Literature DB >> 20329357

Flightless flies: Drosophila models of neuromuscular disease.

Thomas E Lloyd1, J Paul Taylor.   

Abstract

The fruit fly, Drosophila melanogaster, has a long and rich history as an important model organism for biologists. In particular, study of the fruit fly has been essential to much of our fundamental understanding of the development and function of the nervous system. In recent years, studies using fruit flies have provided important insights into the pathogenesis of neurodegenerative and neuromuscular diseases. Fly models of spinal muscular atrophy, spinobulbar muscular atrophy,myotonic dystrophy, dystrophinopathies and other inherited neuromuscular diseases recapitulate many of the key pathologic features of the human disease. The ability to perform genetic screens holds promise for uncovering the molecular mechanisms of disease, and indeed, for identifying novel therapeutic targets. This review will summarize recent progress in developing fly models of neuromuscular diseases and will emphasize the contribution that Drosophila has made to our understanding of these diseases.

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Year:  2010        PMID: 20329357      PMCID: PMC3062507          DOI: 10.1111/j.1749-6632.2010.05432.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  102 in total

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4.  A Drosophila model of Parkinson's disease.

Authors:  M B Feany; W W Bender
Journal:  Nature       Date:  2000-03-23       Impact factor: 49.962

5.  Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy.

Authors:  J W Miller; C R Urbinati; P Teng-Umnuay; M G Stenberg; B J Byrne; C A Thornton; M S Swanson
Journal:  EMBO J       Date:  2000-09-01       Impact factor: 11.598

6.  Genetic suppression of polyglutamine toxicity in Drosophila.

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Journal:  Science       Date:  2000-03-10       Impact factor: 47.728

Review 7.  Glutamine repeats and neurodegeneration.

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Journal:  Annu Rev Neurosci       Date:  2000       Impact factor: 12.449

Review 8.  Molecular basis of muscular dystrophies.

Authors:  R D Cohn; K P Campbell
Journal:  Muscle Nerve       Date:  2000-10       Impact factor: 3.217

9.  Identification of genes that modify ataxin-1-induced neurodegeneration.

Authors:  P Fernandez-Funez; M L Nino-Rosales; B de Gouyon; W C She; J M Luchak; P Martinez; E Turiegano; J Benito; M Capovilla; P J Skinner; A McCall; I Canal; H T Orr; H Y Zoghbi; J Botas
Journal:  Nature       Date:  2000-11-02       Impact factor: 49.962

10.  Disruption of axonal transport and neuronal viability by amyloid precursor protein mutations in Drosophila.

Authors:  S Gunawardena; L S Goldstein
Journal:  Neuron       Date:  2001-11-08       Impact factor: 17.173

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  51 in total

1.  Optical Cross-Sectional Muscle Area Determination of Drosophila Melanogaster Adult Indirect Flight Muscles.

Authors:  Estela Selma-Soriano; Rubén Artero; Beatriz Llamusi
Journal:  J Vis Exp       Date:  2018-03-31       Impact factor: 1.355

2.  A Restrictive Cardiomyopathy Mutation in an Invariant Proline at the Myosin Head/Rod Junction Enhances Head Flexibility and Function, Yielding Muscle Defects in Drosophila.

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Journal:  J Mol Biol       Date:  2016-04-20       Impact factor: 5.469

Review 3.  Axonal transport disruption in peripheral nerve disease: From Jack's discoveries as a resident to recent contributions.

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Journal:  J Peripher Nerv Syst       Date:  2012-12       Impact factor: 3.494

Review 4.  From fat fruit fly to human obesity.

Authors:  Wanli W Smith; Joseph Thomas; Jingnan Liu; Tianxia Li; Timothy H Moran
Journal:  Physiol Behav       Date:  2014-02-06

5.  An improved method for accurate and rapid measurement of flight performance in Drosophila.

Authors:  Daniel T Babcock; Barry Ganetzky
Journal:  J Vis Exp       Date:  2014-02-13       Impact factor: 1.355

Review 6.  Aging and the clock: Perspective from flies to humans.

Authors:  Aliza K De Nobrega; Lisa C Lyons
Journal:  Eur J Neurosci       Date:  2018-10-30       Impact factor: 3.386

Review 7.  Duchenne muscular dystrophy animal models for high-throughput drug discovery and precision medicine.

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Journal:  Expert Opin Drug Discov       Date:  2020-01-30       Impact factor: 6.098

8.  An Efficient and Reliable Assay for Investigating the Effects of Hypoxia/Anoxia on Drosophila.

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Journal:  Neurosci Bull       Date:  2017-09-02       Impact factor: 5.203

Review 9.  Recent advances using zebrafish animal models for muscle disease drug discovery.

Authors:  Lisa Maves
Journal:  Expert Opin Drug Discov       Date:  2014-06-14       Impact factor: 6.098

Review 10.  I Believe I Can Fly!: Use of Drosophila as a Model Organism in Neuropsychopharmacology Research.

Authors:  Anjana S Narayanan; Adrian Rothenfluh
Journal:  Neuropsychopharmacology       Date:  2015-10-30       Impact factor: 7.853

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