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Macrocyclic carbon-linked pyrazoles as novel inhibitors of MCL-1
Demin, S., Peschiulli, A., Velter, A. I., Vos, A., De Boeck, B., Miller, B., … Philippar, U. (2023). Macrocyclic carbon-linked pyrazoles as novel inhibitors of MCL-1. ACS Medicinal Chemistry Letters, 14(7), 955-961. https://doi.org/10.1021/acsmedchemlett.3c00141
Structure-activity relationships, biological evaluation and structural studies of novel pyrrolonaphthoxazepines as antitumor agents
Brindisi, M., Ulivieri, C., Alfano, G., Gemma, S., de Asís Balaguer, F., Khan, T., … Brogi, S. (2019). Structure-activity relationships, biological evaluation and structural studies of novel pyrrolonaphthoxazepines as antitumor agents. European Journal of Medicinal Chemistry, 162, 290-320. https://doi.org/10.1016/j.ejmech.2018.11.004
Evaluation of <sup>99m</sup>Tc-rhAnnexin V-128 SPECT/CT as a diagnostic tool for early stages of interstitial lung disease associated with systemic sclerosis
Schniering, J., Guo, L., Brunner, M., Schibli, R., Ye, S., Distler, O., … Maurer, B. (2018). Evaluation of 99mTc-rhAnnexin V-128 SPECT/CT as a diagnostic tool for early stages of interstitial lung disease associated with systemic sclerosis. Arthritis Research and Therapy, 20(1), 183 (13 pp.). https://doi.org/10.1186/s13075-018-1681-1
The conserved ubiquitin-like protein Hub1 plays a critical role in splicing in human cells
Ammon, T., Mishra, S. K., Kowalska, K., Popowicz, G. M., Holak, T. A., & Jentsch, S. (2014). The conserved ubiquitin-like protein Hub1 plays a critical role in splicing in human cells. Journal of Molecular Cell Biology, 6(4), 312-323. https://doi.org/10.1093/jmcb/mju026
Co-crystallization with conformation-specific designed ankyrin repeat proteins explains the conformational flexibility of BCL-W
Schilling, J., Schöppe, J., Sauer, E., & Plückthun, A. (2014). Co-crystallization with conformation-specific designed ankyrin repeat proteins explains the conformational flexibility of BCL-W. Journal of Molecular Biology, 426(12), 2346-2362. https://doi.org/10.1016/j.jmb.2014.04.010
Discovery of potent and selective spiroindolinone MDM2 inhibitor, RO8994, for cancer therapy
Zhang, Z., Ding, Q., Liu, J. J., Zhang, J., Jiang, N., Chu, X. J., … Graves, B. (2014). Discovery of potent and selective spiroindolinone MDM2 inhibitor, RO8994, for cancer therapy. Bioorganic and Medicinal Chemistry, 22(15), 4001-4009. https://doi.org/10.1016/j.bmc.2014.05.072
The role of the acidity of N-heteroaryl sulfonamides as inhibitors of Bcl-2 family protein-protein interactions
Touré, B. B., Miller-Moslin, K., Yusuff, N., Perez, L., Doré, M., Joud, C., … Visser, M. (2013). The role of the acidity of N-heteroaryl sulfonamides as inhibitors of Bcl-2 family protein-protein interactions. ACS Medicinal Chemistry Letters, 4(2), 186-190. https://doi.org/10.1021/ml300321d
HAX1 deficiency: impact on lymphopoiesis and B-cell development
Peckl-Schmid, D., Wolkerstorfer, S., Königsberger, S., Achatz-Straussberger, G., Feichtner, S., Schwaiger, E., … Achatz, G. (2010). HAX1 deficiency: impact on lymphopoiesis and B-cell development. European Journal of Immunology, 40(11), 3161-3172. https://doi.org/10.1002/eji.200940221
Activation of the lifespan regulator p66<sup>Shc</sup> through reversible disulfide bond formation
Gertz, M., Fischer, F., Wolters, D., & Steegborn, C. (2008). Activation of the lifespan regulator p66Shc through reversible disulfide bond formation. Proceedings of the National Academy of Sciences of the United States of America PNAS, 105(15), 5705-5709. https://doi.org/10.1073/pnas.0800691105
High levels of delayed radiation-induced apoptosis observed in lymphoblastoid cell lines from <em>ataxia-telangiectasia </em>patients
Shi, Y. Q., Li, L., Sanal, O., Tezcan, I., Emery, G. C., Blattmann, H., & Crompton, N. E. A. (2001). High levels of delayed radiation-induced apoptosis observed in lymphoblastoid cell lines from ataxia-telangiectasia patients. International Journal of Radiation Oncology Biology Physics, 49(2), 555-559. https://doi.org/10.1016/S0360-3016(00)01478-4
Wortmannin selectively enhances radiation-induced apoptosis in proliferative but not quiescent cells
Shi, Y. Q., Blattmann, H., & Crompton, N. E. A. (2001). Wortmannin selectively enhances radiation-induced apoptosis in proliferative but not quiescent cells. International Journal of Radiation Oncology Biology Physics, 49(2), 421-425. https://doi.org/10.1016/S0360-3016(00)01479-6