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J S Shane Rountree

Showing results (1-10 of 7) with videos related to

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Organic Letters|January 28, 2009
Synthesis of a novel polyhydroxylated salicylic acid lactone frameworkJ S Shane Rountree, Paul V Murphy
Glycoconjugate Journal|February 27, 2010
Lysosomal storage of oligosaccharide and glycosphingolipid in imino sugar treated cellsStephanie D Boomkamp, J S Shane Rountree, David C A Neville, et al.
Chemmedchem|January 16, 2009
Design, synthesis, and biological evaluation of enantiomeric beta-N-acetylhexosaminidase inhibitors LABNAc and DABNAc as potential agents against Tay-Sachs and Sandhoff diseaseJ S Shane Rountree, Terry D Butters, Mark R Wormald, et al.
Scientific Reports|September 20, 2022
Identification and development of a subtype-selective allosteric AKT inhibitor suitable for clinical developmentNatalie Page, Mark Wappett, Colin R O'Dowd, et al.
Chembiochem : a European Journal of Chemical Biology|March 19, 2009
Synthesis and biological characterisation of novel N-alkyl-deoxynojirimycin alpha-glucosidase inhibitorsAmy J Rawlings, Hannah Lomas, Adam W Pilling, et al.
ACS Medicinal Chemistry Letters|March 16, 2018
Identification and Structure-Guided Development of Pyrimidinone Based USP7 InhibitorsColin R O'Dowd, Matthew D Helm, J S Shane Rountree, et al.
Clinical and Translational Medicine|April 11, 2024
USP7 inhibitors suppress tumour neoangiogenesis and promote synergy with immune checkpoint inhibitors by downregulating fibroblast VEGFAnamarija Jurisic, Pei-Ju Sung, Mark Wappett, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Organic Letters|January 28, 2009
Synthesis of a novel polyhydroxylated salicylic acid lactone frameworkJ S Shane Rountree, Paul V Murphy
Glycoconjugate Journal|February 27, 2010
Lysosomal storage of oligosaccharide and glycosphingolipid in imino sugar treated cellsStephanie D Boomkamp, J S Shane Rountree, David C A Neville, et al.
Chemmedchem|January 16, 2009
Design, synthesis, and biological evaluation of enantiomeric beta-N-acetylhexosaminidase inhibitors LABNAc and DABNAc as potential agents against Tay-Sachs and Sandhoff diseaseJ S Shane Rountree, Terry D Butters, Mark R Wormald, et al.
Scientific Reports|September 20, 2022
Identification and development of a subtype-selective allosteric AKT inhibitor suitable for clinical developmentNatalie Page, Mark Wappett, Colin R O'Dowd, et al.
Chembiochem : a European Journal of Chemical Biology|March 19, 2009
Synthesis and biological characterisation of novel N-alkyl-deoxynojirimycin alpha-glucosidase inhibitorsAmy J Rawlings, Hannah Lomas, Adam W Pilling, et al.
ACS Medicinal Chemistry Letters|March 16, 2018
Identification and Structure-Guided Development of Pyrimidinone Based USP7 InhibitorsColin R O'Dowd, Matthew D Helm, J S Shane Rountree, et al.
Clinical and Translational Medicine|April 11, 2024
USP7 inhibitors suppress tumour neoangiogenesis and promote synergy with immune checkpoint inhibitors by downregulating fibroblast VEGFAnamarija Jurisic, Pei-Ju Sung, Mark Wappett, et al.
Pageof 1