Reversal of phenotypes in MECP2 duplication mice using genetic rescue or antisense oligonucleotides.
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Epigenetic Effect of Environmental Factors on Autism Spectrum DisordersDevelopmental Dynamics of Rett SyndromeInfluenza A induces dysfunctional immunity and death in MeCP2-overexpressing mice.FMRP Expression Levels in Mouse Central Nervous System Neurons Determine Behavioral Phenotype.Restoration of Mecp2 expression in GABAergic neurons is sufficient to rescue multiple disease features in a mouse model of Rett syndrome.MiR-130a regulates neurite outgrowth and dendritic spine density by targeting MeCP2The Role of Epigenetic Mechanisms in the Regulation of Gene Expression in the Nervous System.Distinct Defects in Spine Formation or Pruning in Two Gene Duplication Mouse Models of Autism.Gene-targeting pharmaceuticals for single-gene disorders.Genetic and Pharmacological Reversibility of Phenotypes in Mouse Models of Autism Spectrum Disorder.Genetic Approaches to Understanding Psychiatric Disease.Bridging Autism Spectrum Disorders and Schizophrenia through inflammation and biomarkers - pre-clinical and clinical investigations.An RNA interference screen identifies druggable regulators of MeCP2 stability.Loss-of-function mutation in Mirta22/Emc10 rescues specific schizophrenia-related phenotypes in a mouse model of the 22q11.2 deletion.Excessive UBE3A dosage impairs retinoic acid signaling and synaptic plasticity in autism spectrum disorders.Loss of Capicua alters early T cell development and predisposes mice to T cell lymphoblastic leukemia/lymphoma.Oligonucleotide therapies for disorders of the nervous system.A simplified protocol for differentiation of electrophysiologically mature neuronal networks from human induced pluripotent stem cells.Epigenetic alterations induced by environmental stress associated with metabolic and neurodevelopmental disorders.Depleting Trim28 in adult mice is well tolerated and reduces levels of α-synuclein and tau.Experience-dependent MeCP2 expression in the excitatory cells of mouse visual thalamus.Autism spectrum disorder: prospects for treatment using gene therapy.Pharmacological reactivation of inactive X-linked in cerebral cortical neurons of living miceTranscriptional Regulation by MECP2Early adolescent Rai1 reactivation reverses transcriptional and social interaction deficits in a mouse model of Smith-Magenis syndromeControl of CNS functions by RNA-binding proteins in neurological diseasesGenomics in neurodevelopmental disorders: an avenue to personalized medicine
P2860
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P2860
Reversal of phenotypes in MECP2 duplication mice using genetic rescue or antisense oligonucleotides.
description
2015 nî lūn-bûn
@nan
2015 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年学术文章
@wuu
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
name
Reversal of phenotypes in MECP ...... or antisense oligonucleotides
@nl
Reversal of phenotypes in MECP ...... or antisense oligonucleotides.
@ast
Reversal of phenotypes in MECP ...... or antisense oligonucleotides.
@en
type
label
Reversal of phenotypes in MECP ...... or antisense oligonucleotides
@nl
Reversal of phenotypes in MECP ...... or antisense oligonucleotides.
@ast
Reversal of phenotypes in MECP ...... or antisense oligonucleotides.
@en
prefLabel
Reversal of phenotypes in MECP ...... or antisense oligonucleotides
@nl
Reversal of phenotypes in MECP ...... or antisense oligonucleotides.
@ast
Reversal of phenotypes in MECP ...... or antisense oligonucleotides.
@en
P2093
P2860
P3181
P356
P1433
P1476
Reversal of phenotypes in MECP ...... or antisense oligonucleotides.
@en
P2093
Frank Rigo
Hong-mei Chen
Jianrong Tang
John W Swann
Shuang Hao
Yehezkel Sztainberg
Ying-Wooi Wan
P2860
P2888
P304
P3181
P356
10.1038/NATURE16159
P407
P577
2015-11-25T00:00:00Z
P6179
1002880179