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G Cooke

Showing results (351-360 of 408) with videos related to

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Cancer Cell|January 24, 2012
Pericyte depletion results in hypoxia-associated epithelial-to-mesenchymal transition and metastasis mediated by met signaling pathwayVesselina G Cooke, Valerie S LeBleu, Doruk Keskin, et al.
Journal of Medicinal Chemistry|July 11, 2018
Optimizing a Weakly Binding Fragment into a Potent RORγt Inverse Agonist with Efficacy in an in Vivo Inflammation ModelDavid A Carcache, Anna Vulpetti, Joerg Kallen, et al.
Molecular Medicine (Cambridge, Mass.)|September 30, 2025
Selective inhibition of BRAF and CRAF sensitizes NF1-deficient malignant peripheral nerve sheath tumors to MEK inhibitorsJiawan Wang, Arnab Sarkar, Natalia Garcia, et al.
Science (New York, N.Y.)|February 17, 2007
Starch fossils and the domestication and dispersal of chili peppers (Capsicum spp. L.) in the AmericasLinda Perry, Ruth Dickau, Sonia Zarrillo, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Discovery of BAF312 (Siponimod), a Potent and Selective S1P Receptor ModulatorShifeng Pan, Nathanael S Gray, Wenqi Gao, et al.
Cancer Discovery|July 12, 2013
An F876L mutation in androgen receptor confers genetic and phenotypic resistance to MDV3100 (enzalutamide)Manav Korpal, Joshua M Korn, Xueliang Gao, et al.
Cancer Research|April 22, 2014
Inhibiting Tankyrases sensitizes KRAS-mutant cancer cells to MEK inhibitors via FGFR2 feedback signalingMarie Schoumacher, Kristen E Hurov, Joseph Lehár, et al.
QJM : Monthly Journal of the Association of Physicians|December 14, 2017
Toll-like receptor 3 L412F polymorphism promotes a persistent clinical phenotype in pulmonary sarcoidosisG Cooke, I Kamal, M Strengert, et al.
Biological Psychiatry|September 6, 2005
Vagus nerve stimulation for treatment-resistant depression: a randomized, controlled acute phase trialA John Rush, Lauren B Marangell, Harold A Sackeim, et al.
Journal of Medicinal Chemistry|November 16, 2019
Structure-Based and Property-Driven Optimization of <i>N</i>-Aryl Imidazoles toward Potent and Selective Oral RORγt InhibitorsKlemens Hoegenauer, Joerg Kallen, Eloísa Jiménez-Núñez, et al.
Pageof 41

Showing results (351-360 of 408) with videos related to

Sort By:
Pageof 41
Cancer Cell|January 24, 2012
Pericyte depletion results in hypoxia-associated epithelial-to-mesenchymal transition and metastasis mediated by met signaling pathwayVesselina G Cooke, Valerie S LeBleu, Doruk Keskin, et al.
Journal of Medicinal Chemistry|July 11, 2018
Optimizing a Weakly Binding Fragment into a Potent RORγt Inverse Agonist with Efficacy in an in Vivo Inflammation ModelDavid A Carcache, Anna Vulpetti, Joerg Kallen, et al.
Molecular Medicine (Cambridge, Mass.)|September 30, 2025
Selective inhibition of BRAF and CRAF sensitizes NF1-deficient malignant peripheral nerve sheath tumors to MEK inhibitorsJiawan Wang, Arnab Sarkar, Natalia Garcia, et al.
Science (New York, N.Y.)|February 17, 2007
Starch fossils and the domestication and dispersal of chili peppers (Capsicum spp. L.) in the AmericasLinda Perry, Ruth Dickau, Sonia Zarrillo, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Discovery of BAF312 (Siponimod), a Potent and Selective S1P Receptor ModulatorShifeng Pan, Nathanael S Gray, Wenqi Gao, et al.
Cancer Discovery|July 12, 2013
An F876L mutation in androgen receptor confers genetic and phenotypic resistance to MDV3100 (enzalutamide)Manav Korpal, Joshua M Korn, Xueliang Gao, et al.
Cancer Research|April 22, 2014
Inhibiting Tankyrases sensitizes KRAS-mutant cancer cells to MEK inhibitors via FGFR2 feedback signalingMarie Schoumacher, Kristen E Hurov, Joseph Lehár, et al.
QJM : Monthly Journal of the Association of Physicians|December 14, 2017
Toll-like receptor 3 L412F polymorphism promotes a persistent clinical phenotype in pulmonary sarcoidosisG Cooke, I Kamal, M Strengert, et al.
Biological Psychiatry|September 6, 2005
Vagus nerve stimulation for treatment-resistant depression: a randomized, controlled acute phase trialA John Rush, Lauren B Marangell, Harold A Sackeim, et al.
Journal of Medicinal Chemistry|November 16, 2019
Structure-Based and Property-Driven Optimization of <i>N</i>-Aryl Imidazoles toward Potent and Selective Oral RORγt InhibitorsKlemens Hoegenauer, Joerg Kallen, Eloísa Jiménez-Núñez, et al.
Pageof 41