| Enzyme-synthesized highly branched maltodextrins have slow glucose generation at the mucosal α-glucosidase level and are slowly digestible in vivo BH Lee, L Yan, RJ Phillips, BL Reuhs, K Jones, DR Rose, BL Nichols, ... PloS one 8 (4), e59745, 2013 | 132 | 2013 |
| Mapping the intestinal alpha-glucogenic enzyme specificities of starch digesting maltase-glucoamylase and sucrase-isomaltase K Jones, L Sim, S Mohan, J Kumarasamy, H Liu, S Avery, HY Naim, ... Bioorganic & medicinal chemistry 19 (13), 3929-3934, 2011 | 103 | 2011 |
| Modulation of starch digestion for slow glucose release through “toggling” of activities of mucosal α-glucosidases BH Lee, R Eskandari, K Jones, KR Reddy, R Quezada-Calvillo, ... Journal of Biological Chemistry 287 (38), 31929-31938, 2012 | 91 | 2012 |
| Mucosal C‐terminal maltase‐glucoamylase hydrolyzes large size starch digestion products that may contribute to rapid postprandial glucose generation BH Lee, AHM Lin, BL Nichols, K Jones, DR Rose, R Quezada‐Calvillo, ... Molecular nutrition & food research 58 (5), 1111-1121, 2014 | 42 | 2014 |
| Structural studies of the intestinal α-glucosidases, maltase-glucoamylase and sucrase-isomaltase DR Rose, MM Chaudet, K Jones Journal of pediatric gastroenterology and nutrition 66, S11-S13, 2018 | 33 | 2018 |
| Probing the active-site requirements of human intestinal N-terminal maltase glucoamylase: The effect of replacing the sulfate moiety by a methyl ether in ponkoranol, a … R Eskandari, K Jones, DR Rose, BM Pinto Bioorganic & medicinal chemistry letters 20 (19), 5686-5689, 2010 | 29 | 2010 |
| Probing the intestinal α‐glucosidase enzyme specificities of starch‐digesting maltase‐glucoamylase and sucrase‐isomaltase: synthesis and inhibitory properties of 3′‐and 5 … R Eskandari, K Jones, K Ravinder Reddy, K Jayakanthan, M Chaudet, ... Chemistry–A European Journal 17 (52), 14817-14825, 2011 | 27 | 2011 |
| The effect of heteroatom substitution of sulfur for selenium in glucosidase inhibitors on intestinal α-glucosidase activities R Eskandari, K Jones, DR Rose, BM Pinto Chemical Communications 47 (32), 9134-9136, 2011 | 25 | 2011 |
| Selectivity of 3′-O-methylponkoranol for inhibition of N-and C-terminal maltase glucoamylase and sucrase isomaltase, potential therapeutics for digestive disorders or their … R Eskandari, K Jones, DR Rose, BM Pinto Bioorganic & medicinal chemistry letters 21 (21), 6491-6494, 2011 | 12 | 2011 |
| Discouraging social loafing during team-based assessments K Jones Teaching Innovation Projects 3 (1), 2013 | 6 | 2013 |
| Investigations of the structures and inhibitory properties of intestinal maltase glucoamylase and sucrase isomaltase K Jones, R Eskandari, HY Naim, BM Pinto, DR Rose Journal of pediatric gastroenterology and nutrition 55, S20-S24, 2012 | 6 | 2012 |
| MS53. P11 K Jones, D Rose Acta Cryst 70, C813, 2014 | 1 | 2014 |
| Research progress reported at the 50th anniversary of the discovery of congenital sucrase-isomaltase deficiency workshop M Gilger, B Hamaker, BL Nichols Jr, S Auricchio, WR Treem, HY Naim, ... J Pediatr Gastroenterol Nutr 55 (suppl 2), S1, 2012 | 1 | 2012 |
| Structural evolution and substrate specificity of Family GH31 α-glucosidases and their contribution to starch digestion. Starch digestion is one of the fundamentally important … M Chaudet ACTA CRYSTALLOGRAPHICA A-FOUNDATION AND ADVANCES 73, A72-A72, 2017 | | 2017 |
| Molecular Mechanism of Starch Digestion by Family 31 Glycoside Hydrolases: Structural Characterization and Inhibition Studies of C-terminal Maltase Glycoamylase and Sucrase … KJJ Jones University of Waterloo, 2014 | | 2014 |
| O-SULFONATED PONKORANOL R Eskandari, K Jones, KR Reddy, K Jayakanthan, M Chaudet, DR Rose, ... Declaration of Partial Copyright Licence 17, 179, 2012 | | 2012 |
| The effect of heteroatom substitution of sulfur for selenium R Eskandari, K Jones, DR Rose, BM Pinto Declaration of Partial Copyright Licence, 126, 2012 | | 2012 |
