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B Olsen

Showing results (631-640 of 665) with videos related to

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Bioorganic & Medicinal Chemistry Letters|May 17, 2015
Hydroxy tricyclic 1,5-naphthyridinone oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents-SAR of RHS moiety (Part-3)Sheo B Singh, David E Kaelin, Jin Wu, et al.
Antimicrobial Agents and Chemotherapy|September 25, 2004
A 7-deaza-adenosine analog is a potent and selective inhibitor of hepatitis C virus replication with excellent pharmacokinetic propertiesDavid B Olsen, Anne B Eldrup, Linda Bartholomew, et al.
Genome Biology|October 6, 2004
Complete genome sequence of the industrial bacterium Bacillus licheniformis and comparisons with closely related Bacillus speciesMichael W Rey, Preethi Ramaiya, Beth A Nelson, et al.
Cell Reports|July 2, 2014
Human-chromatin-related protein interactions identify a demethylase complex required for chromosome segregationEdyta Marcon, Zuyao Ni, Shuye Pu, et al.
The Journal of Biological Chemistry|September 11, 2003
Characterization of resistance to non-obligate chain-terminating ribonucleoside analogs that inhibit hepatitis C virus replication in vitroGiovanni Migliaccio, Joanne E Tomassini, Steven S Carroll, et al.
The Journal of Biological Chemistry|April 1, 2015
LLY-507, a Cell-active, Potent, and Selective Inhibitor of Protein-lysine Methyltransferase SMYD2Hannah Nguyen, Abdellah Allali-Hassani, Stephen Antonysamy, et al.
Journal of Medicinal Chemistry|September 9, 2000
Identification of MK-944a: a second clinical candidate from the hydroxylaminepentanamide isostere series of HIV protease inhibitorsB D Dorsey, C McDonough, S L McDaniel, et al.
Nature Structural & Molecular Biology|July 7, 2014
RPRD1A and RPRD1B are human RNA polymerase II C-terminal domain scaffolds for Ser5 dephosphorylationZuyao Ni, Chao Xu, Xinghua Guo, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Discovery of MK-1220: A Macrocyclic Inhibitor of Hepatitis C Virus NS3/4A Protease with Improved Preclinical Plasma ExposureMichael T Rudd, John A McCauley, John W Butcher, et al.
Science (New York, N.Y.)|September 5, 1980
Mount st. Helens ash from the 18 may 1980 eruption: chemical, physical, mineralogical, and biological propertiesJ S Fruchter, D E Robertson, J C Evans, et al.
Pageof 67

Showing results (631-640 of 665) with videos related to

Sort By:
Pageof 67
Bioorganic & Medicinal Chemistry Letters|May 17, 2015
Hydroxy tricyclic 1,5-naphthyridinone oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents-SAR of RHS moiety (Part-3)Sheo B Singh, David E Kaelin, Jin Wu, et al.
Antimicrobial Agents and Chemotherapy|September 25, 2004
A 7-deaza-adenosine analog is a potent and selective inhibitor of hepatitis C virus replication with excellent pharmacokinetic propertiesDavid B Olsen, Anne B Eldrup, Linda Bartholomew, et al.
Genome Biology|October 6, 2004
Complete genome sequence of the industrial bacterium Bacillus licheniformis and comparisons with closely related Bacillus speciesMichael W Rey, Preethi Ramaiya, Beth A Nelson, et al.
Cell Reports|July 2, 2014
Human-chromatin-related protein interactions identify a demethylase complex required for chromosome segregationEdyta Marcon, Zuyao Ni, Shuye Pu, et al.
The Journal of Biological Chemistry|September 11, 2003
Characterization of resistance to non-obligate chain-terminating ribonucleoside analogs that inhibit hepatitis C virus replication in vitroGiovanni Migliaccio, Joanne E Tomassini, Steven S Carroll, et al.
The Journal of Biological Chemistry|April 1, 2015
LLY-507, a Cell-active, Potent, and Selective Inhibitor of Protein-lysine Methyltransferase SMYD2Hannah Nguyen, Abdellah Allali-Hassani, Stephen Antonysamy, et al.
Journal of Medicinal Chemistry|September 9, 2000
Identification of MK-944a: a second clinical candidate from the hydroxylaminepentanamide isostere series of HIV protease inhibitorsB D Dorsey, C McDonough, S L McDaniel, et al.
Nature Structural & Molecular Biology|July 7, 2014
RPRD1A and RPRD1B are human RNA polymerase II C-terminal domain scaffolds for Ser5 dephosphorylationZuyao Ni, Chao Xu, Xinghua Guo, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Discovery of MK-1220: A Macrocyclic Inhibitor of Hepatitis C Virus NS3/4A Protease with Improved Preclinical Plasma ExposureMichael T Rudd, John A McCauley, John W Butcher, et al.
Science (New York, N.Y.)|September 5, 1980
Mount st. Helens ash from the 18 may 1980 eruption: chemical, physical, mineralogical, and biological propertiesJ S Fruchter, D E Robertson, J C Evans, et al.
Pageof 67