Lysosomal accumulation of SCMAS (subunit c of mitochondrial ATP synthase) in neurons of the mouse model of mucopolysaccharidosis III B
- 20 December 2006
- journal article
- Published by Elsevier in Molecular Genetics and Metabolism
- Vol. 90 (4) , 393-401
- https://doi.org/10.1016/j.ymgme.2006.11.006
Abstract
No abstract availableKeywords
This publication has 44 references indexed in Scilit:
- Suppression of basal autophagy in neural cells causes neurodegenerative disease in miceNature, 2006
- Loss of autophagy in the central nervous system causes neurodegeneration in miceNature, 2006
- Validation of a heparan sulfate-derived disaccharide as a marker of accumulation in murine mucopolysaccharidosis type IIIAMolecular Genetics and Metabolism, 2006
- Retrovirally transduced bone marrow has a therapeutic effect on brain in the mouse model of mucopolysaccharidosis IIIBMolecular Genetics and Metabolism, 2004
- Secondary accumulation of gangliosides in lysosomal storage disordersSeminars in Cell & Developmental Biology, 2004
- Intracerebral injection of sulfamidase delays neuropathology in murine MPS-IIIAMolecular Genetics and Metabolism, 2004
- Selective neurodegeneration in murine mucopolysaccharidosis VII is progressive and reversibleAnnals of Neurology, 2002
- Dipeptidyl peptidase II from porcine seminal plasma: Purification, characterization, and its homology to granzymes, cytotoxic cell proteinases (CCP 1–4)Biochimica et Biophysica Acta (BBA) - General Subjects, 1996
- Batten disease and the ATP synthase subunit c turnover pathway: Raising antibodies to subunit cAmerican Journal of Medical Genetics, 1995
- A TECHNIQUE FOR ULTRACRYOTOMY OF CELL SUSPENSIONS AND TISSUESThe Journal of cell biology, 1973