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JOURNAL OF PHYSIOLOGY-LONDON, ISSN 0022-3751, 03/2007, Volume 579, Issue 3, pp. 863 - 876
Rett syndrome (RTT) is an inborn neurodevelopmental disorder caused by mutations in the X-linked methyl-CpG binding protein 2 gene (MECP2). Besides mental... 
PHYSIOLOGY | AUTONOMIC DYSFUNCTION | RETT-SYNDROME | MOUSE MODEL | BIOGENIC-AMINES | KOLLIKER-FUSE NUCLEUS | CPG-BINDING PROTEIN-2 | MECP2-NULL MOUSE | RESPIRATORY RHYTHM GENERATION | BRAIN-STEM NUCLEI | SYNAPTIC PLASTICITY
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2014, Volume 9, Issue 3, p. e92169
Proper brain functioning requires a fine-tuning between excitatory and inhibitory neurotransmission, a balance maintained through the regulation and release of... 
HIPPOCAMPAL SLICES | DECARBOXYLASE | SYNAPTIC CIRCUIT ABNORMALITIES | NEUROTRANSMISSION | RETT-SYNDROME | RAT | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | GAMMA-AMINOBUTYRIC-ACID | 2/3 PYRAMIDAL NEURONS | MECP2-NULL MOUSE | gamma-Aminobutyric Acid - metabolism | Male | Synaptic Transmission | Brain - metabolism | Gene Expression Regulation, Developmental | Nipecotic Acids - pharmacology | Real-Time Polymerase Chain Reaction | gamma-Aminobutyric Acid - genetics | Signal Transduction | Mice, Inbred C57BL | RNA, Messenger - genetics | Cells, Cultured | gamma-Aminobutyric Acid - chemistry | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Mice, Knockout | Brain - drug effects | Rett Syndrome - etiology | Rett Syndrome - metabolism | Methyl-CpG-Binding Protein 2 - physiology | Animals | Rett Syndrome - pathology | GABA Agonists - pharmacology | Brain - pathology | Glutamic Acid - metabolism | Mice | Brain | Nervous system diseases | Neurons | Analysis | GABA | Glutamate | Neurophysiology | Protein binding | mRNA | Neuromodulation | Modulators | Proteins | γ-Aminobutyric acid | Pathways | Methyl-CpG binding protein | Rodents | Age | CpG islands | Pharmacology | Gene expression | Chemical compounds | Studies | Acids | Life span | MeCP2 protein | Multilevel | Rett syndrome | Glutamatergic transmission | Mutation | Laboratory animals | Neurotransmission | Life Sciences | Neurons and Cognition | Neurobiology
Journal Article
Journal of Neuroinflammation, ISSN 1742-2094, 12/2017, Volume 14, Issue 1, pp. 252 - 19
Background: Rett syndrome (RTT) is a pervasive developmental disorder that is progressive and has no effective cure. Immune dysregulation, oxidative stress,... 
Mecp2-null | System Xc | N-Acetyl cysteine | Rett syndrome | Glutamate | PAMAM dendrimer | Microglia | ANTIPORTER SYSTEM X(C)(-) | DRUG | OXIDATIVE STRESS | WILD-TYPE MICROGLIA | CYSTINE UPTAKE | System Xc(-) | ACETYLCYSTEINE | MECHANISMS | IMMUNOLOGY | NEUROSCIENCES | CYSTINE/GLUTAMATE ANTIPORTER | GLUTATHIONE
Journal Article
Biological Psychiatry, ISSN 0006-3223, 2015, Volume 79, Issue 9, pp. 755 - 764
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2014, Volume 9, Issue 7, p. e103906
Originally published, uncorrected article. https://doi.org/10.1371/journal.pone.0103906.s001 (PDF). Ho ECY, Eubanks JH, Zhang L, Skinner FK (2014) Network... 
Animal models | Methyl-CpG binding protein | MeCP2 protein | Rodents | Excitability | Variations | Hippocampus
Journal Article
Journal of Neuroscience Research, ISSN 0360-4012, 10/2016, Volume 94, Issue 10, pp. 896 - 906
Journal Article
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, ISSN 0363-6143, 12/2016, Volume 311, Issue 6, pp. C895 - C909
Rett Syndrome RTT) is an X-linked neurodevelopmental disorder caused mostly by disruption of the MECP2 gene. Among several RTT-like mouse models, one of them... 
MECP2-NULL MICE | Mecp2 | WILD-TYPE | PHYSIOLOGY | breathing | PHENOTYPE | R168X | locus coeruleus | CELL BIOLOGY | electrophysiology | Rett syndrome | MEMBRANE-PROPERTIES | LOCUS-COERULEUS NEURONS | SYNDROME MUTATIONS | Me5 | DEFICITS | EXPRESSION
Journal Article
American Journal of Physiology - Cell Physiology, ISSN 0363-6143, 09/2014, Volume 307, Issue 6, pp. C508 - C520
Journal Article
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2016, Volume 11, Issue 1, p. e0146470
Journal Article
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