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Journal of Proteome Research|May 30, 2008
The mannose 6-phosphate glycoprotein proteomeDavid E Sleat, Maria Cecilia Della Valle, Haiyan Zheng, 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.
Molecular Biology of the Cell|February 23, 2007
Activation of microglia acidifies lysosomes and leads to degradation of Alzheimer amyloid fibrilsAmitabha Majumdar, Dana Cruz, Nikiya Asamoah, et al.
Neurobiology of Aging|January 16, 2007
Degradation of fibrillar forms of Alzheimer's amyloid beta-peptide by macrophagesAmitabha Majumdar, Haeyong Chung, Georgia Dolios, 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|October 5, 2006
NPC2, the protein deficient in Niemann-Pick C2 disease, consists of multiple glycoforms that bind a variety of sterolsHeng-Ling Liou, Sayali S Dixit, Sujuan Xu, et al.
Molecular & Cellular Proteomics : MCP|May 20, 2006
Identification and validation of mannose 6-phosphate glycoproteins in human plasma reveal a wide range of lysosomal and non-lysosomal proteinsDavid E Sleat, Yanhong Wang, Istvan Sohar, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 31, 2018
Lysosomal enzyme tripeptidyl peptidase 1 destabilizes fibrillar Aβ by multiple endoproteolytic cleavages within the β-sheet domainSantiago Solé-Domènech, Ana V Rojas, Gia G Maisuradze, et al.
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