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Aaron Smith

Showing results (141-150 of 170) with videos related to

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Bioorganic & Medicinal Chemistry Letters|November 7, 2017
Imidazo[1,2-a]pyridin-6-yl-benzamide analogs as potent RAF inhibitorsAaron Smith, Zhi-Jie Ni, Daniel Poon, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 18, 2015
The MET Inhibitor AZD6094 (Savolitinib, HMPL-504) Induces Regression in Papillary Renal Cell Carcinoma Patient-Derived Xenograft ModelsAlwin G Schuller, Evan R Barry, Rhys D O Jones, et al.
Cancer Discovery|December 18, 2016
Activating <i>ESR1</i> Mutations Differentially Affect the Efficacy of ER AntagonistsWeiyi Toy, Hazel Weir, Pedram Razavi, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|August 5, 2022
Preclinical Characterization of AZD5305, A Next-Generation, Highly Selective PARP1 Inhibitor and TrapperGiuditta Illuzzi, Anna D Staniszewska, Sonja J Gill, et al.
Cell Metabolism|October 3, 2006
Non-DNA binding, dominant-negative, human PPARgamma mutations cause lipodystrophic insulin resistanceMaura Agostini, Erik Schoenmakers, Catherine Mitchell, et al.
The Journal of Organic Chemistry|April 23, 2024
Challenges with the Synthesis of a Macrocyclic Thioether Peptide: From Milligram to Multigram Using Solid Phase Peptide Synthesis (SPPS)James Kempson, Rulin Zhao, Joseph Pawluczyk, et al.
Molecular Cancer Therapeutics|February 2, 2026
Preclinical to clinical translation of pharmacokinetic-pharmacodynamic relationship in EGFR Exon20Ins mutations: a modelling framework for irreversible inhibitorsAdriana Savoca, Diana Zindel, Radoslaw Polanski, et al.
Molecular Cancer Therapeutics|September 20, 2019
Pharmacology of the ATM Inhibitor AZD0156: Potentiation of Irradiation and Olaparib Responses PreclinicallyLucy C Riches, Antonio G Trinidad, Gareth Hughes, et al.
Cell Reports. Medicine|August 26, 2025
AZ14289671 is a highly selective and blood-brain barrier penetrant irreversible TKI that targets EGFRExon20 insertionsAisha M Swaih, Sara Talbot, Adriana Savoca, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Chemical Probe Identification Platform for Orphan GPCRs Using Focused Compound Screening: GPR39 as a Case ExampleMarkus Boehm, David Hepworth, Paula M Loria, et al.
Pageof 17

Showing results (141-150 of 170) with videos related to

Sort By:
Pageof 17
Bioorganic & Medicinal Chemistry Letters|November 7, 2017
Imidazo[1,2-a]pyridin-6-yl-benzamide analogs as potent RAF inhibitorsAaron Smith, Zhi-Jie Ni, Daniel Poon, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 18, 2015
The MET Inhibitor AZD6094 (Savolitinib, HMPL-504) Induces Regression in Papillary Renal Cell Carcinoma Patient-Derived Xenograft ModelsAlwin G Schuller, Evan R Barry, Rhys D O Jones, et al.
Cancer Discovery|December 18, 2016
Activating <i>ESR1</i> Mutations Differentially Affect the Efficacy of ER AntagonistsWeiyi Toy, Hazel Weir, Pedram Razavi, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|August 5, 2022
Preclinical Characterization of AZD5305, A Next-Generation, Highly Selective PARP1 Inhibitor and TrapperGiuditta Illuzzi, Anna D Staniszewska, Sonja J Gill, et al.
Cell Metabolism|October 3, 2006
Non-DNA binding, dominant-negative, human PPARgamma mutations cause lipodystrophic insulin resistanceMaura Agostini, Erik Schoenmakers, Catherine Mitchell, et al.
The Journal of Organic Chemistry|April 23, 2024
Challenges with the Synthesis of a Macrocyclic Thioether Peptide: From Milligram to Multigram Using Solid Phase Peptide Synthesis (SPPS)James Kempson, Rulin Zhao, Joseph Pawluczyk, et al.
Molecular Cancer Therapeutics|February 2, 2026
Preclinical to clinical translation of pharmacokinetic-pharmacodynamic relationship in EGFR Exon20Ins mutations: a modelling framework for irreversible inhibitorsAdriana Savoca, Diana Zindel, Radoslaw Polanski, et al.
Molecular Cancer Therapeutics|September 20, 2019
Pharmacology of the ATM Inhibitor AZD0156: Potentiation of Irradiation and Olaparib Responses PreclinicallyLucy C Riches, Antonio G Trinidad, Gareth Hughes, et al.
Cell Reports. Medicine|August 26, 2025
AZ14289671 is a highly selective and blood-brain barrier penetrant irreversible TKI that targets EGFRExon20 insertionsAisha M Swaih, Sara Talbot, Adriana Savoca, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Chemical Probe Identification Platform for Orphan GPCRs Using Focused Compound Screening: GPR39 as a Case ExampleMarkus Boehm, David Hepworth, Paula M Loria, et al.
Pageof 17