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P C Tyler

Showing results (11-20 of 18) with videos related to

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Bioorganic & Medicinal Chemistry|July 10, 1999
Prostaglandin E2-bisphosphonate conjugates: potential agents for treatment of osteoporosisL Gil, Y Han, E E Opas, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 5, 2001
Immucillin H, a powerful transition-state analog inhibitor of purine nucleoside phosphorylase, selectively inhibits human T lymphocytesG A Kicska, L Long, H Hörig, et al.
The Journal of Organic Chemistry|August 21, 2001
Addition of lithiated 9-deazapurine derivatives to a carbohydrate cyclic imine: convergent synthesis of the aza-C-nucleoside immucillinsG B Evans, R H Furneaux, T L Hutchison, et al.
Nature Structural Biology|June 9, 1999
Transition-state analogs as inhibitors of human and malarial hypoxanthine-guanine phosphoribosyltransferasesC M Li, P C Tyler, R H Furneaux, et al.
Biochemistry|July 11, 2001
Structures of purine nucleoside phosphorylase from Mycobacterium tuberculosis in complexes with immucillin-H and its piecesW Shi, L A Basso, D S Santos, et al.
Biochemistry|June 8, 2000
Crystal structures of Giardia lamblia guanine phosphoribosyltransferase at 1.75 A(,)W Shi, N R Munagala, C C Wang, et al.
Biochemistry|August 6, 1999
The 2.0 A structure of malarial purine phosphoribosyltransferase in complex with a transition-state analogue inhibitorW Shi, C M Li, P C Tyler, et al.
Biochemistry|February 15, 2001
Transition state structure of purine nucleoside phosphorylase and principles of atomic motion in enzymatic catalysisA Fedorov, W Shi, G Kicska, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Bioorganic & Medicinal Chemistry|July 10, 1999
Prostaglandin E2-bisphosphonate conjugates: potential agents for treatment of osteoporosisL Gil, Y Han, E E Opas, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 5, 2001
Immucillin H, a powerful transition-state analog inhibitor of purine nucleoside phosphorylase, selectively inhibits human T lymphocytesG A Kicska, L Long, H Hörig, et al.
The Journal of Organic Chemistry|August 21, 2001
Addition of lithiated 9-deazapurine derivatives to a carbohydrate cyclic imine: convergent synthesis of the aza-C-nucleoside immucillinsG B Evans, R H Furneaux, T L Hutchison, et al.
Nature Structural Biology|June 9, 1999
Transition-state analogs as inhibitors of human and malarial hypoxanthine-guanine phosphoribosyltransferasesC M Li, P C Tyler, R H Furneaux, et al.
Biochemistry|July 11, 2001
Structures of purine nucleoside phosphorylase from Mycobacterium tuberculosis in complexes with immucillin-H and its piecesW Shi, L A Basso, D S Santos, et al.
Biochemistry|June 8, 2000
Crystal structures of Giardia lamblia guanine phosphoribosyltransferase at 1.75 A(,)W Shi, N R Munagala, C C Wang, et al.
Biochemistry|August 6, 1999
The 2.0 A structure of malarial purine phosphoribosyltransferase in complex with a transition-state analogue inhibitorW Shi, C M Li, P C Tyler, et al.
Biochemistry|February 15, 2001
Transition state structure of purine nucleoside phosphorylase and principles of atomic motion in enzymatic catalysisA Fedorov, W Shi, G Kicska, et al.
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