Disrupted intricacy of histone H3K4 methylation in neurodevelopmental disorders.
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Landmarks in the Evolution of (t)-RNAs from the Origin of Life up to Their Present Role in Human CognitionLongitudinal assessment of neuronal 3D genomes in mouse prefrontal cortex.Haploinsufficiency of KMT2B, Encoding the Lysine-Specific Histone Methyltransferase 2B, Results in Early-Onset Generalized Dystonia.TXNIP mediates the differential responses of A549 cells to sodium butyrate and sodium 4-phenylbutyrate treatment.Touch, act and go: landing and operating on nucleosomes.CHARGE and Kabuki Syndromes: Gene-Specific DNA Methylation Signatures Identify Epigenetic Mechanisms Linking These Clinically Overlapping Conditions.Toward development of epigenetic drugs for central nervous system disorders: Modulating neuroplasticity via H3K4 methylation.Yin-yang actions of histone methylation regulatory complexes in the brain.The epigenomics of schizophrenia, in the mouse.The Histone Demethylase KDM5 Activates Gene Expression by Recognizing Chromatin Context through Its PHD Reader Motif.New insight into LSD1 function in human cortical neurogenesis.Studies on the Interaction of the Histone Demethylase KDM5B with Tricarboxylic Acid Cycle Intermediates.Transcriptome analysis revealed impaired cAMP responsiveness in PHF21A-deficient human cells.KDM5B overexpression predicts a poor prognosis in patients with squamous cell carcinoma of the head and neck.Loss of Kdm5c Causes Spurious Transcription and Prevents the Fine-Tuning of Activity-Regulated Enhancers in Neurons.Epigenetic Etiology of Intellectual Disability.The Identification of Key Genes and Pathways in Glioma by Bioinformatics Analysis.A Drosophila Model of Intellectual Disability Caused by Mutations in the Histone Demethylase KDM5.Altered Gene-Regulatory Function of KDM5C by a Novel Mutation Associated With Autism and Intellectual Disability.An inactivating mutation in the histone deacetylase SIRT6 causes human perinatal lethality.Refining the clinical phenotype of Okur-Chung neurodevelopmental syndrome.A direct regulatory link between microRNA-137 and SHANK2: implications for neuropsychiatric disorders.The Histone Demethylase KDM5 Is Essential for Larval Growth in Drosophila.Searching the overlap between network modules with specific betweeness (S2B) and its application to cross-disease analysis
P2860
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P2860
Disrupted intricacy of histone H3K4 methylation in neurodevelopmental disorders.
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name
Disrupted intricacy of histone H3K4 methylation in neurodevelopmental disorders.
@ast
Disrupted intricacy of histone H3K4 methylation in neurodevelopmental disorders.
@en
type
label
Disrupted intricacy of histone H3K4 methylation in neurodevelopmental disorders.
@ast
Disrupted intricacy of histone H3K4 methylation in neurodevelopmental disorders.
@en
prefLabel
Disrupted intricacy of histone H3K4 methylation in neurodevelopmental disorders.
@ast
Disrupted intricacy of histone H3K4 methylation in neurodevelopmental disorders.
@en
P2860
P356
P1433
P1476
Disrupted intricacy of histone H3K4 methylation in neurodevelopmental disorders.
@en
P2093
Christina N Vallianatos
Shigeki Iwase
P2860
P304
P356
10.2217/EPI.15.1
P577
2015-01-01T00:00:00Z