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Proteomics. Clinical Applications|December 8, 2010
Lysosomal proteomics and diseaseDavid E Sleat, Michel Jadot, Peter LobelThe Biochemical Journal|April 8, 2010
Glial fibrillary acidic protein is elevated in the lysosomal storage disease classical late-infantile neuronal ceroid lipofuscinosis, but is not a component of the storage materialSu Xu, David E Sleat, Michel Jadot, et al.Proceedings of the National Academy of Sciences of the United States of America|October 23, 2008
Acid phosphatase 5 is responsible for removing the mannose 6-phosphate recognition marker from lysosomal proteinsPengling Sun, David E Sleat, Michèle Lecocq, et al.Plos One|September 3, 2011
Loss of Niemann-Pick C1 or C2 protein results in similar biochemical changes suggesting that these proteins function in a common lysosomal pathwaySayali S Dixit, Michel Jadot, Istvan Sohar, et al.Molecular & Cellular Proteomics : MCP|January 22, 2011
Classification of subcellular location by comparative proteomic analysis of native and density-shifted lysosomesMaria Cecilia Della Valle, David E Sleat, Haiyan Zheng, et al.The Journal of Biological Chemistry|September 7, 2006
Demonstration of lysosomal localization for the mammalian ependymin-related protein using classical approaches combined with a novel density shift methodMaria Cecilia Della Valle, David E Sleat, Istvan Sohar, et al.Biochimica Et Biophysica Acta|November 4, 2008
Proteomics of the lysosomeTorben Lübke, Peter Lobel, David E SleatBiochimica Et Biophysica Acta|January 30, 2007
The human urine mannose 6-phosphate glycoproteomeDavid E Sleat, Haiyan Zheng, Peter LobelJournal of Proteome Research|March 6, 2020
Comparative Analysis of Quantitative Mass Spectrometric Methods for Subcellular ProteomicsAbla Tannous, Marielle Boonen, Haiyan Zheng, et al.Journal of Proteome Research|May 6, 2022
A Method to Estimate the Distribution of Proteins across Multiple Compartments Using Data from Quantitative Proteomics Subcellular Fractionation ExperimentsDirk F Moore, David E Sleat, Peter LobelPageof 10