Cerebellar defects in a mouse model of juvenile neuronal ceroid lipofuscinosis
- 17 April 2009
- journal article
- Published by Elsevier BV in Brain Research
- Vol. 1266, 93-107
- https://doi.org/10.1016/j.brainres.2009.02.009
Abstract
No abstract availableKeywords
Funding Information
- National Institutes of Health (NS40580, NS41930, T32 MH065181, NS44310)
- Batten Disease Support and Research Association (NS40580, NS41930, T32 MH065181, NS44310)
This publication has 56 references indexed in Scilit:
- Interactions between the juvenile Batten disease gene, CLN3, and the Notch and JNK signalling pathwaysHuman Molecular Genetics, 2008
- Transcript and in silico analysis of CLN3 in juvenile neuronal ceroid lipofuscinosis and associated mouse modelsHuman Molecular Genetics, 2008
- GABAA α6-Containing Receptors Are Selectively Compromised in Cerebellar Granule Cells of the Ataxic Mouse, StargazerPublished by Elsevier BV ,2007
- Neuroanatomical phenotypes in the Reeler mouseNeuroImage, 2007
- Selectively increased sensitivity of cerebellar granule cells to AMPA receptor-mediated excitotoxicity in a mouse model of Batten diseaseNeurobiology of Disease, 2006
- Barhl1Regulates Migration and Survival of Cerebellar Granule Cells by Controlling Expression of the Neurotrophin-3 GeneJournal of Neuroscience, 2004
- A new mathematical model for relative quantification in real-time RT-PCRNucleic Acids Research, 2001
- Purkinje cell fate instaggerer mutants: Agenesis versus cell deathJournal of Neurobiology, 2000
- Biochemical Characterization and Localization of a Non‐N‐Methyl‐D‐Aspartate Glutamate Receptor in Rat BrainJournal of Neurochemistry, 1992
- Initiation and growth of ectopic neurites and meganeurites during postnatal cortical development in ganglioside storage diseaseDevelopmental Brain Research, 1990