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Cancers|August 26, 2023
Synthesis and Biological Evaluation of Cyclobutane-Based β3 Integrin Antagonists: A Novel Approach to Targeting Integrins for Cancer TherapyMark Sutherland, Andrew Gordon, Fatemah O F O Al-Shammari, et al.Journal of Thrombosis and Thrombolysis|April 11, 2023
Prediction of blood pressure variability during thrombectomy using supervised machine learning and outcomes of patients with ischemic stroke from large vessel occlusionDaniel Najafali, Thomas Johnstone, Melissa Pergakis, et al.RSC Medicinal Chemistry|September 16, 2024
Sidechain structure-activity relationships of cyclobutane-based small molecule αvβ3 antagonistsAdam Throup, Manar Saleh Zraikat, Andrew Gordon, et al.Molecular Cancer Therapeutics|October 4, 2012
Antitumor activity of a duocarmycin analogue rationalized to be metabolically activated by cytochrome P450 1A1 in human transitional cell carcinoma of the bladderMark Sutherland, Jason H Gill, Paul M Loadman, et al.Scientific Reports|September 24, 2021
Cytochrome P450 isoforms 1A1, 1B1 AND 2W1 as targets for therapeutic intervention in head and neck cancerDaniela Presa, Syed A Khurram, Amir Z A Zubir, et al.Life Sciences|October 9, 2022
Matrix metalloproteinase 2 is a target of the RAN-GTP pathway and mediates migration, invasion and metastasis in human breast cancerMohamed El-Tanani, Angela Platt-Higgins, Yin-Fai Lee, et al.Journal of Medicinal Chemistry|July 13, 2013
Re-engineering of the duocarmycin structural architecture enables bioprecursor development targeting CYP1A1 and CYP2W1 for biological activityHelen M Sheldrake, Sandra Travica, Inger Johansson, et al.Plos One|August 17, 2013
Pharmacological inhibition of polysialyltransferase ST8SiaII modulates tumour cell migrationYousef M J Al-Saraireh, Mark Sutherland, Bradley R Springett, et al.JAMA Network Open|May 22, 2025
Identification of Long-Term Care Facility Residence From Admission Notes Using Large Language ModelsKatherine E Goodman, Matthew L Robinson, Seyed M Shams, et al.Pageof 4