Emerging major synaptic signaling pathways involved in intellectual disability.
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SYNGAP1: Mind the GapBRaf signaling principles unveiled by large-scale human mutation analysis with a rapid lentivirus-based gene replacement method.Impaired Dendritic Development and Memory in Sorbs2 Knock-Out Mice.The pseudokinase CaMKv is required for the activity-dependent maintenance of dendritic spines.Human post-mortem synapse proteome integrity screening for proteomic studies of postsynaptic complexesHuman intellectual disability genes form conserved functional modules in Drosophila.BRF1 mutations alter RNA polymerase III-dependent transcription and cause neurodevelopmental anomalies.Psychopathology and cognitive performance in individuals with membrane-associated guanylate kinase mutations: a functional network phenotyping study.δ-Catenin Regulates Spine Architecture via Cadherin and PDZ-dependent Interactions.Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules.Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigreeFMRP regulates actin filament organization via the armadillo protein p0071.Molecular mechanisms of dendrite morphogenesis.Genetic architecture of cognitive traits.Targeted deep resequencing identifies MID2 mutation for X-linked intellectual disability with varied disease severity in a large kindred from India.Euchromatin histone methyltransferase 1 regulates cortical neuronal network development.Ring finger protein 10 is a novel synaptonuclear messenger encoding activation of NMDA receptors in hippocampusInvolvement of the kinesin family members KIF4A and KIF5C in intellectual disability and synaptic function.Hippocampal dysfunction in the Euchromatin histone methyltransferase 1 heterozygous knockout mouse model for Kleefstra syndrome.Spatiotemporal profile of postsynaptic interactomes integrates components of complex brain disorders.Sestd1 Encodes a Developmentally Dynamic Synapse Protein That Complexes With BCR Rac1-GAP to Regulate Forebrain Dendrite, Spine and Synapse Formation.Improvement of Self-Injury With Dopamine and Serotonin Replacement Therapy in a Patient With a Hemizygous PAK3 Mutation: A New Therapeutic Strategy for Neuropsychiatric Features of an Intellectual Disability Syndrome.The molecular and phenotypic spectrum of IQSEC2-related epilepsy.Supporting the generalist genes hypothesis for intellectual ability/disability: the case of SNAP25.Fasudil treatment in adult reverses behavioural changes and brain ventricular enlargement in Oligophrenin-1 mouse model of intellectual disability.The Multifarious Hippocampal Functions of MicroRNA-137.Early-onset epileptic encephalopathy and severe developmental delay in an association with de novo double mutations in NF1 and MAGEL2.
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Emerging major synaptic signaling pathways involved in intellectual disability.
description
article científic
@ca
article scientifique
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articol științific
@ro
articolo scientifico
@it
artigo científico
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artigo científico
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artigo científico
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artikel ilmiah
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artikull shkencor
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artículo científico
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name
Emerging major synaptic signaling pathways involved in intellectual disability.
@en
Emerging major synaptic signaling pathways involved in intellectual disability.
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type
label
Emerging major synaptic signaling pathways involved in intellectual disability.
@en
Emerging major synaptic signaling pathways involved in intellectual disability.
@nl
prefLabel
Emerging major synaptic signaling pathways involved in intellectual disability.
@en
Emerging major synaptic signaling pathways involved in intellectual disability.
@nl
P2860
P356
P1433
P1476
Emerging major synaptic signaling pathways involved in intellectual disability.
@en
P2093
P2860
P2888
P304
P356
10.1038/MP.2011.139
P407
P577
2011-10-25T00:00:00Z