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V Thieu

Showing results (1-10 of 10) with videos related to

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Journal of Synchrotron Radiation|August 22, 2001
Local structure of guest molecules in gas hydrates--a model study of Kr and Xe clathratesP A Montano, J Linton, V Thieu, et al.
Journal of the American Chemical Society|December 26, 2001
Time-resolved in situ neutron diffraction studies of gas hydrate: transformation of structure II (sII) to structure I (sI)Y Halpern, V Thieu, R W Henning, et al.
The Science of the Total Environment|June 5, 2021
Biogeochemical functioning of an urbanized tropical estuary: Implementing the generic C-GEM (reactive transport) modelA T Nguyen, J Némery, N Gratiot, et al.
The Science of the Total Environment|May 2, 2018
Reducing marine eutrophication may require a paradigmatic changeX Desmit, V Thieu, G Billen, et al.
Frontiers in Immunology|February 2, 2018
<i>Salmonella</i> Typhi Bactericidal Antibodies Reduce Disease Severity but Do Not Protect against Typhoid Fever in a Controlled Human Infection ModelHelene B Juel, Helena B Thomaides-Brears, Thomas C Darton, et al.
Journal of Medicinal Chemistry|December 28, 2007
7-fluoroindazoles as potent and selective inhibitors of factor XaYu-Kai Lee, Daniel J Parks, Tianbao Lu, et al.
Bioorganic & Medicinal Chemistry Letters|November 2, 2011
2,7-Pyrrolo[2,1-f][1,2,4]triazines as JAK2 inhibitors: modification of target structure to minimize reactive metabolite formationLinda R Weinberg, Mark S Albom, Thelma S Angeles, et al.
Journal of Medicinal Chemistry|August 24, 2011
2,7-disubstituted-pyrrolo[2,1-f][1,2,4]triazines: new variant of an old template and application to the discovery of anaplastic lymphoma kinase (ALK) inhibitors with in vivo antitumor activityGregory R Ott, Gregory J Wells, Tho V Thieu, et al.
Bioorganic & Medicinal Chemistry Letters|December 16, 2011
Optimization of a novel kinase inhibitor scaffold for the dual inhibition of JAK2 and FAK kinasesCraig A Zificsak, Diane E Gingrich, Henry J Breslin, et al.
Journal of Medicinal Chemistry|December 7, 2011
Strategies to mitigate the bioactivation of 2-anilino-7-aryl-pyrrolo[2,1-f][1,2,4]triazines: identification of orally bioavailable, efficacious ALK inhibitorsEugen F Mesaros, Tho V Thieu, Gregory J Wells, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Journal of Synchrotron Radiation|August 22, 2001
Local structure of guest molecules in gas hydrates--a model study of Kr and Xe clathratesP A Montano, J Linton, V Thieu, et al.
Journal of the American Chemical Society|December 26, 2001
Time-resolved in situ neutron diffraction studies of gas hydrate: transformation of structure II (sII) to structure I (sI)Y Halpern, V Thieu, R W Henning, et al.
The Science of the Total Environment|June 5, 2021
Biogeochemical functioning of an urbanized tropical estuary: Implementing the generic C-GEM (reactive transport) modelA T Nguyen, J Némery, N Gratiot, et al.
The Science of the Total Environment|May 2, 2018
Reducing marine eutrophication may require a paradigmatic changeX Desmit, V Thieu, G Billen, et al.
Frontiers in Immunology|February 2, 2018
<i>Salmonella</i> Typhi Bactericidal Antibodies Reduce Disease Severity but Do Not Protect against Typhoid Fever in a Controlled Human Infection ModelHelene B Juel, Helena B Thomaides-Brears, Thomas C Darton, et al.
Journal of Medicinal Chemistry|December 28, 2007
7-fluoroindazoles as potent and selective inhibitors of factor XaYu-Kai Lee, Daniel J Parks, Tianbao Lu, et al.
Bioorganic & Medicinal Chemistry Letters|November 2, 2011
2,7-Pyrrolo[2,1-f][1,2,4]triazines as JAK2 inhibitors: modification of target structure to minimize reactive metabolite formationLinda R Weinberg, Mark S Albom, Thelma S Angeles, et al.
Journal of Medicinal Chemistry|August 24, 2011
2,7-disubstituted-pyrrolo[2,1-f][1,2,4]triazines: new variant of an old template and application to the discovery of anaplastic lymphoma kinase (ALK) inhibitors with in vivo antitumor activityGregory R Ott, Gregory J Wells, Tho V Thieu, et al.
Bioorganic & Medicinal Chemistry Letters|December 16, 2011
Optimization of a novel kinase inhibitor scaffold for the dual inhibition of JAK2 and FAK kinasesCraig A Zificsak, Diane E Gingrich, Henry J Breslin, et al.
Journal of Medicinal Chemistry|December 7, 2011
Strategies to mitigate the bioactivation of 2-anilino-7-aryl-pyrrolo[2,1-f][1,2,4]triazines: identification of orally bioavailable, efficacious ALK inhibitorsEugen F Mesaros, Tho V Thieu, Gregory J Wells, et al.
Pageof 1