Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient
about
Dynamic DNA methylation in the brain: a new epigenetic mark for experience-dependent plasticityNew answers to old questions from genome-wide maps of DNA methylation in hematopoietic cellsAbnormalities of the DNA methylation mark and its machinery: an emerging cause of neurologic dysfunctionA Novel Mutation in a Critical Region for the Methyl Donor Binding in DNMT3B Causes Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome (ICF).Germline genes hypomethylation and expression define a molecular signature in peripheral blood of ICF patients: implications for diagnosis and etiology.DNA methylation modulates HRES1/p28 expression in B cells from patients with Lupus.ICF-specific DNMT3B dysfunction interferes with intragenic regulation of mRNA transcription and alternative splicing.New strategy to control cell migration and metastasis regulated by CCN2/CTGF.Aberrant signature methylome by DNMT1 hot spot mutation in hereditary sensory and autonomic neuropathy 1EAcute hypersensitivity of pluripotent testicular cancer-derived embryonal carcinoma to low-dose 5-aza deoxycytidine is associated with global DNA Damage-associated p53 activation, anti-pluripotency and DNA demethylation.TET proteins and the control of cytosine demethylation in cancer.Understanding the relationship between DNA methylation and histone lysine methylation.Post-conversion targeted capture of modified cytosines in mammalian and plant genomes.Genome-Wide DNA Methylation Analysis Identifies Novel Hypomethylated Non-Pericentromeric Genes with Potential Clinical Implications in ICF Syndrome.Evaluation of single CpG sites as proxies of CpG island methylation states at the genome scale.Characterization and rescue of telomeric abnormalities in ICF syndrome type I fibroblasts.Regionally specific and genome-wide analyses conclusively demonstrate the absence of CpG methylation in human mitochondrial DNA.TET1 inhibits gastric cancer growth and metastasis by PTEN demethylation and re-expressionGenetic syndromes caused by mutations in epigenetic genes.Epigenetic biomarkers in laboratory diagnostics: emerging approaches and opportunities.Epigenetic profiling joins personalized cancer medicine.Non-coding RNAs in chromatin disease involving neurological defectsDevelopmental ORIgins of Healthy and Unhealthy AgeiNg: the role of maternal obesity--introduction to DORIAN.Genetic alterations of DNA methylation machinery in human diseases.A DNA methylation map of human cancer at single base-pair resolution.Dissecting Epigenetic Dysregulation of Primary Antibody Deficiencies.Validation of a DNA methylation microarray for 850,000 CpG sites of the human genome enriched in enhancer sequences.Induced pluripotent stem cells as a model for telomeric abnormalities in ICF type I syndrome.Converging disease genes in ICF syndrome: ZBTB24 controls expression of CDCA7 in mammals.No evidence for cumulative effects in a Dnmt3b hypomorph across multiple generations.Developmentally linked human DNA hypermethylation is associated with down-modulation, repression, and upregulation of transcription.
P2860
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P2860
Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient
description
2012 nî lūn-bûn
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2012年の論文
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2012年論文
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2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
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2012年论文
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2012年论文
@zh-cn
name
Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient
@ast
Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient
@en
type
label
Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient
@ast
Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient
@en
prefLabel
Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient
@ast
Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient
@en
P2093
P2860
P50
P356
P1433
P1476
Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient
@en
P2093
Dori Huertas
Karolina Szczesna
Laia Simó-Riudalbas
Maria R Matarazzo
Sole Gatto
P2860
P304
P356
10.4161/EPI.20523
P50
P577
2012-06-01T00:00:00Z