Heritable germline epimutation of MSH2 in a family with hereditary nonpolyposis colorectal cancer. - Test2 - elhamkhani - TriplyDB

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

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

http://www.wikidata.org/entity/Q34563305

about

BRCA1 promoter methylation in peripheral blood DNA of mutation negative familial breast cancer patients with a BRCA1 tumour phenotype Epimutation and cancer: a new carcinogenic mechanism of Lynch syndrome (Review)Epigenetics of colorectal cancer A decade of exploring the cancer epigenome - biological and translational implications Hybrid vigor and transgenerational epigenetic effects on early mouse embryo phenotype Microsatellite instability in colorectal cancer Epigenetic changes during disease progression in a murine model of human chronic lymphocytic leukemia The clinical value of aberrant epigenetic changes of DNA damage repair genes in human cancer Molecular approach to genetic and epigenetic pathogenesis of early-onset colorectal cancer Carcinogenesis and microsatellite instability: the interrelationship between genetics and epigenetics Allele-specific chromatin immunoprecipitation studies show genetic influence on chromatin state in human genome Evidence for transgenerational transmission of epigenetic tumor susceptibility in Drosophila Dnmt3b promotes tumorigenesis in vivo by gene-specific de novo methylation and transcriptional silencing Coevolution between simple sequence repeats (SSRs) and virus genome size Environmental epigenomics and disease susceptibility An Sp1/Sp3 binding polymorphism confers methylation protection.Human placental-specific epipolymorphism and its association with adverse pregnancy outcomes Natural single-nucleosome epi-polymorphisms in yeast.LINE-1 methylation is inherited in familial testicular cancer kindreds.Allele-specific CDH1 downregulation and hereditary diffuse gastric cancer.Performance of clinical guidelines compared with molecular tumour screening methods in identifying possible Lynch syndrome among colorectal cancer patients: a Norwegian population-based study Correlation of global and gene-specific DNA methylation in maternal-infant pairs.Constitutional promoter methylation and risk of familial melanoma Somatic hypermethylation of MSH2 is a frequent event in Lynch Syndrome colorectal cancers A DNA methyltransferase inhibitor and all-trans retinoic acid reduce oral cavity carcinogenesis induced by the carcinogen 4-nitroquinoline 1-oxide.Epigenome mapping in normal and disease States.Application of molecular diagnostics for the detection of Lynch syndrome.Differential Features of Microsatellite-Unstable Colorectal Carcinomas Depending on EPCAM Expression Status.EPCAM germ line deletions as causes of Lynch syndrome in Spanish patients Epigenetics in sports.Differential MSH2 promoter methylation in blood cells of Neurofibromatosis type 1 (NF1) patients Epigenetic remodelling and dysregulation of DLGAP4 is linked with early-onset cerebellar ataxia Germline allele-specific expression of DAPK1 in chronic lymphocytic leukemia.Scrutinizing the epigenetics revolution.Genome-wide epigenetic modifications in cancer.Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated Lynch syndrome cases.The A/G allele of rs16906252 predicts for MGMT methylation and is selectively silenced in premalignant lesions from smokers and in lung adenocarcinomas.Integrative analysis of hereditary nonpolyposis colorectal cancer: the contribution of allele-specific expression and other assays to diagnostic algorithms.Environmental epigenetics Germline variants in POLE are associated with early onset mismatch repair deficient colorectal cancer

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P2860

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

http://www.wikidata.org/entity/Q34563305

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2006 nî lūn-bûn

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2006 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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Heritable germline epimutation ...... onpolyposis colorectal cancer.

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Heritable germline epimutation ...... onpolyposis colorectal cancer.

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Heritable germline epimutation ...... onpolyposis colorectal cancer.

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Heritable germline epimutation ...... onpolyposis colorectal cancer.

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Heritable germline epimutation ...... onpolyposis colorectal cancer.

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Heritable germline epimutation ...... onpolyposis colorectal cancer.

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Nature Genetics

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Heritable germline epimutation ...... onpolyposis colorectal cancer.

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P2093

Annie S Y Chan

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Chi Kwan Kong

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Michelle W S Lo

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Siu Tsan Yuen

http://www.w3.org/2001/XMLSchema#string

Suet Yi Leung

http://www.w3.org/2001/XMLSchema#string

Tsun Leung Chan

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Vivian S W Li

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Wai Fu Ng

http://www.w3.org/2001/XMLSchema#string

Wai Yin Tsui

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Wing Yip Tam

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P2860

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma

An epigenetic mutation responsible for natural variation in floral symmetry.

MSH2 c.1452-1455delAATG is a founder mutation and an important cause of hereditary nonpolyposis colorectal cancer in the southern Chinese population.

Downregulation of ID4 by promoter hypermethylation in gastric adenocarcinoma.

Epigenetic reprogramming in mammals.

Proximal adenomas in hereditary non-polyposis colorectal cancer are prone to rapid malignant transformation

Epigenetic germline inheritance.

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

Germline epimutation of MLH1 in individuals with multiple cancers.

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1178-1183

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10.1038/NG1866

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10

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38

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2006-09-03T00:00:00Z

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6837667

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16951683

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colorectal cancer