Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice. - Wikidata - awgldk - TriplyDB

Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice.

Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice.

http://www.wikidata.org/entity/Q36737172

about

Neuropathology and animal models of autism: genetic and environmental factors mTOR is a key modulator of ageing and age-related disease Congenital hypoplasia of the cerebellum: developmental causes and behavioral consequences Clinical and Neurobiological Relevance of Current Animal Models of Autism Spectrum Disorders.RELN Mutations in Autism Spectrum Disorder Cortico-Cerebellar Connectivity in Autism Spectrum Disorder: What Do We Know So Far?Ribosomal Protein S6 Phosphorylation in the Nervous System: From Regulation to Function Behavioral phenotypes of genetic mouse models of autism.Genes, circuits, and precision therapies for autism and related neurodevelopmental disorders The role of cerebellar circuitry alterations in the pathophysiology of autism spectrum disorders Roles of mTOR Signaling in Brain Development The neurology of mTOR Autism spectrum disorders and neuropathology of the cerebellum The cerebellum and psychiatric disorders Channelopathy pathogenesis in autism spectrum disorders Potential for treatment of severe autism in tuberous sclerosis complex Behavioral and Neuroanatomical Phenotypes in Mouse Models of Autism Reinstating aberrant mTORC1 activity in Huntington's disease mice improves disease phenotypes.Seizure-dependent mTOR activation in 5-HT neurons promotes autism-like behaviors in mice PX-RICS-deficient mice mimic autism spectrum disorder in Jacobsen syndrome through impaired GABAA receptor trafficking Dysfunctional cerebellar Purkinje cells contribute to autism-like behaviour in Shank2-deficient mice.Crystal structure of the yeast TSC1 core domain and implications for tuberous sclerosis pathological mutations Genetic aspects of autism spectrum disorders: insights from animal models Modulation, Plasticity and Pathophysiology of the Parallel Fiber-Purkinje Cell Synapse.Advancing the understanding of autism disease mechanisms through genetics LTD-like molecular pathways in developmental synaptic pruning A Subset of Autism-Associated Genes Regulate the Structural Stability of Neurons.Loss of mTOR-dependent macroautophagy causes autistic-like synaptic pruning deficits GABAB Receptor Agonist R-Baclofen Reverses Social Deficits and Reduces Repetitive Behavior in Two Mouse Models of Autism Translational Mouse Models of Autism: Advancing Toward Pharmacological Therapeutics.Neuronal Tsc1/2 complex controls autophagy through AMPK-dependent regulation of ULK1 Autism-related deficits via dysregulated eIF4E-dependent translational control.ASD-relevant Animal Models of the Foxp Family of Transcription Factors The neuroanatomy of autism - a developmental perspective A Critical Period in Purkinje Cell Development Is Mediated by Local Estradiol Synthesis, Disrupted by Inflammation, and Has Enduring Consequences Only for Males.Primary Cilia as a Possible Link between Left-Right Asymmetry and Neurodevelopmental Diseases.Rare deleterious mutations of the gene EFR3A in autism spectrum disorders.Tricornered Kinase Regulates Synapse Development by Regulating the Levels of Wiskott-Aldrich Syndrome Protein The cerebellum, sensitive periods, and autism.In vivo synaptic transmission and morphology in mouse models of Tuberous sclerosis, Fragile X syndrome, Neurofibromatosis type 1, and Costello syndrome

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P2860

Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice.

http://www.wikidata.org/entity/Q36737172

description

2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

@zh-tw

2012年论文

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2012年论文

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2012年论文

@zh-cn

name

Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice.

@ast

Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice.

@en

type

label

Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice.

@ast

Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice.

@en

prefLabel

Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice.

@ast

Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice.

@en

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Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice.

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Abbey R Sadowski

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Emily Greene-Colozzi

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Jacqueline N Crawley

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Jarrett M Leech

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Jason Steinberg

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Peter T Tsai

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Wade G Regehr

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YunXiang Chu

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P2860

Neuroanatomy of autism

The study of autism as a distributed disorder

Disorders of the Cerebellum: Ataxia, Dysmetria of Thought, and the Cerebellar Cognitive Affective Syndrome

A mouse model of TSC1 reveals sex-dependent lethality from liver hemangiomas, and up-regulation of p70S6 kinase activity in Tsc1 null cells

Prevalence of autism spectrum disorders - Autism and Developmental Disabilities Monitoring Network, United States, 2006

A mouse model of tuberous sclerosis: neuronal loss of Tsc1 causes dysplastic and ectopic neurons, reduced myelination, seizure activity, and limited survival

Regulation of neuronal morphology and function by the tumor suppressors Tsc1 and Tsc2

Tuberous sclerosis complex proteins control axon formation

Sociability and motor functions in Shank1 mutant mice

Automated three-chambered social approach task for mice

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