The dystrobrevin-binding protein 1 gene: features and networks - Wikidata - awgldk - TriplyDB

The dystrobrevin-binding protein 1 gene: features and networks

The dystrobrevin-binding protein 1 gene: features and networks

http://www.wikidata.org/entity/Q33809026

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The dysbindin-containing complex (BLOC-1) in brain: developmental regulation, interaction with SNARE proteins and role in neurite outgrowth Schizophrenia susceptibility gene dysbindin regulates glutamatergic and dopaminergic functions via distinctive mechanisms in Drosophila A comparative study of cancer proteins in the human protein-protein interaction network Dissecting bipolar disorder complexity through epigenomic approach Autoimmune diseases, gastrointestinal disorders and the microbiome in schizophrenia: more than a gut feeling Database of genetic studies of bipolar disorder Impaired long-term memory retention and working memory in sdy mutant mice with a deletion in Dtnbp1, a susceptibility gene for schizophrenia Animal Models of Psychosis: Current State and Future Directions.Dysbindin-1 mutant mice implicate reduced fast-phasic inhibition as a final common disease mechanism in schizophrenia.Scents and nonsense: olfactory dysfunction in schizophrenia Dysbindin-1 loss compromises NMDAR-dependent synaptic plasticity and contextual fear conditioning.In vivo imaging of adult human hippocampal neurogenesis: progress, pitfalls and promise Schizophrenia gene networks and pathways and their applications for novel candidate gene selection Genetic modifiers of abnormal organelle biogenesis in a Drosophila model of BLOC-1 deficiency.Common variants conferring risk of schizophrenia: a pathway analysis of GWAS data.Neurodevelopmental disorders: mechanisms and boundary definitions from genomes, interactomes and proteomes.GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia Genetics of schizophrenia from a clinicial perspective.Reduced rate of neural differentiation in the dentate gyrus of adult dysbindin null (sandy) mouse SNP-based pathway enrichment analysis for genome-wide association studies The DTNBP1 (dysbindin-1) gene variant rs2619522 is associated with variation of hippocampal and prefrontal grey matter volumes in humans.Network analysis of EtOH-related candidate genes.Linking neurodevelopmental and synaptic theories of mental illness through DISC1 Lack of change in markers of presynaptic terminal abundance alongside subtle reductions in markers of presynaptic terminal plasticity in prefrontal cortex of schizophrenia patients.Neuroplasticity signaling pathways linked to the pathophysiology of schizophrenia.Dysbindin-associated proteome in the p2 synaptosome fraction of mouse brain Dysbindin-1 genotype effects on emotional working memory Reduced occipital and prefrontal brain volumes in dysbindin-associated schizophrenia Association study of 167 candidate genes for schizophrenia selected by a multi-domain evidence-based prioritization algorithm and neurodevelopmental hypothesis.Transcriptome sequencing and genome-wide association analyses reveal lysosomal function and actin cytoskeleton remodeling in schizophrenia and bipolar disorder.Disrupted-in-schizophrenia 1 (DISC1) regulates dysbindin function by enhancing its stability Common variants in the MKL1 gene confer risk of schizophrenia.Exploring schizophrenia drug-gene interactions through molecular network and pathway modeling Cell biology of the BLOC-1 complex subunit dysbindin, a schizophrenia susceptibility gene.Genetic association of single nucleotide polymorphisms in dystrobrevin binding protein 1 gene with schizophrenia in a Malaysian population.Network-assisted Causal Gene Detection in Genome-wide Association Studies: An Improved Module Search Algorithm Schizophrenia genomics and proteomics: are we any closer to biomarker discovery?Neuregulin 1-erbB4 pathway in schizophrenia: From genes to an interactome Contrast features of CpG islands in the promoter and other regions in the dog genome Mutation of the 3-phosphoinositide-dependent protein kinase-1 (PDK1) substrate-docking site in the developing brain causes microcephaly with abnormal brain morphogenesis independently of Akt, leading to impaired cognition and disruptive behaviors.

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P2860

The dystrobrevin-binding protein 1 gene: features and networks

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2008 nî lūn-bûn

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2008 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2008 թվականի հուլիսին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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name

The dystrobrevin-binding protein 1 gene: features and networks

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The dystrobrevin-binding protein 1 gene: features and networks

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The dystrobrevin-binding protein 1 gene: features and networks

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The dystrobrevin-binding protein 1 gene: features and networks

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The dystrobrevin-binding protein 1 gene: features and networks

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The dystrobrevin-binding protein 1 gene: features and networks

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Molecular Psychiatry

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The dystrobrevin-binding protein 1 gene: features and networks

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A Y Guo

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B P Riley

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D L Thiselton

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J Sun

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Z Zhao

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P2860

AceView: a comprehensive cDNA-supported gene and transcripts annotation

Association between the DTNBP1 gene and intelligence: a case-control study in young patients with schizophrenia and related disorders and unaffected siblings

A map of recent positive selection in the human genome

Snapin: a SNARE-associated protein implicated in synaptic transmission

Recent advances in the genetics of schizophrenia

Dysbindin-1 is a synaptic and microtubular protein that binds brain snapin

Disrupted in Schizophrenia 1 Interactome: evidence for the close connectivity of risk genes and a potential synaptic basis for schizophrenia

Identification of snapin and three novel proteins (BLOS1, BLOS2, and BLOS3/reduced pigmentation) as subunits of biogenesis of lysosome-related organelles complex-1 (BLOC-1)

Reinvestigation of the dysbindin subunit of BLOC-1 (biogenesis of lysosome-related organelles complex-1) as a dystrobrevin-binding protein

EBAG9 adds a new layer of control on large dense-core vesicle exocytosis via interaction with Snapin

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10.1038/MP.2008.88

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1

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14

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Kenneth S. Kendler

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