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Bauer, M. S., Gruber, S., Hausch, A., Gomes, Psfc, Milles, L. F., Nicolaus, T., Schendel, L. C., Navajas, P. L., Procko, E., Lietha, D., Melo, M. C. R., Bernardi, R. C., Gaub, H. E., Lipfert, J.
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[2022]. TDP-43 Modulation by Tau-Tubulin Kinase 1 Inhibitors: A New Avenue for Future Amyotrophic Lateral Sclerosis Therapy. J Med Chem. 65:1585-1607-.
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[2020]. Design, Synthesis, and Biological Evaluation of Covalent Inhibitors of Focal Adhesion Kinase (FAK) against Human Malignant Glioblastoma. J Med Chem. 63(21):12707-12724
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[2020]. A Synergistic Anticancer FAK and HDAC Inhibitor Combination Discovered by a Novel Chemical-Genetic High-Content Phenotypic Screen. Mol Cancer Ther. 19:637-649-.
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[2018]. Exome Sequencing of Plasma DNA Portrays the Mutation Landscape of Colorectal Cancer and Discovers Mutated VEGFR2 Receptors as Modulators of Antiangiogenic Therapies. Clin Cancer Res. 24:3550-3559-.
Le Coq, J., Camacho-Artacho, M., Velazquez, J. V., Santiveri, C. M., Gallego, L. H., Campos-Olivas, R., Dolker, N., Lietha, D.
[2017]. Structural basis for interdomain communication in SHIP2 providing high phosphatase activity. Elife. 6:-.
Yen-Pon, E., Li, B., Acebron-Garcia-de-Eulate, M., Tomkiewicz-Raulet, C., Dawson, J., Lietha, D., Frame, M. C., Coumoul, X., Garbay, C., Etheve-Quelquejeu, M., Chen, H.
[2018]. Structure-Based Design, Synthesis, and Characterization of the First Irreversible Inhibitor of Focal Adhesion Kinase. ACS Chem Biol. 13:2067-2073-.
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