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Journal Article
PLoS ONE, ISSN 1932-6203, 09/2011, Volume 6, Issue 9, p. e25065
Injury to the glomerular podocyte is a key mechanism in human glomerular disease and podocyte repair is an important therapeutic target. In Fabry disease,... 
RAT-KIDNEY | MULTIDISCIPLINARY SCIENCES | RENAL PATHOLOGY | HUMAN FIBROBLASTS | GLOMERULAR EPITHELIAL-CELLS | GROWTH-FACTOR-II | ENZYME REPLACEMENT THERAPY | HEYMANN NEPHRITIS ANTIGEN | AGALSIDASE-BETA THERAPY | L-IDURONIDASE | LYSOSOMAL-ENZYME | Surface Plasmon Resonance | alpha-Galactosidase - genetics | Cell Membrane | Iodine Radioisotopes | Fabry Disease - genetics | Humans | Adaptor Proteins, Vesicular Transport - genetics | Male | alpha-Galactosidase - metabolism | Adaptor Proteins, Vesicular Transport - metabolism | Immunoenzyme Techniques | Receptor, IGF Type 2 - metabolism | Receptor, IGF Type 2 - genetics | Kidney - metabolism | Insulin-Like Growth Factor II - genetics | Adult | Low Density Lipoprotein Receptor-Related Protein-2 - genetics | Recombinant Proteins - metabolism | Trihexosylceramides - metabolism | Podocytes - metabolism | RNA, Messenger - genetics | Cells, Cultured | Low Density Lipoprotein Receptor-Related Protein-2 - metabolism | Kidney - cytology | Recombinant Proteins - genetics | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Insulin-Like Growth Factor II - metabolism | Endocytosis - physiology | Podocytes - cytology | Fabry Disease - metabolism | Phosphates | Globotriaosylceramide | Drug delivery systems | Disease | Galactosidase | Biochemistry | Mannose | Biology | Drug delivery | Insulin-like growth factors | Proteins | Receptors | Endocytosis | Labeling | Localization | Carbohydrates | Antigens | Enzymes | Kidneys | Organs | Insulin | Patients | Fabry's disease | Biopsy | Intracellular | Kidney transplantation
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
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Journal Article
Clinical Genetics, ISSN 0009-9163, 01/2016, Volume 89, Issue 1, pp. 44 - 54
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