Literature DB >> 12175807

Mouse and fly models of neurodegeneration.

Huda Y Zoghbi1, Juan Botas.   

Abstract

One of the most surprising discoveries of the past decade (at least in the field of neurodegeneration) was that protein misfolding underlies several seemingly disparate neurological diseases. Animal models were crucial to this discovery. In this article, we will discuss the CAG repeat diseases, the tauopathies and Parkinson disease, highlighting how mouse and fly models have contributed to our understanding of pathogenesis. In each case, we will stress what has been learned about the role of protein clearance and the questions that remain about how misfolded proteins acquire their toxicity.

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Year:  2002        PMID: 12175807     DOI: 10.1016/s0168-9525(02)02729-4

Source DB:  PubMed          Journal:  Trends Genet        ISSN: 0168-9525            Impact factor:   11.639


  29 in total

Review 1.  Protein misfolding, aggregation, and degradation in disease.

Authors:  Niels Gregersen; Lars Bolund; Peter Bross
Journal:  Mol Biotechnol       Date:  2005-10       Impact factor: 2.695

2.  The dominant cold-sensitive Out-cold mutants of Drosophila melanogaster have novel missense mutations in the voltage-gated sodium channel gene paralytic.

Authors:  Helen A Lindsay; Richard Baines; Richard ffrench-Constant; Kathryn Lilley; Howard T Jacobs; Kevin M C O'Dell
Journal:  Genetics       Date:  2008-08-24       Impact factor: 4.562

Review 3.  Protein aggregation and aggregate toxicity: new insights into protein folding, misfolding diseases and biological evolution.

Authors:  Massimo Stefani; Christopher M Dobson
Journal:  J Mol Med (Berl)       Date:  2003-08-27       Impact factor: 4.599

4.  Novel alternatively spliced endoplasmic reticulum retention signal in the cytoplasmic loop of Proteolipid Protein-1.

Authors:  Cherie Southwood; Kevin Olson; Chia-Yen Wu; Alexander Gow
Journal:  J Neurosci Res       Date:  2007-02-15       Impact factor: 4.164

5.  Chemical screen reveals small molecules suppressing fragile X premutation rCGG repeat-mediated neurodegeneration in Drosophila.

Authors:  Abrar Qurashi; Huijie Liu; Laurie Ray; David L Nelson; Ranhui Duan; Peng Jin
Journal:  Hum Mol Genet       Date:  2012-02-01       Impact factor: 6.150

Review 6.  Pathways to neurodegeneration: lessons learnt from unbiased genetic screens in Drosophila.

Authors:  Neha Singhal; Manish Jaiswal
Journal:  J Genet       Date:  2018-07       Impact factor: 1.166

Review 7.  RNA-mediated neurodegeneration in fragile X-associated tremor/ataxia syndrome.

Authors:  Yujing Li; Peng Jin
Journal:  Brain Res       Date:  2012-03-09       Impact factor: 3.252

8.  An antisense CAG repeat transcript at JPH3 locus mediates expanded polyglutamine protein toxicity in Huntington's disease-like 2 mice.

Authors:  Brian Wilburn; Dobrila D Rudnicki; Jing Zhao; Tara Murphy Weitz; Yin Cheng; Xiaofeng Gu; Erin Greiner; Chang Sin Park; Nan Wang; Bryce L Sopher; Albert R La Spada; Alex Osmand; Russell L Margolis; Yi E Sun; X William Yang
Journal:  Neuron       Date:  2011-05-12       Impact factor: 17.173

9.  Suppression of Huntington's disease pathology in Drosophila by human single-chain Fv antibodies.

Authors:  William J Wolfgang; Todd W Miller; Jack M Webster; James S Huston; Leslie M Thompson; J Lawrence Marsh; Anne Messer
Journal:  Proc Natl Acad Sci U S A       Date:  2005-08-01       Impact factor: 11.205

10.  Multiple measures of functionality exhibit progressive decline in a parallel, stochastic fashion in Drosophila Sod2 null mutants.

Authors:  Nicole Piazza; Michael Hayes; Ian Martin; Atanu Duttaroy; Mike Grotewiel; Robert Wessells
Journal:  Biogerontology       Date:  2009-01-16       Impact factor: 4.277

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