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Journal Article
Cellular and Molecular Life Sciences, ISSN 1420-682X, 5/2013, Volume 70, Issue 9, pp. 1543 - 1573
Epigenetic mechanisms play an important role in gene regulation during development. DNA methylation, which is probably the most important and best-studied... 
Life Sciences | Biochemistry, general | Life Sciences, general | Disease | Epigenetics | Mutation | Biomedicine general | Cell Biology | SYSTEMIC-LUPUS-ERYTHEMATOSUS | RUBINSTEIN-TAYBI-SYNDROME | BIOCHEMISTRY & MOLECULAR BIOLOGY | S-ADENOSYLMETHIONINE SYNTHETASE | CPG-BINDING-PROTEIN | XNP/ATR-X GENE | METHIONINE ADENOSYLTRANSFERASE 1A | CELL BIOLOGY | FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY | COFFIN-LOWRY-SYNDROME | SINGLE NUCLEOTIDE POLYMORPHISM | GLYCINE N-METHYLTRANSFERASE | Coffin-Lowry Syndrome - genetics | Neoplasms - metabolism | Epigenesis, Genetic | Humans | Lupus Erythematosus, Systemic - metabolism | Muscular Dystrophy, Facioscapulohumeral - genetics | alpha-Thalassemia - metabolism | DNA Methylation | Mental Retardation, X-Linked - genetics | Rubinstein-Taybi Syndrome - genetics | Neoplasms - genetics | Sotos Syndrome - metabolism | Coffin-Lowry Syndrome - metabolism | alpha-Thalassemia - genetics | Muscular Dystrophy, Facioscapulohumeral - metabolism | Sotos Syndrome - genetics | DNA Modification Methylases - metabolism | Cockayne Syndrome - metabolism | DNA - metabolism | Rubinstein-Taybi Syndrome - metabolism | DNA - genetics | Rett Syndrome - metabolism | DNA Modification Methylases - genetics | Animals | Histones - genetics | CHARGE Syndrome - metabolism | Lupus Erythematosus, Systemic - genetics | Cockayne Syndrome - genetics | CHARGE Syndrome - genetics | Histones - metabolism | Rett Syndrome - genetics | Mental Retardation, X-Linked - metabolism | Liver cancer | Gene mutations | Genes | Transferases | Immunodeficiency | Physiological aspects | Methylation | Glycine | Mental illness | S-adenosylmethionine | CHARGE syndrome
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 | MESSENGER-RNA | COMPLEX-I | MOUSE MODEL | BEHAVIORAL SCIENCES | MENTAL-RETARDATION PROTEIN | 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