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Nature (London), ISSN 1476-4687, 2010, Volume 468, Issue 7321, pp. 263 - 269
Mutations in the X-linked MECP2 gene, which encodes the transcriptional regulator methyl-CpG-binding protein 2 (MeCP2), cause Rett syndrome and several... 
GLUTAMIC-ACID DECARBOXYLASE | GENE | 67 KDA | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | MUTATION | NEURONAL MECP2 | SCHIZOPHRENIA | MICE | CPG-BINDING PROTEIN-2 | YOUNG GIRLS | Autistic Disorder - physiopathology | gamma-Aminobutyric Acid - metabolism | Methyl-CpG-Binding Protein 2 - metabolism | Male | Psychomotor Disorders - complications | Methyl-CpG-Binding Protein 2 - deficiency | Compulsive Behavior - physiopathology | Neurons - metabolism | Disease Models, Animal | Autistic Disorder - genetics | Signal Transduction | Compulsive Behavior - genetics | Genotype | Mice, Transgenic | Survival Rate | Hippocampus - pathology | Rett Syndrome - physiopathology | Self-Injurious Behavior - genetics | Phenotype | Neuronal Plasticity | Long-Term Potentiation | Stereotypic Movement Disorder - genetics | Compulsive Behavior - complications | Glutamate Decarboxylase - metabolism | Mice | Hippocampus - physiopathology | Autistic Disorder - pathology | Rett Syndrome - complications | Neural Inhibition | Stereotypic Movement Disorder - pathology | Reflex, Startle - genetics | Electroencephalography | Methyl-CpG-Binding Protein 2 - genetics | Synaptic Transmission | Psychomotor Disorders - genetics | Self-Injurious Behavior - complications | Psychomotor Disorders - physiopathology | Inhibitory Postsynaptic Potentials | Stereotypic Movement Disorder - physiopathology | Brain - cytology | Homeodomain Proteins - genetics | Stereotypic Movement Disorder - complications | Self-Injurious Behavior - physiopathology | Animals | Rett Syndrome - pathology | Vesicular Inhibitory Amino Acid Transport Proteins - genetics | Presynaptic Terminals - metabolism | Autistic Disorder - complications | Respiration | Rett Syndrome - genetics | Autism | Care and treatment | Rett syndrome | Schizophrenia | GABA | Genetic aspects | Diagnosis | Cognition disorders | Seizures (Medicine) | Health aspects | Studies | Anxieties | Social interaction | Neurons | Rodents | Bipolar disorder | Behavior | Gene expression
Journal Article
Biological psychiatry (1969), ISSN 0006-3223, 2016, Volume 80, Issue 4, pp. 302 - 311
Abstract Background CDKL5 (cyclin-dependent kinase-like 5) is mutated in many severe neurodevelopmental disorders, including atypical Rett syndrome. CDKL5 was... 
Psychiatry | IGF-1 | CDKL5 | PSD-95 | dendritic spines | imaging | Rett syndrome | LONG-TERM | NEOCORTEX IN-VIVO | RETT-SYNDROME | STRUCTURAL PLASTICITY | PSYCHIATRY | CRANIAL WINDOW | PROTEIN-SYNTHESIS | NEUROSCIENCES | MECP2 | SIGNALING PATHWAY | DYSREGULATION | MICE | Disks Large Homolog 4 Protein | Protein-Serine-Threonine Kinases - deficiency | Age Factors | Gene Expression Regulation, Developmental - genetics | Green Fluorescent Proteins - genetics | Spasms, Infantile - genetics | Synapses - pathology | Somatosensory Cortex - pathology | Rett Syndrome - drug therapy | Long-Term Potentiation - drug effects | Dendritic Spines - drug effects | Membrane Proteins - metabolism | Phosphorylation - drug effects | Insulin-Like Growth Factor I - therapeutic use | Pyramidal Cells - ultrastructure | Disease Models, Animal | Animals, Newborn | Green Fluorescent Proteins - metabolism | Synapses - drug effects | Epileptic Syndromes | Gene Expression Regulation, Developmental - drug effects | Protein-Serine-Threonine Kinases - genetics | Mice, Transgenic | Long-Term Potentiation - genetics | Spasms, Infantile - pathology | Patch-Clamp Techniques | Animals | Spasms, Infantile - drug therapy | Dendritic Spines - pathology | Rett Syndrome - pathology | Guanylate Kinases - metabolism | Pyramidal Cells - pathology | Mice | Rett Syndrome - genetics | Proteins | Neurosciences | Molecular biology | Analysis
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 12/2005, Volume 25, Issue 50, pp. 11521 - 11530
Journal Article
PloS one, ISSN 1932-6203, 2014, Volume 9, Issue 10, p. e109527
Rett syndrome (RTT) is an autism spectrum disorder (ASD) caused by mutations in the X-linked MECP2 gene that encodes methyl-CpG binding protein 2 (MeCP2).... 
PHOSPHOENOLPYRUVATE CARBOXYKINASE | ENTERAL METABOLISM | RETT-SYNDROME | FAT OXIDATION DISORDERS | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | REPERFUSION INJURY | DISEASE | DYSFUNCTION | CPG-BINDING PROTEIN-2 | PERMEABILITY TRANSITION | Gene Expression | Longevity - drug effects | Humans | Mice, Inbred C57BL | Rett Syndrome - psychology | Citric Acid Cycle - drug effects | Motor Activity - drug effects | Male | Methyl-CpG-Binding Protein 2 - deficiency | Methyl-CpG-Binding Protein 2 - genetics | Rett Syndrome - physiopathology | Mice, Knockout | Triglycerides - administration & dosage | Citric Acid Cycle - genetics | Phenotype | Animals | Diet | Metabolome - drug effects | Rett Syndrome - diet therapy | Lipid Metabolism - drug effects | Behavior, Animal - drug effects | Mice | Rett Syndrome - genetics | Disease Models, Animal | Metabolites | Leptin | Liver | Glucose | Social aspects | Dextrose | Protein binding | Tricarboxylic acid cycle | Brain | Therapy | Metabolomics | Neurosciences | Adipose tissue | Homeostasis | Disabilities | Adiponectin | Proteins | Genotype & phenotype | Mitochondria | Energy | Methyl-CpG binding protein | Rodents | Ataxia | Supplementation | Seizures | CpG islands | Obesity | Phenotypes | Nutrient deficiency | Dietary supplements | Muscles | Metabolism | Gene expression | Insulin | Fatty acids | Substrates | Skeletal muscle | Intermediates | Medicine | Glucose tolerance | Autism | Brain research | Nutrient utilization | Life span | MeCP2 protein | Morphology | Rett syndrome | Mutation | Critical period | Nutrient cycles
Journal Article
Scientific reports, ISSN 2045-2322, 2016, Volume 6, Issue 1, p. 19796
Journal Article
Neuroscience, ISSN 0306-4522, 2016, Volume 324, pp. 496 - 508
Journal Article