(Q57316220)

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Molecular characterization of the spectrum of genomic deletions in the mismatch repair genesMSH2,MLH1,MSH6, andPMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC)

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scholarly article

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Molecular characterization of the spectrum of genomic deletions in the mismatch repair genesMSH2,MLH1,MSH6, andPMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC) (English)

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cancer research

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colorectal cancer

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colorectal carcinoma

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DNA mismatch repair

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object named as

John Burn

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object named as

Riccardo Fodde

18

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object named as

Hans Vasen

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William David Foulkes

object named as

William Foulkes

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object named as

Pal Moller

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author name string

Heleen van der Klift

1

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Juul Wijnen

2

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Anja Wagner

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Paul Verkuilen

4

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Carli Tops

5

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Robyn Otway

6

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Maija Kohonen-Corish

7

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Cristina Oliani

9

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Daniela Barana

10

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Celia DeLozier-Blanchet

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Pierre Hutter

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Henry Lynch

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Gabriela Möslein

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publication date

2005

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Genes, Chromosomes and Cancer

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44

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123-138

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2

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Cancer risk in mutation carriers of DNA-mismatch-repair genes

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https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Spectrum of genetic alterations in Muir-Torre syndrome is the same as in HNPCC

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https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer.

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https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

based on heuristic

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Diet and cancer prevention: the Concerted Action Polyp Prevention (CAPP) Studies

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https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

based on heuristic

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Unequal homologous recombination between LINE-1 elements as a mutational mechanism in human genetic disease

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https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Topoisomerase-I- and Alu-mediated genomic deletions of the APC gene in familial adenomatous polyposis.

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https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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A novel germline 1.8-kb deletion of hMLH1 mimicking alternative splicing: a founder mutation in the Chinese population

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https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Prediction of a mismatch repair gene defect by microsatellite instability and immunohistochemical analysis in endometrial tumours from HNPCC patients

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https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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

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https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Screening for genomic rearrangements of the MMR genes must be included in the routine diagnosis of HNPCC.

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https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer

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https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach

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https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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The molecular basis of Turcot's syndrome

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https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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PMS2 mutations in HNPCC

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https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Genome maintenance mechanisms for preventing cancer

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https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Revision of consensus sequence of human Alu repeats--a review

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https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Chromosome 2p linkage analysis in hereditary non-polyposis colon cancer

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https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Evolutionary analyses of the human genome

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https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Hereditary nonpolyposis colorectal cancer (HNPCC).

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

based on heuristic

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A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United States

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

based on heuristic

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Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Identification and characterization of genomic rearrangements of MSH2 and MLH1 in Lynch syndrome (HNPCC) by novel techniques

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

based on heuristic

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Mismatch repair gene PMS2: disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Recombination at the human alpha-globin gene cluster: sequence features and topological constraints

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

based on heuristic

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Mutations of two PMS homologues in hereditary nonpolyposis colon cancer

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Founding mutations and Alu-mediated recombination in hereditary colon cancer

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Evaluation of enzymatic mutation detectiontrade mark in hereditary nonpolyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Mutations predisposing to hereditary nonpolyposis colorectal cancer: Database and results of a collaborative study. The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

based on heuristic

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Genomic rearrangements of hMSH6 contribute to the genetic predisposition in suspected hereditary non-polyposis colorectal cancer syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

based on heuristic

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One short well conserved region of Alu-sequences is involved in human gene rearrangements and has homology with prokaryotic chi.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

based on heuristic

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LINE-1 elements at the sites of molecular rearrangements in Alport syndrome-diffuse leiomyomatosis

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Relevance of sequence and structure elements for deletion events in the dystrophin gene major hot-spot

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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The origin of interspersed repeats in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Molecular cloning of cDNA for the carcinoma-associated antigen GA733-2.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrent deletions by MLPA.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Hereditary non-polyposis colorectal cancer and the role of hPMS2 and hEXO1 mutations

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

based on heuristic

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Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

based on heuristic

inferred from DOI database lookup

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/10.1002%2FGCC.20219

7 January 2021

based on heuristic

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Different molecular mechanisms underlie genomic deletions in the MLH1 Gene.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

based on heuristic

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Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

based on heuristic

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A 10-Mb paracentric inversion of chromosome arm 2p inactivatesMSH2 and is responsible for hereditary nonpolyposis colorectal cancer in a North-American kindred

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

based on heuristic

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Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

based on heuristic

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Hereditary nonpolyposis colorectal cancer: frequent occurrence of large genomic deletions in MSH2 and MLH1 genes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

based on heuristic

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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/10.1002%2FGCC.20219

7 January 2021

based on heuristic

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MSH2 genomic deletions are a frequent cause of HNPCC

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Familial endometrial cancer in female carriers of MSH6 germline mutations

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Conversion of diploidy to haploidy

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20219

7 January 2021

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Identifiers

10.1002/GCC.20219

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