neuron-specific protein with cysteine-rich and SH3 domains

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Roles of MGMT and MLH1 proteins in alkylation-induced apoptosis and mutagenesis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Tumorigenesis in colorectal tumors from patients with hereditary non-polyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

CpG island methylator phenotype in colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Influence of template DNA degradation on the genotyping of SNPs and STR polymorphisms from forensic materials by PCR

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Biallelic inactivation of hMLH1 by epigenetic gene silencing, a novel mechanism causing human MSI cancers.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

The role of hypermethylation of the hMLH1 promoter region in HNPCC versus MSI+ sporadic colorectal cancers

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Familial endometrial cancer in female carriers of MSH6 germline mutations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Germline, somatic and epigenetic events underlying mismatch repair deficiency in colorectal and HNPCC-related cancers.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Gene conversion is a frequent mechanism of inactivation of the wild-type allele in cancers from MLH1/MSH2 deletion carriers.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210236

7 January 2021

Identifiers

DOI

10.1038/SJ.ONC.1210236

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Dimensions Publication ID

24 July 2017

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