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J L Meek

Showing results (51-60 of 55) with videos related to

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Molecular Pharmacology|September 1, 1984
Enkephalin biosynthesis in adrenal medulla. Modulation of proenkephalin mRNA content of cultured chromaffin cells by 8-bromo-adenosine 3',5'-monophosphateT T Quach, F Tang, H Kageyama, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1982
Isolation, characterization, and purification to homogeneity of a rat brain protein (GABA-modulin)A Guidotti, D R Konkel, B Ebstein, et al.
Science (New York, N.Y.)|January 21, 1994
Rational design of potent, bioavailable, nonpeptide cyclic ureas as HIV protease inhibitorsP Y Lam, P K Jadhav, C J Eyermann, et al.
Journal of Medicinal Chemistry|May 23, 1998
Nonpeptide cyclic cyanoguanidines as HIV-1 protease inhibitors: synthesis, structure-activity relationships, and X-ray crystal structure studiesP K Jadhav, F J Woerner, P Y Lam, et al.
Chemistry & Biology|April 1, 1996
Improved cyclic urea inhibitors of the HIV-1 protease: synthesis, potency, resistance profile, human pharmacokinetics and X-ray crystal structure of DMP 450C N Hodge, P E Aldrich, L T Bacheler, et al.
Pageof 6

Showing results (51-60 of 55) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 55 results.
Molecular Pharmacology|September 1, 1984
Enkephalin biosynthesis in adrenal medulla. Modulation of proenkephalin mRNA content of cultured chromaffin cells by 8-bromo-adenosine 3',5'-monophosphateT T Quach, F Tang, H Kageyama, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1982
Isolation, characterization, and purification to homogeneity of a rat brain protein (GABA-modulin)A Guidotti, D R Konkel, B Ebstein, et al.
Science (New York, N.Y.)|January 21, 1994
Rational design of potent, bioavailable, nonpeptide cyclic ureas as HIV protease inhibitorsP Y Lam, P K Jadhav, C J Eyermann, et al.
Journal of Medicinal Chemistry|May 23, 1998
Nonpeptide cyclic cyanoguanidines as HIV-1 protease inhibitors: synthesis, structure-activity relationships, and X-ray crystal structure studiesP K Jadhav, F J Woerner, P Y Lam, et al.
Chemistry & Biology|April 1, 1996
Improved cyclic urea inhibitors of the HIV-1 protease: synthesis, potency, resistance profile, human pharmacokinetics and X-ray crystal structure of DMP 450C N Hodge, P E Aldrich, L T Bacheler, et al.
Pageof 6