Synaptic Dysfunction in Neurodevelopmental Disorders Associated with Autism and Intellectual Disabilities

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Items 201–300 of 797

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18. The autism associated MET receptor tyrosine kinase engages early neuronal growth mechanism and controls glutamatergic circuits development in the forebrain
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26. Leveraging large genomic datasets to illuminate the pathobiology of autism spectrum disorders
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31. Systematic reconstruction of autism biology from massive genetic mutation profiles
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32. Synapse-Selective Control of Cortical Maturation and Plasticity by Parvalbumin-Autonomous Action of SynCAM 1
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33. Mechanisms Underlying Circuit Dysfunction in Neurodevelopmental Disorders
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35. Towards understanding sex differences in autism spectrum disorders
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36. Possible Implication of the CA2 Hippocampal Circuit in Social Cognition Deficits Observed in the Neuroligin 3 Knock-Out Mouse, a Non-Syndromic Animal Model of Autism
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37. Human Intellectual Disability Genes Form Conserved Functional Modules in Drosophila
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39. Resolving the Synaptic versus Developmental Dichotomy of Autism Risk Genes
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40. Synaptic plasticity and cognitive function are disrupted in the absence of Lrp4
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41. ARID1B controls transcriptional programs of axon projection in an organoid model of the human corpus callosum
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44. MeCP2 Regulates the Synaptic Expression of a Dysbindin-BLOC-1 Network Component in Mouse Brain and Human Induced Pluripotent Stem Cell-Derived Neurons
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45. Alleviation of N-Methyl-d-Aspartate Receptor-Dependent Long-Term Depression via Regulation of the Glycogen Synthase Kinase-3β Pathway in the Amygdala of a Valproic Acid-Induced Animal Model of Autism
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46. Abnormal behaviours relevant to neurodevelopmental disorders in Kirrel3-knockout mice
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48. Loss of Mecp2 Causes Atypical Synaptic and Molecular Plasticity of Parvalbumin-Expressing Interneurons Reflecting Rett Syndrome–Like Sensorimotor Defects
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50. Investigating mechanisms underlying neurodevelopmental phenotypes of autistic and intellectual disability disorders: a perspective
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51. Roles of Glial Cells in Sculpting Inhibitory Synapses and Neural Circuits
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52. Probing disrupted neurodevelopment in autism using human stem cell‐derived neurons and organoids: An outlook into future diagnostics and drug development
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54. Apparent bias toward long gene misregulation in MeCP2 syndromes disappears after controlling for baseline variations
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56. Sarm1 deficiency impairs synaptic function and leads to behavioral deficits, which can be ameliorated by an mGluR allosteric modulator
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57. A review of gene–environment correlations and their implications for autism: A conceptual model.
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58. Ablation of TFR1 in Purkinje Cells Inhibits mGlu1 Trafficking and Impairs Motor Coordination, But Not Autistic-Like Behaviors
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