Multilocus loss of DNA methylation in individuals with mutations in the histone H3 lysine 4 demethylase KDM5C.
about
Methamphetamine-associated memory is regulated by a writer and an eraser of permissive histone methylation.X chromosome regulation: diverse patterns in development, tissues and disease.Mutations in the intellectual disability gene KDM5C reduce protein stability and demethylase activity.Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsy.Mutations in the KDM5C ARID Domain and Their Plausible Association with Syndromic Claes-Jensen-Type Disease.COHCAP: an integrative genomic pipeline for single-nucleotide resolution DNA methylation analysis.Biological and biochemical modulation of DNA methylation.DNA methylation analysis in constitutional disorders: Clinical implications of the epigenome.CHARGE and Kabuki Syndromes: Gene-Specific DNA Methylation Signatures Identify Epigenetic Mechanisms Linking These Clinically Overlapping Conditions.Constitutional Epi/Genetic Conditions: Genetic, Epigenetic, and Environmental Factors.Identification of epigenetic signature associated with alpha thalassemia/mental retardation X-linked syndrome.The defining DNA methylation signature of Floating-Harbor Syndrome.Studies on the Interaction of the Histone Demethylase KDM5B with Tricarboxylic Acid Cycle Intermediates.NSD1 mutations generate a genome-wide DNA methylation signature.A deep ensemble model to predict miRNA-disease association.Loss of Kdm5c Causes Spurious Transcription and Prevents the Fine-Tuning of Activity-Regulated Enhancers in Neurons.X chromosome dosage and presence of SRY shape sex-specific differences in DNA methylation at an autosomal region in human cells.Peripheral blood epi-signature of Claes-Jensen syndrome enables sensitive and specific identification of patients and healthy carriers with pathogenic mutations in KDM5C.Allelic expression analysis in the brain suggests a role for heterogeneous insults affecting epigenetic processes in autism spectrum disorders.A Drosophila Model of Intellectual Disability Caused by Mutations in the Histone Demethylase KDM5.
P2860
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P2860
Multilocus loss of DNA methylation in individuals with mutations in the histone H3 lysine 4 demethylase KDM5C.
description
2013 nî lūn-bûn
@nan
2013 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Multilocus loss of DNA methyla ...... H3 lysine 4 demethylase KDM5C.
@ast
Multilocus loss of DNA methyla ...... H3 lysine 4 demethylase KDM5C.
@en
Multilocus loss of DNA methyla ...... H3 lysine 4 demethylase KDM5C.
@nl
type
label
Multilocus loss of DNA methyla ...... H3 lysine 4 demethylase KDM5C.
@ast
Multilocus loss of DNA methyla ...... H3 lysine 4 demethylase KDM5C.
@en
Multilocus loss of DNA methyla ...... H3 lysine 4 demethylase KDM5C.
@nl
prefLabel
Multilocus loss of DNA methyla ...... H3 lysine 4 demethylase KDM5C.
@ast
Multilocus loss of DNA methyla ...... H3 lysine 4 demethylase KDM5C.
@en
Multilocus loss of DNA methyla ...... H3 lysine 4 demethylase KDM5C.
@nl
P2093
P2860
P356
P1433
P1476
Multilocus loss of DNA methyla ...... H3 lysine 4 demethylase KDM5C.
@en
P2093
Andrei L Turinsky
Barian H Y Chung
Carolyn A Bondy
Charles E Schwartz
Chunhua Zhao
Cindy Skinner
Darci T Butcher
Daria Grafodatskaya
Fatima E Abidi
James Stavropoulos
P2860
P2888
P356
10.1186/1755-8794-6-1
P577
2013-01-28T00:00:00Z
P5875
P6179
1011277564