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Neurexin Dysfunction in Adult Neurons Results in Autistic-like Behavior in Mice

https://doi.org/10.1016/j.celrep.2014.06.022
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Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.

1 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.

The 47 checked references that resolve
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Neuroligin-1 Deletion Results in Impaired Spatial Memory and Increased Repetitive Behavior
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A Splice Code for trans-Synaptic Cell Adhesion Mediated by Binding of Neuroligin 1 to α- and β-Neurexins
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Mutations affecting synaptic levels of neurexin-1β in autism and mental retardation
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Rare variants analysis of neurexin-1β in autism reveals a novel start codon mutation affecting protein levels at synapses
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Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
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Deletions of <i>NRXN1</i> (neurexin‐1) predispose to a wide spectrum of developmental disorders
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Neurexin-Neuroligin Transsynaptic Interaction Mediates Learning-Related Synaptic Remodeling and Long-Term Facilitation in Aplysia
resolves10.1021/bi0614131
Gene Selection, Alternative Splicing, and Post-translational Processing Regulate Neuroligin Selectivity for β-Neurexins
resolves10.1038/nn1074
Neurexin mediates the assembly of presynaptic terminals
resolves10.1038/ng1933
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
resolves10.1371/journal.pgen.1003474
The Tissue-Specific RNA Binding Protein T-STAR Controls Regional Splicing Patterns of Neurexin Pre-mRNAs in the Brain
resolves10.1073/pnas.0910297106
Mouse neurexin-1α deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments
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Polarized Targeting of Neurexins to Synapses Is Regulated by their C-Terminal Sequences
resolves10.1038/nn1837
Retrograde modulation of presynaptic release probability through signaling mediated by PSD-95–neuroligin
resolves10.1007/s00439-011-0975-z
Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia
resolves10.1038/nature11628
Autism-related deficits via dysregulated eIF4E-dependent translational control
resolves10.1523/JNEUROSCI.1232-13.2013
Membrane-Tethered Monomeric Neurexin LNS-Domain Triggers Synapse Formation
resolves10.1016/j.neuron.2006.08.029
Clathrin-Mediated Endocytosis Is the Dominant Mechanism of Vesicle Retrieval at Hippocampal Synapses
resolves10.1371/journal.pone.0067114
Altered Social Behaviours in Neurexin 1α Knockout Mice Resemble Core Symptoms in Neurodevelopmental Disorders
resolves10.1126/science.1138389
Reversal of Neurological Defects in a Mouse Model of Rett Syndrome
resolves10.1016/j.cell.2011.11.028
SAM68 Regulates Neuronal Activity-Dependent Alternative Splicing of Neurexin-1
resolves10.1038/ng1136
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
resolves10.1016/j.neuron.2006.03.023
Pten Regulates Neuronal Arborization and Social Interaction in Mice
resolves10.1523/JNEUROSCI.1245-12.2012
Activity-Dependent Regulation of Inhibition via GAD67
resolves10.1086/382137
X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family
resolves10.1203/PDR.0b013e3182130c54
Sensory Processing in Autism: A Review of Neurophysiologic Findings
resolves10.1126/science.274.5293.1678
Control of Memory Formation Through Regulated Expression of a CaMKII Transgene
resolves10.1126/science.1206593
Adult Neural Function Requires MeCP2
resolves10.1038/nature01755
α-Neurexins couple Ca2+ channels to synaptic vesicle exocytosis
resolves10.1016/j.cell.2013.10.031
Integrative Functional Genomic Analyses Implicate Specific Molecular Pathways and Circuits in Autism
resolves10.1016/j.cell.2011.08.040
Absence of CNTNAP2 Leads to Epilepsy, Neuronal Migration Abnormalities, and Core Autism-Related Deficits
resolves10.1523/JNEUROSCI.15-04-02849.1995
Neurexins are differentially expressed in the embryonic nervous system of mice
resolves10.1038/ejhg.2012.95
Phenotypic spectrum and genotype–phenotype correlations of NRXN1 exon deletions
resolves10.1016/S0092-8674(00)80877-6
Neuroligin Expressed in Nonneuronal Cells Triggers Presynaptic Development in Contacting Axons
resolves10.1038/nrn3469
Corticostriatal connectivity and its role in disease
resolves10.1038/nrn2851
Behavioural phenotyping assays for mouse models of autism
resolves10.1038/nature07456
Neuroligins and neurexins link synaptic function to cognitive disease
resolves10.1038/ng1985
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
resolves10.1006/geno.2002.6780
Structure and Evolution of Neurexin Genes: Insight into the Mechanism of Alternative Splicing
resolves10.1073/pnas.1403244111
Cartography of neurexin alternative splicing mapped by single-molecule long-read mRNA sequencing
resolves10.1038/nature11310
Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice
resolves10.1126/science.1621094
Neurexins: Synaptic Cell Surface Proteins Related to the α-Latrotoxin Receptor and Laminin
resolves10.1016/j.cell.2013.10.020
Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism
resolves10.1002/ajmg.b.31064
Intragenic rearrangements in <i>NRXN1</i> in three families with autism spectrum disorder, developmental delay, and speech delay
resolves10.1038/nature11208
Autistic-like social behaviour in Shank2-mutant mice improved by restoring NMDA receptor function
resolves10.1002/0471142301.ns0826s56
Automated Three‐Chambered Social Approach Task for Mice
The 1 reference without a DOI — listed, not checked
no DOI — not checkedYang, M., and Crawley, J.N. (2009). Simple behavioral assessment of mouse olfaction. Curr. Protoc. Neurosci. (New York: John Wiley & Sons), Chapter 8, Unit 8.24.
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