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Plos One
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July 1, 2022
Assumptions about patients seeking PrEP: Exploring the effects of patient and sexual partner race and gender identity and the moderating role of implicit racism
Samuel R Bunting, Brian A Feinstein, Sarah K Calabrese, et al.
Antimicrobial Agents and Chemotherapy
|
December 1, 1993
In vitro anti-human immunodeficiency virus (HIV) activity of XM323, a novel HIV protease inhibitor
M J Otto, C D Reid, S Garber, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 24, 2001
3,3a-Dihydropyrano[4,3,2-de]quinazolin-2(1H)-ones are potent non-nucleoside reverse transcriptase inhibitors
J W Corbett, S Pan, J A Markwalder, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 15, 1993
In vitro isolation and identification of human immunodeficiency virus (HIV) variants with reduced sensitivity to C-2 symmetrical inhibitors of HIV type 1 protease
M J Otto, S Garber, D L Winslow, et al.
Clinical Radiology
|
November 1, 1989
Non-operative management of gallstones--a preliminary review
S N Jones, W R Lees, S Garber, et al.
In Vitro Cellular & Developmental Biology : Journal of the Tissue Culture Association
|
November 1, 1992
A transformed human epithelial cell line that retains tight junctions post crisis
A L Cozens, M J Yezzi, M Yamaya, et al.
LGBT Health
|
April 11, 2022
Evaluating Medical Students' Views of the Complexity of Sexual Minority Patients and Implications for Care
Samuel R Bunting, Sarah K Calabrese, Sabina T Spigner, et al.
Chemistry & Biology
|
January 5, 2002
Drug design with a new transition state analog of the hydrated carbonyl: silicon-based inhibitors of the HIV protease
C A Chen, S M Sieburth, A Glekas, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 1, 1999
The synthesis of symmetrical and unsymmetrical P1/P1' cyclic ureas as HIV protease inhibitors
M Patel, R F Kaltenbach, D A Nugiel, et al.
Antimicrobial Agents and Chemotherapy
|
October 16, 2001
DPC 681 and DPC 684: potent, selective inhibitors of human immunodeficiency virus protease active against clinically relevant mutant variants
R F Kaltenbach, G Trainor, D Getman, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 86) with videos related to
Sort By:
Page
of 9
Plos One
|
July 1, 2022
Assumptions about patients seeking PrEP: Exploring the effects of patient and sexual partner race and gender identity and the moderating role of implicit racism
Samuel R Bunting, Brian A Feinstein, Sarah K Calabrese, et al.
Antimicrobial Agents and Chemotherapy
|
December 1, 1993
In vitro anti-human immunodeficiency virus (HIV) activity of XM323, a novel HIV protease inhibitor
M J Otto, C D Reid, S Garber, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 24, 2001
3,3a-Dihydropyrano[4,3,2-de]quinazolin-2(1H)-ones are potent non-nucleoside reverse transcriptase inhibitors
J W Corbett, S Pan, J A Markwalder, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 15, 1993
In vitro isolation and identification of human immunodeficiency virus (HIV) variants with reduced sensitivity to C-2 symmetrical inhibitors of HIV type 1 protease
M J Otto, S Garber, D L Winslow, et al.
Clinical Radiology
|
November 1, 1989
Non-operative management of gallstones--a preliminary review
S N Jones, W R Lees, S Garber, et al.
In Vitro Cellular & Developmental Biology : Journal of the Tissue Culture Association
|
November 1, 1992
A transformed human epithelial cell line that retains tight junctions post crisis
A L Cozens, M J Yezzi, M Yamaya, et al.
LGBT Health
|
April 11, 2022
Evaluating Medical Students' Views of the Complexity of Sexual Minority Patients and Implications for Care
Samuel R Bunting, Sarah K Calabrese, Sabina T Spigner, et al.
Chemistry & Biology
|
January 5, 2002
Drug design with a new transition state analog of the hydrated carbonyl: silicon-based inhibitors of the HIV protease
C A Chen, S M Sieburth, A Glekas, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 1, 1999
The synthesis of symmetrical and unsymmetrical P1/P1' cyclic ureas as HIV protease inhibitors
M Patel, R F Kaltenbach, D A Nugiel, et al.
Antimicrobial Agents and Chemotherapy
|
October 16, 2001
DPC 681 and DPC 684: potent, selective inhibitors of human immunodeficiency virus protease active against clinically relevant mutant variants
R F Kaltenbach, G Trainor, D Getman, et al.
Page
of 9