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Pedro M Campos

Showing results (1-10 of 6) with videos related to

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Cell Cycle (Georgetown, Tex.)|March 14, 2007
Interfering with MAP kinase docking interactions: implications and perspective for the p38 routeFederico Mayor, Maria Jurado-Pueyo, Pedro M Campos, et al.
Plos One|November 30, 2016
Identification of a Novel Inhibitory Allosteric Site in p38αPatricia Gomez-Gutierrez, Pedro M Campos, Miguel Vega, et al.
Current Medicinal Chemistry|December 21, 2021
Structure-Activity Studies of Novel Di-substituted [1,2,5]oxadiazolo [3,4-b]pyrazine Analogs Targeting the A-loop Regulatory Site of p38 MAP KinaseEsther Carrasco, Patricia Gomez-Gutierrez, Pedro M Campos, et al.
European Journal of Medicinal Chemistry|June 29, 2021
Discovery of novel 2,3,5-trisubstituted pyridine analogs as potent inhibitors of IL-1β via modulation of the p38 MAPK signaling pathwayEsther Carrasco, Patricia Gomez-Gutierrez, Pedro M Campos, et al.
Current Biology : CB|October 24, 2006
Phosphorylation of p38 by GRK2 at the docking groove unveils a novel mechanism for inactivating p38MAPKSandra Peregrin, Maria Jurado-Pueyo, Pedro M Campos, et al.
The Biochemical Journal|February 13, 2014
A novel p38 MAPK docking-groove-targeted compound is a potent inhibitor of inflammatory hyperalgesiaHanneke L D M Willemen, Pedro M Campos, Elisa Lucas, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Cell Cycle (Georgetown, Tex.)|March 14, 2007
Interfering with MAP kinase docking interactions: implications and perspective for the p38 routeFederico Mayor, Maria Jurado-Pueyo, Pedro M Campos, et al.
Plos One|November 30, 2016
Identification of a Novel Inhibitory Allosteric Site in p38αPatricia Gomez-Gutierrez, Pedro M Campos, Miguel Vega, et al.
Current Medicinal Chemistry|December 21, 2021
Structure-Activity Studies of Novel Di-substituted [1,2,5]oxadiazolo [3,4-b]pyrazine Analogs Targeting the A-loop Regulatory Site of p38 MAP KinaseEsther Carrasco, Patricia Gomez-Gutierrez, Pedro M Campos, et al.
European Journal of Medicinal Chemistry|June 29, 2021
Discovery of novel 2,3,5-trisubstituted pyridine analogs as potent inhibitors of IL-1β via modulation of the p38 MAPK signaling pathwayEsther Carrasco, Patricia Gomez-Gutierrez, Pedro M Campos, et al.
Current Biology : CB|October 24, 2006
Phosphorylation of p38 by GRK2 at the docking groove unveils a novel mechanism for inactivating p38MAPKSandra Peregrin, Maria Jurado-Pueyo, Pedro M Campos, et al.
The Biochemical Journal|February 13, 2014
A novel p38 MAPK docking-groove-targeted compound is a potent inhibitor of inflammatory hyperalgesiaHanneke L D M Willemen, Pedro M Campos, Elisa Lucas, et al.
Pageof 1