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Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autismIntegrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genesEpigenetic mechanisms in diurnal cycles of metabolism and neurodevelopmentMultiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disordersImmunologic and neurodevelopmental susceptibilities of autismRAB22 and RAB163/mouse BRCA2: proteins that specifically interact with the RAD51 proteinPlacental methylome analysis from a prospective autism studyLoss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome.Epigenetic regulation of UBE3A and roles in human neurodevelopmental disorders.Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number.Long-lived epigenetic interactions between perinatal PBDE exposure and Mecp2308 mutation.Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome.X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain.Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation.Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patientsReduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylationGender influences monoallelic expression of ATP10A in human brainMethylation and gene expression responses to ethanol feeding and betaine supplementation in the cystathionine beta synthase-deficient mouseCharacterization of timed changes in hepatic copper concentrations, methionine metabolism, gene expression, and global DNA methylation in the Jackson toxic milk mouse model of Wilson disease.The role of MeCP2 in brain development and neurodevelopmental disordersNeuronal chromatin dynamics of imprinting in development and diseaseMeCP2 is required for global heterochromatic and nucleolar changes during activity-dependent neuronal maturation.15q11.2-13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain.Large-scale methylation domains mark a functional subset of neuronally expressed genes.Paradoxical role of methyl-CpG-binding protein 2 in Rett syndrome.Early Developmental and Evolutionary Origins of Gene Body DNA Methylation Patterns in Mammalian Placentas.Chimeric MicroRNA-1291 Biosynthesized Efficiently in Escherichia coli Is Effective to Reduce Target Gene Expression in Human Carcinoma Cells and Improve Chemosensitivity.Phosphorylation of distinct sites in MeCP2 modifies cofactor associations and the dynamics of transcriptional regulationRett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctionsSequence features accurately predict genome-wide MeCP2 binding in vivo.MECP2 promoter methylation and X chromosome inactivation in autismEpigenetic layers and players underlying neurodevelopment.R-loop formation at Snord116 mediates topotecan inhibition of Ube3a-antisense and allele-specific chromatin decondensation.The landscape of DNA methylation amid a perfect storm of autism aetiologies.A Prader-Willi locus lncRNA cloud modulates diurnal genes and energy expenditureImprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size.Cumulative Impact of Polychlorinated Biphenyl and Large Chromosomal Duplications on DNA Methylation, Chromatin, and Expression of Autism Candidate Genes.How has the study of the human placenta aided our understanding of partially methylated genes?
P50
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P50
description
researcher
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wetenschapper
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հետազոտող
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name
Janine M. LaSalle
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Janine M. LaSalle
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Janine M. LaSalle
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Janine M. LaSalle
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Janine M. LaSalle
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type
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Janine M. LaSalle
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Janine M. LaSalle
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Janine M. LaSalle
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Janine M. LaSalle
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Janine M. LaSalle
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Janine M. LaSalle
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Janine M. LaSalle
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Janine M. LaSalle
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Janine M. LaSalle
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Janine M. LaSalle
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P1053
A-4643-2008
P106
P1153
7005702015
P31
P3829
P3835
janine-lasalle
P496
0000-0002-3480-2031