Flightless flies: Drosophila models of neuromuscular disease.
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The Presynaptic Microtubule Cytoskeleton in Physiological and Pathological Conditions: Lessons from Drosophila Fragile X Syndrome and Hereditary Spastic ParaplegiasGenetic Engineering of Dystroglycan in Animal Models of Muscular DystrophyFrom fat fruit fly to human obesityAxonal transport disruption in peripheral nerve disease: From Jack's discoveries as a resident to recent contributionsModel organisms in the fight against muscular dystrophy: lessons from drosophila and ZebrafishAnimal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapyRecent advances using zebrafish animal models for muscle disease drug discoveryThe study of muscle remodeling in Drosophila metamorphosis using in vivo microscopy and bioimage informaticsAn improved method for accurate and rapid measurement of flight performance in DrosophilaInvertebrate models of spinal muscular atrophy: insights into mechanisms and potential therapeutics.The alternative oxidase AOX does not rescue the phenotype of tko25t mutant fliesHuman disease models in Drosophila melanogaster and the role of the fly in therapeutic drug discovery.A Drosophila model of FUS-related neurodegeneration reveals genetic interaction between FUS and TDP-43.A fruitful endeavor: modeling ALS in the fruit flyA Drosophila model for genetic analysis of influenza viral/host interactions.Assaying locomotor, learning, and memory deficits in Drosophila models of neurodegeneration.A cis-regulatory mutation in troponin-I of Drosophila reveals the importance of proper stoichiometry of structural proteins during muscle assembly.A genome-wide CRISPR library for high-throughput genetic screening in Drosophila cells.Dominant, toxic gain-of-function mutations in gars lead to non-cell autonomous neuropathology.Asparagus cochinchinensis Extract Alleviates Metal Ion-Induced Gut Injury in Drosophila: An In Silico Analysis of Potential Active Constituents.I Believe I Can Fly!: Use of Drosophila as a Model Organism in Neuropsychopharmacology Research.A Restrictive Cardiomyopathy Mutation in an Invariant Proline at the Myosin Head/Rod Junction Enhances Head Flexibility and Function, Yielding Muscle Defects in DrosophilaSmall heat shock proteins mediate cell-autonomous and -nonautonomous protection in a Drosophila model for environmental-stress-induced degeneration.Drosophila melanogaster: a model organism for controlling Dipteran vectors and pests.Dissection and imaging of active zones in the Drosophila neuromuscular junction.Genetics of alcohol consumption in Drosophila melanogaster.A conserved role for the zinc finger polyadenosine RNA binding protein, ZC3H14, in control of poly(A) tail length.Drosophila melanogaster as a suitable in vivo model to determine potential side effects of nanomaterials: A review.Development of a Drosophila melanogaster spliceosensor system for in vivo high-throughput screening in myotonic dystrophy type 1.Transcriptome Analysis of Male Drosophila melanogaster Exposed to Ethylparaben Using Digital Gene Expression Profiling.The Little Fly that Could: Wizardry and Artistry of Drosophila Genomics.A fruit fly in the nanoworld: once again Drosophila contributes to environment and human health.Drosophila: An Emergent Model for Delineating Interactions between the Circadian Clock and Drugs of Abuse.An Efficient and Reliable Assay for Investigating the Effects of Hypoxia/Anoxia on Drosophila.Drosophila in the Heart of Understanding Cardiac Diseases: Modeling Channelopathies and Cardiomyopathies in the Fruitfly.Estimation of changes in fitness components and antioxidant defense of Drosophila subobscura (Insecta, Diptera) after exposure to 2.4 T strong static magnetic field.Loss of the Drosophila m-AAA mitochondrial protease paraplegin results in mitochondrial dysfunction, shortened lifespan, and neuronal and muscular degeneration.Optical Cross-Sectional Muscle Area Determination of Drosophila Melanogaster Adult Indirect Flight Muscles.A novel lipid nanocarrier for insulin delivery: production, characterization and toxicity testing.Overexpression of ter94, Drosophila VCP, improves motor neuron degeneration induced by knockdown of TBPH, Drosophila TDP-43.
P2860
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P2860
Flightless flies: Drosophila models of neuromuscular disease.
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
name
Flightless flies: Drosophila models of neuromuscular disease.
@ast
Flightless flies: Drosophila models of neuromuscular disease.
@en
Flightless flies: Drosophila models of neuromuscular disease.
@nl
type
label
Flightless flies: Drosophila models of neuromuscular disease.
@ast
Flightless flies: Drosophila models of neuromuscular disease.
@en
Flightless flies: Drosophila models of neuromuscular disease.
@nl
prefLabel
Flightless flies: Drosophila models of neuromuscular disease.
@ast
Flightless flies: Drosophila models of neuromuscular disease.
@en
Flightless flies: Drosophila models of neuromuscular disease.
@nl
P2860
P1476
Flightless flies: Drosophila models of neuromuscular disease.
@en
P2093
J Paul Taylor
Thomas E Lloyd
P2860
P356
10.1111/J.1749-6632.2010.05432.X
P407
P577
2010-01-01T00:00:00Z