Chapter 21 Monitoring Autophagy in Lysosomal Storage Disorders
- 11 February 2009
- book chapter
- Published by Elsevier
- Vol. 453, 417-449
- https://doi.org/10.1016/s0076-6879(08)04021-4
Abstract
No abstract availableKeywords
This publication has 76 references indexed in Scilit:
- Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotesAutophagy, 2008
- Neurologic, Gastric, and Opthalmologic Pathologies in a Murine Model of Mucolipidosis Type IVAmerican Journal of Human Genetics, 2007
- Cathepsin D deficiency and NCL/Batten disease: there's more to death than apoptosis.Autophagy, 2007
- Impairment of starvation-induced and constitutive autophagy in Atg7-deficient miceThe Journal of cell biology, 2005
- The Genetic Spectrum of Human Neuronal Ceroid‐lipofuscinosesBrain Pathology, 2004
- The Multiple Sulfatase Deficiency Gene Encodes an Essential and Limiting Factor for the Activity of SulfatasesCell, 2003
- Multiple Sulfatase Deficiency Is Caused by Mutations in the Gene Encoding the Human Cα-Formylglycine Generating EnzymeCell, 2003
- Insights Into the Diagnosis and Treatment of Lysosomal Storage DiseasesArchives of Neurology, 2003
- Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)Nature, 2000
- Lysosomal glycogen storage disease with normal acid maltaseNeurology, 1981