Enhanced autophagy and mitochondrial aberrations in murine GM1-gangliosidosis

Author:

Takamura Ayumi,Higaki Katsumi,Kajimaki Kenya,Otsuka Susumu,Ninomiya Haruaki,Matsuda Junichiro,Ohno Kousaku,Suzuki Yoshiyuki,Nanba Eiji

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference25 articles.

1. A. Oshima, E. Nanba, J. Matsuda, Y. Suzuki, β-Galactosidase deficiency (β-galactosidosis): GM1-gangliosidosis and Morquio B disease. In: D. Valle, A.L. Baudet, B. Vogelstein, et al., (Eds.), The Online Metabolic and Molecular Bases of Inherited Disease. 8th ed. McGraw-Hill, New York, 2007, Available from. .

2. Morphological, histological and biochemical studies on a case of systemic late infantile lipidosis (generalized gangliosidosis);Suzuki;J. Neuropathol. Exp. Neurol.,1968

3. β-Galactosidase-deficient mouse as an animal model for GM1-gangliosidosis;Matsuda;Glycoconj. J.,1997

4. Generalized CNS disease and massive GM1-ganglioside accumulation in mice defective in lysosomal acid β-galactosidase;Hahn;Hum. Mol. Genet.,1997

5. Chronic GM1 gangliosidosis presenting as dystonia: I. Clinical and pathological features;Goldman;Ann. Neurol.,1981

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