Analysis of cerebellar function in Ube3a-deficient mice reveals novel genotype-specific behaviors - Wikidata - wikimedia - TriplyDB

Analysis of cerebellar function in Ube3a-deficient mice reveals novel genotype-specific behaviors

Analysis of cerebellar function in Ube3a-deficient mice reveals novel genotype-specific behaviors

http://www.wikidata.org/entity/Q33985870

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Angelman syndrome: insights into genomic imprinting and neurodevelopmental phenotypes Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3.Seizure-like activity in a juvenile Angelman syndrome mouse model is attenuated by reducing Arc expression.Behavioral deficits in an Angelman syndrome model: effects of genetic background and age.Comprehensive analysis of ultrasonic vocalizations in a mouse model of fragile X syndrome reveals limited, call type specific deficits Nitrosamine exposure causes insulin resistance diseases: relevance to type 2 diabetes mellitus, non-alcoholic steatohepatitis, and Alzheimer's disease Cerebellar plasticity and motor learning deficits in a copy-number variation mouse model of autism.si-RNA inhibition of brain insulin or insulin-like growth factor receptors causes developmental cerebellar abnormalities: relevance to fetal alcohol spectrum disorder.Normal social seeking behavior, hypoactivity and reduced exploratory range in a mouse model of Angelman syndrome Mitochondrial dysfunction in CA1 hippocampal neurons of the UBE3A deficient mouse model for Angelman syndrome Tissue-specific variation of Ube3a protein expression in rodents and in a mouse model of Angelman syndrome Adeno-associated virus-mediated rescue of the cognitive defects in a mouse model for Angelman syndrome.Role of aspartyl-(asparaginyl)-β-hydroxylase mediated notch signaling in cerebellar development and function.Altered serotonin, dopamine and norepinepherine levels in 15q duplication and Angelman syndrome mouse models Disruption of the LTD dialogue between the cerebellum and the cortex in Angelman syndrome model: a timing hypothesis.Prenatal infection decreases calbindin, decreases Purkinje cell volume and density and produces long-term motor deficits in Sprague-Dawley rats.Imbalanced mechanistic target of rapamycin C1 and C2 activity in the cerebellum of Angelman syndrome mice impairs motor function.E46K human alpha-synuclein transgenic mice develop Lewy-like and tau pathology associated with age-dependent, detrimental motor impairment Toward a Broader View of Ube3a in a Mouse Model of Angelman Syndrome: Expression in Brain, Spinal Cord, Sciatic Nerve and Glial Cells.The neurobiology of mouse models syntenic to human chromosome 15q.Angelman Syndrome.Variation in Dube3a expression affects neurotransmission at the Drosophila neuromuscular junction.Understanding the pathogenesis of Angelman syndrome through animal models LKB1 Regulates Cerebellar Development by Controlling Sonic Hedgehog-mediated Granule Cell Precursor Proliferation and Granule Cell Migration.Dissociation of locomotor and cerebellar deficits in a murine Angelman syndrome model.Comprehensive motor testing in Fmr1-KO mice exposes temporal defects in oromotor coordination Potential therapeutic approaches for Angelman syndrome.The fine temporal structure of the rat licking pattern: what causes the variabiliy in the interlick intervals and how is it affected by the drinking solution?The neuronal code(s) of the cerebellum A technique for stereotaxic recordings of neuronal activity in awake, head-restrained mice.Activity-dependent changes in MAPK activation in the Angelman Syndrome mouse model.Allelic specificity of Ube3a expression in the mouse brain during postnatal development.Genomic imprinting in development, growth, behavior and stem cells Behavioral profiles of mouse models for autism spectrum disorders.E6AP in the brain: one protein, dual function, multiple diseases.Gene discovery and functional assessment of rare copy-number variants in neurodevelopmental disorders.Cerebellar and Striatal Pathologies in Mouse Models of Autism Spectrum Disorder.mTORC1-S6K1 inhibition or mTORC2 activation improves hippocampal synaptic plasticity and learning in Angelman syndrome mice Touchscreen learning deficits in Ube3a, Ts65Dn and Mecp2 mouse models of neurodevelopmental disorders with intellectual disabilities.Reversal of reduced parvalbumin neurons in hippocampus and amygdala of Angelman syndrome model mice by chronic treatment of fluoxetine.

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P2860

Analysis of cerebellar function in Ube3a-deficient mice reveals novel genotype-specific behaviors

http://www.wikidata.org/entity/Q33985870

description

2008 nî lūn-bûn

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2008 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2008 թվականի ապրիլին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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Analysis of cerebellar functio ...... el genotype-specific behaviors

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Analysis of cerebellar functio ...... el genotype-specific behaviors

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Analysis of cerebellar functio ...... el genotype-specific behaviors

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Analysis of cerebellar functio ...... el genotype-specific behaviors

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Analysis of cerebellar functio ...... el genotype-specific behaviors

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Human Molecular Genetics

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Analysis of cerebellar functio ...... el genotype-specific behaviors

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P2093

Mark S LeDoux

http://www.w3.org/2001/XMLSchema#string

Snigdha Roy

http://www.w3.org/2001/XMLSchema#string

Yu Zhao

http://www.w3.org/2001/XMLSchema#string

P2860

UBE3A/E6-AP mutations cause Angelman syndrome

Neural correlates of the emergence of consciousness of thirst

Behavioral phenotyping of transgenic and knockout mice: experimental design and evaluation of general health, sensory functions, motor abilities, and specific behavioral tests.

Clinical profile of Angelman syndrome at different ages.

Neuroimaging evidence implicating cerebellum in support of sensory/cognitive processes associated with thirst

Epigenetics and human disease.

A low-cost solution to measure mouse licking in an electrophysiological setup with a standard analog-to-digital converter.

Molecular epigenetics of Angelman syndrome.

Advances in behavioral genetics: mouse models of autism.

Expression of the Rho-GEF Pbl/ECT2 is regulated by the UBE3A E3 ubiquitin ligase

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10.1093/HMG/DDN117

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14

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17

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Lawrence T Reiter

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2008-04-15T00:00:00Z

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5439978

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18413322

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2902285

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