Drosophila as an In Vivo Model for Human Neurodegenerative Disease
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Modelling amyotrophic lateral sclerosis: progress and possibilitiesPhosphorylation of the 19S regulatory particle ATPase subunit, Rpt6, modifies susceptibility to proteotoxic stress and protein aggregation.Drosophila lines with mutant and wild type human TDP-43 replacing the endogenous gene reveals phosphorylation and ubiquitination in mutant lines in the absence of viability or lifespan defects.Opposite effects of 5-HT/AKH and octopamine on the crop contractions in adult Drosophila melanogaster: Evidence of a double brain-gut serotonergic circuitry.Small heat shock proteins mediate cell-autonomous and -nonautonomous protection in a Drosophila model for environmental-stress-induced degeneration.PINK1-dependent phosphorylation of PINK1 and Parkin is essential for mitochondrial quality control.Drosophila melanogaster As a Model Organism to Study RNA Toxicity of Repeat Expansion-Associated Neurodegenerative and Neuromuscular DiseasesA Simple Neuronal Mechanical Injury Methodology to Study Drosophila Motor Neuron Degeneration.The Sustained Impact of Model Organisms-in Genetics and Epigenetics.Autophagy and Human Neurodegenerative Diseases-A Fly's Perspective.Neuroligins Nlg2 and Nlg4 Affect Social Behavior in Drosophila melanogaster.Model Organisms Facilitate Rare Disease Diagnosis and Therapeutic Research.Different responses of Drosophila subobscura isofemale lines to extremely low frequency magnetic field (50 Hz, 0.5 mT): fitness components and locomotor activity.Drosophila melanogaster: Deciphering Alzheimer’s Disease.Novel genetic approaches to behavior in Drosophila.Glial contributions to neuronal health and disease: new insights from Drosophila.Varied pathological and therapeutic response effects associated with CHCHD2 mutant and risk variants.Mutations in the Drosophila homolog of human PLA2G6 give rise to age-dependent loss of psychomotor activity and neurodegeneration.Drosophila melanogaster: Deciphering Alzheimer's Disease.A Drosophila model of ALS reveals a partial loss of function of causative human PFN1 mutants.A Statistically Representative Atlas for Mapping Neuronal Circuits in the Drosophila Adult Brain.Monitoring Cell-to-cell Transmission of Prion-like Protein Aggregates in Drosophila Melanogaster.Role of Glial Immunity in Lifespan Determination: A Drosophila Perspective.Aberrant activation of non-coding RNA targets of transcriptional elongation complexes contributes to TDP-43 toxicity
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P2860
Drosophila as an In Vivo Model for Human Neurodegenerative Disease
description
2015 nî lūn-bûn
@nan
2015 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Drosophila as an In Vivo Model for Human Neurodegenerative Disease
@ast
Drosophila as an In Vivo Model for Human Neurodegenerative Disease
@en
Drosophila as an In Vivo Model for Human Neurodegenerative Disease
@nl
type
label
Drosophila as an In Vivo Model for Human Neurodegenerative Disease
@ast
Drosophila as an In Vivo Model for Human Neurodegenerative Disease
@en
Drosophila as an In Vivo Model for Human Neurodegenerative Disease
@nl
prefLabel
Drosophila as an In Vivo Model for Human Neurodegenerative Disease
@ast
Drosophila as an In Vivo Model for Human Neurodegenerative Disease
@en
Drosophila as an In Vivo Model for Human Neurodegenerative Disease
@nl
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Drosophila as an In Vivo Model for Human Neurodegenerative Disease
@en
P2093
Nancy M Bonini
P2860
P304
P3181
P356
10.1534/GENETICS.115.179457
P407
P577
2015-10-01T00:00:00Z