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Nature, ISSN 0028-0836, 11/2010, 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
Journal Article
Neuroscience and Biobehavioral Reviews, ISSN 0149-7634, 10/2014, Volume 46, Issue 2, pp. 202 - 217
Clinical manifestations typical of mitochondrial diseases are often present in various genetic syndromes associated with intellectual disability, a condition... 
Neuroplasticity | Oxidative stress | Epigallocatechine-3-gallate | Mitochondrial dysfunction | Down syndrome | Drug development | Neurogenesis | Autism | Mitochondria | Intellectual disability | Oxidative phosphorylation | Rett syndrome | Fragile X | ALZHEIMERS-DISEASE | SPECTRUM DISORDERS | ELEMENT-BINDING PROTEIN | SYNAPTIC PLASTICITY | NEUROSCIENCES | REACTIVE OXYGEN | COMPLEX-I | MOUSE MODEL | BEHAVIORAL SCIENCES | MENTAL-RETARDATION PROTEIN | DOSAGE EFFECT HYPOTHESIS | Mitochondrial Diseases - pathology | Rett Syndrome - complications | Autistic Disorder - physiopathology | Autistic Disorder - metabolism | Down Syndrome - metabolism | Fragile X Syndrome - physiopathology | Humans | Mitochondrial Diseases - metabolism | Intellectual Disability - complications | Down Syndrome - physiopathology | Fragile X Syndrome - drug therapy | Intellectual Disability - metabolism | Mitochondrial Diseases - complications | Neuronal Plasticity - physiology | Down Syndrome - complications | Molecular Targeted Therapy - methods | Oxidative Phosphorylation | Fragile X Syndrome - metabolism | Mitochondria - metabolism | Antioxidants - pharmacology | Mitochondria - pathology | Fragile X Syndrome - complications | Rett Syndrome - physiopathology | Intellectual Disability - physiopathology | Rett Syndrome - metabolism | Antioxidants - therapeutic use | Models, Biological | Neurogenesis - physiology | Oxidative Stress - drug effects | Autistic Disorder - complications | Mitochondrial Diseases - physiopathology | Neurosciences | Actors | Actresses | Cells
Journal Article
Epilepsia, ISSN 0013-9580, 02/2016, Volume 57, Issue 2, pp. 182 - 193
Autism and epilepsy are two associated disorders that are highly prevalent, share common developmental origins, and demonstrate substantial heritability. In... 
Gamma‐aminobutyric acid | Epileptic encephalopathy | Epilepsy | Cortical interneuron | Autism spectrum disorder | Gamma-aminobutyric acid | RETT-SYNDROME | CLINICAL NEUROLOGY | CHILDREN | LANDAU-KLEFFNER | SEIZURES | DE-NOVO MUTATIONS | MOUSE MODEL | FRAGILE-X-SYNDROME | DRAVET-SYNDROME | SEVERE MYOCLONIC EPILEPSY | MICE | Landau-Kleffner Syndrome - physiopathology | Neural Inhibition | Spasms, Infantile - physiopathology | gamma-Aminobutyric Acid - metabolism | Humans | Autism Spectrum Disorder - complications | Child, Preschool | Infant | Aicardi Syndrome - genetics | Epilepsy - physiopathology | Spasms, Infantile - genetics | Cerebral Cortex - metabolism | Lennox Gastaut Syndrome - genetics | Lennox Gastaut Syndrome - psychology | Cerebral Cortex - physiopathology | Landau-Kleffner Syndrome - psychology | Epilepsy - genetics | Neurons - metabolism | Spasms, Infantile - complications | Child | Epilepsies, Myoclonic - genetics | Autism Spectrum Disorder - genetics | Epilepsy - psychology | Aicardi Syndrome - complications | Epilepsies, Myoclonic - physiopathology | Spasms, Infantile - psychology | Autism Spectrum Disorder - psychology | Landau-Kleffner Syndrome - genetics | Epilepsies, Myoclonic - complications | Epilepsy - complications | Landau-Kleffner Syndrome - complications | Aicardi Syndrome - psychology | Epilepsies, Myoclonic - psychology | Interneurons - metabolism | Aicardi Syndrome - physiopathology | Lennox Gastaut Syndrome - complications | Lennox Gastaut Syndrome - physiopathology | Autism Spectrum Disorder - physiopathology | GABA | Autism | Neurosciences
Journal Article
European Journal of Neuroscience, ISSN 0953-816X, 07/2009, Volume 30, Issue 1, pp. 1 - 8
Epigenetic mechanisms are not only essential for biological functions requiring stable molecular changes such as the establishment of cell identity and tissue... 
Neurodevelopment | Schizophrenia | Reversibility | Neurodegeneration | Epigenetic codes | RUBINSTEIN-TAYBI-SYNDROME | LONG-TERM-MEMORY | ALZHEIMERS-DISEASE | neurodegeneration | TRANSCRIPTIONAL COACTIVATOR CBP | schizophrenia | CPG-BINDING PROTEIN-2 | SYNAPTIC PLASTICITY | NEUROSCIENCES | neurodevelopment | epigenetic codes | MOUSE MODEL | reversibility | FRAGILE-X-SYNDROME | HISTONE DEACETYLASE INHIBITORS | HUNTINGTONS-DISEASE | Epigenesis, Genetic | Fragile X Syndrome - physiopathology | Humans | Fragile X Syndrome - drug therapy | Rett Syndrome - drug therapy | Rubinstein-Taybi Syndrome - genetics | Schizophrenia - genetics | Schizophrenia - physiopathology | Huntington Disease - drug therapy | Huntington Disease - physiopathology | Fragile X Syndrome - genetics | Alzheimer Disease - physiopathology | Cognition Disorders - physiopathology | Rubinstein-Taybi Syndrome - drug therapy | Brain - physiopathology | Alzheimer Disease - drug therapy | Cognition Disorders - genetics | Cognition Disorders - drug therapy | Rett Syndrome - physiopathology | Animals | Huntington Disease - genetics | Histones - metabolism | Schizophrenia - drug therapy | Alzheimer Disease - genetics | Rett Syndrome - genetics | DNA Methylation - drug effects | Rubinstein-Taybi Syndrome - physiopathology | Gene expression | Alzheimer's disease
Journal Article
Annual Review of Medicine, ISSN 0066-4219, 02/2011, Volume 62, Issue 1, pp. 411 - 429