Mutations and epimutations in the origin of cancer (Q37969849)

26 August 2017

title

Mutations and epimutations in the origin of cancer (English)

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26 August 2017

Päivi Peltomäki

1

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language of work or name

English

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publication date

13 December 2011

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Experimental Cell Research

26 August 2017

published in

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26 August 2017

volume

318

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26 August 2017

issue

4

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26 August 2017

page(s)

299-310

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Inherited susceptibility to common cancers

26 August 2017

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Genome-wide profiling of histone h3 lysine 4 and lysine 27 trimethylation reveals an epigenetic signature in prostate carcinogenesis

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A comprehensive catalogue of somatic mutations from a human cancer genome

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Interplay between microRNAs and the epigenetic machinery: an intricate network

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Germline epigenetic silencing of the tumor suppressor gene PTPRJ in early-onset familial colorectal cancer

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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′UTR

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Large genomic rearrangements and germline epimutations in Lynch syndrome

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Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome

7 January 2021

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Germline epigenetic regulation of KILLIN in Cowden and Cowden-like syndrome

7 January 2021

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Germline and somatic DNA methylation and epigenetic regulation of KILLIN in renal cell carcinoma.

7 January 2021

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MLH1 Germline Epimutations as a Factor in Hereditary Nonpolyposis Colorectal Cancer

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Inheritance of a Cancer-AssociatedMLH1Germ-Line Epimutation

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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Distinct genetic and epigenetic signatures of colorectal cancers according to ethnic origin

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Profiling CpG island field methylation in both morphologically normal and neoplastic human colonic mucosa

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Sequential DNA methylation changes are associated with DNMT3B overexpression in colorectal neoplastic progression

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7 January 2021

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7 January 2021

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7 January 2021

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Positional cloning of the gene for multiple endocrine neoplasia-type 1

7 January 2021

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Constitutional mutations of the hSNF5/INI1 gene predispose to a variety of cancers

7 January 2021

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Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer

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Growing Y-junction carbon nanotubes

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Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease

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Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss

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7 January 2021

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Epigenetic inactivation of the Sotos overgrowth syndrome gene histone methyltransferase NSD1 in human neuroblastoma and glioma

7 January 2021

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ARID1A mutations in endometriosis-associated ovarian carcinomas

7 January 2021

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Somatic mutations of the histone methyltransferase gene EZH2 in myelodysplastic syndromes

7 January 2021

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Deregulation of H3K27 methylation in cancer

7 January 2021

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

7 January 2021

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Deletions removing the last exon of TACSTD1 constitute a distinct class of mutations predisposing to Lynch syndrome.

7 January 2021

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Allele-specific CDH1 downregulation and hereditary diffuse gastric cancer

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Mutation of the DNA methyltransferase (DNMT) 1 gene in human colorectal cancers.

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DNMT3A Mutations in Acute Myeloid Leukemia

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Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma

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Frequent alteration of MLL3 frameshift mutations in microsatellite deficient colorectal cancer

7 January 2021

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Menin, the product of the MEN1 gene, is a nuclear protein

7 January 2021

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DAXX/ATRX, MEN1, and mTOR pathway genes are frequently altered in pancreatic neuroendocrine tumors

7 January 2021

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Candidate tumor suppressor RIZ is frequently involved in colorectal carcinogenesis

7 January 2021

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Tumor formation and inactivation of RIZ1, an Rb-binding member of a nuclear protein-methyltransferase superfamily

7 January 2021

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Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin

7 January 2021

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Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes

7 January 2021

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CREBBP mutations in relapsed acute lymphoblastic leukaemia

7 January 2021

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Inactivating mutations of acetyltransferase genes in B-cell lymphoma

7 January 2021

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Mutations truncating the EP300 acetylase in human cancers

7 January 2021

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A role for p300/CREB binding protein genes in promoting cancer progression in colon cancer cell lines with microsatellite instability

7 January 2021

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A truncating mutation of HDAC2 in human cancers confers resistance to histone deacetylase inhibition

7 January 2021

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Genomic analysis using high-density single nucleotide polymorphism-based oligonucleotide arrays and multiplex ligation-dependent probe amplification provides a comprehensive analysis of INI1/SMARCB1 in malignant rhabdoid tumors

7 January 2021

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Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma

7 January 2021

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https://api.crossref.org/works/10.1016/J.YEXCR.2011.12.001

Frequent mutations of chromatin remodeling gene ARID1A in ovarian clear cell carcinoma

7 January 2021

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10.1016/J.YEXCR.2011.12.001

7 January 2021

Identifiers

DOI

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26 August 2017

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