Prospects for Improving Brain Function in Individuals with Down Syndrome
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Timing of therapies for Down syndrome: the sooner, the betterRegulation of emotional response in juvenile monkeys treated with fluoxetine: MAOA interactionsSleep disturbance as detected by actigraphy in pre-pubertal juvenile monkeys receiving therapeutic doses of fluoxetineModulation of GABAergic transmission in development and neurodevelopmental disorders: investigating physiology and pathology to gain therapeutic perspectives.Long-term effect of neonatal inhibition of APP gamma-secretase on hippocampal development in the Ts65Dn mouse model of Down syndrome.Identification of a DYRK1A Inhibitor that Induces Degradation of the Target Kinase using Co-chaperone CDC37 fused with Luciferase nanoKAZ.DS-Connect: A Promising Tool to Improve Lives and Engage Down Syndrome Communities WorldwideInhibition of APP gamma-secretase restores Sonic Hedgehog signaling and neurogenesis in the Ts65Dn mouse model of Down syndromeCognitive Impairment, Neuroimaging, and Alzheimer Neuropathology in Mouse Models of Down Syndrome.Integrated care for Down syndrome.Generation of Integration-Free Induced Pluripotent Stem Cells from Urine-Derived Cells Isolated from Individuals with Down Syndrome.A quantitative transcriptome reference map of the normal human brain.Developmental excitatory-to-inhibitory GABA-polarity switch is disrupted in 22q11.2 deletion syndrome: a potential target for clinical therapeutics.Epigallocatechin gallate: A useful therapy for cognitive disability in Down syndrome?Infantile spasms in down syndrome: Rescue by knockdown of the GIRK2 channel.Epigallocatechin-3-gallate (EGCG) consumption in the Ts65Dn model of Down syndrome fails to improve behavioral deficits and is detrimental to skeletal phenotypes.Three-Dimensional Hyaluronic Acid Hydrogel-Based Models for In Vitro Human iPSC-Derived NPC Culture and Differentiation.Intracellular chloride accumulation: a possible mechanism for cognitive deficits in Down syndrome.Pharmacological interventions to improve cognition and adaptive functioning in Down syndrome: Strides to date.Pharmacological Modulation of Three Modalities of CA1 Hippocampal Long-Term Potentiation in the Ts65Dn Mouse Model of Down Syndrome.
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P2860
Prospects for Improving Brain Function in Individuals with Down Syndrome
description
2013 nî lūn-bûn
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2013 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հուլիսին հրատարակված գիտական հոդված
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2013年の論文
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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
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name
Prospects for Improving Brain Function in Individuals with Down Syndrome
@ast
Prospects for Improving Brain Function in Individuals with Down Syndrome
@en
Prospects for Improving Brain Function in Individuals with Down Syndrome
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type
label
Prospects for Improving Brain Function in Individuals with Down Syndrome
@ast
Prospects for Improving Brain Function in Individuals with Down Syndrome
@en
Prospects for Improving Brain Function in Individuals with Down Syndrome
@nl
altLabel
Prospects for improving brain function in individuals with Down syndrome
@en
prefLabel
Prospects for Improving Brain Function in Individuals with Down Syndrome
@ast
Prospects for Improving Brain Function in Individuals with Down Syndrome
@en
Prospects for Improving Brain Function in Individuals with Down Syndrome
@nl
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Prospects for improving brain function in individuals with Down syndrome
@en
P2093
Alberto C. S. Costa
Jonah J. Scott-McKean
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P2888
P304
P356
10.1007/S40263-013-0089-3
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P577
2013-09-01T00:00:00Z
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P6179
1038649250