Cellular pathogenesis in sphingolipid storage disorders: the quest for new therapeutic approaches
Author:
Affiliation:
1. Department of Biological Chemistry, Weizmann Institute of Science, Rehovot 76100, Israel
Publisher
Informa UK Limited
Subject
Cardiology and Cardiovascular Medicine,Endocrinology, Diabetes and Metabolism
Link
https://www.tandfonline.com/doi/pdf/10.2217/clp.10.13
Reference73 articles.
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2. Dierks T, Schlotawa L, Frese MA, Radhakrishnan K, von Figura K, Schmidt B: Molecular basis of multiple sulfatase deficiency, mucolipidosis II/III and Niemann-Pick Cl disease – lysosomal storage disorders caused by defects of non-lysosomal proteins. Biochim. Biophys. Acta 1793, 710–725 (2009).
3. Lahiri S, Futerman AH: The metabolism and function of sphingolipids and glycosphingolipids. Cell. Mol. Life Sci. 64, 2270–2284 (2007).
4. Futerman AH, Hannun YA: The complex life of simple sphingolipids. EMBO Rep. 5, 777–782 (2004).
5. DAngelo G, Polishchuk E, Di Tullio G et al.: Glycosphingolipid synthesis requires FAPP2 transfer of glucosylceramide. Nature. 449, 62–67 (2007).
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