Pages that link to "Q24328996"
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The following pages link to Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments (Q24328996):
Displaying 50 items.
- Genetic-background modulation of core and variable autistic-like symptoms in Fmr1 knock-out mice (Q21135541) (← links)
- Neurexin-1 (Q21207908) (← links)
- Neurexin-1 (Q21990403) (← links)
- Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia (Q24297920) (← links)
- Rare deletions at the neurexin 3 locus in autism spectrum disorder (Q24300898) (← links)
- Calsyntenins function as synaptogenic adhesion molecules in concert with neurexins (Q24338932) (← links)
- Shank3 mutant mice display autistic-like behaviours and striatal dysfunction (Q24597501) (← links)
- Autism-associated neuroligin-3 mutations commonly disrupt tonic endocannabinoid signaling (Q24621853) (← links)
- Neurexins and neuroligins: recent insights from invertebrates (Q24632787) (← links)
- The structure of neurexin 1α reveals features promoting a role as synaptic organizer (Q24633681) (← links)
- Behavioral and cerebellar transmission deficits in mice lacking the autism-linked gene islet brain-2 (Q24634643) (← links)
- Autism-associated neuroligin-3 mutations commonly impair striatal circuits to boost repetitive behaviors (Q26269833) (← links)
- Region-specific deletions of RIM1 reproduce a subset of global RIM1α(-/-) phenotypes (Q26269877) (← links)
- Neurexins physically and functionally interact with GABA(A) receptors (Q26269882) (← links)
- Synaptic cell adhesion (Q26269885) (← links)
- An autism-associated point mutation in the neuroligin cytoplasmic tail selectively impairs AMPA receptor-mediated synaptic transmission in hippocampus (Q26269889) (← links)
- Autism-linked neuroligin-3 R451C mutation differentially alters hippocampal and cortical synaptic function (Q26269895) (← links)
- RIM1alpha and interacting proteins involved in presynaptic plasticity mediate prepulse inhibition and additional behaviors linked to schizophrenia (Q26269908) (← links)
- Neuroligin-1 deletion results in impaired spatial memory and increased repetitive behavior (Q26269923) (← links)
- Clinical and Neurobiological Relevance of Current Animal Models of Autism Spectrum Disorders (Q26748761) (← links)
- Mouse Genetic Models of Human Brain Disorders (Q26752246) (← links)
- Autism Spectrum Disorders and Drug Addiction: Common Pathways, Common Molecules, Distinct Disorders? (Q26768231) (← links)
- Behavioral phenotypes of genetic mouse models of autism (Q26781456) (← links)
- Modeling psychiatric disorders for developing effective treatments (Q26784269) (← links)
- Excitatory/Inhibitory Balance and Circuit Homeostasis in Autism Spectrum Disorders (Q26796321) (← links)
- Following the genes: a framework for animal modeling of psychiatric disorders (Q26830603) (← links)
- The molecular basis of cognitive deficits in pervasive developmental disorders (Q26991872) (← links)
- CNVs: harbingers of a rare variant revolution in psychiatric genetics (Q27022289) (← links)
- Behavioral and Neuroanatomical Phenotypes in Mouse Models of Autism (Q27025227) (← links)
- NMDA receptor agonists reverse impaired psychomotor and cognitive functions associated with hippocampal Hbegf-deficiency in mice (Q27300850) (← links)
- Missense mutation in DISC1 C-terminal coiled-coil has GSK3β signaling and sex-dependent behavioral effects in mice (Q27302920) (← links)
- Negative allosteric modulation of the mGluR5 receptor reduces repetitive behaviors and rescues social deficits in mouse models of autism (Q27329063) (← links)
- Heterozygous deletion of α-neurexin I or α-neurexin II results in behaviors relevant to autism and schizophrenia (Q27334217) (← links)
- Deletion of JMJD2B in neurons leads to defective spine maturation, hyperactive behavior and memory deficits in mouse (Q27339100) (← links)
- Advancing the understanding of autism disease mechanisms through genetics (Q28069757) (← links)
- Neuronal mechanisms and circuits underlying repetitive behaviors in mouse models of autism spectrum disorder (Q28071696) (← links)
- A Subset of Autism-Associated Genes Regulate the Structural Stability of Neurons. (Q28079929) (← links)
- Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development (Q28081179) (← links)
- Common mechanisms of excitatory and inhibitory imbalance in schizophrenia and autism spectrum disorders (Q28086869) (← links)
- Deletion of α-neurexin II results in autism-related behaviors in mice (Q28252135) (← links)
- Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disorders (Q28259910) (← links)
- Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications (Q28304430) (← links)
- Using mouse models of autism spectrum disorders to study the neurotoxicology of gene-environment interactions (Q28392778) (← links)
- Translational Mouse Models of Autism: Advancing Toward Pharmacological Therapeutics (Q28394524) (← links)
- LRRTM1-deficient mice show a rare phenotype of avoiding small enclosures--a tentative mouse model for claustrophobia-like behaviour. (Q28507356) (← links)
- Association of mouse Dlg4 (PSD-95) gene deletion and human DLG4 gene variation with phenotypes relevant to autism spectrum disorders and Williams' syndrome (Q28586842) (← links)
- Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission (Q28590192) (← links)
- Sociability and motor functions in Shank1 mutant mice (Q28592494) (← links)
- Using Gene Ontology to describe the role of the neurexin-neuroligin-SHANK complex in human, mouse and rat and its relevance to autism (Q28645671) (← links)
- Genetic targeting of NRXN2 in mice unveils role in excitatory cortical synapse function and social behaviors (Q28649716) (← links)