Genome-wide copy neutral LOH is infrequent in familial and sporadic microsatellite unstable carcinomas. (Q38426909)

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5 January 2020

title

Genome-wide copy neutral LOH is infrequent in familial and sporadic microsatellite unstable carcinomas (English)

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5 January 2020

4

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Hans Vasen

6

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5 January 2020

Tom Van Wezel

10

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5 January 2020

author name string

Marjo van Puijenbroek

1

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Anneke Middeldorp

2

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Carli M J Tops

3

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5 January 2020

Heleen M van der Klift

5

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Juul Th Wijnen

7

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Frederik J Hes

8

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Jan Oosting

9

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5 January 2020

Hans Morreau

11

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publication date

15 April 2008

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5 January 2020

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5 January 2020

volume

7

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issue

4

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5 January 2020

page(s)

319-330

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https://scigraph.springernature.com/pub.10.1007/s10689-008-9194-8

5 January 2020

exact match

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cites work

Features of colorectal cancers with high-level microsatellite instability occurring in familial and sporadic settings: parallel pathways of tumorigenesis

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Loss or somatic mutations of hMSH2 occur in hereditary nonpolyposis colorectal cancers with hMSH2 germline mutations.

21 January 2018

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

21 January 2018

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Chromosomal imbalances in the colorectal carcinomas with microsatellite instability

21 January 2018

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Bias in detection of instability of the (C)8 mononucleotide repeat of MSH6 in tumours from HNPCC patients

21 January 2018

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12 December 2020

Cloning, characterization and chromosomal assignment of the human genes homologous to yeast PMS1, a member of mismatch repair genes

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12 December 2020

High-resolution analysis of DNA copy number alterations in colorectal cancer by array-based comparative genomic hybridization.

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12 December 2020

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

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Reliable High-Throughput Genotyping and Loss-of-Heterozygosity Detection in Formalin-Fixed, Paraffin-Embedded Tumors Using Single Nucleotide Polymorphism Arrays

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

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12 December 2020

A common genetic risk factor for colorectal and prostate cancer

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Comparative genomic hybridization reveals differences in DNA copy number changes between sporadic gastric carcinomas and gastric carcinomas from patients with hereditary nonpolyposis colorectal cancer

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12 December 2020

Variants on 9p24 and 8q24 are associated with risk of colorectal cancer: results from the Colon Cancer Family Registry

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12 December 2020

Methylation-specific MLPA (MS-MLPA): simultaneous detection of CpG methylation and copy number changes of up to 40 sequences

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Extensive gene conversion at the PMS2 DNA mismatch repair locus

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12 December 2020

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

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Classification of colorectal cancer based on correlation of clinical, morphological and molecular features

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The order of genetic events associated with colorectal cancer progression inferred from meta-analysis of copy number changes

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Analysis of genetic alterations, classified according to their DNA ploidy pattern, in the progression of colorectal adenomas and early colorectal carcinomas

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Trends in right and left-sided colon cancer

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Cancer of the microsatellite mutator phenotype.

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12 December 2020

Microsatellite instability in cancer of the proximal colon

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12 December 2020

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

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12 December 2020

Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis

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12 December 2020

Array comparative genomic hybridization analysis of colorectal cancer cell lines and primary carcinomas

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12 December 2020

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

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12 December 2020

Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome).

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12 December 2020

Different genetic features associated with colon and rectal carcinogenesis.

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12 December 2020

Hypermutability and mismatch repair deficiency in RER+ tumor cells

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12 December 2020

Microsatellite instability, immunohistochemistry, and additional PMS2 staining in suspected hereditary nonpolyposis colorectal cancer

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12 December 2020

Hereditary nonpolyposis colorectal cancer (Lynch syndrome). An updated review

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12 December 2020

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

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12 December 2020

Chromosomal instability in microsatellite-unstable and stable colon cancer

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12 December 2020

Genome-wide differences between microsatellite stable and unstable colorectal tumors.

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12 December 2020

Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24.

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12 December 2020

A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21

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12 December 2020

Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex changes and multiple forms of chromosomal instability in colorectal cancers

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12 December 2020

Genomic organization of the human PMS2 gene family.

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12 December 2020

Causes of microsatellite instability in colorectal tumors

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12 December 2020

No evidence for dual role of loss of heterozygosity in hereditary non-polyposis colorectal cancer

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12 December 2020

High-resolution copy number analysis of paraffin-embedded archival tissue using SNP BeadArrays.

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12 December 2020

Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome

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12 December 2020

Diploid predominance in hereditary nonpolyposis colorectal carcinoma evaluated by flow cytometry

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12 December 2020

DNA ploidy of colorectal carcinoma by tumour site, gender and history of noncolorectal malignancies

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12 December 2020

Mechanisms of oncogenesis in colon versus rectal cancer.

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12 December 2020

Progression and tumor heterogeneity analysis in early rectal cancer.

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12 December 2020

10.1007/S10689-008-9194-8

Identifiers

DOI

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Dimensions Publication ID

5 January 2020

1045983059

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Fatcat ID

release_somw2rz4ijhf3dy7p5zgh6ihbq

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Fatcat

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24 November 2022

mapped directly with Wikidata item

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