22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia. - Wikidata - wikimedia - TriplyDB

22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.

22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.

http://www.wikidata.org/entity/Q30478713

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The shock of the new: progress in schizophrenia genomics The schizophrenia susceptibility factor dysbindin and its associated complex sort cargoes from cell bodies to the synapse The PHR proteins: intracellular signaling hubs in neuronal development and axon degeneration Hippocampal-Prefrontal Interactions in Cognition, Behavior and Psychiatric Disease Characterizing autism spectrum disorders by key biochemical pathways.Synaptic plasticity, neural circuits, and the emerging role of altered short-term information processing in schizophrenia.Following the genes: a framework for animal modeling of psychiatric disorders Noncoding RNAs and neurobehavioral mechanisms in psychiatric disease Two patients walk into a clinic...a genomics perspective on the future of schizophrenia Triangulating perspectives on functional neuroimaging for disorders of mental health Impaired cognitive function and altered hippocampal synapse morphology in mice lacking Lrrtm1, a gene associated with schizophrenia miR-185 plays an anti-hypertrophic role in the heart via multiple targets in the calcium-signaling pathways Characterization of the past and current duplication activities in the human 22q11.2 region Animal models of neuropsychiatric disorders Exome sequencing supports a de novo mutational paradigm for schizophrenia.Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.Modeling resilience to schizophrenia in genetically modified mice: a novel approach to drug discovery.Comprehensive neurocognitive endophenotyping strategies for mouse models of genetic disorders Evidence for association of hyperprolinemia with schizophrenia and a measure of clinical outcome The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders.Schizophrenia risk gene CAV1 is both pro-psychotic and required for atypical antipsychotic drug actions in vivo.Zic2 hypomorphic mutant mice as a schizophrenia model and ZIC2 mutations identified in schizophrenia patients Evidence for altered hippocampal function in a mouse model of the human 22q11.2 microdeletion.Genomic structural variation in psychiatric disorders.Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson's disease.Mutations in the BLOC-1 subunits dysbindin and muted generate divergent and dosage-dependent phenotypes.Neurodevelopmental disorders: mechanisms and boundary definitions from genomes, interactomes and proteomes.No evidence for the presence of genetic variants predisposing to psychotic disorders on the non-deleted 22q11.2 allele of VCFS patients.Examining the Overlap between Autism Spectrum Disorder and 22q11.2 Deletion Syndrome.Mouse Models of 22q11.2-Associated Autism Spectrum Disorder Decreased DGCR8 expression and miRNA dysregulation in individuals with 22q11.2 deletion syndrome.Mitochondrial dysfunction and pathology in bipolar disorder and schizophrenia.Three phases of DiGeorge/22q11 deletion syndrome pathogenesis during brain development: patterning, proliferation, and mitochondrial functions of 22q11 genes Default mode network connectivity and reciprocal social behavior in 22q11.2 deletion syndrome.Modeling motivational deficits in mouse models of schizophrenia: behavior analysis as a guide for neuroscience.Avoiding mouse traps in schizophrenia genetics: lessons and promises from current and emerging mouse models.Translational neuroscience of schizophrenia: seeking a meeting of minds between mouse and man.Animal models of psychiatric disorders that reflect human copy number variation.Systematic prioritization and integrative analysis of copy number variations in schizophrenia reveal key schizophrenia susceptibility genes.The genomics of schizophrenia: update and implications.

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22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.

http://www.wikidata.org/entity/Q30478713

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2010 nî lūn-bûn

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2010 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2010 թվականի հունիսին հրատարակված գիտական հոդված

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2010年の論文

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Nature Reviews Neuroscience

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22q11.2 microdeletions: linkin ...... dysfunction and schizophrenia.

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Joseph A Gogos

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Maria Karayiorgou

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Tony J Simon

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P2860

Copy-number variations associated with neuropsychiatric conditions

Rare chromosomal deletions and duplications increase risk of schizophrenia

Intracellular localization and tissue-specific distribution of human and yeast DHHC cysteine-rich domain-containing proteins

A mutation in SNAP29, coding for a SNARE protein involved in intracellular trafficking, causes a novel neurocutaneous syndrome characterized by cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma

Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia

Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome.

Genetic variation in the 22q11 locus and susceptibility to schizophrenia

High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays.

SNAP-29: a general SNARE protein that inhibits SNARE disassembly and is implicated in synaptic transmission

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

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