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ACS Chemical Biology|January 6, 2016
Expanding the 3-O-Sulfate Proteome--Enhanced Binding of Neuropilin-1 to 3-O-Sulfated Heparan Sulfate Modulates Its ActivityBryan E Thacker, Emylie Seamen, Roger Lawrence, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|July 13, 2013
Hepatic remnant lipoprotein clearance by heparan sulfate proteoglycans and low-density lipoprotein receptors depend on dietary conditions in miceErin M Foley, Philip L S M Gordts, Kristin I Stanford, et al.
The Journal of Biological Chemistry|September 7, 2012
A genetic model of substrate reduction therapy for mucopolysaccharidosisWilliam C Lamanna, Roger Lawrence, Stéphane Sarrazin, et al.
The Journal of Biological Chemistry|June 14, 2012
Metabolism of vertebrate amino sugars with N-glycolyl groups: incorporation of N-glycolylhexosamines into mammalian glycans by feeding N-glycolylgalactosamineAnne K Bergfeld, Oliver M T Pearce, Sandra L Diaz, et al.
Nature Chemical Biology|January 11, 2012
Disease-specific non-reducing end carbohydrate biomarkers for mucopolysaccharidosesRoger Lawrence, Jillian R Brown, Kanar Al-Mafraji, et al.
Glycobiology|January 4, 2020
Characterization of disease-specific chondroitin sulfate nonreducing end accumulation in mucopolysaccharidosis IVARoger Lawrence, Heather Prill, Preejith P Vachali, et al.
Plos One|December 1, 2020
Natural history study of glycan accumulation in large animal models of GM2 gangliosidosesCatlyn Cavender, Linley Mangini, Jeremy L Van Vleet, et al.
The Journal of Biological Chemistry|March 2, 2011
Lacrimal gland development and Fgf10-Fgfr2b signaling are controlled by 2-O- and 6-O-sulfated heparan sulfateXiuxia Qu, Christian Carbe, Chenqi Tao, et al.
Molecular Genetics and Metabolism|April 11, 2021
Biochemical evaluation of intracerebroventricular rhNAGLU-IGF2 enzyme replacement therapy in neonatal mice with Sanfilippo B syndromeShih-Hsin Kan, Ibrahim Elsharkawi, Steven Q Le, et al.
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