The fly as a model for neurodegenerative diseases: is it worth the jump?
about
Alzheimer's disease: the silver tsunami of the 21(st) centuryTriplet repeat-derived siRNAs enhance RNA-mediated toxicity in a Drosophila model for myotonic dystrophyCharacterization of the proteostasis roles of glycerol accumulation, protein degradation and protein synthesis during osmotic stress in C. elegansAn integrated micro- and macroarchitectural analysis of the Drosophila brain by computer-assisted serial section electron microscopy.Drosophila melanogaster in the study of human neurodegeneration.Conserved requirement for DEAD-box RNA helicase Gemin3 in Drosophila oogenesisModels for LRRK2-Linked Parkinsonism.Homeotic Gene teashirt (tsh) has a neuroprotective function in amyloid-beta 42 mediated neurodegeneration.The Gemin associates of survival motor neuron are required for motor function in Drosophila.Drosophila Eye Model to Study Neuroprotective Role of CREB Binding Protein (CBP) in Alzheimer's Disease.Computational approaches for understanding the diagnosis and treatment of Parkinson's disease.A Drosophila model for LRRK2-linked parkinsonism.Suppression of neurodegeneration and increased neurotransmission caused by expanded full-length huntingtin accumulating in the cytoplasmIdentification of novel genes that modify phenotypes induced by Alzheimer's beta-amyloid overexpression in DrosophilaGenome-wide RNAi screen and in vivo protein aggregation reporters identify degradation of damaged proteins as an essential hypertonic stress response.Drosophila melanogaster as a model organism of brain diseasesDrosophila protein kinase CK2 is rendered temperature-sensitive by mutations of highly conserved residues flanking the activation segment.Mutations in palmitoyl-protein thioesterase 1 alter exocytosis and endocytosis at synapses in Drosophila larvae.Drosophila, a golden bug, for the dissection of the genetic basis of tolerance and susceptibility to hypoxia.Gem depletion: amyotrophic lateral sclerosis and spinal muscular atrophy crossover.A Drosophila model for the Zellweger spectrum of peroxisome biogenesis disorders.RNA processing-associated molecular mechanisms of neurodegenerative diseases.Analyses of mental dysfunction-related ACSl4 in Drosophila reveal its requirement for Dpp/BMP production and visual wiring in the brain.Novel interactors of the Drosophila Survival Motor Neuron (SMN) Complex suggest its full conservation.Gem formation upon constitutive Gemin3 overexpression in Drosophila.Acute exposure of Drosophila melanogaster to paraquat causes oxidative stress and mitochondrial dysfunction.Could the detection of visual disturbances associated with Parkinson's disease genes in flies lead to new treatments for the disease?Genetic screen identifies a requirement for SMN in mRNA localisation within the Drosophila oocyte.A soy protein Lunasin can ameliorate amyloid-beta 42 mediated neurodegeneration in Drosophila eye
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P2860
The fly as a model for neurodegenerative diseases: is it worth the jump?
description
2006 nî lūn-bûn
@nan
2006年の論文
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2006年論文
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2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
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2006年论文
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2006年论文
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name
The fly as a model for neurodegenerative diseases: is it worth the jump?
@ast
The fly as a model for neurodegenerative diseases: is it worth the jump?
@en
type
label
The fly as a model for neurodegenerative diseases: is it worth the jump?
@ast
The fly as a model for neurodegenerative diseases: is it worth the jump?
@en
prefLabel
The fly as a model for neurodegenerative diseases: is it worth the jump?
@ast
The fly as a model for neurodegenerative diseases: is it worth the jump?
@en
P2860
P356
P1476
The fly as a model for neurodegenerative diseases: is it worth the jump?
@en
P2093
Marcel van den Heuvel
P2860
P304
P356
10.1159/000097303
P577
2006-01-01T00:00:00Z