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M A Murcko

Showing results (21-30 of 29) with videos related to

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Cell|June 14, 1996
Structure and mechanism of inosine monophosphate dehydrogenase in complex with the immunosuppressant mycophenolic acidM D Sintchak, M A Fleming, O Futer, et al.
Structure (London, England : 1993)|March 11, 1998
Hepatitis C virus NS3 RNA helicase domain with a bound oligonucleotide: the crystal structure provides insights into the mode of unwindingJ L Kim, K A Morgenstern, J P Griffith, et al.
Chemistry & Biology|June 1, 1997
The structural basis for the specificity of pyridinylimidazole inhibitors of p38 MAP kinaseK P Wilson, P G McCaffrey, K Hsiao, et al.
Journal of Medicinal Chemistry|December 1, 1989
Thienothiopyran-2-sulfonamides: novel topically active carbonic anhydrase inhibitors for the treatment of glaucomaJ J Baldwin, G S Ponticello, P S Anderson, et al.
Journal of Medicinal Chemistry|June 1, 1991
New isomeric classes of topically active ocular hypotensive carbonic anhydrase inhibitors: 5-substituted thieno[2,3-b]thiophene-2-sulfonamides and 5-substituted thieno[3,2-b]thiophene-2-sulfonamidesJ D Prugh, G D Hartman, P J Mallorga, et al.
Acta Crystallographica. Section D, Biological Crystallography|July 1, 1995
Comparative X-ray structures of the major binding protein for the immunosuppressant FK506 (tacrolimus) in unliganded form and in complex with FK506 and rapamycinK P Wilson, M M Yamashita, M D Sintchak, et al.
Nature|July 28, 1994
Structure and mechanism of interleukin-1 beta converting enzymeK P Wilson, J A Black, J A Thomson, et al.
Acta Crystallographica. Section D, Biological Crystallography|July 1, 1995
Design, synthesis and structure of non-macrocyclic inhibitors of FKBP12, the major binding protein for the immunosuppressant FK506D M Armistead, M C Badia, D D Deininger, et al.
Cell|October 18, 1996
Crystal structure of the hepatitis C virus NS3 protease domain complexed with a synthetic NS4A cofactor peptideJ L Kim, K A Morgenstern, C Lin, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Cell|June 14, 1996
Structure and mechanism of inosine monophosphate dehydrogenase in complex with the immunosuppressant mycophenolic acidM D Sintchak, M A Fleming, O Futer, et al.
Structure (London, England : 1993)|March 11, 1998
Hepatitis C virus NS3 RNA helicase domain with a bound oligonucleotide: the crystal structure provides insights into the mode of unwindingJ L Kim, K A Morgenstern, J P Griffith, et al.
Chemistry & Biology|June 1, 1997
The structural basis for the specificity of pyridinylimidazole inhibitors of p38 MAP kinaseK P Wilson, P G McCaffrey, K Hsiao, et al.
Journal of Medicinal Chemistry|December 1, 1989
Thienothiopyran-2-sulfonamides: novel topically active carbonic anhydrase inhibitors for the treatment of glaucomaJ J Baldwin, G S Ponticello, P S Anderson, et al.
Journal of Medicinal Chemistry|June 1, 1991
New isomeric classes of topically active ocular hypotensive carbonic anhydrase inhibitors: 5-substituted thieno[2,3-b]thiophene-2-sulfonamides and 5-substituted thieno[3,2-b]thiophene-2-sulfonamidesJ D Prugh, G D Hartman, P J Mallorga, et al.
Acta Crystallographica. Section D, Biological Crystallography|July 1, 1995
Comparative X-ray structures of the major binding protein for the immunosuppressant FK506 (tacrolimus) in unliganded form and in complex with FK506 and rapamycinK P Wilson, M M Yamashita, M D Sintchak, et al.
Nature|July 28, 1994
Structure and mechanism of interleukin-1 beta converting enzymeK P Wilson, J A Black, J A Thomson, et al.
Acta Crystallographica. Section D, Biological Crystallography|July 1, 1995
Design, synthesis and structure of non-macrocyclic inhibitors of FKBP12, the major binding protein for the immunosuppressant FK506D M Armistead, M C Badia, D D Deininger, et al.
Cell|October 18, 1996
Crystal structure of the hepatitis C virus NS3 protease domain complexed with a synthetic NS4A cofactor peptideJ L Kim, K A Morgenstern, C Lin, et al.
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