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Journal of Medicinal Chemistry, ISSN 0022-2623, 04/2013, Volume 56, Issue 7, pp. 2705 - 2725
Journal Article
Chemical communications (Cambridge, England), ISSN 1359-7345, 04/2016, Volume 52, Issue 32, pp. 5497 - 5515
Lysosomal storage disorders (LSDs) are often caused by mutations that destabilize native folding and impair the trafficking of enzymes, leading to premature... 
Gangliosidosis, GM1 - metabolism | Molecular Mimicry | Carbohydrates - chemistry | Gaucher Disease - metabolism | Fabry Disease - metabolism | Humans | Molecular Chaperones - therapeutic use | Fabry Disease - drug therapy | Gangliosidosis, GM1 - drug therapy | Gaucher Disease - drug therapy
Journal Article
Journal Article
Journal Article
Expert Reviews in Molecular Medicine, ISSN 1462-3994, 06/2007, Volume 9, Issue 16, pp. 1 - 18
Proteins that are exported from the cell, or targeted to the cell surface or other organelles, are synthesised and assembled in the endoplasmic reticulum and... 
Humans | Molecular Chaperones - therapeutic use | Genetic Diseases, Inborn - drug therapy | Protein Folding | Protein Renaturation - drug effects
Journal Article
Journal Article