Lurcher mouse
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11140%2F16%3A10330496" target="_blank" >RIV/00216208:11140/16:10330496 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.1007/978-3-319-24551-5" target="_blank" >http://dx.doi.org/10.1007/978-3-319-24551-5</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1007/978-3-319-24551-5" target="_blank" >10.1007/978-3-319-24551-5</a>
Alternative languages
Result language
angličtina
Original language name
Lurcher mouse
Original language description
Lurcher mutant mouse is a natural model of hereditary cerebellar degeneration which is caused by a mutation in the δ2 glutamate receptor encoding gene. heterozygous Lurcher mice suffer from vitrually complete loss of Purkinje cells and the degeneration of cerebellar interneurons, deep cerebellar nuclei and inferior olive neurons. Progressive cerebellar degeneration in Lurcher mice affects motor and cognitive functions as well as emotional processing.
Czech name
—
Czech description
—
Classification
Type
C - Chapter in a specialist book
CEP classification
FH - Neurology, neuro-surgery, nuero-sciences
OECD FORD branch
—
Result continuities
Project
—
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2016
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Book/collection name
Essentials of Cerebellum and Cerebellar Disorders
ISBN
978-3-319-24549-2
Number of pages of the result
7
Pages from-to
429-435
Number of pages of the book
656
Publisher name
Springer
Place of publication
Neuveden
UT code for WoS chapter
—