Phenotypic characterization of a mouse model of juvenile neuronal ceroid lipofuscinosis

This publication has 35 references indexed in Scilit:

• The Novel Neuronal Ceroid Lipofuscinosis Gene MFSD8 Encodes a Putative Lysosomal Transporter
  American Journal of Human Genetics, 2007
• Ocular phenotype in a mouse gene knockout model for infantile neuronal ceroid lipofuscinosis
  Journal of Neuroscience Research, 2006
• Cathepsin D Deficiency Is Associated with a Human Neurodegenerative Disorder
  American Journal of Human Genetics, 2006
• Visual deficits in a mouse model of Batten disease are the result of optic nerve degeneration and loss of dorsal lateral geniculate thalamic neurons
  Neurobiology of Disease, 2006
• Behavioral assessment in mouse models of neuronal ceroid lipofuscinosis using a light-cued T-maze
  Behavioural Brain Research, 2005
• CLN3P, the Batten disease protein, localizes to membrane lipid rafts (detergent-resistant membranes)
  Biochemical and Biophysical Research Communications, 2004
• Optic Nerve Degeneration in a Murine Model of Juvenile Ceroid Lipofuscinosis
  Investigative Opthalmology & Visual Science, 2003
• Retinal Pathology and Function in a Cln3 Knockout Mouse Model of Juvenile Neuronal Ceroid Lipofuscinosis (Batten Disease)
  Molecular and Cellular Neuroscience, 2002
• The Gene Mutated in Variant Late-Infantile Neuronal Ceroid Lipofuscinosis (CLN6) and in nclf Mutant Mice Encodes a Novel Predicted Transmembrane Protein
  American Journal of Human Genetics, 2002
• Histopathologic and immunocytochemical analysis of the retina and ocular tissues in batten disease
  Ophthalmology, 2000