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Journal Article
Nature Neuroscience, ISSN 1097-6256, 06/2005, Volume 8, Issue 6, pp. 828 - 834
Carriers of the short allele of a functional 5' promoter polymorphism of the serotonin transporter gene have increased anxiety-related temperamental traits,... 
SEROTONIN TRANSPORTER | HUMAN BRAIN | GLUCOSE-METABOLISM | MOOD DISORDERS | AFFECTIVE-DISORDERS | ANTERIOR CINGULATE | FUNCTIONAL CONNECTIVITY | PROMOTER POLYMORPHISM | MAJOR DEPRESSION | NEUROSCIENCES | PREFRONTAL CORTEX | Amygdala - physiopathology | Depressive Disorder - pathology | Anthropometry | Humans | Atrophy - pathology | Serotonin Plasma Membrane Transport Proteins | Neural Pathways - pathology | Fear - physiology | Anxiety Disorders - pathology | Membrane Transport Proteins - genetics | Gyrus Cinguli - pathology | Atrophy - genetics | Fear - psychology | Surveys and Questionnaires | Anxiety Disorders - metabolism | Neural Pathways - physiopathology | Brain Chemistry - genetics | Depressive Disorder - genetics | Genetic Predisposition to Disease - genetics | Amygdala - metabolism | Mutation - genetics | Depressive Disorder - metabolism | Nerve Tissue Proteins - genetics | Amygdala - pathology | Gyrus Cinguli - metabolism | Membrane Glycoproteins - genetics | Neuropsychological Tests | Magnetic Resonance Imaging | Serotonin - metabolism | Brain Mapping | Gyrus Cinguli - physiopathology | Neural Pathways - metabolism | Anxiety Disorders - genetics | Polymorphism, Genetic - genetics | Atrophy - metabolism | Depression, Mental | Physiological aspects | Genetic aspects | Research | Diagnosis | Amygdala (Brain) | Risk factors | Genetic polymorphisms | Index Medicus
Journal Article
Nature, ISSN 0028-0836, 04/2008, Volume 452, Issue 7190, pp. 997 - 1001
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2011, Volume 6, Issue 10, pp. e26203 - e26203
Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability. In addition to cognitive deficits, FXS patients exhibit hyperactivity,... 
METHYLATION | ALLELES | REPEAT EXPANSION | PROTEIN | INSTABILITY | MESSENGER-RNA | MECHANISM | MULTIDISCIPLINARY SCIENCES | INVOLVEMENT | DIFFERENTIATION | EXPRESSION | Neurons - pathology | Epigenesis, Genetic | Humans | Middle Aged | Nervous System - metabolism | Child, Preschool | Male | Fragile X Mental Retardation Protein - metabolism | RNA, Messenger - metabolism | Case-Control Studies | Cell Differentiation - genetics | Nervous System - growth & development | Nervous System - pathology | Adult | Neurons - metabolism | Cellular Reprogramming - genetics | Infant, Newborn | Fibroblasts - metabolism | Induced Pluripotent Stem Cells - metabolism | Fragile X Syndrome - genetics | Induced Pluripotent Stem Cells - pathology | RNA, Messenger - genetics | Cells, Cultured | DNA Methylation - genetics | Fibroblasts - pathology | Mutation - genetics | Models, Biological | CpG Islands - genetics | Trinucleotide Repeat Expansion - genetics | Mosaicism | Fragile X Mental Retardation Protein - genetics | Tissue Donors | Epigenetic inheritance | Autism | Analysis | Genes | Stem cells | Genetic aspects | Fragile X syndrome | Methylation | Mental illness | Neurophysiology | Cell culture | Synaptogenesis | Disease | Pathogenesis | Hyperactivity | Intellectual disabilities | Cognitive ability | Cases (containers) | Mental retardation | Medical schools | Neuronal-glial interactions | Proteins | Fragile X mental retardation protein | Cell cycle | Fibroblasts | DNA methylation | Ataxia | Anxiety | Chromosomes | CpG islands | Neurons | Cloning | Attention | Gene expression | Patients | Hospitals | Epigenetics | Genetic research | Mutation | Aberration | Differentiation | Pluripotency | FMR1 protein | Inhibitory postsynaptic potentials | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2014, Volume 9, Issue 4, pp. e93400 - e93400
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 05/2016, Volume 98, Issue 5, pp. 898 - 908
Journal Article
Current topics in behavioral neurosciences, ISSN 1866-3370, 2010, Volume 2, p. 63
Journal Article
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 | Index Medicus
Journal Article