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。Trans-Synaptic Interaction of GluRδ2 and Neurexin through Cbln1 Mediates Synapse Formation in the Cerebellum
Takeshi Uemura et al.
CELL (2010)
LRRTMs and Neuroligins Bind Neurexins with a Differential Code to Cooperate in Glutamate Synapse Development
Tabrez J. Siddiqui et al.
JOURNAL OF NEUROSCIENCE (2010)
Functional impact of global rare copy number variation in autism spectrum disorders
Dalila Pinto et al.
NATURE (2010)
De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia
Julie Gauthier et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Recurrent Rearrangements in Synaptic and Neurodevelopmental Genes and Shared Biologic Pathways in Schizophrenia, Autism, and Mental Retardation
Audrey Guilmatre et al.
ARCHIVES OF GENERAL PSYCHIATRY (2009)
A Neuroligin-4 Missense Mutation Associated with Autism Impairs Neuroligin-4 Folding and Endoplasmic Reticulum Export
Chen Zhang et al.
JOURNAL OF NEUROSCIENCE (2009)
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
Joseph T. Glessner et al.
NATURE (2009)
LRRTM2 Interacts with Neurexin1 and Regulates Excitatory Synapse Formation
Joris de Wit et al.
NEURON (2009)
LRRTM2 Functions as a Neurexin Ligand in Promoting Excitatory Synapse Formation
Jaewon Ko et al.
NEURON (2009)
Mutations in SYNGAP1 in Autosomal nonsyndromic Mental Retardation
Fadi F. Hamdan et al.
NEW ENGLAND JOURNAL OF MEDICINE (2009)
Mouse neurexin-1α deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments
Mark R. Etherton et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Structural variation of chromosomes in autism spectrum disorder
Christian R. Marshall et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Disruption of neurexin 1 associated with autism spectrum disorder
Hyung-Goo Kim et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Neuroligins and neurexins link synaptic function to cognitive disease
Thomas C. Sudhof
NATURE (2008)
Neurexin 1α structural variants associated with autism
Jin Yan et al.
NEUROSCIENCE LETTERS (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)
A patient with vertebral, cognitive and behavioural abnormalities and a de novo deletion of NRXN1α
F. R. Zahir et al.
JOURNAL OF MEDICAL GENETICS (2008)
Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia
George Kirov et al.
HUMAN MOLECULAR GENETICS (2008)
Induction of GABAergic postsynaptic differentiation by α-neurexins
Yunhee Kang et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Contribution of SHANK3 mutations to autism spectrum disorder
Rainald Moessner et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia
C. Francks et al.
MOLECULAR PSYCHIATRY (2007)
Deletion of α-neurexins does not cause a major impairment of axonal pathfinding or synapse formation
Irina Dudanova et al.
JOURNAL OF COMPARATIVE NEUROLOGY (2007)
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Peter Szatmari et al.
NATURE GENETICS (2007)
Neurexin-neuroligin signaling in synapse development
Ann Marie Craig et al.
CURRENT OPINION IN NEUROBIOLOGY (2007)
Mixed-culture assays for analyzing neuronal synapse formation
Thomas Biederer et al.
NATURE PROTOCOLS (2007)
High frequency of neurexin 1β signal peptide structural variants in patients with autism
Jinong Feng et al.
NEUROSCIENCE LETTERS (2006)
How to build a central synapse: clues from cell culture
AM Craig et al.
TRENDS IN NEUROSCIENCES (2006)
A splice code for trans-synaptic cell adhesion mediated by binding of neuroligin 1 to α- and β-neurexins
AA Boucard et al.
NEURON (2005)
X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family
F Laumonnier et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms
HL Wilson et al.
JOURNAL OF MEDICAL GENETICS (2003)
α-neurexins couple Ca2+ channels to synaptic vesicle exocytosis
M Missler et al.
NATURE (2003)
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
S Jamain et al.
NATURE GENETICS (2003)
A stoichiometric complex of neurexins and dystroglycan in brain
S Sugita et al.
JOURNAL OF CELL BIOLOGY (2001)
分享论文
