[Baran lab]
[1]

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  • J. Hu, B. Hu, M. Wang, F. Xu, B. Miao, C. Yang, M. Wang, Z. Liu, D.F. Hayes, K. Chinnaswamy, J. Delproposto, J. Stuckey, and S. Wang, "Discovery of ERD-308 as a Highly Potent Proteolysis Targeting Chimera (PROTAC) Degrader of Estrogen Receptor (ER)", Journal of Medicinal Chemistry, vol. 62, pp. 1420-1442, 2019. http://dx.doi.org/10.1021/acs.jmedchem.8b01572

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  • S. Scheer, S. Ackloo, T.S. Medina, M. Schapira, F. Li, J.A. Ward, A.M. Lewis, J.P. Northrop, P.L. Richardson, H.. Kaniskan, Y. Shen, J. Liu, D. Smil, D. McLeod, C.A. Zepeda-Velazquez, M. Luo, J. Jin, D. Barsyte-Lovejoy, K.V.M. Huber, D.D. De Carvalho, M. Vedadi, C. Zaph, P.J. Brown, and C.H. Arrowsmith, "A chemical biology toolbox to study protein methyltransferases and epigenetic signaling", Nature Communications, vol. 10, 2019. http://dx.doi.org/10.1038/s41467-018-07905-4

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  • V. Zoppi, S.J. Hughes, C. Maniaci, A. Testa, T. Gmaschitz, C. Wieshofer, M. Koegl, K.M. Riching, D.L. Daniels, A. Spallarossa, and A. Ciulli, "Iterative Design and Optimization of Initially Inactive Proteolysis Targeting Chimeras (PROTACs) Identify VZ185 as a Potent, Fast, and Selective von Hippel–Lindau (VHL) Based Dual Degrader Probe of BRD9 and BRD7", Journal of Medicinal Chemistry, vol. 62, pp. 699-726, 2018. http://dx.doi.org/10.1021/acs.jmedchem.8b01413