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Justin Du Bois

Showing results (1-10 of 12) with videos related to

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Angewandte Chemie (International Ed. in English)|September 16, 2004
Rh-catalyzed amination of ethereal Calpha-H bonds: a versatile strategy for the synthesis of complex aminesKristin Williams Fiori, James J Fleming, Justin Du Bois
Chemical Society Reviews|March 11, 2011
C-H functionalization in organic synthesisHuw M L Davies, Justin Du Bois, Jin-Quan Yu
ACS Chemical Biology|September 24, 2013
The Stanford Institute for Chemical BiologyJames K Chen, Justin Du Bois, Jeffrey Glenn, et al.
Tetrahedron Letters|June 30, 2015
An expedient synthesis of maraviroc (UK-427,857) <i>via</i> C-H functionalizationT Aaron Bedell, Graham A B Hone, Justin Du Bois, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 24, 2012
Capturing fleeting intermediates in a catalytic C-H amination reaction cycleRichard H Perry, Thomas J Cahill, Jennifer L Roizen, et al.
Aquatic Toxicology (Amsterdam, Netherlands)|July 16, 2017
The paralytic shellfish toxin, saxitoxin, enters the cytoplasm and induces apoptosis of oyster immune cells through a caspase-dependent pathwayCelina Abi-Khalil, Darren S Finkelstein, Genevieve Conejero, et al.
Molecular Pharmacology|June 9, 2022
Lubiprostone is non-selective activator of cAMP-gated ion channels and Clc-2 has a minor role in its prosecretory effect in intestinal epithelial cellsApurva A Oak, Tifany Chu, Pattareeya Yottasan, et al.
Nature Communications|March 15, 2024
Dual receptor-sites reveal the structural basis for hyperactivation of sodium channels by poison-dart toxin batrachotoxinLige Tonggu, Goragot Wisedchaisri, Tamer M Gamal El-Din, et al.
Journal of the American Chemical Society|April 9, 2014
Visualizing dermal permeation of sodium channel modulators by mass spectrometric imagingLivia S Eberlin, John V Mulcahy, Alexander Tzabazis, et al.
British Journal of Pharmacology|May 8, 2024
ST-2560, a selective inhibitor of the Na<sub>V</sub>1.7 sodium channel, affects nocifensive and cardiovascular reflexes in non-human primatesJohn V Mulcahy, Jacob T Beckley, Sheri D Klas, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Angewandte Chemie (International Ed. in English)|September 16, 2004
Rh-catalyzed amination of ethereal Calpha-H bonds: a versatile strategy for the synthesis of complex aminesKristin Williams Fiori, James J Fleming, Justin Du Bois
Chemical Society Reviews|March 11, 2011
C-H functionalization in organic synthesisHuw M L Davies, Justin Du Bois, Jin-Quan Yu
ACS Chemical Biology|September 24, 2013
The Stanford Institute for Chemical BiologyJames K Chen, Justin Du Bois, Jeffrey Glenn, et al.
Tetrahedron Letters|June 30, 2015
An expedient synthesis of maraviroc (UK-427,857) <i>via</i> C-H functionalizationT Aaron Bedell, Graham A B Hone, Justin Du Bois, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 24, 2012
Capturing fleeting intermediates in a catalytic C-H amination reaction cycleRichard H Perry, Thomas J Cahill, Jennifer L Roizen, et al.
Aquatic Toxicology (Amsterdam, Netherlands)|July 16, 2017
The paralytic shellfish toxin, saxitoxin, enters the cytoplasm and induces apoptosis of oyster immune cells through a caspase-dependent pathwayCelina Abi-Khalil, Darren S Finkelstein, Genevieve Conejero, et al.
Molecular Pharmacology|June 9, 2022
Lubiprostone is non-selective activator of cAMP-gated ion channels and Clc-2 has a minor role in its prosecretory effect in intestinal epithelial cellsApurva A Oak, Tifany Chu, Pattareeya Yottasan, et al.
Nature Communications|March 15, 2024
Dual receptor-sites reveal the structural basis for hyperactivation of sodium channels by poison-dart toxin batrachotoxinLige Tonggu, Goragot Wisedchaisri, Tamer M Gamal El-Din, et al.
Journal of the American Chemical Society|April 9, 2014
Visualizing dermal permeation of sodium channel modulators by mass spectrometric imagingLivia S Eberlin, John V Mulcahy, Alexander Tzabazis, et al.
British Journal of Pharmacology|May 8, 2024
ST-2560, a selective inhibitor of the Na<sub>V</sub>1.7 sodium channel, affects nocifensive and cardiovascular reflexes in non-human primatesJohn V Mulcahy, Jacob T Beckley, Sheri D Klas, et al.
Pageof 2