Abnormal social behaviors and altered gene expression rates in a mouse model for Potocki-Lupski syndrome. - Wikidata - wikimedia - TriplyDB

Abnormal social behaviors and altered gene expression rates in a mouse model for Potocki-Lupski syndrome.

Abnormal social behaviors and altered gene expression rates in a mouse model for Potocki-Lupski syndrome.

http://www.wikidata.org/entity/Q34777768

about

Phenotypic consequences of copy number variation: insights from Smith-Magenis and Potocki-Lupski syndrome mouse models Negative allosteric modulation of the mGluR5 receptor reduces repetitive behaviors and rescues social deficits in mouse models of autism.A duplication CNV that conveys traits reciprocal to metabolic syndrome and protects against diet-induced obesity in mice and men Translational Mouse Models of Autism: Advancing Toward Pharmacological Therapeutics.Found in translation: Understanding the biology and behavior of experimental traumatic brain injury Using transcription modules to identify expression clusters perturbed in Williams-Beuren syndrome Behavioural phenotyping assays for mouse models of autism Automated three-chambered social approach task for mice Multiple autism-like behaviors in a novel transgenic mouse model.Enriched rearing improves behavioral responses of an animal model for CNV-based autistic-like traits.Genetic background modulates phenotypes of serotonin transporter Ala56 knock-in mice The effect of translocation-induced nuclear reorganization on gene expression.Rai1 Haploinsufficiency Is Associated with Social Abnormalities in Mice.Retinoic Acid Induced 1, RAI1: A Dosage Sensitive Gene Related to Neurobehavioral Alterations Including Autistic Behavior Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.Overview of mouse models of autism spectrum disorders Copy number variation modifies expression time courses Absence of preference for social novelty and increased grooming in integrin β3 knockout mice: initial studies and future directions.Mouse models of genomic syndromes as tools for understanding the basis of complex traits: an example with the smith-magenis and the potocki-lupski syndromes Genomic sister-disorders of neurodevelopment: an evolutionary approach Sensitized phenotypic screening identifies gene dosage sensitive region on chromosome 11 that predisposes to disease in mice Rare copy number variation in cerebral palsy.Smith-Magenis syndrome: haploinsufficiency of RAI1 results in altered gene regulation in neurological and metabolic pathways.Autism spectrum disorders: the quest for genetic syndromes.Social dysfunction after pediatric traumatic brain injury: A translational perspective.Autism genetics - an overview.Yin-yang actions of histone methylation regulatory complexes in the brain.Trans-acting epigenetic effects of chromosomal aneuploidies: lessons from Down syndrome and mouse models.Deficits in social behavior emerge during development after pediatric traumatic brain injury in mice Searching for Potocki-Lupski syndrome phenotype: a patient with language impairment and no autism.Reciprocal deletion and duplication of 17p11.2-11.2: Korean patients with Smith-Magenis syndrome and Potocki-Lupski syndrome.The behavioural phenotype of Potocki-Lupski syndrome: a cross-syndrome comparison.A candidate circuit approach to investigating autism.Enhanced aggressive behaviour in a mouse model of depression.Segmental copy number variation shapes tissue transcriptomes.Inactivation of the catalytic phosphatase domain of PTPRT/RPTPρ increases social interaction in mice.Definition of a critical genetic interval related to kidney abnormalities in the Potocki-Lupski syndrome.Opposing phenotypes in mice with Smith-Magenis deletion and Potocki-Lupski duplication syndromes suggest gene dosage effects on fluid consumption behavior.

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P2860

Abnormal social behaviors and altered gene expression rates in a mouse model for Potocki-Lupski syndrome.

http://www.wikidata.org/entity/Q34777768

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2008 nî lūn-bûn

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2008 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2008 թվականի մայիսին հրատարակված գիտական հոդված

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2008年の論文

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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Abnormal social behaviors and ...... l for Potocki-Lupski syndrome.

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Abnormal social behaviors and ...... l for Potocki-Lupski syndrome.

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Abnormal social behaviors and ...... l for Potocki-Lupski syndrome.

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Abnormal social behaviors and ...... l for Potocki-Lupski syndrome.

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Abnormal social behaviors and ...... l for Potocki-Lupski syndrome.

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Abnormal social behaviors and ...... l for Potocki-Lupski syndrome.

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Human Molecular Genetics

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Abnormal social behaviors and ...... l for Potocki-Lupski syndrome.

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P2093

César P Canales

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Jacqueline Chrast

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James R Lupski

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Jessica Molina

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Paola M Krall

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P2860

Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes

Strong association of de novo copy number mutations with autism

Genes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouse

Rai1 duplication causes physical and behavioral phenotypes in a mouse model of dup(17)(p11.2p11.2).

Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

Mapping autism risk loci using genetic linkage and chromosomal rearrangements.

Molecular mechanism for duplication 17p11.2- the homologous recombination reciprocal of the Smith-Magenis microdeletion

Genotype-phenotype correlation in Smith-Magenis syndrome: evidence that multiple genes in 17p11.2 contribute to the clinical spectrum

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2486-2495

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scholarly article

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10.1093/HMG/DDN148

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16

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P478

17

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Alexandre Reymond

Paulina Carmona-Mora

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2008-05-10T00:00:00Z

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5382902

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18469339

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