A chromosome 16p13.11 microduplication causes hyperactivity through dysregulation of miR-484/protocadherin-19 signaling.
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The RNA-binding protein MARF1 promotes cortical neurogenesis through its RNase activity domainδ-Protocadherins: Organizers of neural circuit assembly.Modeling Fragile X syndrome in neurogenesis: An unexpected phenotype and a novel tool for future therapies.Regulation of neural circuit formation by protocadherins.Quantitative trait locus mapping and analysis of heritable variation in affiliative social behavior and co-occurring traits.The NDE1 genomic locus can affect treatment of psychiatric illness through gene expression changes related to microRNA-484.The female epilepsy protein PCDH19 is a new GABAAR binding partner that regulates GABAergic transmission as well as migration and morphological maturation of hippocampal neurons.The Cadherin Superfamily in Neural Circuit Assembly.Identification of MS-specific serum miRNAs in an international multicenter study
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A chromosome 16p13.11 microduplication causes hyperactivity through dysregulation of miR-484/protocadherin-19 signaling.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 05 July 2016
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
A chromosome 16p13.11 microdup ...... 84/protocadherin-19 signaling.
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A chromosome 16p13.11 microdup ...... 84/protocadherin-19 signaling.
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label
A chromosome 16p13.11 microdup ...... 84/protocadherin-19 signaling.
@en
A chromosome 16p13.11 microdup ...... 84/protocadherin-19 signaling.
@nl
prefLabel
A chromosome 16p13.11 microdup ...... 84/protocadherin-19 signaling.
@en
A chromosome 16p13.11 microdup ...... 84/protocadherin-19 signaling.
@nl
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A chromosome 16p13.11 microdup ...... 84/protocadherin-19 signaling.
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10.1038/MP.2016.106
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2016-07-05T00:00:00Z
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1019653935