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Journal of Biotechnology
|
August 2, 2003
Identifying and modulating disulfide formation in the biopharmaceutical production of a recombinant protein vaccine candidate
Anne Bouvier, Jaymi Chapline, Renee Boerner, et al.
Clinical and Vaccine Immunology : CVI
|
July 28, 2010
Inhalational botulism in rhesus macaques exposed to botulinum neurotoxin complex serotypes A1 and B1
Daniel C Sanford, Roy E Barnewall, Michelle L Vassar, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
May 17, 2006
Discovery and characterization of triaminotriazine aniline amides as highly selective p38 kinase inhibitors
Tsung H Lin, Axel Metzger, David J Diller, et al.
Bioorganic & Medicinal Chemistry
|
January 7, 2009
Solid-phase parallel synthesis and SAR of 4-amidofuran-3-one inhibitors of cathepsin S: effect of sulfonamides P3 substituents on potency and selectivity
Susana Ayesa, Charlotta Lindquist, Tatiana Agback, et al.
Pflugers Archiv : European Journal of Physiology
|
August 7, 2012
Proteolytic activation of the epithelial sodium channel (ENaC) by the cysteine protease cathepsin-S
Silke Haerteis, Matteus Krappitz, Marko Bertog, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
June 24, 2016
Selective Cathepsin S Inhibition with MIV-247 Attenuates Mechanical Allodynia and Enhances the Antiallodynic Effects of Gabapentin and Pregabalin in a Mouse Model of Neuropathic Pain
Ellen Hewitt, Thomas Pitcher, Biljana Rizoska, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 24, 2007
Discovery and preliminary evaluation of 5-(4-phenylbenzyl)oxazole-4-carboxamides as prostacyclin receptor antagonists
Marc-Raleigh Brescia, Laura L Rokosz, Andrew G Cole, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 3, 2009
Synthesis and SAR studies of trisubstituted purinones as potent and selective adenosine A2A receptor antagonists
Yuefei Shao, Andrew G Cole, Marc-Raleigh Brescia, et al.
The Plant Cell
|
February 11, 2021
Spatiotemporal control of miR398 biogenesis, via chromatin remodeling and kinase signaling, ensures proper ovule development
Hanyang Cai, Liping Liu, Man Zhang, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 12, 2020
Discovery of USP7 small-molecule allosteric inhibitors
Olof Engström, Oscar Belda, Mari Kullman-Magnusson, et al.
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of 9
Search research articles
Search
Showing results (51-60 of 87) with videos related to
Sort By:
Page
of 9
Journal of Biotechnology
|
August 2, 2003
Identifying and modulating disulfide formation in the biopharmaceutical production of a recombinant protein vaccine candidate
Anne Bouvier, Jaymi Chapline, Renee Boerner, et al.
Clinical and Vaccine Immunology : CVI
|
July 28, 2010
Inhalational botulism in rhesus macaques exposed to botulinum neurotoxin complex serotypes A1 and B1
Daniel C Sanford, Roy E Barnewall, Michelle L Vassar, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
May 17, 2006
Discovery and characterization of triaminotriazine aniline amides as highly selective p38 kinase inhibitors
Tsung H Lin, Axel Metzger, David J Diller, et al.
Bioorganic & Medicinal Chemistry
|
January 7, 2009
Solid-phase parallel synthesis and SAR of 4-amidofuran-3-one inhibitors of cathepsin S: effect of sulfonamides P3 substituents on potency and selectivity
Susana Ayesa, Charlotta Lindquist, Tatiana Agback, et al.
Pflugers Archiv : European Journal of Physiology
|
August 7, 2012
Proteolytic activation of the epithelial sodium channel (ENaC) by the cysteine protease cathepsin-S
Silke Haerteis, Matteus Krappitz, Marko Bertog, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
June 24, 2016
Selective Cathepsin S Inhibition with MIV-247 Attenuates Mechanical Allodynia and Enhances the Antiallodynic Effects of Gabapentin and Pregabalin in a Mouse Model of Neuropathic Pain
Ellen Hewitt, Thomas Pitcher, Biljana Rizoska, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 24, 2007
Discovery and preliminary evaluation of 5-(4-phenylbenzyl)oxazole-4-carboxamides as prostacyclin receptor antagonists
Marc-Raleigh Brescia, Laura L Rokosz, Andrew G Cole, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 3, 2009
Synthesis and SAR studies of trisubstituted purinones as potent and selective adenosine A2A receptor antagonists
Yuefei Shao, Andrew G Cole, Marc-Raleigh Brescia, et al.
The Plant Cell
|
February 11, 2021
Spatiotemporal control of miR398 biogenesis, via chromatin remodeling and kinase signaling, ensures proper ovule development
Hanyang Cai, Liping Liu, Man Zhang, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 12, 2020
Discovery of USP7 small-molecule allosteric inhibitors
Olof Engström, Oscar Belda, Mari Kullman-Magnusson, et al.
Page
of 9