Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders.
about
Super resolution microscopy is poised to reveal new insights into the formation and maturation of dendritic spinesAxon initial segments: diverse and dynamic neuronal compartmentsWnt signaling networks in autism spectrum disorder and intellectual disabilitySodium channel β subunits: emerging targets in channelopathiesNeurodevelopmental disorders: mechanisms and boundary definitions from genomes, interactomes and proteomes.Synaptic Interactome Mining Reveals p140Cap as a New Hub for PSD Proteins Involved in Psychiatric and Neurological Disorders.Ankyrin-G regulates neurogenesis and Wnt signaling by altering the subcellular localization of β-cateninGlial ankyrins facilitate paranodal axoglial junction assemblyMeCP2 regulates the synaptic expression of a Dysbindin-BLOC-1 network component in mouse brain and human induced pluripotent stem cell-derived neurons.Giant ankyrin-G stabilizes somatodendritic GABAergic synapses through opposing endocytosis of GABAA receptors.Giant ankyrin-G: a critical innovation in vertebrate evolution of fast and integrated neuronal signalingStructural basis of diverse membrane target recognitions by ankyrins.The contribution of protein intrinsic disorder to understand the role of genetic variants uncovered by autism spectrum disorders exome studies.A New Fiji-Based Algorithm That Systematically Quantifies Nine Synaptic Parameters Provides Insights into Drosophila NMJ MorphometryComputational dissection of human episodic memory reveals mental process-specific genetic profiles.Nucleotide diversity inflation as a genome-wide response to experimental lifespan extension in Drosophila melanogaster.Integrative Variation Analysis Reveals that a Complex Genotype May Specify Phenotype in Siblings with Syndromic Autism Spectrum Disorder.A novel phenotype in N-glycosylation disorders: Gillessen-Kaesbach-Nishimura skeletal dysplasia due to pathogenic variants in ALG9Structural basis for the membrane association of ankyrinG via palmitoylationConditional deletion of L1CAM in human neurons impairs both axonal and dendritic arborization and action potential generation.Long-Term Memory in Drosophila Is Influenced by Histone Deacetylase HDAC4 Interacting with SUMO-Conjugating Enzyme Ubc9.Association of a risk allele of ANK3 with cognitive performance and cortical thickness in patients with first-episode psychosis.NF-κB regulates neuronal ankyrin-G via a negative feedback loop.Ankyrin-3 as a molecular marker of early-life stress and vulnerability to psychiatric disorders.The node of Ranvier in CNS pathologySubcellular patterning: axonal domains with specialized structure and function.The Molecular Genetics of Autosomal Recessive Nonsyndromic Intellectual Disability: a Mutational Continuum and Future Recommendations.An update on the comorbidity of ADHD and ASD: a focus on clinical management.The ANK3 gene and facial affect processing: An ERP study.Hierarchical microtubule organization controls axon caliber and transport and determines synaptic structure and stability.Psychiatric risk factor ANK3/ankyrin-G nanodomains regulate the structure and function of glutamatergic synapses.Genetic disruption of ankyrin-G in adult mouse forebrain causes cortical synapse alteration and behavior reminiscent of bipolar disorderTwo Algorithms for High-throughput and Multi-parametric Quantification of Drosophila Neuromuscular Junction Morphology.The molecular classification of astrocytic tumors.L1 coupling to ankyrin and the spectrin-actin cytoskeleton modulates ethanol inhibition of L1 adhesion and ethanol teratogenesis.Autoinhibition of ankyrin-B/G membrane target bindings by intrinsically disordered segments from the tail regions.Drosophila Studies on Autism Spectrum Disorders.GABA/Glutamate synaptic pathways targeted by integrative genomic and electrophysiological explorations distinguish autism from intellectual disability.Ankyrin-G isoform imbalance and interneuronopathy link epilepsy and bipolar disorder.A novel genetic syndrome with STARD9 mutation and abnormal spindle morphology.
P2860
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P2860
Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders.
description
2013 nî lūn-bûn
@nan
2013 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Homozygous and heterozygous di ...... tal and psychiatric disorders.
@ast
Homozygous and heterozygous di ...... tal and psychiatric disorders.
@en
Homozygous and heterozygous di ...... tal and psychiatric disorders.
@nl
type
label
Homozygous and heterozygous di ...... tal and psychiatric disorders.
@ast
Homozygous and heterozygous di ...... tal and psychiatric disorders.
@en
Homozygous and heterozygous di ...... tal and psychiatric disorders.
@nl
prefLabel
Homozygous and heterozygous di ...... tal and psychiatric disorders.
@ast
Homozygous and heterozygous di ...... tal and psychiatric disorders.
@en
Homozygous and heterozygous di ...... tal and psychiatric disorders.
@nl
P2093
P50
P356
P1476
Homozygous and heterozygous di ...... ntal and psychiatric disorders
@en
P2093
Anneke T Vulto-van Silfhout
Arjan P M de Brouwer
Bonnie Nijhof
Jamie M Kramer
Judith A Besseling
Laura Tomas Roca
Liesbeth Rooms
Muhammad Yasir Zahoor
Nathalie Van der Aa
R Frank Kooy
P304
P356
10.1093/HMG/DDT043
P50
P577
2013-02-05T00:00:00Z