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Convulsing toward the pathophysiology of autismThe comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13Angelman syndrome: insights into genomic imprinting and neurodevelopmental phenotypesProteostasis and RNA Binding Proteins in Synaptic Plasticity and in the Pathogenesis of Neuropsychiatric Disorders"Seq-ing" insights into the epigenetics of neuronal gene regulationThe molecular basis of cognitive deficits in pervasive developmental disordersThe prospect of molecular therapy for Angelman syndrome and other monogenic neurologic disordersImmunologic and neurodevelopmental susceptibilities of autismToxic environmental chemicals: the role of reproductive health professionals in preventing harmful exposuresCellular epigenetic modifications of neural stem cell differentiation[Genetic and brain structure anomalies in autism spectrum disorders. Towards an understanding of the aetiopathogenesis?].From microscopes to microarrays: dissecting recurrent chromosomal rearrangements.Characterization of the Brain 26S Proteasome and its Interacting ProteinsAnalysis of cerebellar function in Ube3a-deficient mice reveals novel genotype-specific behaviorsImprinted loci in domestic livestock species as epigenomic targets for artificial selection of complex traits.Drosophila Ube3a regulates monoamine synthesis by increasing GTP cyclohydrolase I activity via a non-ubiquitin ligase mechanism.Epigenetic regulation of neuronal dendrite and dendritic spine developmentAlcohol modulates expression of DNA methyltranferases and methyl CpG-/CpG domain-binding proteins in murine embryonic fibroblastsImbalanced mechanistic target of rapamycin C1 and C2 activity in the cerebellum of Angelman syndrome mice impairs motor function.Epigenetic mechanisms of pulmonary hypertension.Altered GABA(A) receptor subunit expression and pharmacology in human Angelman syndrome cortex.Maternal Ube3a Loss Disrupts Sleep Homeostasis But Leaves Circadian Rhythmicity Largely Intact.Dissociation of locomotor and cerebellar deficits in a murine Angelman syndrome model.Ube3a-ATS is an atypical RNA polymerase II transcript that represses the paternal expression of Ube3aProtein Delivery of an Artificial Transcription Factor Restores Widespread Ube3a Expression in an Angelman Syndrome Mouse BrainThe role of redox signaling in epigenetics and cardiovascular disease.Potential therapeutic approaches for Angelman syndrome.In vivo and in vitro differentiation of uniparental embryonic stem cells into hematopoietic and neural cell typesThe Drosophila homologue of the Angelman syndrome ubiquitin ligase regulates the formation of terminal dendritic branches.Failure of neuronal homeostasis results in common neuropsychiatric phenotypes.Epigenetics, autism spectrum, and neurodevelopmental disorders.DNA methylation and methyl-CpG binding proteins: developmental requirements and function.Allelic specificity of Ube3a expression in the mouse brain during postnatal development.Evolving role of MeCP2 in Rett syndrome and autism.Role of H3K4 demethylases in complex neurodevelopmental diseases.Epilepsy in four genetically determined syndromes of intellectual disability.Epigenetic factors and autism spectrum disorders.E6AP in the brain: one protein, dual function, multiple diseases.Angelman syndrome: review of clinical and molecular aspects.Genetic architecture, epigenetic influence and environment exposure in the pathogenesis of Autism.
P2860
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P2860
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Molecular epigenetics of Angelman syndrome.
@ast
Molecular epigenetics of Angelman syndrome.
@en
type
label
Molecular epigenetics of Angelman syndrome.
@ast
Molecular epigenetics of Angelman syndrome.
@en
prefLabel
Molecular epigenetics of Angelman syndrome.
@ast
Molecular epigenetics of Angelman syndrome.
@en
P1476
Molecular epigenetics of Angelman syndrome.
@en
P2093
M A Calciano
P2888
P304
P356
10.1007/S00018-007-6460-0
P577
2007-04-01T00:00:00Z