Identification and functional characterization of rare SHANK2 variants in schizophrenia. - Test2 - elhamkhani - TriplyDB

Identification and functional characterization of rare SHANK2 variants in schizophrenia.

Identification and functional characterization of rare SHANK2 variants in schizophrenia.

http://www.wikidata.org/entity/Q36301065

about

Whole-genome sequencing in multiplex families with psychoses reveals mutations in the SHANK2 and SMARCA1 genes segregating with illness.Investigation of SHANK3 in schizophrenia.Transcriptome sequencing study implicates immune-related genes differentially expressed in schizophrenia: new data and a meta-analysis.Selective Localization of Shanks to VGLUT1-Positive Excitatory Synapses in the Mouse Hippocampus.Emerging Synaptic Molecules as Candidates in the Etiology of Neurological Disorders.Therapeutic Potential of Selectively Targeting the α2C-Adrenoceptor in Cognition, Depression, and Schizophrenia-New Developments and Future Perspective.Treating the Synapse in Major Psychiatric Disorders: The Role of Postsynaptic Density Network in Dopamine-Glutamate Interplay and Psychopharmacologic Drugs Molecular Actions Social Preference and Glutamatergic Dysfunction: Underappreciated Prerequisites for Social Dysfunction in Schizophrenia.Novel functions for ADF/cofilin in excitatory synapses - lessons from gene-targeted mice Differential sensory fMRI signatures in autism and schizophrenia: Analysis of amplitude and trial-to-trial variability.The Synapse as a Central Target for Neurodevelopmental Susceptibility to Pesticides Rare SHANK2 variants in schizophrenia.Hippocampal Regulation of Postsynaptic Density Homer1 by Associative Learning.Deficiency of Shank2 causes mania-like behavior that responds to mood stabilizers.Impaired Object Recognition but Normal Social Behavior and Ultrasonic Communication in Cofilin1 Mutant Mice.nArgBP2-SAPAP-SHANK, the core postsynaptic triad associated with psychiatric disorders.Shank2 Deletion in Parvalbumin Neurons Leads to Moderate Hyperactivity, Enhanced Self-Grooming and Suppressed Seizure Susceptibility in Mice.Genetic variability in scaffolding proteins and risk for schizophrenia and autism-spectrum disorders: a systematic review.Distinct Phenotypes of Mouse Models Reflect Neuropsychiatric Spectrum Disorders of Human Patients With Variants

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Identification and functional characterization of rare SHANK2 variants in schizophrenia.

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Identification and functional characterization of rare SHANK2 variants in schizophrenia.

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Identification and functional characterization of rare SHANK2 variants in schizophrenia.

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Identification and functional characterization of rare SHANK2 variants in schizophrenia.

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Identification and functional characterization of rare SHANK2 variants in schizophrenia.

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Identification and functional characterization of rare SHANK2 variants in schizophrenia.

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Identification and functional characterization of rare SHANK2 variants in schizophrenia.

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Molecular Psychiatry

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Identification and functional characterization of rare SHANK2 variants in schizophrenia.

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Shank, a novel family of postsynaptic density proteins that binds to the NMDA receptor/PSD-95/GKAP complex and cortactin

Rare chromosomal deletions and duplications increase risk of schizophrenia

Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation

SHANK1 Deletions in Males with Autism Spectrum Disorder

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

Autistic-like social behaviour in Shank2-mutant mice improved by restoring NMDA receptor function

Biological insights from 108 schizophrenia-associated genetic loci

Functional impact of global rare copy number variation in autism spectrum disorders

Paternal age and sporadic schizophrenia: evidence for de novo mutations

Common variants conferring risk of schizophrenia

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