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Article

Dominantly Inherited Constitutional Epigenetic Silencing of MLH1 in a Cancer-Affected Family Is Linked to a Single Nucleotide Variant within the 5′UTR

1 Aug 2011

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 21840485
DOI: 10.1016/j.ccr.2011.07.003

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Related research

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Dominantly Inherited Constitutional Epigenetic Silencing of MLH1 in a Cancer-Affected Family Is Linked to a Single Nucleotide Variant within the 5′UTRPMID 21840485Read ↗

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Diversity of genetic events associated with MLH1 promoter methylation in Lynch syndrome families with heritable constitutional epimutation.Semantic proximity Read ↗

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Inheritance of epigenetic aberrations (constitutional epimutations) in cancer susceptibility.Semantic proximity Read ↗

Constitutional epimutation as a mechanism for cancer causality and heritability?Semantic proximity Read ↗

Lynch syndrome associated with two MLH1 promoter variants and allelic imbalance of MLH1 expression.Semantic proximity Read ↗

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