Literature DB >> 11331185

C. elegans: a novel pharmacogenetic model to study Parkinson's disease.

R Nass1, D M. Miller, R D. Blakely.   

Abstract

Parkinson's disease (PD) is characterized by the degeneration of dopaminergic neurons in the substantia nigra pars compacta. Although the use of vertebrate and tissue culture systems continue to provide valuable insight into the pathology of the neurodegeneration, the molecular determinants involved in the etiology of the disease remain elusive. Because of the high conservation of genes and metabolic pathways between invertebrates and humans, as well as the availability of genetic strategies to identify novel proteins, protein interactions and drug targets, genetic analysis using invertebrate model systems has enormous potential in deducing the factors involved in neuronal disease. In this article, we discuss the opportunities for the use of the nematode Caenorhabditis elegans (C. elegans) for gaining insight into the molecular mechanisms and pathways involved in PD.

Entities:  

Year:  2001        PMID: 11331185     DOI: 10.1016/s1353-8020(00)00056-0

Source DB:  PubMed          Journal:  Parkinsonism Relat Disord        ISSN: 1353-8020            Impact factor:   4.891


  26 in total

Review 1.  A predictable worm: application of Caenorhabditis elegans for mechanistic investigation of movement disorders.

Authors:  Paige M Dexter; Kim A Caldwell; Guy A Caldwell
Journal:  Neurotherapeutics       Date:  2012-04       Impact factor: 7.620

Review 2.  Caenorhabditis elegans as an emerging model system in environmental epigenetics.

Authors:  Caren Weinhouse; Lisa Truong; Joel N Meyer; Patrick Allard
Journal:  Environ Mol Mutagen       Date:  2018-08-09       Impact factor: 3.216

3.  The Caenorhabditis elegans snf-11 gene encodes a sodium-dependent GABA transporter required for clearance of synaptic GABA.

Authors:  Gregory P Mullen; Eleanor A Mathews; Paurush Saxena; Stephen D Fields; John R McManus; Gary Moulder; Robert J Barstead; Michael W Quick; James B Rand
Journal:  Mol Biol Cell       Date:  2006-04-26       Impact factor: 4.138

4.  A programmable microvalve-based microfluidic array for characterization of neurotoxin-induced responses of individual C. elegans.

Authors:  Hui Ma; Lei Jiang; Weiwei Shi; Jianhua Qin; Bingcheng Lin
Journal:  Biomicrofluidics       Date:  2009-12-23       Impact factor: 2.800

5.  Neurotoxin-induced degeneration of dopamine neurons in Caenorhabditis elegans.

Authors:  Richard Nass; David H Hall; David M Miller; Randy D Blakely
Journal:  Proc Natl Acad Sci U S A       Date:  2002-02-26       Impact factor: 11.205

6.  Two novel DEG/ENaC channel subunits expressed in glia are needed for nose-touch sensitivity in Caenorhabditis elegans.

Authors:  Lu Han; Ying Wang; Rachele Sangaletti; Giulia D'Urso; Yun Lu; Shai Shaham; Laura Bianchi
Journal:  J Neurosci       Date:  2013-01-16       Impact factor: 6.167

Review 7.  Use of non-mammalian alternative models for neurotoxicological study.

Authors:  Randall T Peterson; Richard Nass; Windy A Boyd; Jonathan H Freedman; Ke Dong; Toshio Narahashi
Journal:  Neurotoxicology       Date:  2008-04-25       Impact factor: 4.294

8.  The metal transporter SMF-3/DMT-1 mediates aluminum-induced dopamine neuron degeneration.

Authors:  Natalia VanDuyn; Raja Settivari; Jennifer LeVora; Shaoyu Zhou; Jason Unrine; Richard Nass
Journal:  J Neurochem       Date:  2012-11-21       Impact factor: 5.372

9.  Characterization of the effects of methylmercury on Caenorhabditis elegans.

Authors:  Kirsten J Helmcke; Tore Syversen; David M Miller; Michael Aschner
Journal:  Toxicol Appl Pharmacol       Date:  2009-03-31       Impact factor: 4.219

10.  The divalent metal transporter homologues SMF-1/2 mediate dopamine neuron sensitivity in caenorhabditis elegans models of manganism and parkinson disease.

Authors:  Raja Settivari; Jennifer Levora; Richard Nass
Journal:  J Biol Chem       Date:  2009-12-18       Impact factor: 5.157

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