S. Duplock

发表

Lipid composition of microdomains is altered in a cell model of Gaucher disease** This work was supported by a National Health and Medical Research Council project grant in Australia. Published, JLR Papers in Press, April 21, 2008.

J. Hopwood, L. Hein, M. Fuller, 2008, Journal of Lipid Research.

Selective reduction of bis(monoacylglycero)phosphate ameliorates the storage burden in a THP-1 macrophage model of Gaucher disease[S]

L. Hein, M. Fuller, S. Duplock, 2013, Journal of Lipid Research.

Mass spectrometric quantification of glycogen to assess primary substrate accumulation in the Pompe mouse.

P. Meikle, D. Brooks, J. Hopwood, 2012, Analytical biochemistry.

Synthesis of siloxanes containing reactive side chains

J. Matisons, R. Warren, S. Duplock, 1991 .

Effect of lysosomal storage on bis(monoacylglycero)phosphate.

P. Meikle, J. Hopwood, P. Whitfield, 2008, The Biochemical journal.

Low-dose, continual enzyme delivery ameliorates some aspects of established brain disease in a mouse model of a childhood-onset neurodegenerative disorder

P. Trim, M. Snel, J. Hopwood, 2016, Experimental Neurology.

Delivery of therapeutic protein for prevention of neurodegenerative changes: Comparison of different CSF-delivery methods

P. Trim, M. Snel, J. Hopwood, 2015, Experimental Neurology.

Glycosphingolipid analysis in a naturally occurring ovine model of acute neuronopathic Gaucher disease

L. Karageorgos, M. Snel, J. Hopwood, 2016, Neurobiology of Disease.

Plasma lipids are altered in Gaucher disease: biochemical markers to evaluate therapeutic intervention.

P. Meikle, J. Hopwood, D. Elstein, 2008, Blood cells, molecules & diseases.

Synthesis and reactions of methacryl-substituted siloxane macromers

G. George, S. Duplock, A. Swincer, 1991 .

Is SGSH heterozygosity a risk factor for early‐onset neurodegenerative disease?

P. Trim, M. Snel, J. Hopwood, 2021, Journal of inherited metabolic disease.

A novel conditional Sgsh knockout mouse model recapitulates phenotypic and neuropathic deficits of Sanfilippo syndrome

P. Trim, M. Snel, J. Hopwood, 2017, Journal of Inherited Metabolic Disease.

Early disease course is unaltered in mucopolysaccharidosis type IIIA (MPS IIIA) mice lacking α‐synuclein

P. Trim, M. Snel, J. Hopwood, 2019, Neuropathology and applied neurobiology.

Evaluation of Disease Lesions in the Developing Canine MPS IIIA Brain.

P. Trim, M. Snel, K. Hemsley, 2018, JIMD reports.

Liquid chromatography/electrospray ionisation-tandem mass spectrometry quantification of GM2 gangliosides in human peripheral cells and plasma.

D. Mahuran, L. Hein, M. Fuller, 2014, Analytical biochemistry.