Lowering mutant huntingtin by small molecules relieves Huntington’s disease symptoms and progression von Bahat, Anat, Itzhaki, Elad, Weiss, Benjamin, Tolmasov, Michael, Tsoory, Michael, Kuperman, Yael, Brandis, Alexander, Shurrush, Khriesto A, Dikstein, Rivka

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Non-quaternary oximes detoxify nerve agents and reactivate nerve agent-inhibited human butyrylcholinesterase von Amitai, Gabriel, Plotnikov, Alexander, Chapman, Shira, Lazar, Shlomi, Gez, Rellie, Loewenthal, Dan, Shurrush, Khriesto A., Cohen, Galit, Solmesky, Leonardo J., Barr, Haim, Russell, Alan J.

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PRMT1 inhibition induces differentiation of colon cancer cells von Plotnikov, Alexander, Kozer, Noga, Cohen, Galit, Carvalho, Silvia, Duberstein, Shirly, Almog, Ofir, Solmesky, Leonardo Javier, Shurrush, Khriesto A., Babaev, Ilana, Benjamin, Sima, Gilad, Shlomit, Kupervaser, Meital, Levin, Yishai, Gershovits, Michael, Ben-Avraham, Danny, Barr, Haim Michael

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5-Bromomethyl-4,5-dihydroisoxazoles von Mosher, Michael D., Norman, Amber L., Shurrush, Khriesto A.

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Enantioselective total synthesis of macrolide (+)-neopeltolideElectronic supplementary information (ESI) available: Characterization of selected compounds; copies of 1H and 13C NMR... von Ghosh, Arun K, Shurrush, Khriesto A, Dawson, Zachary L

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ChemInform Abstract: Preparation and Reactivity of Acyclic Chiral Allylzinc Species by a Zinc‐Brook Rearrangement von Leibeling, Markus, Shurrush, Khriesto A., Werner, Veronika, Perrin, Lionel, Marek, Ilan

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ChemInform Abstract: 5-Bromomethyl-4,5-dihydroisoxazoles von Mosher, Michael D., Norman, Amber L., Shurrush, Khriesto A.

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Specific quinone reductase 2 inhibitors reduce metabolic burden and reverse Alzheimer's disease phenotype in mice von Gould, Nathaniel L, Scherer, Gila R, Carvalho, Silvia, Shurrush, Khriesto, Kayyal, Haneen, Edry, Efrat, Elkobi, Alina, David, Orit, Foqara, Maria, Thakar, Darshit, Pavesi, Tommaso, Sharma, Vijendra, Walker, Matthew, Maitland, Matthew, Dym, Orly, Albeck, Shira, Peleg, Yoav, Germain, Nicolas, Babaev, Ilana, Sharir, Haleli, Lalzar, Maya, Shklyar, Boris, Hazut, Neta, Khamaisy, Mohammad, Lévesque, Maxime, Lajoie, Gilles, Avoli, Massimo, Amitai, Gabriel, Lefker, Bruce, Subramanyam, Chakrapani, Shilton, Brian, Barr, Haim, Rosenblum, Kobi

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Covalent Docking Identifies a Potent and Selective MKK7 Inhibitor von Shraga, Amit, Olshvang, Evgenia, Davidzohn, Natalia, Khoshkenar, Payam, Germain, Nicolas, Shurrush, Khriesto, Carvalho, Silvia, Avram, Liat, Albeck, Shira, Unger, Tamar, Lefker, Bruce, Subramanyam, Chakrapani, Hudkins, Robert L., Mitchell, Amir, Shulman, Ziv, Kinoshita, Takayoshi, London, Nir

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Small molecule inhibitor of Igf2bp1 represses Kras and a pro-oncogenic phenotype in cancer cells von Wallis, Nadav, Oberman, Froma, Shurrush, Khriesto, Germain, Nicolas, Greenwald, Gila, Gershon, Tehila, Pearl, Talia, Abis, Giancarlo, Singh, Vikash, Singh, Amandeep, Sharma, Arun K., Barr, Haim M., Ramos, Andres, Spiegelman, Vladimir S., Yisraeli, Joel K.

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Asymmetric Synthesis of anti-Aldol Segments via a Nonaldol Route: Synthetic Applications to Statines and (−)-Tetrahydrolipstatin von Ghosh, Arun K, Shurrush, Khriesto, Kulkarni, Sarang

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Optimization of Covalent MKK7 Inhibitors via Crude Nanomole-Scale Libraries von Gehrtz, Paul, Marom, Shir, Bührmann, Mike, Hardick, Julia, Kleinbölting, Silke, Shraga, Amit, Dubiella, Christian, Gabizon, Ronen, Wiese, Jan N., Müller, Matthias P., Cohen, Galit, Babaev, Ilana, Shurrush, Khriesto, Avram, Liat, Resnick, Efrat, Barr, Haim, Rauh, Daniel, London, Nir

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Turning high-throughput structural biology into predictive inhibitor design von Saar, Kadi L, McCorkindale, William, Fearon, Daren, Boby, Melissa, Barr, Haim, Ben-Shmuel, Amir, London, Nir, von Delft, Frank, Chodera, John D, Lee, Alpha A

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Asymmetric multi-component reactions: convenient access to acyclic stereocenters and functionalized cyclopentenoids von Ghosh, Arun K, Kulkarni, Sarang S, Xu, Chun-Xiao, Shurrush, Khriesto

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Fragment-Based Hit Discovery via Unsupervised Learning of Fragment-Protein Complexes von McCorkindale, William, Ahel, Ivan, Barr, Haim, Correy, Galen, Fraser, James, London, Nir, Schuller, Marion, Shurrush, Khriesto, Lee, Alpha

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ChemInform Abstract: Asymmetric Synthesis of anti-Aldol Segments via a Nonaldol Route: Synthetic Applications to Statines and (-)-Tetrahydrolipstatin von Ghosh, Arun K., Shurrush, Khriesto, Kulkarni, Sarang

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