IL1RAPL1 knockout mice show spine density decrease, learning deficiency, hyperactivity and reduced anxiety-like behaviours
出版年份 2014 全文链接
标题
IL1RAPL1 knockout mice show spine density decrease, learning deficiency, hyperactivity and reduced anxiety-like behaviours
作者
关键词
-
出版物
Scientific Reports
Volume 4, Issue 1, Pages -
出版商
Springer Nature
发表日期
2014-10-14
DOI
10.1038/srep06613
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- The hippocampo-amygdala control of contextual fear expression is affected in a model of intellectual disability
- (2014) Chun-Lei Zhang et al. Brain Structure & Function
- Contextual and Cued Fear Conditioning Test Using a Video Analyzing System in Mice
- (2014) Hirotaka Shoji et al. Jove-Journal of Visualized Experiments
- Intragenic ILRAPL1 deletion in a male patient with intellectual disability, mild dysmorphic signs, deafness, and behavioral problems
- (2013) Chiara Barone et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- New innovations: Therapeutic opportunities for intellectual disabilities
- (2013) Jonathan D. Picker et al. ANNALS OF NEUROLOGY
- Target-Specific Vulnerability of Excitatory Synapses Leads to Deficits in Associative Memory in a Model of Intellectual Disorder
- (2013) X. Houbaert et al. JOURNAL OF NEUROSCIENCE
- Correction: Construction and Characterization of Normalized cDNA Libraries by 454 Pyrosequencing and Estimation of DNA Methylation Levels in Three Distantly Related Termite Species
- (2013) Yoshinobu Hayashi et al. PLoS One
- Slitrks control excitatory and inhibitory synapse formation with LAR receptor protein tyrosine phosphatases
- (2013) Y. S. Yim et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Genetic Basis of Intellectual Disability
- (2012) Jay W. Ellison et al. Annual Review of Medicine
- Interleukin-1 Receptor Accessory Protein Organizes Neuronal Synaptogenesis as a Cell Adhesion Molecule
- (2012) T. Yoshida et al. JOURNAL OF NEUROSCIENCE
- Selective control of inhibitory synapse development by Slitrk3-PTPδ trans-synaptic interaction
- (2012) Hideto Takahashi et al. NATURE NEUROSCIENCE
- Comprehensive behavioral analysis of pituitary adenylate cyclase-activating polypeptide (PACAP) knockout mice
- (2012) Satoko Hattori et al. Frontiers in Behavioral Neuroscience
- T-maze Forced Alternation and Left-right Discrimination Tasks for Assessing Working and Reference Memory in Mice
- (2012) Hirotaka Shoji et al. Jove-Journal of Visualized Experiments
- Deletion of the immunoglobulin domain of IL1RAPL1 results in nonsyndromic X-linked intellectual disability associated with behavioral problems and mild dysmorphism
- (2011) Karl J. Franek et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Genetic and Epigenetic Networks in Intellectual Disabilities
- (2011) Hans van Bokhoven Annual Review of Genetics
- IL1RAPL1 gene deletion as a cause of X-linked intellectual disability and dysmorphic features
- (2011) Erin L. Youngs et al. European Journal of Medical Genetics
- The X-linked intellectual disability protein IL1RAPL1 regulates excitatory synapse formation by binding PTPδ and RhoGAP2
- (2011) Pamela Valnegri et al. HUMAN MOLECULAR GENETICS
- IL-1 Receptor Accessory Protein-Like 1 Associated with Mental Retardation and Autism Mediates Synapse Formation by Trans-Synaptic Interaction with Protein Tyrosine Phosphatase
- (2011) T. Yoshida et al. JOURNAL OF NEUROSCIENCE
- Intragenic deletions of IL1RAPL1: Report of two cases and review of the literature
- (2010) Anne Behnecke et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- A Postsynaptic Signaling Pathway that May Account for the Cognitive Defect Due to IL1RAPL1 Mutation
- (2010) Alice Pavlowsky et al. CURRENT BIOLOGY
- Trans-synaptic Adhesions between Netrin-G Ligand-3 (NGL-3) and Receptor Tyrosine Phosphatases LAR, Protein-tyrosine Phosphatase δ (PTPδ), and PTPσ via Specific Domains Regulate Excitatory Synapse Formation
- (2010) Seok-Kyu Kwon et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- The genetic basis of non-syndromic intellectual disability: a review
- (2010) Liana Kaufman et al. Journal of Neurodevelopmental Disorders
- Abnormal Behavior in a Chromosome- Engineered Mouse Model for Human 15q11-13 Duplication Seen in Autism
- (2009) Jin Nakatani et al. CELL
- IL1RAPL1 controls inhibitory networks during cerebellar development in mice
- (2009) Frédéric Gambino et al. EUROPEAN JOURNAL OF NEUROSCIENCE
- Trans-synaptic adhesion between NGL-3 and LAR regulates the formation of excitatory synapses
- (2009) Jooyeon Woo et al. NATURE NEUROSCIENCE
- Fmr1 knockout mice show reduced anxiety and alterations in neurogenesis that are specific to the ventral dentate gyrus
- (2009) B.D. Eadie et al. NEUROBIOLOGY OF DISEASE
- Abnormal social behavior, hyperactivity, impaired remote spatial memory, and increased D1-mediated dopaminergic signaling in neuronal nitric oxide synthase knockout mice
- (2009) Koichi Tanda et al. Molecular Brain
- Elevated Plus Maze for Mice
- (2009) Munekazu Komada et al. Jove-Journal of Visualized Experiments
- Novel mutation ofIL1RAPL1gene in a nonspecific X-linked mental retardation (MRX) family
- (2008) Magdalena Nawara et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Mutations in the calcium-related gene IL1RAPL1 are associated with autism
- (2008) A. Piton et al. HUMAN MOLECULAR GENETICS
- Zebrafish orthologue of mental retardation protein IL1RAPL1 regulates presynaptic differentiation
- (2008) Tomoyuki Yoshida et al. MOLECULAR AND CELLULAR NEUROSCIENCE
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