Further evidence for heritability of an epimutation in one of 12 cases with MLH1 promoter methylation in blood cells clinically displaying HNPCC (Q80776609)

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scientific article published on 27 February 2008

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English	Further evidence for heritability of an epimutation in one of 12 cases with MLH1 promoter methylation in blood cells clinically displaying HNPCC	scientific article published on 27 February 2008

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3 January 2020

Further evidence for heritability of an epimutation in one of 12 cases with MLH1 promoter methylation in blood cells clinically displaying HNPCC (English)

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Elke Holinski-Feder

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Elke Holinski-Feder

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Brigitte Royer-Pokora

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Brigitte Royer-Pokora

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Monika Morak

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Hans Konrad Schackert

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Nils Rahner

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Beate Betz

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Matthias Ebert

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Constanze Walldorf

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Karsten Schulmann

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Magnus von Knebel-Doeberitz

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Wolfgang Dietmaier

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Gisela Keller

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Brigitte Kerker

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Gertraud Leitner

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publication date

27 February 2008

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European Journal of Human Genetics

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804-811

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7

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3 January 2020

https://scigraph.springernature.com/pub.10.1038/ejhg.2008.25

0 references

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

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

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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%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

Imprinting mechanisms.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

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Densely methylated MLH1 promoter correlates with decreased mRNA expression in sporadic colorectal cancers

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

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%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

Distinct methylation pattern and microsatellite instability in sporadic gastric cancer

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

Transcriptional regulation of the mismatch repair gene hMLH1

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

CpG island methylator phenotype in colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

The epigenetics of colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

Germline epimutation of MLH1 in individuals with multiple cancers.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

Extensive but hemiallelic methylation of the hMLH1 promoter region in early-onset sporadic colon cancers with microsatellite instability.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

MLH1 Germline Epimutations as a Factor in Hereditary Nonpolyposis Colorectal Cancer

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

MLH1 germline epimutations in selected patients with early-onset non-polyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

Inheritance of a Cancer-AssociatedMLH1Germ-Line Epimutation

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

Hereditary non-polyposis colorectal cancer: clinical and molecular evidence for a new entity of hereditary colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

Deletions account for 17% of pathogenic germline alterations in MLH1 and MSH2 in hereditary nonpolyposis colorectal cancer (HNPCC) families

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

Methylation in hMLH1 promoter interferes with its binding to transcription factor CBF and inhibits gene expression

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

'Touchdown' PCR to circumvent spurious priming during gene amplification

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

The epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

MS-MLPA: an attractive alternative laboratory assay for robust, reliable, and semiquantitative detection of MGMT promoter hypermethylation in gliomas

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

A core promoter and a frequent single-nucleotide polymorphism of the mismatch repair gene hMLH1.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

MethPrimer: designing primers for methylation PCRs

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

EMBOSS: the European Molecular Biology Open Software Suite

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

The human genome browser at UCSC

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

Extensive methylation of hMLH1 promoter region predominates in proximal colon cancer with microsatellite instability.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

Demethylation of the zygotic paternal genome

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

Genomic imprinting: parental influence on the genome

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

Evolution of imprinting mechanisms: the battle of the sexes begins in the zygote

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

Heritable germline epimutation of MSH2 in a family with hereditary nonpolyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

Addendum: Germline epimutation of MLH1 in individuals with multiple cancers

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

CpG island methylator phenotype in cancer

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

Genotype-phenotype comparison of German MLH1 and MSH2 mutation carriers clinically affected with Lynch syndrome: a report by the German HNPCC Consortium.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.25

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/EJHG.2008.25

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18301449%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18301449%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

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