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。Loss of Functional A-Type Potassium Channels in the Dendrites of CA1 Pyramidal Neurons from a Mouse Model of Fragile X Syndrome
Brandy N. Routh et al.
JOURNAL OF NEUROSCIENCE (2013)
Activity-dependent neuronal signalling and autism spectrum disorder
Daniel H. Ebert et al.
NATURE (2013)
Progress toward treatments for synaptic defects in autism
Richard Delorme et al.
NATURE MEDICINE (2013)
Dysregulation of synaptic plasticity precedes appearance of morphological defects in a Pten conditional knockout mouse model of autism
Koichi Takeuchi et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2013)
Development and Characterization of NEX-Pten, a Novel Forebrain Excitatory Neuron-Specific Knockout Mouse
Tatiana M. Kazdoba et al.
DEVELOPMENTAL NEUROSCIENCE (2012)
Phosphatase and tensin homologue (PTEN) regulates synaptic plasticity independently of its effect on neuronal morphology and migration
Margaret Sperow et al.
JOURNAL OF PHYSIOLOGY-LONDON (2012)
Kv4.2 knockout mice have hippocampal-dependent learning and memory deficits
Joaquin N. Lugo et al.
LEARNING & MEMORY (2012)
Genetic Removal of p70 S6 Kinase 1 Corrects Molecular, Synaptic, and Behavioral Phenotypes in Fragile X Syndrome Mice
Aditi Bhattacharya et al.
NEURON (2012)
Chronic Pharmacological mGlu5 Inhibition Corrects Fragile X in Adult Mice
Aubin Michalon et al.
NEURON (2012)
Behavioral Profiles of Mouse Models for Autism Spectrum Disorders
Elodie Ey et al.
AUTISM RESEARCH (2011)
FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism
Jennifer C. Darnell et al.
CELL (2011)
Fragile X Mental Retardation Protein Regulates Protein Expression and mRNA Translation of the Potassium Channel Kv4.2
Christina Gross et al.
JOURNAL OF NEUROSCIENCE (2011)
Bidirectional Regulation of Dendritic Voltage-Gated Potassium Channels by the Fragile X Mental Retardation Protein
Hye Young Lee et al.
NEURON (2011)
Association of Mouse Dlg4 (PSD-95) Gene Deletion and Human DLG4 Gene Variation With Phenotypes Relevant to Autism Spectrum Disorders and Williams' Syndrome
Michael Feyder et al.
AMERICAN JOURNAL OF PSYCHIATRY (2010)
Dysregulation of mTOR Signaling in Fragile X Syndrome
Ali Sharma et al.
JOURNAL OF NEUROSCIENCE (2010)
Targeted treatments for cognitive and neurodevelopmental disorders in tuberous sclerosis complex
Petrus J. Vries
Neurotherapeutics (2010)
The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly
Elizabeth A. Varga et al.
GENETICS IN MEDICINE (2009)
The Autistic Neuron: Troubled Translation?
Raymond J. Kelleher et al.
CELL (2008)
S6K1 phosphorylates and regulates fragile X mental retardation protein (FMRP) with the neuronal protein synthesis-dependent mammalian target of rapamycin (mTOR) signaling cascade
Usha Narayanan et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Altered phosphorylation and localization of the A-type channel, Kv4.2 in status epilepticus
Joaquin N. Lugo et al.
JOURNAL OF NEUROCHEMISTRY (2008)
Response of a neuronal model of tuberous sclerosis to mammalian target of rapamycin (mTOR) inhibitors: Effects on mTORC1 and Akt signaling lead to improved survival and function
Lynsey Meikle et al.
JOURNAL OF NEUROSCIENCE (2008)
Advances in autism genetics: on the threshold of a new neurobiology
Brett S. Abrahams et al.
NATURE REVIEWS GENETICS (2008)
Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function
Gary J. Bassell et al.
NEURON (2008)
Removal of FKBP12 Enhances mTOR-Raptor Interactions, LTP, Memory, and Perseverative/Repetitive Behavior
Charles A. Hoeffer et al.
NEURON (2008)
Unusual Repertoire of Vocalizations in the BTBR T plus tf/J Mouse Model of Autism
Maria Luisa Scattoni et al.
PLOS ONE (2008)
Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism
Stephane Jamain et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Metabotropic Glutamate Receptors and Fragile X Mental Retardation Protein: Partners in Translational Regulation at the Synapse
Jennifer A. Ronesi et al.
SCIENCE SIGNALING (2008)
Scent marking behavior in male C57BL/6J mice: Sexual and developmental determination
Hiroyuki Arakawa et al.
BEHAVIOURAL BRAIN RESEARCH (2007)
Dysregulated metabotropic glutamate receptor-dependent translation of AMPA receptor and postsynaptic density-95 mRNAs at Synapses in a mouse model of fragile X syndrome
Ravi S. Muddashetty et al.
JOURNAL OF NEUROSCIENCE (2007)
A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability
Francesca Zalfa et al.
NATURE NEUROSCIENCE (2007)
Autistic behavior in children with fragile X syndrome: Prevalence, stability, and the impact of FMRP
Deborah D. Hatton et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2006)
Pten regulates neuronal arborization and social interaction in mice
Chang-Hyuk Kwon et al.
NEURON (2006)
The PTEN phosphatase is essential for long-term depression of hippocampal synapses
Yue Wang et al.
NEUROMOLECULAR MEDICINE (2006)
The role of the MAGUK protein CASK in neural development and synaptic function
YP Hsueh
CURRENT MEDICINAL CHEMISTRY (2006)
Altered anxiety-related and social behaviors in the Fmr1 knockout mouse model of fragile X syndrome
CM Spencer et al.
GENES BRAIN AND BEHAVIOR (2005)
Cav1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism
I Splawski et al.
CELL (2004)
Automated apparatus for quantitation of social approach behaviors in mice
JJ Nadler et al.
GENES BRAIN AND BEHAVIOR (2004)
A postsynaptic transient K+ current modulated by arachidonic acid regulates synaptic integration and threshold for LTP induction in hippocampal pyramidal cells
GMJ Ramakers et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
Pten regulates neuronal soma size: a mouse model of Lhermitte-Duclos disease
CH Kwon et al.
NATURE GENETICS (2001)
Deletion of Pten in mouse brain causes seizures, ataxia and defects in soma size resembling Lhermitte-Duclos disease
SA Backman et al.
NATURE GENETICS (2001)
Social amnesia in mice lacking the oxytocin gene
JN Ferguson et al.
NATURE GENETICS (2000)