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.
The 47 checked references that resolve
resolves10.1016/j.neuron.2005.08.026A Splice Code for trans-Synaptic Cell Adhesion Mediated by Binding of Neuroligin 1 to α- and β-Neurexins
resolves10.1016/S0092-8674(00)81736-5A Tripartite Protein Complex with the Potential to Couple Synaptic Vesicle Exocytosis to Cell Adhesion in Brain
resolves10.1097/YPG.0000000000000013Rare variants analysis of neurexin-1β in autism reveals a novel start codon mutation affecting protein levels at synapses
resolves10.1038/85906Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
resolves10.1002/ajmg.b.31063Deletions of <i>NRXN1</i> (neurexin‐1) predispose to a wide spectrum of developmental disorders
resolves10.1016/j.neuron.2011.03.020Neurexin-Neuroligin Transsynaptic Interaction Mediates Learning-Related Synaptic Remodeling and Long-Term Facilitation in Aplysia
resolves10.1021/bi0614131Gene Selection, Alternative Splicing, and Post-translational Processing Regulate Neuroligin Selectivity for β-Neurexins
resolves10.1038/nn1074Neurexin mediates the assembly of presynaptic terminals
resolves10.1038/ng1933Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
resolves10.1371/journal.pgen.1003474The Tissue-Specific RNA Binding Protein T-STAR Controls Regional Splicing Patterns of Neurexin Pre-mRNAs in the Brain
resolves10.1073/pnas.0910297106Mouse neurexin-1α deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments
resolves10.1038/nn1837Retrograde modulation of presynaptic release probability through signaling mediated by PSD-95–neuroligin
resolves10.1038/nature11628Autism-related deficits via dysregulated eIF4E-dependent translational control
resolves10.1371/journal.pone.0067114Altered Social Behaviours in Neurexin 1α Knockout Mice Resemble Core Symptoms in Neurodevelopmental Disorders
resolves10.1038/ng1136Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
resolves10.1086/382137X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family
resolves10.1016/j.cell.2013.10.031Integrative Functional Genomic Analyses Implicate Specific Molecular Pathways and Circuits in Autism
resolves10.1016/j.cell.2011.08.040Absence of CNTNAP2 Leads to Epilepsy, Neuronal Migration Abnormalities, and Core Autism-Related Deficits
resolves10.1038/ejhg.2012.95Phenotypic spectrum and genotype–phenotype correlations of NRXN1 exon deletions
resolves10.1038/nrn3469Corticostriatal connectivity and its role in disease
resolves10.1038/nrn2851Behavioural phenotyping assays for mouse models of autism
resolves10.1038/nature07456Neuroligins and neurexins link synaptic function to cognitive disease
resolves10.1038/ng1985Mapping autism risk loci using genetic linkage and chromosomal rearrangements
resolves10.1006/geno.2002.6780Structure and Evolution of Neurexin Genes: Insight into the Mechanism of Alternative Splicing
resolves10.1073/pnas.1403244111Cartography of neurexin alternative splicing mapped by single-molecule long-read mRNA sequencing
resolves10.1038/nature11310Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice
resolves10.1126/science.1621094Neurexins: Synaptic Cell Surface Proteins Related to the α-Latrotoxin Receptor and Laminin
resolves10.1016/j.cell.2013.10.020Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism
resolves10.1002/ajmg.b.31064Intragenic rearrangements in <i>NRXN1</i> in three families with autism spectrum disorder, developmental delay, and speech delay
resolves10.1038/nature11208Autistic-like social behaviour in Shank2-mutant mice improved by restoring NMDA receptor function
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