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Molecular Genetics and Metabolism|November 11, 2018
Dissociation of globotriaosylceramide and impaired endothelial function in α-galactosidase-A deficient EA.hy926 cellsNayiri Kaissarian, Justin Kang, Liming Shu, et al.American Journal of Physiology. Renal Physiology|October 9, 2015
Developing novel chemical entities for the treatment of lysosomal storage disorders: an academic perspectiveJames A ShaymanExpert Review of Endocrinology & Metabolism|February 10, 2019
Eliglustat tartrate, a prototypic glucosylceramide synthase inhibitorJames A ShaymanAmerican Journal of Physiology. Renal Physiology|October 12, 2007
Mapping mechanisms and charting the time course of premature cell senescence and apoptosis: lysosomal dysfunction and ganglioside accumulation in endothelial cellsSusann Patschan, Jun Chen, Olga Gealekman, et al.Seminars in Nephrology|April 1, 2018
Targeting Glucosylceramide Synthesis in the Treatment of Rare and Common Renal DiseaseJames A ShaymanFrontiers in Cardiovascular Medicine|May 11, 2026
A new approach methodology for studying intrinsic ventricular arrhythmias in Fabry diseaseAndre Monteiro da Rocha, Liming Shu, Prakaimuk Saraithong, et al.Cell Chemical Biology|October 22, 2016
Adding Lyso-Lipids to Arachidonate Metabolism Sets the Stage for New BiologyJames A ShaymanTransactions of the American Clinical and Climatological Association|July 23, 2013
The design and clinical development of inhibitors of glycosphingolipid synthesis: will invention be the mother of necessity?James A ShaymanPageof 13