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Journal of Medicinal Chemistry
|
December 19, 1998
Prediction of binding affinities for TIBO inhibitors of HIV-1 reverse transcriptase using Monte Carlo simulations in a linear response method
R H Smith, W L Jorgensen, J Tirado-Rives, et al.
Chemical Research in Toxicology
|
May 11, 1991
1,3-Dialkyltriazenes: reactive intermediates and DNA alkylation
M B Kroeger-Koepke, R H Smith, E A Goodnow, et al.
Chemical Research in Toxicology
|
March 1, 1996
Specificity of DNA alkylation by 1-(2-chloroethyl)-3-alkyl-3-acyltriazenes depends on the structure of the acyl group: kinetic and product studies
M B Smith, B F Schmidt, G Czerwinski, et al.
Chemical Research in Toxicology
|
November 1, 1990
Stereoselectivity in the microsomal conversion of N-nitrosodimethylamine to formaldehyde
L K Keefer, M B Kroeger-Koepke, H Ishizaki, et al.
Journal of Leukocyte Biology
|
July 17, 1998
Small molecule inhibitor of HIV-1 cell fusion blocks chemokine receptor-mediated function
O M Howard, T Korte, N I Tarasova, et al.
Protein Engineering
|
May 23, 1998
Molecular modeling of HIV-1 reverse transcriptase drug-resistant mutant strains: implications for the mechanism of polymerase action
M B Kroeger Smith, C J Michejda, S H Hughes, et al.
Biochemical Pharmacology
|
July 6, 1993
An unexpected pathway for the metabolic degradation of 1,3-dialkyl-3-acyltriazenes
C A Rouzer, E J Thompson, T L Skinner, et al.
The Journal of Biological Chemistry
|
June 6, 1997
Visualization of G protein-coupled receptor trafficking with the aid of the green fluorescent protein. Endocytosis and recycling of cholecystokinin receptor type A
N I Tarasova, R H Stauber, J K Choi, et al.
Chemical Research in Toxicology
|
January 1, 1996
Oxidative metabolism of 1-(2-chloroethyl)-3-alkyl-3- (methylcarbamoyl)triazenes: formation of chloroacetaldehyde and relevance to biological activity
C A Rouzer, M Sabourin, T L Skinner, et al.
Antimicrobial Agents and Chemotherapy
|
March 28, 1998
Inhibition of acute-, latent-, and chronic-phase human immunodeficiency virus type 1 (HIV-1) replication by a bistriazoloacridone analog that selectively inhibits HIV-1 transcription
J A Turpin, R W Buckheit, D Derse, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 51) with videos related to
Sort By:
Page
of 6
Journal of Medicinal Chemistry
|
December 19, 1998
Prediction of binding affinities for TIBO inhibitors of HIV-1 reverse transcriptase using Monte Carlo simulations in a linear response method
R H Smith, W L Jorgensen, J Tirado-Rives, et al.
Chemical Research in Toxicology
|
May 11, 1991
1,3-Dialkyltriazenes: reactive intermediates and DNA alkylation
M B Kroeger-Koepke, R H Smith, E A Goodnow, et al.
Chemical Research in Toxicology
|
March 1, 1996
Specificity of DNA alkylation by 1-(2-chloroethyl)-3-alkyl-3-acyltriazenes depends on the structure of the acyl group: kinetic and product studies
M B Smith, B F Schmidt, G Czerwinski, et al.
Chemical Research in Toxicology
|
November 1, 1990
Stereoselectivity in the microsomal conversion of N-nitrosodimethylamine to formaldehyde
L K Keefer, M B Kroeger-Koepke, H Ishizaki, et al.
Journal of Leukocyte Biology
|
July 17, 1998
Small molecule inhibitor of HIV-1 cell fusion blocks chemokine receptor-mediated function
O M Howard, T Korte, N I Tarasova, et al.
Protein Engineering
|
May 23, 1998
Molecular modeling of HIV-1 reverse transcriptase drug-resistant mutant strains: implications for the mechanism of polymerase action
M B Kroeger Smith, C J Michejda, S H Hughes, et al.
Biochemical Pharmacology
|
July 6, 1993
An unexpected pathway for the metabolic degradation of 1,3-dialkyl-3-acyltriazenes
C A Rouzer, E J Thompson, T L Skinner, et al.
The Journal of Biological Chemistry
|
June 6, 1997
Visualization of G protein-coupled receptor trafficking with the aid of the green fluorescent protein. Endocytosis and recycling of cholecystokinin receptor type A
N I Tarasova, R H Stauber, J K Choi, et al.
Chemical Research in Toxicology
|
January 1, 1996
Oxidative metabolism of 1-(2-chloroethyl)-3-alkyl-3- (methylcarbamoyl)triazenes: formation of chloroacetaldehyde and relevance to biological activity
C A Rouzer, M Sabourin, T L Skinner, et al.
Antimicrobial Agents and Chemotherapy
|
March 28, 1998
Inhibition of acute-, latent-, and chronic-phase human immunodeficiency virus type 1 (HIV-1) replication by a bistriazoloacridone analog that selectively inhibits HIV-1 transcription
J A Turpin, R W Buckheit, D Derse, et al.
Page
of 6