Search results (53)
« Back to PublicationsCompartmentalization proteomics revealed endolysosomal protein network changes in a goat model of atrial fibrillation.
Journal article
Ayagama T. et al, (2024), iScience, 27
A Mouse Systems Genetics Approach Reveals Common and Uncommon Genetic Modifiers of Hepatic Lysosomal Enzyme Activities and Glycosphingolipids.
Journal article
Durán A. et al, (2023), Int J Mol Sci, 24
Glucosamine amends CNS pathology in mucopolysaccharidosis IIIC mouse expressing misfolded HGSNAT.
Journal article
Pan X. et al, (2022), J Exp Med, 219
Glycosphingolipid metabolism and its role in ageing and Parkinson's disease.
Journal article
Wallom K-L. et al, (2022), Glycoconj J, 39, 39 - 53
An iPSC model of Hereditary Sensory Neuropathy type-1 reveals Serine responsive deficits in neuronal ganglioside composition and axoglial interactions
Journal article
CLARK A., (2021), Cell Reports Medicine
Upregulating β-hexosaminidase activity in rodents prevents α-synuclein lipid associations and protects dopaminergic neurons from α-synuclein-mediated neurotoxicity.
Journal article
Brekk OR. et al, (2020), Acta Neuropathol Commun, 8
Systemic AAV9 gene therapy using the synapsin I promoter rescues a mouse model of neuronopathic Gaucher disease but with limited cross-correction potential to astrocytes.
Journal article
Massaro G. et al, (2020), Hum Mol Genet, 29, 1933 - 1949
Brain Pathology in Mucopolysaccharidoses (MPS) Patients with Neurological Forms.
Journal article
Viana GM. et al, (2020), J Clin Med, 9
Brain pathology in mucopolysaccharidoses (MPS) patients with neurological forms
Journal article
Viana GM. et al, (2020), Journal of Clinical Medicine, 9
Correction to: Reduced sphingolipid hydrolase activities, substrate accumulation and ganglioside decline in Parkinson's disease.
Journal article
Huebecker M. et al, (2020), Mol Neurodegener, 15
Molecular basis for a new bovine model of Niemann-Pick type C disease.
Journal article
Woolley SA. et al, (2020), PLoS One, 15
Sterile activation of invariant natural killer T cells by ER-stressed antigen-presenting cells.
Journal article
Bedard M. et al, (2019), Proc Natl Acad Sci U S A, 116, 23671 - 23681
Reduced sphingolipid hydrolase activities, substrate accumulation and ganglioside decline in Parkinson's disease.
Journal article
Huebecker M. et al, (2019), Mol Neurodegener, 14
TLR9-mediated dendritic cell activation uncovers mammalian ganglioside species with specific ceramide backbones that activate invariant natural killer T cells.
Journal article
Paget C. et al, (2019), PLoS Biol, 17
TLR9-mediated dendritic cell activation uncovers mammalian ganglioside species with specific ceramide backbones that activate invariant Natural Killer T cells
Journal article
PRIESTMAN D., (2019), PLoS Biology
