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Molecular Genetics and Metabolism|August 30, 2017
A simple method for quantification of plasma globotriaosylsphingosine: Utility for Fabry diseaseAndrew Talbot, Kathy Nicholls, Janice M Fletcher, et al.
International Journal of Molecular Sciences|April 12, 2013
Aberrant lipid metabolism: an emerging diagnostic and therapeutic target in ovarian cancerCarmen E Pyragius, Maria Fuller, Carmela Ricciardelli, et al.
Journal of Veterinary Diagnostic Investigation : Official Publication of the American Association of Veterinary Laboratory Diagnosticians, Inc|October 18, 2018
Globoid cell leukodystrophy (Krabbe disease) in a Merino sheepEffie Lee, Maria Fuller, Mandi Carr, et al.
Journal of Lipid Research|April 23, 2008
Lipid composition of microdomains is altered in a cell model of Gaucher diseaseLeanne K Hein, Stephen Duplock, John J Hopwood, et al.
Molecular Genetics and Metabolism|December 15, 2005
Validation of a heparan sulfate-derived disaccharide as a marker of accumulation in murine mucopolysaccharidosis type IIIABarbara King, Peter Savas, Maria Fuller, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 1, 2018
Disease and subtype specific signatures enable precise diagnosis of the mucopolysaccharidosesJennifer T Saville, Belinda K McDermott, Janice M Fletcher, et al.
Analytical Chemistry|July 1, 2006
Characterization of sulfated oligosaccharides in mucopolysaccharidosis type IIIA by electrospray ionization mass spectrometryKerryn E Mason, Peter J Meikle, John J Hopwood, et al.
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