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Nucleic Acids Research
|
October 11, 1994
Genetic Bit Analysis: a solid phase method for typing single nucleotide polymorphisms
T T Nikiforov, R B Rendle, P Goelet, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 7, 1999
Purin-8-ones as corticotropin-releasing hormone (CRH-R1) receptor antagonists
J P Beck, A G Arvanitis, M A Curry, et al.
Nucleic Acids Research
|
May 15, 1996
Potent antisense oligonucleotides to the human multidrug resistance-1 mRNA are rationally selected by mapping RNA-accessible sites with oligonucleotide libraries
S P Ho, D H Britton, B A Stone, et al.
Journal of Medicinal Chemistry
|
December 7, 2010
Trends in kinase selectivity: insights for target class-focused library screening
Shana L Posy, Mark A Hermsmeier, Wayne Vaccaro, et al.
Pediatric Annals
|
May 31, 2013
A 15-year-old boy with dyspnea with exertion
Robert Listernick, Jennifer L Trainor, Susanna A McColley, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 17, 2001
Synthesis and evaluation of efavirenz (Sustiva) analogues as HIV-1 reverse transcriptase inhibitors: replacement of the cyclopropylacetylene side chain
A J Cocuzza, D R Chidester, B C Cordova, et al.
Science (New York, N.Y.)
|
October 16, 1987
A system for rapid DNA sequencing with fluorescent chain-terminating dideoxynucleotides
J M Prober, G L Trainor, R J Dam, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 28, 2009
Benzo[d]imidazole inhibitors of Coactivator Associated Arginine Methyltransferase 1 (CARM1)--Hit to Lead studies
Honghe Wan, Tram Huynh, Suhong Pang, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 22, 2005
Synthesis and evaluation of 2-anilino-3-phenylsulfonyl-6-methylpyridines as corticotropin-releasing factor1 receptor ligands
Richard A Hartz, Argyrios G Arvanitis, Charles Arnold, 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.
Page
of 11
Search research articles
Search
Showing results (31-40 of 104) with videos related to
Sort By:
Page
of 11
Nucleic Acids Research
|
October 11, 1994
Genetic Bit Analysis: a solid phase method for typing single nucleotide polymorphisms
T T Nikiforov, R B Rendle, P Goelet, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 7, 1999
Purin-8-ones as corticotropin-releasing hormone (CRH-R1) receptor antagonists
J P Beck, A G Arvanitis, M A Curry, et al.
Nucleic Acids Research
|
May 15, 1996
Potent antisense oligonucleotides to the human multidrug resistance-1 mRNA are rationally selected by mapping RNA-accessible sites with oligonucleotide libraries
S P Ho, D H Britton, B A Stone, et al.
Journal of Medicinal Chemistry
|
December 7, 2010
Trends in kinase selectivity: insights for target class-focused library screening
Shana L Posy, Mark A Hermsmeier, Wayne Vaccaro, et al.
Pediatric Annals
|
May 31, 2013
A 15-year-old boy with dyspnea with exertion
Robert Listernick, Jennifer L Trainor, Susanna A McColley, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 17, 2001
Synthesis and evaluation of efavirenz (Sustiva) analogues as HIV-1 reverse transcriptase inhibitors: replacement of the cyclopropylacetylene side chain
A J Cocuzza, D R Chidester, B C Cordova, et al.
Science (New York, N.Y.)
|
October 16, 1987
A system for rapid DNA sequencing with fluorescent chain-terminating dideoxynucleotides
J M Prober, G L Trainor, R J Dam, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 28, 2009
Benzo[d]imidazole inhibitors of Coactivator Associated Arginine Methyltransferase 1 (CARM1)--Hit to Lead studies
Honghe Wan, Tram Huynh, Suhong Pang, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 22, 2005
Synthesis and evaluation of 2-anilino-3-phenylsulfonyl-6-methylpyridines as corticotropin-releasing factor1 receptor ligands
Richard A Hartz, Argyrios G Arvanitis, Charles Arnold, 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.
Page
of 11