about
Animal models of polyglutamine diseases and therapeutic approachesBiology of ageing and role of dietary antioxidantsLoss of Polo ameliorates APP-induced Alzheimer's disease-like symptoms in DrosophilaQuantifying and predicting Drosophila larvae crawling phenotypes.Guide to understanding Drosophila models of neurodegenerative diseases.Role of X11 and ubiquilin as in vivo regulators of the amyloid precursor protein in DrosophilaDrosophotoxicology: the growing potential for Drosophila in neurotoxicologyDevelopmental toxicity assays using the Drosophila model.Analysis of axonal trafficking via a novel live-imaging technique reveals distinct hedgehog transport kineticsTransgenic Drosophila models of Alzheimer's disease and tauopathiesDrosophila melanogaster in the study of human neurodegeneration.Neurodegenerative models in Drosophila: polyglutamine disorders, Parkinson disease, and amyotrophic lateral sclerosis.Grape-seed polyphenolic extract improves the eye phenotype in a Drosophila model of tauopathy.Expression of human Gaucher disease gene GBA generates neurodevelopmental defects and ER stress in Drosophila eyeRNAi screening in Drosophila cells identifies new modifiers of mutant huntingtin aggregation.β-N-methylamino-L-alanine induces neurological deficits and shortened life span in DrosophilaPathogenic chaperone-like RNA induces congophilic aggregates and facilitates neurodegeneration in DrosophilaA high throughput and sensitive method correlates neuronal disorder genotypes to Drosophila larvae crawling phenotypesSuppression of neurodegeneration and increased neurotransmission caused by expanded full-length huntingtin accumulating in the cytoplasmIntroducing Pitt-Hopkins syndrome-associated mutations of TCF4 to Drosophila daughterless.The etiopathogenesis of Parkinson disease and suggestions for future research. Part II.Drosophila melanogaster As a Model Organism to Study RNA Toxicity of Repeat Expansion-Associated Neurodegenerative and Neuromuscular DiseasesModifiers and mechanisms of multi-system polyglutamine neurodegenerative disorders: lessons from fly models.Bar-coding neurodegeneration: identifying subcellular effects of human neurodegenerative disease proteins using Drosophila leg neurons.BMAA neurotoxicity in Drosophila.ubiquilin antagonizes presenilin and promotes neurodegeneration in Drosophila.GULP1/CED-6 ameliorates amyloid-β toxicity in a Drosophila model of Alzheimer's disease.Cell type-specific processing of human Tau proteins in Drosophila.The commonly used eye-specific sev-GAL4 and GMR-GAL4 drivers in Drosophila melanogaster are expressed in tissues other than eyes also.A fly model for the CCUG-repeat expansion of myotonic dystrophy type 2 reveals a novel interaction with MBNL1.Naphthoquinone-Tryptophan Hybrid Inhibits Aggregation of the Tau-Derived Peptide PHF6 and Reduces Neurotoxicity.
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
name
Drosophila models of neurodegenerative disease
@ast
Drosophila models of neurodegenerative disease
@en
type
label
Drosophila models of neurodegenerative disease
@ast
Drosophila models of neurodegenerative disease
@en
prefLabel
Drosophila models of neurodegenerative disease
@ast
Drosophila models of neurodegenerative disease
@en
P2860
P356
P1433
P1476
Drosophila models of neurodegenerative disease
@en
P2093
George R Jackson
Tzu-Kang Sang
P2860
P304
P356
10.1602/NEURORX.2.3.438
P577
2005-07-01T00:00:00Z