Comprehensive characterization of HNPCC-related colorectal cancers reveals striking molecular features in families with no germline mismatch repair gene mutations. (Q53361302)

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English	Comprehensive characterization of HNPCC-related colorectal cancers reveals striking molecular features in families with no germline mismatch repair gene mutations.	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/15674332

Comprehensive characterization of HNPCC-related colorectal cancers reveals striking molecular features in families with no germline mismatch repair gene mutations. (English)

1 reference

Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/15674332

DNA mismatch repair

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based on heuristic

inferred from title

6

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Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/15674332

Päivi Peltomäki

8

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Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/15674332

Wael M Abdel-Rahman

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Wael M Abdel-Rahman

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Miina Ollikainen

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Miina Ollikainen

2

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Jukka-Pekka Mecklin

5

object named as

Jukka-Pekka Mecklin

1 reference

Europe PubMed Central

PubMed publication ID

13 May 2018

author name string

Reetta Kariola

3

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Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/15674332

Heikki J Järvinen

4

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Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/15674332

Sakari Knuutila

7

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Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/15674332

language of work or name

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1 February 2005

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Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/15674332

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Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/15674332

24

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Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/15674332

9

1 reference

Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/15674332

1542-1551

1 reference

Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/15674332

Spectral karyotyping suggests additional subsets of colorectal cancers characterized by pattern of chromosome rearrangement.

1 reference

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21 January 2018

CDX2 is mutated in a colorectal cancer with normal APC/beta-catenin signaling

1 reference

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21 January 2018

BRAF mutation is frequently present in sporadic colorectal cancer with methylated hMLH1, but not in hereditary nonpolyposis colorectal cancer

1 reference

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21 January 2018

Accumulated clonal genetic alterations in familial and sporadic colorectal carcinomas with widespread instability in microsatellite sequences

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21 January 2018

Beta-catenin expression and allelic loss at APC in sporadic colorectal carcinogenesis.

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21 January 2018

Silencing of CDX2 expression in colon cancer via a dominant repression pathway

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21 January 2018

Loss of CDX2 expression and microsatellite instability are prominent features of large cell minimally differentiated carcinomas of the colon

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21 January 2018

APC mutations in colorectal tumors with mismatch repair deficiency

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21 January 2018

Beta-catenin mutations in cell lines established from human colorectal cancers

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21 January 2018

Expression of beta-catenin and full-length APC protein in normal and neoplastic colonic tissues.

1 reference

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21 January 2018

Molecular nature of colon tumors in hereditary nonpolyposis colon cancer, familial polyposis, and sporadic colon cancer.

1 reference

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21 January 2018

Endometrial and colorectal tumors from patients with hereditary nonpolyposis colon cancer display different patterns of microsatellite instability

1 reference

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21 January 2018

Activating BRAF and N-Ras mutations in sporadic primary melanomas: an inverse association with allelic loss on chromosome 9.

1 reference

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21 January 2018

Genetic instability in colorectal cancers

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1208387

21 January 2018

APC and CTNNB1 mutations in a large series of sporadic colorectal carcinomas stratified by the microsatellite instability status.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1208387

21 January 2018

Activation of beta-catenin-Tcf signaling in colon cancer by mutations in beta-catenin or APC

1 reference

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21 January 2018

Founding mutations and Alu-mediated recombination in hereditary colon cancer

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Role of DNA mismatch repair defects in the pathogenesis of human cancer

1 reference

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21 January 2018

Expression of CDX2 in normal and neoplastic human colon tissue and during differentiation of an in vitro model system

1 reference

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21 January 2018

APC mutations in sporadic colorectal tumors: A mutational "hotspot" and interdependence of the "two hits"

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1208387

21 January 2018

New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1208387

21 January 2018

Surfing the p53 network

1 reference

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21 January 2018

CDX2, a human homologue of Drosophila caudal, is mutated in both alleles in a replication error positive colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1208387

21 January 2018

Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1208387

21 January 2018

Genomic structure and alterations of homeobox gene CDX2 in colorectal carcinomas

1 reference

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21 January 2018

Early-onset colorectal cancer with stable microsatellite DNA and near-diploid chromosomes

1 reference

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21 January 2018

A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: Meeting Highlights and Bethesda Guidelines

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1208387

21 January 2018

BRAF mutations characterize colon but not gastric cancer with mismatch repair deficiency

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1208387

21 January 2018

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

1 reference

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21 January 2018

p53 gene point mutations in relation to p53 nuclear protein accumulation in colorectal cancers

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1208387

7 January 2021

based on heuristic

inferred from DOI database lookup

Specific patterns of chromosomal abnormalities are associated with RER status in sporadic colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1208387

7 January 2021

based on heuristic

inferred from DOI database lookup

Predominance of normal karyotype in colorectal tumors from hereditary non-polyposis colorectal cancer patients

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1208387

7 January 2021

based on heuristic

inferred from DOI database lookup

Colorectal cancer with and without microsatellite instability involves different genes

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1208387

7 January 2021

based on heuristic

inferred from DOI database lookup

The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1208387

7 January 2021

based on heuristic

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Identifiers

10.1038/SJ.ONC.1208387

1 reference

Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/15674332

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/15674332

ResearchGate publication ID

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