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Neuron, ISSN 0896-6273, 03/2012, Volume 73, Issue 6, pp. 1143 - 1158
Mutations in TSPAN7—a member of the tetraspanin protein superfamily—are implicated in some forms of X-linked intellectual disability. Here we show that TSPAN7... 
DENDRITIC SPINES | GLUTAMATE RECEPTORS | MENTAL-RETARDATION | TRANSMEMBRANE 4 SUPERFAMILY | KINASE-C-ALPHA | RECEPTOR TRAFFICKING | PICK1 | ACTIVITY-DEPENDENT REGULATION | HIPPOCAMPAL-NEURONS | NEUROSCIENCES | TETRASPANIN PROTEINS | Disks Large Homolog 4 Protein | Electric Stimulation | Embryo, Mammalian | Humans | Green Fluorescent Proteins - genetics | Intracellular Signaling Peptides and Proteins - metabolism | Protein Transport - drug effects | Synapses - genetics | Long-Term Potentiation - drug effects | Time Factors | Tetraspanins - genetics | Excitatory Postsynaptic Potentials - genetics | Receptors, AMPA - metabolism | Dendritic Spines - physiology | Gene Expression Regulation, Developmental - drug effects | Rats | Protein Transport - genetics | Hydrazones - pharmacology | Microscopy, Confocal | Patch-Clamp Techniques | Analysis of Variance | RNA, Small Interfering - metabolism | Immunoprecipitation | Cercopithecus aethiops | Gene Expression Regulation, Developmental - genetics | Excitatory Postsynaptic Potentials - drug effects | Pseudopodia - drug effects | Transfection | Dendritic Spines - drug effects | Neurons - physiology | Membrane Proteins - metabolism | Tetraspanins - metabolism | Green Fluorescent Proteins - metabolism | Synapses - physiology | RNA, Small Interfering - pharmacology | Cells, Cultured | Nuclear Proteins - metabolism | Long-Term Potentiation - genetics | Biophysics | Hippocampus - cytology | Nerve Tissue Proteins - genetics | Integrin beta1 - metabolism | Nerve Tissue Proteins - metabolism | Two-Hybrid System Techniques | Animals | Carrier Proteins - metabolism | Pseudopodia - genetics | Dendritic Spines - genetics | In Vitro Techniques | Neurons | Neurosciences | Proteins | Brain | Brain research | Mutation | Rodents | alpha -Amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptors | Head | Synaptogenesis | X chromosome | Pseudopodia | Embryos | Mental retardation | Dendritic spines | Development | Glutamatergic transmission | Protein transport | Hippocampus | Synapses
Journal Article
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 757 - 17
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 2018, Volume 293, Issue 3, pp. 1040 - 1053
L-type voltage-gated Ca V 1.2 calcium channels (Ca V 1.2) are key regulators of neuronal excitability, synaptic plasticity, and excitation-transcription... 
Ser1928 | Molecular Biophysics | fluorescence | dihydropyridine receptor (DHPR) | excitatory | neuron | Ser1700 | molecular dynamics | imaging | trafficking | L-type Ca2+ channels
Journal Article
Frontiers in Molecular Neuroscience, ISSN 1662-5099, 09/2018, Volume 11
Fragile X syndrome (FXS), the most common form of inherited intellectual disability (ID) and a leading cause of autism, results from the loss of expression of... 
Fragile X syndrome | 2.1 | Ratiometric calcium imaging | Cacna1a | Calcium homeostasis | Causes of | Autism | Cell membranes | Research | Protein binding | calcium homeostasis | ratiometric calcium imaging | Cav2.1
Journal Article
Journal Article
Cerebral Cortex, ISSN 1047-3211, 11/2017, Volume 27, Issue 11, pp. 5369 - 5384
Intellectual disability affects 2-3% of the world's population and typically begins during childhood, causing impairments in social skills and cognitive... 
ampakine | hippocampus | animal model | TSPAN7 | Original
Journal Article
Frontiers in Molecular Neuroscience, ISSN 1662-5099, 01/2016, Volume 9, p. 1
Myosin IXa (Myo9a) is a motor protein that is highly expressed in the brain. However, the role of Myo9a in neurons remains unknown. Here, we investigated Myo9a... 
PSD | LTP | Hippocampal synapses | AMPAR | Myosin IXa | PROTEIN | hippocampal synapses | NEUROSCIENCES | GTPASES | SYNAPSES | RECEPTOR TRAFFICKING | NEURONS | OBJECT RECOGNITION | LONG-TERM POTENTIATION | RAT-BRAIN | EXPRESSION | PLASTICITY | Cognition | Muscle proteins | Health aspects | Myosin
Journal Article
Frontiers in molecular neuroscience, ISSN 1662-5099, 2018, Volume 11, p. 342
Fragile X syndrome (FXS), the most common form of inherited intellectual disability (ID) and a leading cause of autism, results from the loss of expression of... 
Journal Article
The Journal of biological chemistry, 01/2018, Volume 293, Issue 3, p. 1040
L-type voltage-gated Ca 1.2 calcium channels (Ca 1.2) are key regulators of neuronal excitability, synaptic plasticity, and excitation-transcription coupling.... 
Journal Article