Genetic diseases of sphingolipid metabolism: Pathological mechanisms and therapeutic options von Kacher, Yaacov, Futerman, Anthony H.

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The pathogenesis of glycosphingolipid storage disorders von Ginzburg, Luba, Kacher, Yaacov, Futerman, Anthony H

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Impaired IL-10 transcription and release in animal models of Gaucher disease macrophages von Kacher, Yaacov, Futerman, Anthony H.

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Acid β-glucosidase: insights from structural analysis and relevance to Gaucher disease therapy von Kacher, Yaacov, Brumshtein, Boris, Boldin-Adamsky, Swetlana, Toker, Lilly, Shainskaya, Alla, Silman, Israel, Sussman, Joel L., Futerman, Anthony H.

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Glycosphingolipidoses: beyond the enzymatic defect von Raas-Rothschild, Annick, Pankova-Kholmyansky, Irene, Kacher, Yaacov, Futerman, Anthony H

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Changes in macrophage morphology in a Gaucher disease model are dependent on CTP:phosphocholine cytidylyltransferase α von Kacher, Yaacov, Golan, Avner, Pewzner-Jung, Yael, Futerman, Anthony H.

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