Rett Syndrome: Crossing the Threshold to Clinical Translation - Wikidata - wikimedia - TriplyDB

Rett Syndrome: Crossing the Threshold to Clinical Translation

Rett Syndrome: Crossing the Threshold to Clinical Translation

http://www.wikidata.org/entity/Q26772909

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Rett syndrome - biological pathways leading from MECP2 to disorder phenotypes Insulin-Like Growth Factor 1 and Related Compounds in the Treatment of Childhood-Onset Neurodevelopmental Disorders FMRP Expression Levels in Mouse Central Nervous System Neurons Determine Behavioral Phenotype.Therapeutic Potential of Transcranial Focused Ultrasound for Rett Syndrome.Autonomic breathing abnormalities in Rett syndrome: caregiver perspectives in an international database study.N-Methyl-D-Aspartate Receptors, Ketamine, and Rett Syndrome: Something Special on the Road to Treatments?Neurobiologically-based treatments in Rett syndrome: opportunities and challenges.Development of the Tailored Rett Intervention and Assessment Longitudinal (TRIAL) database and the Rett Evaluation of Symptoms and Treatments (REST) Questionnaire.The Role of Noncoding RNAs in Neurodevelopmental Disorders: The Case of Rett Syndrome.Modeling Rett Syndrome Using TALEN-Edited MECP2 Mutant Cynomolgus Monkeys Pathogenesis of Lethal Aspiration Pneumonia in Mecp2-null Mouse Model for Rett Syndrome MeCP2 mutations: progress towards understanding and treating Rett syndrome Retention of Mitochondria in Mature Human Red Blood Cells as the Result of Autophagy Impairment in Rett Syndrome.Whole genome sequencing in psychiatric disorders: the WGSPD consortium.A mixed modality approach towards Xi reactivation for Rett syndrome and other X-linked disorders.Common pathophysiology in multiple mouse models of Pitt-Hopkins syndrome.Activation of the Medial Prefrontal Cortex Reverses Cognitive and Respiratory Symptoms in a Mouse Model of Rett Syndrome Environmental enrichment intervention for Rett syndrome: an individually randomised stepped wedge trial.Stem Cell Technology for (Epi)genetic Brain Disorders.Increased Mitochondrial Mass and Cytosolic Redox Imbalance in Hippocampal Astrocytes of a Mouse Model of Rett Syndrome: Subcellular Changes Revealed by Ratiometric Imaging of JC-1 and roGFP1 Fluorescence.Developmental timing and critical windows for the treatment of psychiatric disorders.NMDA Receptors in the Central Nervous System.Neurogenetic research: of mice and men … and misunderstanding.Neurobiology: Domains to the rescue for Rett syndrome.Effect of desipramine on patients with breathing disorders in RETT syndrome.Autism spectrum disorder: prospects for treatment using gene therapy.Apparent bias toward long gene misregulation in MeCP2 syndromes disappears after controlling for baseline variations Tsix-Mecp2 female mouse model for Rett syndrome reveals that low-level MECP2 expression extends life and improves neuromotor function The Way Forward for Mechanism-Based Therapeutics in Genetically Defined Neurodevelopmental Disorders

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Rett Syndrome: Crossing the Threshold to Clinical Translation

http://www.wikidata.org/entity/Q26772909

description

2016 nî lūn-bûn

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2016 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2016 թվականի փետրվարին հրատարակված գիտական հոդված

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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name

Rett Syndrome: Crossing the Threshold to Clinical Translation

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Rett Syndrome: Crossing the Threshold to Clinical Translation

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Rett Syndrome: Crossing the Threshold to Clinical Translation

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Rett Syndrome: Crossing the Threshold to Clinical Translation

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Rett Syndrome: Crossing the Threshold to Clinical Translation

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Rett Syndrome: Crossing the Threshold to Clinical Translation

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Rett Syndrome: Crossing the Threshold to Clinical Translation

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Rett Syndrome: Crossing the Threshold to Clinical Translation

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Rett Syndrome: Crossing the Threshold to Clinical Translation

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J.TINS.2015.12.008

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Trends in Neurosciences

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Rett Syndrome: Crossing the Threshold to Clinical Translation

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Benjamin D Philpot

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Daniel C Tarquinio

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David M Katz

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Monica Coenraads

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Steven J Gray

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The nuclear DNA base 5-hydroxymethylcytosine is present in Purkinje neurons and the brain

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

Reduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett syndrome

Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice

Topoisomerase inhibitors unsilence the dormant allele of Ube3a in neurons

Pathophysiology of locus ceruleus neurons in a mouse model of Rett syndrome

Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2

MeCP2, a key contributor to neurological disease, activates and represses transcription

Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities

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10.1016/J.TINS.2015.12.008

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2

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Adrian Peter Bird

Debashish Menon

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2016-02-01T00:00:00Z

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