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Sleat, David E; Sun, Pengling; Wiseman, Jennifer A et al. (2013) Extending the mannose 6-phosphate glycoproteome by high resolution/accuracy mass spectrometry analysis of control and acid phosphatase 5-deficient mice. Mol Cell Proteomics 12:1806-17
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Della Valle, Maria Cecilia; Sleat, David E; Zheng, Haiyan et al. (2011) Classification of subcellular location by comparative proteomic analysis of native and density-shifted lysosomes. Mol Cell Proteomics 10:M110.006403
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Xu, Su; Sleat, David E; Jadot, Michel et al. (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 material. Biochem J 428:355-62
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Sleat, David E; Ding, Lin; Wang, Shudan et al. (2009) Mass spectrometry-based protein profiling to determine the cause of lysosomal storage diseases of unknown etiology. Mol Cell Proteomics 8:1708-18
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Guhaniyogi, Jayita; Sohar, Istvan; Das, Kalyan et al. (2009) Crystal structure and autoactivation pathway of the precursor form of human tripeptidyl-peptidase 1, the enzyme deficient in late infantile ceroid lipofuscinosis. J Biol Chem 284:3985-97
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Sleat, David E; Della Valle, Maria Cecilia; Zheng, Haiyan et al. (2008) The mannose 6-phosphate glycoprotein proteome. J Proteome Res 7:3010-21
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Sleat, David E; Zheng, Haiyan; Lobel, Peter (2007) The human urine mannose 6-phosphate glycoproteome. Biochim Biophys Acta 1774:368-72
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Showing the most recent 10 out of 14 publications
