about
Modeling anorexia nervosa: transcriptional insights from human iPSC-derived neuronsWilliams syndrome-specific neuroanatomical profile and its associations with behavioral featuresThe Wnt receptor Ryk is a negative regulator of mammalian dendrite morphogenesisPrecursors to language development in typically and atypically developing infants and toddlers: the importance of embracing complexity.Modeling Williams syndrome with induced pluripotent stem cells.Modeling neurodevelopmental and psychiatric diseases with human iPSCs.Human induced pluripotent stem cells for modelling neurodevelopmental disorders.Application of CRISPR/Cas9 to the study of brain development and neuropsychiatric disease.Modeling of TREX1-Dependent Autoimmune Disease using Human Stem Cells Highlights L1 Accumulation as a Source of Neuroinflammation.Increased overall cortical connectivity with syndrome specific local decreases suggested by atypical sleep-EEG synchronization in Williams syndrome.Basal Dendritic Morphology of Cortical Pyramidal Neurons in Williams Syndrome: Prefrontal Cortex and BeyondA Polymer Physics Investigation of the Architecture of the Murine Orthologue of the 7q11.23 Human Locus.Quantitative trait locus mapping and analysis of heritable variation in affiliative social behavior and co-occurring traits.Autism spectrum disorders and disease modeling using stem cells.A postmortem stereological study of the amygdala in Williams syndrome.The contribution of GTF2I haploinsufficiency to Williams syndrome.Prospects of Pluripotent and Adult Stem Cells for Rare Diseases.Blocking Zika virus vertical transmission.Modeling neurological diseases using iPSC-derived neural cells : iPSC modeling of neurological diseases.Strategies to advance drug discovery in rare monogenic intellectual disability syndromes.Serotonin in psychiatry: in vitro disease modeling using patient-derived neurons.The role of TGF-β superfamily signaling in neurological disorders.OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion Syndrome.Uncovering True Cellular Phenotypes: Using Induced Pluripotent Stem Cell-Derived Neurons to Study Early Insults in Neurodevelopmental Disorders.In situ characterization of stem cells-like biomarkers in meningiomas.Williams Syndrome neuroanatomical score associates with GTF2IRD1 in large-scale magnetic resonance imaging cohorts: a proof of concept for multivariate endophenotypes.
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P2860
description
2016 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
article publié dans la revue scientifique Nature
@fr
artículu científicu espublizáu en 2016
@ast
scientific journal article
@en
vedecký článok (publikovaný 2016/08/18)
@sk
vědecký článek publikovaný v roce 2016
@cs
wetenschappelijk artikel (gepubliceerd op 2016/08/18)
@nl
наукова стаття, опублікована в серпні 2016
@uk
مقالة علمية (نشرت في 18-8-2016)
@ar
name
A human neurodevelopmental model for Williams syndrome
@ast
A human neurodevelopmental model for Williams syndrome
@en
A human neurodevelopmental model for Williams syndrome
@nl
type
label
A human neurodevelopmental model for Williams syndrome
@ast
A human neurodevelopmental model for Williams syndrome
@en
A human neurodevelopmental model for Williams syndrome
@nl
prefLabel
A human neurodevelopmental model for Williams syndrome
@ast
A human neurodevelopmental model for Williams syndrome
@en
A human neurodevelopmental model for Williams syndrome
@nl
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P2860
P4510
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P921
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A human neurodevelopmental model for Williams syndrome
@en
P2093
Alysson R. Muotri
Anna Järvinen
Beatriz C. Freitas
Bob Jacobs
Branka Hrvoj-Mihic
Cedric Bardy
Cleber A. Trujillo
Diana X. Yu
Eric Halgren
Fred H. Gage
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P2888
P304
P356
10.1038/NATURE19067
P407
P577
2016-08-18T00:00:00Z
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1003402465