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Cell
|
June 14, 1996
Structure and mechanism of inosine monophosphate dehydrogenase in complex with the immunosuppressant mycophenolic acid
M 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 unwinding
J 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 kinase
K 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 glaucoma
J 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-sulfonamides
J 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 rapamycin
K P Wilson, M M Yamashita, M D Sintchak, et al.
Nature
|
July 28, 1994
Structure and mechanism of interleukin-1 beta converting enzyme
K 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 FK506
D 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 peptide
J L Kim, K A Morgenstern, C Lin, et al.
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of 3
Search research articles
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Showing results (21-30 of 29) with videos related to
Sort By:
Page
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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 acid
M 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 unwinding
J 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 kinase
K 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 glaucoma
J 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-sulfonamides
J 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 rapamycin
K P Wilson, M M Yamashita, M D Sintchak, et al.
Nature
|
July 28, 1994
Structure and mechanism of interleukin-1 beta converting enzyme
K 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 FK506
D 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 peptide
J L Kim, K A Morgenstern, C Lin, et al.
Page
of 3