Modeling Autism by SHANK Gene Mutations in Mice

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Items 201–300 of 496

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8. Prefrontal circuits guiding social preference: Implications in autism spectrum disorder
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10. Shank3‐deficient rats exhibit degraded cortical responses to sound
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13. Shank3 Binds to and Stabilizes the Active Form of Rap1 and HRas GTPases via Its NTD-ANK Tandem with Distinct Mechanisms
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15. Dormant state of quiescent neural stem cells links Shank3 mutation to autism development
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16. Postnatal age-differential ASD-like transcriptomic, synaptic, and behavioral deficits in Myt1l-mutant mice
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17. Functional genomics analysis of Phelan-McDermid syndrome 22q13 region during human neurodevelopment
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18. SHANK3 Downregulation in the Ventral Tegmental Area Accelerates the Extinction of Contextual Associations Induced by Juvenile Non-familiar Conspecific Interaction
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19. The Yin and Yang of nucleic acid-based therapy in the brain
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20. Aberrant cognitive phenotypes and altered hippocampal BDNF expression related to epigenetic modifications in mice lacking the post‐synaptic scaffolding protein SHANK1: Implications for autism spectrum disorder
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21. Myosin Va Brain-Specific Mutation Alters Mouse Behavior and Disrupts Hippocampal Synapses
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22. A Presynaptic Function of Shank Protein inDrosophila
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23. Activity and circadian rhythm influence synaptic Shank3 protein levels in mice
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24. An urgent need of experimental animal model of autism in drug development
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25. Early and Late Corrections in Mouse Models of Autism Spectrum Disorder
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26. Acute and crucial requirement for MeCP2 function upon transition from early to late adult stages of brain maturation
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27. Shank2 Binds to aPKC and Controls Tight Junction Formation with Rap1 Signaling during Establishment of Epithelial Cell Polarity
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28. Social propinquity in rodents as measured by tube cooccupancy differs between inbred and outbred genotypes
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29. Alternative polyadenylation and differential expression of Shank mRNAs in the synaptic neuropil
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30. Uncovering True Cellular Phenotypes: Using Induced Pluripotent Stem Cell-Derived Neurons to Study Early Insults in Neurodevelopmental Disorders
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31. Behavioral phenotypes and neurobiological mechanisms in the Shank1 mouse model for autism spectrum disorder: A translational perspective
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32. Identification of two novel Shank3 transcripts in the developing mouse neocortex
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33. Age-dependent decrease of GAD65/67 mRNAs but normal densities of GABAergic interneurons in the brain regions of Shank3 -overexpressing manic mouse model
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34. Novel Therapeutic Approach for Autism Spectrum Disorder: Focus on SHANK3
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35. The enteric nervous system deficits in autism spectrum disorder
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36. Sapap3 deletion causes dynamic synaptic density abnormalities: a longitudinal [11C]UCB-J PET study in a model of obsessive–compulsive disorder-like behaviour
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37. Complete or partial reduction of the Met receptor tyrosine kinase in distinct circuits differentially impacts mouse behavior
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38. Mental disorders and an acidic glycan-from the perspective of polysialic acid (PSA/polySia) and the synthesizing enzyme, ST8SIA2
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39. Social Deficits and Repetitive Behaviors Are Improved by Early Postnatal Low-Dose VPA Intervention in a Novel shank3-Deficient Zebrafish Model
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40. Expression of mutant DISC1 in Purkinje cells increases their spontaneous activity and impairs cognitive and social behaviors in mice
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41. Cognitive impairment and autistic-like behaviour in SAPAP4-deficient mice
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42. POSH regulates assembly of the NMDAR/PSD-95/Shank complex and synaptic function
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43. Age, brain region, and gene dosage-differential transcriptomic changes in Shank3-mutant mice
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44. CaMKII Phosphorylation Regulates Synaptic Enrichment of Shank3
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45. Sam Domains in Multiple Diseases
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46. Defective Synapse Maturation and Enhanced Synaptic Plasticity in Shank2 Δex7 –/– Mice
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47. Neurodevelopmental Disorders: Functional Role of Ambra1 in Autism and Schizophrenia
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48. Mouse models as a tool for discovering new neurological diseases
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49. Neural Stem Cells from Shank3-ko Mouse Model Autism Spectrum Disorders
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50. Diffusion Tensor Imaging Abnormalities in the Uncinate Fasciculus and Inferior Longitudinal Fasciculus in Phelan-McDermid Syndrome
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51. Brain physiome: A concept bridging in vitro 3D brain models and in silico models for predicting drug toxicity in the brain
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52. CRISPR activation rescues abnormalities in SCN2A haploinsufficiency-associated autism spectrum disorder
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54. Defective AMPA-mediated synaptic transmission and morphology in human neurons with hemizygous SHANK3 deletion engrafted in mouse prefrontal cortex
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55. Phenanthrene induces autism-like behavior by promoting oxidative stress and mTOR pathway activation
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56. Limited impact of Cntn4 mutation on autism-related traits in developing and adult C57BL/6J mice
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58. SHANK family on stem cell fate and development
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59. IRSp53 Deletion in Glutamatergic and GABAergic Neurons and in Male and Female Mice Leads to Distinct Electrophysiological and Behavioral Phenotypes
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60. Advancing the discovery of medications for autism spectrum disorder using new technologies to reveal social brain circuitry in rodents
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62. Shank is a dose-dependent regulator of Cav1 calcium current and CREB target expression
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63. The Gut-Microbiota-Brain Axis in Autism Spectrum Disorder
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64. Learning-dependent chromatin remodeling highlights noncoding regulatory regions linked to autism
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67. 40-Hz Auditory Steady-State Response (ASSR) as a Biomarker of Genetic Defects in the SHANK3 Gene: A Case Report of 15-Year-Old Girl with a Rare Partial SHANK3 Duplication
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70. Brain mGluR5 in Shank3B−/− Mice Studied With in vivo [18F]FPEB PET Imaging and ex vivo Immunoblotting
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71. Altered striatum centered brain structures in SHANK3 deficient Chinese children with genotype and phenotype profiling
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74. Sensitivity to isoflurane anesthesia increases in autism spectrum disorder Shank3+/∆c mutant mouse model
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76. Autism Spectrum Disorder
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77. Impaired synaptic function and hyperexcitability of the pyramidal neurons in the prefrontal cortex of autism-associated Shank3 mutant dogs
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78. Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders
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79. Case report: an unexpected link between partial deletion of the SHANK3 gene and Heller’s dementia infantilis, a rare subtype of autism spectrum disorder
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80. Diminished social interaction incentive contributes to social deficits in mouse models of autism spectrum disorder
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81. The Neomycin Resistance Cassette in the Targeted Allele of Shank3B Knock-Out Mice Has Potential Off-Target Effects to Produce an Unusual Shank3 Isoform
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83. Unexpected Compensatory Increase in Shank3 Transcripts in Shank3 Knock-Out Mice Having Partial Deletions of Exons
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84. Apparent Genetic Rescue of AdultShank3Exon 21 Insertion Mutation Mice Tempered by Appropriate Control Experiments
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85. SHANK3 Antibody Validation: Differential Performance in Western Blotting, Immunocyto- and Immunohistochemistry
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93. Postsynaptic Protein Shank3a Deficiency Synergizes with Alzheimer's Disease Neuropathology to Impair Cognitive Performance in the 3xTg-AD Murine Model
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94. SHANK3 in vagal sensory neurons regulates body temperature, systemic inflammation, and sepsis
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95. Glutamatergic agents in Autism Spectrum Disorders: Current trends
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98. Cluster Analysis of Short Sensory Profile Data Reveals Sensory-Based Subgroups in Autism Spectrum Disorder
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99. A blueprint for research on Shankopathies: A view from research on autism spectrum disorder
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