Parkinson’s disease mouse models in translational research
Identifieur interne : 000219 ( Main/Curation ); précédent : 000218; suivant : 000220Parkinson’s disease mouse models in translational research
Auteurs : Paul Antony [Luxembourg (pays)] ; Nico Diederich [Luxembourg (pays)] ; Rudi Balling [Luxembourg (pays)]Source :
- Mammalian Genome [ 0938-8990 ] ; 2011.
Abstract
Animal models with high predictive power are a prerequisite for translational research. The closer the similarity of a model to Parkinson’s disease (PD), the higher is the predictive value for clinical trials. An ideal PD model should present behavioral signs and pathology that resemble the human disease. The increasing understanding of PD stratification and etiology, however, complicates the choice of adequate animal models for preclinical studies. An ultimate mouse model, relevant to address all PD-related questions, is yet to be developed. However, many of the existing models are useful in answering specific questions. An appropriate model should be chosen after considering both the context of the research and the model properties. This review addresses the validity, strengths, and limitations of current PD mouse models for translational research.
Url:
DOI: 10.1007/s00335-011-9330-x
PubMed: 21559878
PubMed Central: 3151483
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Luxembourg</wicri:noRegion></affiliation></author><author><name sortKey="Diederich, Nico J" sort="Diederich, Nico J" uniqKey="Diederich N" first="Nico" last="Diederich">Nico Diederich</name><affiliation wicri:level="1"><nlm:aff id="Aff1">Luxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, 162, a Avenue de la Faïencerie, 1511 Luxembourg, Luxembourg</nlm:aff><country xml:lang="fr">Luxembourg (pays)</country><wicri:regionArea>Luxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, 162, a Avenue de la Faïencerie, 1511 Luxembourg</wicri:regionArea><wicri:noRegion>1511 Luxembourg</wicri:noRegion></affiliation><affiliation wicri:level="1"><nlm:aff id="Aff2">Department of Neuroscience, Centre Hospitalier de Luxembourg, 4, rue Ernest Barblé, 1210 Luxembourg, Luxembourg</nlm:aff><country xml:lang="fr">Luxembourg (pays)</country><wicri:regionArea>Department of Neuroscience, Centre Hospitalier de Luxembourg, 4, rue Ernest Barblé, 1210 Luxembourg</wicri:regionArea><wicri:noRegion>1210 Luxembourg</wicri:noRegion></affiliation></author><author><name sortKey="Balling, Rudi" sort="Balling, Rudi" uniqKey="Balling R" first="Rudi" last="Balling">Rudi Balling</name><affiliation wicri:level="1"><nlm:aff id="Aff1">Luxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, 162, a Avenue de la Faïencerie, 1511 Luxembourg, Luxembourg</nlm:aff><country xml:lang="fr">Luxembourg (pays)</country><wicri:regionArea>Luxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, 162, a Avenue de la Faïencerie, 1511 Luxembourg</wicri:regionArea><wicri:noRegion>1511 Luxembourg</wicri:noRegion></affiliation></author></analytic><series><title level="j">Mammalian Genome</title><idno type="ISSN">0938-8990</idno><idno type="e-ISSN">1432-1777</idno><imprint><date when="2011">2011</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Animal models with high predictive power are a prerequisite for translational research. The closer the similarity of a model to Parkinson’s disease (PD), the higher is the predictive value for clinical trials. An ideal PD model should present behavioral signs and pathology that resemble the human disease. The increasing understanding of PD stratification and etiology, however, complicates the choice of adequate animal models for preclinical studies. An ultimate mouse model, relevant to address all PD-related questions, is yet to be developed. However, many of the existing models are useful in answering specific questions. An appropriate model should be chosen after considering both the context of the research and the model properties. 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Duff</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Zhou, W" uniqKey="Zhou W">W Zhou</name></author><author><name sortKey="Milder, Jb" uniqKey="Milder J">JB Milder</name></author><author><name sortKey="Freed, Cr" uniqKey="Freed C">CR Freed</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Zhu, Xr" uniqKey="Zhu X">XR Zhu</name></author><author><name sortKey="Maskri, L" uniqKey="Maskri L">L Maskri</name></author><author><name sortKey="Herold, C" uniqKey="Herold C">C Herold</name></author><author><name sortKey="Bader, V" uniqKey="Bader V">V Bader</name></author><author><name sortKey="Stichel, Cc" uniqKey="Stichel C">CC Stichel</name></author><author><name sortKey="Gunturkun, O" uniqKey="Gunturkun O">O Gunturkun</name></author><author><name sortKey="Lubbert, H" uniqKey="Lubbert H">H Lubbert</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Zimprich, A" uniqKey="Zimprich A">A Zimprich</name></author><author><name sortKey="Biskup, S" uniqKey="Biskup S">S Biskup</name></author><author><name sortKey="Leitner, P" uniqKey="Leitner P">P Leitner</name></author><author><name sortKey="Lichtner, P" uniqKey="Lichtner P">P Lichtner</name></author><author><name sortKey="Farrer, M" uniqKey="Farrer M">M Farrer</name></author><author><name sortKey="Lincoln, S" uniqKey="Lincoln S">S Lincoln</name></author><author><name sortKey="Kachergus, J" uniqKey="Kachergus J">J Kachergus</name></author><author><name sortKey="Hulihan, M" uniqKey="Hulihan M">M Hulihan</name></author><author><name sortKey="Uitti, Rj" uniqKey="Uitti R">RJ Uitti</name></author><author><name sortKey="Calne, Db" uniqKey="Calne D">DB Calne</name></author></analytic></biblStruct></listBibl></div1></back></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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