Ganesh Venkataraman
Affiliations: | 1993 | Massachusetts Institute of Technology, Cambridge, MA, United States |
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"Ganesh Venkataraman"Mean distance: 8.87 | S | N | B | C | P |
Parents
Sign in to add mentorKaren Klincewicz Gleason | grad student | 1993 | MIT | |
(Proteins at charged interfaces) |
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Publications
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Shriver Z, Capila I, Venkataraman G, et al. (2012) Heparin and heparan sulfate: analyzing structure and microheterogeneity. Handbook of Experimental Pharmacology. 159-76 |
Schultes BC, Chu CL, Long A, et al. (2012) Abstract 2336: M402, a heparan sulfate mimetic, inhibits tumor revascularization and invasiveness after high-dose taxane treatment in a mouse breast cancer model Cancer Research. 72: 2336-2336 |
Zhou H, Roy S, Cochran E, et al. (2011) M402, a novel heparan sulfate mimetic, targets multiple pathways implicated in tumor progression and metastasis. Plos One. 6: e21106 |
Roy S, Lai H, Zouaoui R, et al. (2011) Bioactivity screening of partially desulfated low-molecular-weight heparins: a structure/activity relationship study. Glycobiology. 21: 1194-205 |
Beccati D, Roy S, Yu F, et al. (2010) Identification of a novel structure in heparin generated by potassium permanganate oxidation. Carbohydrate Polymers. 82: 699-705 |
Zhou H, Roy S, Cochran E, et al. (2010) Abstract 2269: M402 - A novel heparan sulfate proteoglycan mimetic targeting tumor-host interactions Cancer Research. 70: 2269-2269 |
Galcheva-Gargova Z, Zhidkova N, Geisler S, et al. (2008) Overexpression of Merlin in B16F10 mouse melanoma cells reduces their metastatic activity: role of the cell surface heparan sulfate glycosaminoglycans. International Journal of Oncology. 32: 1237-43 |
Yang Y, MacLeod V, Dai Y, et al. (2007) The syndecan-1 heparan sulfate proteoglycan is a viable target for myeloma therapy. Blood. 110: 2041-8 |
Shaya D, Tocilj A, Li Y, et al. (2006) Crystal structure of heparinase II from Pedobacter heparinus and its complex with a disaccharide product. The Journal of Biological Chemistry. 281: 15525-35 |
Dai Y, Yang Y, MacLeod V, et al. (2005) HSulf-1 and HSulf-2 are potent inhibitors of myeloma tumor growth in vivo. The Journal of Biological Chemistry. 280: 40066-73 |