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Structure (London, England : 1993)|January 31, 2017
Allosteric Mutant IDH1 Inhibitors Reveal Mechanisms for IDH1 Mutant and Isoform SelectivityXiaoling Xie, Daniel Baird, Kimberly Bowen, et al.Communications Chemistry|March 23, 2025
Structural insight into the cGAS active site explains differences between therapeutically relevant speciesAlexander M Skeldon, Li Wang, Nicolas Sgarioto, et al.Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|May 29, 2024
The Fight Tumour Blindness Registry: Efficient capture of high-quality real-world data in uveal melanomaRoderick F O'Day, R Max Conway, Li-Anne Lim, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 23, 2020
LXH254, a Potent and Selective ARAF-Sparing Inhibitor of BRAF and CRAF for the Treatment of MAPK-Driven TumorsKelli-Ann Monaco, Scott Delach, Jing Yuan, et al.Pageof 3