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。Synaptic Dysfunction in Neurodevelopmental Disorders Associated with Autism and Intellectual Disabilities
Huda Y. Zoghbi et al.
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2012)
Mutations causing syndromic autism define an axis of synaptic pathophysiology
Benjamin D. Auerbach et al.
NATURE (2011)
Reevaluating the Role of LTD in Cerebellar Motor Learning
Martijn Schonewille et al.
NEURON (2011)
Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders
Dan Levy et al.
NEURON (2011)
Rare De Novo Variants Associated with Autism Implicate a Large Functional Network of Genes Involved in Formation and Function of Synapses
Sarah R. Gilman et al.
NEURON (2011)
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
Stephan J. Sanders et al.
NEURON (2011)
Autism-linked neuroligin-3 R451C mutation differentially alters hippocampal and cortical synaptic function
Mark Etherton et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Ubiquitination in Postsynaptic Function and Plasticity
Angela M. Mabb et al.
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, VOL 26 (2010)
Flexible Accelerated STOP Tetracycline Operator-Knockin (FAST): A Versatile and Efficient New Gene Modulating System
Kenji F. Tanaka et al.
BIOLOGICAL PSYCHIATRY (2010)
Group 1 mGIuR-Dependent Synaptic Long-Term Depression: Mechanisms and Implications for Circuitry and Disease
Christian Luscher et al.
NEURON (2010)
Key role for gene dosage and synaptic homeostasis in autism spectrum disorders
Roberto Toro et al.
TRENDS IN GENETICS (2010)
Decreased connectivity and cerebellar activity in autism during motor task performance
Stewart H. Mostofsky et al.
BRAIN (2009)
Neuroligin-3-deficient mice: model of a monogenic heritable form of autism with an olfactory deficit
K. Radyushkin et al.
GENES BRAIN AND BEHAVIOR (2009)
AXONAL COMPETITION IN THE SYNAPTIC WIRING OF THE CEREBELLAR CORTEX DURING DEVELOPMENT AND IN THE MATURE CEREBELLUM
R. Cesa et al.
NEUROSCIENCE (2009)
Minimal Aberrant Behavioral Phenotypes of Neuroligin-3 R451C Knockin Mice
Kathryn K. Chadman et al.
AUTISM RESEARCH (2008)
Neuroligins and neurexins link synaptic function to cognitive disease
Thomas C. Sudhof
NATURE (2008)
Role of olivary electrical coupling in cerebellar motor learning
Ruben S. Van Der Giessen et al.
NEURON (2008)
Type-1 metabotropic glutamate receptor in cerebellar Purkinje cells: a key molecule responsible for long-term depression, endocannabinoid signalling and synapse elimination
Masanobu Kano et al.
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES (2008)
Neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice
Katsuhiko Tabuchi et al.
SCIENCE (2007)
Neuroligin-3 is a neuronal adhesion protein at GABAergic and glutamatergic synapses
Elaine C. Budreck et al.
EUROPEAN JOURNAL OF NEUROSCIENCE (2007)
The neuropsychiatry of the cerebellum - insights from the clinic
Jeremy D. Schmahmann et al.
CEREBELLUM (2007)
Neuroligins determine synapse maturation and function
Frederique Varoqueaux et al.
NEURON (2006)
Targeted in vivo mutations of the AMPA receptor subunit GluR2 and its interacting protein PICK1 eliminate cerebellar long-term depression
JP Steinberg et al.
NEURON (2006)
Deletion of FMR1 in Purkinje cells enhances parallel fiber LTD, enlarges spines, and attenuates cerebellar eyelid conditioning in fragile X syndrome
SKE Koekkoek et al.
NEURON (2005)
Control of excitatory and inhibitory synapse formation by neuroligins
B Chih et al.
SCIENCE (2005)
Disorder-associated mutations lead to functional inactivation of neuroligins
B Chih et al.
HUMAN MOLECULAR GENETICS (2004)
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
S Jamain et al.
NATURE GENETICS (2003)