Replicable in vivo physiological and behavioral phenotypes of the Shank3B null mutant mouse model of autism
出版年份 2017 全文链接
标题
Replicable in vivo physiological and behavioral phenotypes of the Shank3B null mutant mouse model of autism
作者
关键词
<em class=EmphasisTypeItalic >Shank3B</em>, Pentylenetetrazol, Gamma oscillations, Repetitive behavior, Social behavior, Autism, Anxiety
出版物
Molecular Autism
Volume 8, Issue 1, Pages -
出版商
Springer Nature
发表日期
2017-06-15
DOI
10.1186/s13229-017-0142-z
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Novel Shank3 mutant exhibits behaviors with face validity for autism and altered striatal and hippocampal function
- (2016) Thomas C. Jaramillo et al. Autism Research
- Considerations in biomarker development for neurodevelopmental disorders
- (2016) James C. McPartland CURRENT OPINION IN NEUROLOGY
- The spectrum of epilepsy and electroencephalographic abnormalities due toSHANK3loss-of-function mutations
- (2016) J. Lloyd Holder et al. EPILEPSIA
- Identification and validation of biomarkers for autism spectrum disorders
- (2016) Eva Loth et al. NATURE REVIEWS DRUG DISCOVERY
- Recent Advances in Resting-State Electroencephalography Biomarkers for Autism Spectrum Disorder—A Review of Methodological and Clinical Challenges
- (2016) Tosca-Marie Heunis et al. PEDIATRIC NEUROLOGY
- Altered mGluR5-Homer scaffolds and corticostriatal connectivity in a Shank3 complete knockout model of autism
- (2016) Xiaoming Wang et al. Nature Communications
- Defining Precision Medicine Approaches to Autism Spectrum Disorders: Concepts and Challenges
- (2016) Eva Loth et al. Frontiers in Psychiatry
- EEG biomarkers of target engagement, therapeutic effect, and disease process
- (2015) Robert E. Featherstone et al. Annals of the New York Academy of Sciences
- Recent Advances in Autism Research as Reflected in DSM-5 Criteria for Autism Spectrum Disorder
- (2015) Catherine Lord et al. Annual Review of Clinical Psychology
- 16p11.2 Deletion Syndrome Mice Display Sensory and Ultrasonic Vocalization Deficits During Social Interactions
- (2015) Mu Yang et al. Autism Research
- Altered Striatal Synaptic Function and Abnormal Behaviour inShank3Exon4-9 Deletion Mouse Model of Autism
- (2015) Thomas C. Jaramillo et al. Autism Research
- Huperzine A prophylaxis against pentylenetetrazole-induced seizures in rats is associated with increased cortical inhibition
- (2015) R. Gersner et al. EPILEPSY RESEARCH
- The 16p11.2 Deletion Mouse Model of Autism Exhibits Altered Cortical Progenitor Proliferation and Brain Cytoarchitecture Linked to the ERK MAPK Pathway
- (2015) J. Pucilowska et al. JOURNAL OF NEUROSCIENCE
- Autism-Associated Insertion Mutation (InsG) of Shank3 Exon 21 Causes Impaired Synaptic Transmission and Behavioral Deficits
- (2015) H. E. Speed et al. JOURNAL OF NEUROSCIENCE
- 16p11.2 Deletion mice display cognitive deficits in touchscreen learning and novelty recognition tasks
- (2015) M. Yang et al. LEARNING & MEMORY
- From the genetic architecture to synaptic plasticity in autism spectrum disorder
- (2015) Thomas Bourgeron NATURE REVIEWS NEUROSCIENCE
- GABAB Receptor Agonist R-Baclofen Reverses Social Deficits and Reduces Repetitive Behavior in Two Mouse Models of Autism
- (2015) J L Silverman et al. NEUROPSYCHOPHARMACOLOGY
- Behavioral assessment of NIH Swiss mice acutely intoxicated with tetramethylenedisulfotetramine
- (2015) Brenna M. Flannery et al. NEUROTOXICOLOGY AND TERATOLOGY
- Autism spectrum disorder in Phelan-McDermid syndrome: initial characterization and genotype-phenotype correlations
- (2015) Lindsay M. Oberman et al. Orphanet Journal of Rare Diseases
- Evaluation of the neuroactive steroid ganaxolone on social and repetitive behaviors in the BTBR mouse model of autism
- (2015) Tatiana M. Kazdoba et al. PSYCHOPHARMACOLOGY
- Genes, circuits, and precision therapies for autism and related neurodevelopmental disorders
- (2015) M. Sahin et al. SCIENCE
- Autism-like Deficits in Shank3-Deficient Mice Are Rescued by Targeting Actin Regulators
- (2015) Lara J. Duffney et al. Cell Reports
- The Parvalbumin/Somatostatin Ratio Is Increased in Pten Mutant Mice and by Human PTEN ASD Alleles
- (2015) Daniel Vogt et al. Cell Reports
- Phenotypic and functional analysis of SHANK3 stop mutations identified in individuals with ASD and/or ID
- (2015) Daniela M Cochoy et al. Molecular Autism
- Ultrastructural analyses in the hippocampus CA1 field in Shank3-deficient mice
- (2015) Neha Uppal et al. Molecular Autism
- Whole Genome Sequencing Reveals a De Novo SHANK3 Mutation in Familial Autism Spectrum Disorder
- (2015) Sergio I. Nemirovsky et al. PLoS One
- Association study between autistic-like traits and polymorphisms in the autism candidate regions RELN, CNTNAP2, SHANK3, and CDH9/10
- (2015) Lina Jonsson et al. Molecular Autism
- Absence of strong strain effects in behavioral analyses of Shank3-deficient mice
- (2014) E. Drapeau et al. Disease Models & Mechanisms
- Cellular origins of auditory event-related potential deficits in Rett syndrome
- (2014) Darren Goffin et al. NATURE NEUROSCIENCE
- Behavioral Abnormalities and Circuit Defects in the Basal Ganglia of a Mouse Model of 16p11.2 Deletion Syndrome
- (2014) Thomas Portmann et al. Cell Reports
- Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments
- (2014) Claire S. Leblond et al. PLoS Genetics
- Loss of Predominant Shank3 Isoforms Results in Hippocampus-Dependent Impairments in Behavior and Synaptic Transmission
- (2013) M. Kouser et al. JOURNAL OF NEUROSCIENCE
- SHANK3 overexpression causes manic-like behaviour with unique pharmacogenetic properties
- (2013) Kihoon Han et al. NATURE
- NINDS epilepsy and autism spectrum disorders workshop report
- (2013) R. Tuchman et al. NEUROLOGY
- Modeling Autism by SHANK Gene Mutations in Mice
- (2013) Yong-hui Jiang et al. NEURON
- SHANK3 haploinsufficiency: a “common” but underdiagnosed highly penetrant monogenic cause of autism spectrum disorders
- (2013) Catalina Betancur et al. Molecular Autism
- Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency
- (2013) Latha Soorya et al. Molecular Autism
- Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders
- (2012) Luigi Boccuto et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Reduced Excitatory Neurotransmission and Mild Autism-Relevant Phenotypes in Adolescent Shank3 Null Mutant Mice
- (2012) M. Yang et al. JOURNAL OF NEUROSCIENCE
- Early Behavioral Intervention Is Associated With Normalized Brain Activity in Young Children With Autism
- (2012) Geraldine Dawson et al. JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
- AMPAKINE enhancement of social interaction in the BTBR mouse model of autism
- (2012) J.L. Silverman et al. NEUROPHARMACOLOGY
- Autism-Relevant Social Abnormalities and Cognitive Deficits in Engrailed-2 Knockout Mice
- (2012) Jennifer Brielmaier et al. PLoS One
- Negative Allosteric Modulation of the mGluR5 Receptor Reduces Repetitive Behaviors and Rescues Social Deficits in Mouse Models of Autism
- (2012) J. L. Silverman et al. Science Translational Medicine
- RETRACTED: Enhanced Polyubiquitination of Shank3 and NMDA Receptor in a Mouse Model of Autism
- (2011) M Ali Bangash et al. CELL
- Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3
- (2011) Xiaoming Wang et al. HUMAN MOLECULAR GENETICS
- Shank3 mutant mice display autistic-like behaviours and striatal dysfunction
- (2011) João Peça et al. NATURE
- Novel variants of the SHANK3 gene in Japanese autistic patients with severe delayed speech development
- (2011) Chikako Waga et al. PSYCHIATRIC GENETICS
- Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication
- (2011) Ozlem Bozdagi et al. Molecular Autism
- Analysis of a purported SHANK3 mutation in a boy with autism: Clinical impact of rare variant research in neurodevelopmental disabilities
- (2010) Alexander Kolevzon et al. BRAIN RESEARCH
- Sociability and motor functions in Shank1 mutant mice
- (2010) Jill L. Silverman et al. BRAIN RESEARCH
- Unusual repertoire of vocalizations in adult BTBR T+tf/J mice during three types of social encounters
- (2010) M. L. Scattoni et al. GENES BRAIN AND BEHAVIOR
- Behavioural phenotyping assays for mouse models of autism
- (2010) Jill L. Silverman et al. NATURE REVIEWS NEUROSCIENCE
- Low stress reactivity and neuroendocrine factors in the BTBR T+tf/J mouse model of autism
- (2010) J.L. Silverman et al. NEUROSCIENCE
- Association study of SHANK3 gene polymorphisms with autism in Chinese Han population
- (2009) Jian Qin et al. BMC Medical Genetics
- A synaptic trek to autism
- (2009) Thomas Bourgeron CURRENT OPINION IN NEUROBIOLOGY
- Common circuit defect of excitatory-inhibitory balance in mouse models of autism
- (2009) Nadine Gogolla et al. Journal of Neurodevelopmental Disorders
- Parvalbumin neurons and gamma rhythms enhance cortical circuit performance
- (2009) Vikaas S. Sohal et al. NATURE
- Driving fast-spiking cells induces gamma rhythm and controls sensory responses
- (2009) Jessica A. Cardin et al. NATURE
- Marble burying reflects a repetitive and perseverative behavior more than novelty-induced anxiety
- (2009) Alexia Thomas et al. PSYCHOPHARMACOLOGY
- Novel de novo SHANK3 mutation in autistic patients
- (2008) Julie Gauthier et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- Minimal aberrant behavioral phenotypes of neuroligin-3 R451C knockin mice
- (2008) Kathryn K. Chadman et al. Autism Research
- Petilla terminology: nomenclature of features of GABAergic interneurons of the cerebral cortex
- (2008) NATURE REVIEWS NEUROSCIENCE
- Autism-like behavioral phenotypes in BTBR T+tf/J mice
- (2007) H. G. McFarlane et al. GENES BRAIN AND BEHAVIOR
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started