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Hölter, S.M. ; Glasl, L.

High-troughput mouse phenotyping.

In: Animal Models of Movement Disorders. Volume I. Berlin: Springer, 2011. 109-133 (Neuromethods ; 61)
DOI
Here, we describe the systematic mouse phenotyping approach of the German Mouse Clinic (GMC), that works as an open-access phenotyping platform, and of the European Mouse Disease Clinic, which is an EU-funded multi-centre project characterising mutants generated by the large-scale mouse mutagenesis project European Conditional Mouse Mutagenesis Program. We explain the aims and the general framework of these large-scale projects and the resulting consequences for the phenotyping strategies. Then, we focus on the description of the behavioural tests used in the GMC to detect motor and nonmotor symptoms in mouse mutants that are genetic models of human movement disorders or neurodegenerative diseases.
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Publikationstyp Artikel: Sammelbandbeitrag/Buchkapitel
Herausgeber Lane, E.L.* ; Dunnett, S.B.*
Schlagwörter Behavioural phenotyping, Mouse, Functional genomics, Comprehensive screening, Motor abilities, Parkinson’s disease, Gait, Non-motor symptoms
ISSN (print) / ISBN 1940-6045
ISBN 978-1-6177-9297-7
Bandtitel Animal Models of Movement Disorders. Volume I
Zeitschrift Neuromethods
Quellenangaben Band: 61, Heft: , Seiten: 109-133 Artikelnummer: , Supplement: ,
Verlag Springer
Verlagsort Berlin
Institut(e) Institute of Developmental Genetics (IDG)