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Neurobiology of Disease, ISSN 0969-9961, 2014, Volume 68, Issue 100, pp. 66 - 77
Abstract Rett syndrome (RTT) is a rare neurodevelopmental disorder affecting almost exclusively females, caused in the overwhelming majority of the cases by... 
Neurology | Lipid peroxidation | Oxidative stress | Brain damage | Neurodevelopmental disorder | Murine models | Rett syndrome | IRON | CPG-BINDING PROTEIN-2 | NEUROSCIENCES | CHOLESTEROL-METABOLISM | MECP2 MUTANT MICE | MOUSE MODEL | DISEASE | ANIMAL-MODELS | DISORDER | DYSFUNCTION | STRESS | Arachidonic Acid - metabolism | Rett Syndrome - complications | Gas Chromatography-Mass Spectrometry | Mice, Inbred C57BL | Neuroprostanes - metabolism | Oxidative Stress - physiology | Male | Mice, Transgenic | Aldehydes - metabolism | Mutation - genetics | Methyl-CpG-Binding Protein 2 - genetics | Animals | Isoprostanes - metabolism | Analysis of Variance | Nestin - genetics | Brain Injuries - blood | Female | Mice | Brain Injuries - etiology | Rett Syndrome - blood | Rett Syndrome - genetics | Brain Injuries - pathology | Disease Models, Animal | Docosahexaenoic Acids - metabolism | Models | Analysis | Protein binding | Organic chemistry | Chemical Sciences | OS, oxidative stress | Mecp2 | y, hemizygous null mice | NPBI, non-protein-bound iron | Mecp2, methyl-CpG-binding protein 2 — mouse protein | CRE, Cre-Recombinase | AdA, adrenic acid | AUs, arbitrary units | ARA, arachidonic acid | 4-HNE PAs, 4-HNE protein adducts | PSV, Preserved Speech Variant | Mecp2, methyl-CpG-binding protein 2 — mouse gene | wt, wild type | wt-Cre, wild type expressing Cre recombinase | MECP2, methyl-CpG-binding protein 2 — human gene | y, symptomatic Mecp2 308-mutated hemizygous males | ROS, reactive oxygen species | F2-IsoPs, F2-isoprostanes | MeCP2, methyl-CpG-binding protein 2 — human protein | y, Lox | F2-dihomo-IsoPs, F2-dihomo-isoprostanes | 4-HNE PAs, 4-hydroxy-2-nonenal protein adducts | Mecp2 stop | y NestinCre, rescued Lox | ASDs, autism spectrum disorders | F4-NeuroPs, F4-neuroprostanes | Mecp2 308 | stop pre-symptomatic hemizygous mice | x, symptomatic Mecp2 308-mutated females | DHA, docosahexaenoic acid | PUFAs, polyunsaturated fatty acids | BDNF, brain-derived neurotrophic factor | IsoPs, isoprostanes | RTT, Rett syndrome | stop mice (Mecp2 reactivated in the nervous tissue) | 4-HNE, 4-hydroxy-2-nonenal
Journal Article
11/2009
Rett syndrome is a neurological condition that affects primarily girls. Approximately 40% of Rett syndrome cases arise from nonsense mutations. Several studies... 
MeCP2 | Rett syndrome | 0719 | aminoglycosides
Dissertation
BBA - Gene Regulatory Mechanisms, ISSN 1874-9399, 09/2019, Volume 1862, Issue 9, p. 194409
MeCP2 is an abundant protein, involved in transcriptional repression by binding to CG and non-CG methylated DNA. However, MeCP2 might also function as a... 
Non-CG methylated DNA | X-ray crystallography | MeCP2 | MARs | Rett syndrome | GTG containing DNA | BIOCHEMISTRY & MOLECULAR BIOLOGY | SCAFFOLD ATTACHMENT REGION | TRANSCRIPTION | METHYLATED DNA | NEURONAL MECP2 | BIOPHYSICS | GENE | STRUCTURAL BASIS | PURIFICATION | RETT-SYNDROME MUTATIONS | PROTEIN MECP2 | EXPRESSION
Journal Article
Neuropharmacology, ISSN 0028-3908, 06/2019, pp. 107664 - 107664
Post-traumatic stress disorder (PTSD) is a mental disorder characterized by symptoms of persistent anxiety arising after exposure to traumatic events. Stress... 
Journal Article
11/2010
Methyl-CpG-binding proteins (MeCP2, MBD1-MBD3) recruit transcriptional co-repressor molecules to methylated regions and silence transcription. The role of MBD2... 
MeCP2 | behavioral impairments | EEG | MBD2 | 0719
Dissertation
02/2008
Rett syndrome is a rare genetic X-linked dominant disorder. This syndrome is the most frequent cause of mental retardation in girls. In the classical form of... 
MeCP2 | Genetic counseling | Rett syndrome
Web Resource
06/2010
Intractable epilepsy remains one of the top issues affecting the quality of living in Rett children. While several MeCP2-deficient mouse models of Rett... 
Rett Syndrome EEG mice MeCP2 | 0564
Dissertation
Developmental Medicine & Child Neurology, ISSN 0012-1622, 09/2018, Volume 60, Issue 9, pp. 951 - 957
Aim Respiratory illness is a major cause of morbidity and mortality in Rett syndrome. This study investigated respiratory morbidity and relationships with age,... 
MECP2 | PEDIATRICS | CLINICAL NEUROLOGY | CHILDREN
Journal Article
Molecular Syndromology, ISSN 1661-8769, 04/2012, Volume 2, Issue 3-5, pp. 113 - 127
Rett syndrome is one of the most common causes of complex disability in girls. It is characterized by early neurological regression that severely affects... 
Paper | MeCP2 | Rett syndrome
Journal Article