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M Szewczyk

Showing results (131-140 of 157) with videos related to

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ACS Medicinal Chemistry Letters|July 24, 2018
LLY-283, a Potent and Selective Inhibitor of Arginine Methyltransferase 5, PRMT5, with Antitumor ActivityZahid Q Bonday, Guillermo S Cortez, Michael J Grogan, et al.
Journal of Medicinal Chemistry|February 1, 2021
Discovery of Small-Molecule Antagonists of the PWWP Domain of NSD2Renato Ferreira de Freitas, Yanli Liu, Magdalena M Szewczyk, et al.
Communications Biology|December 9, 2021
Huntingtin structure is orchestrated by HAP40 and shows a polyglutamine expansion-specific interaction with exon 1Rachel J Harding, Justin C Deme, Johannes F Hevler, et al.
Journal of the American Chemical Society|March 28, 2023
Discovery of a Potent and Selective Targeted NSD2 Degrader for the Reduction of H3K36me2Ronan P Hanley, David Y Nie, John R Tabor, et al.
Journal of Medicinal Chemistry|July 27, 2023
Discovery and Characterization of a Chemical Probe Targeting the Zinc-Finger Ubiquitin-Binding Domain of HDAC6Rachel J Harding, Ivan Franzoni, Mandeep K Mann, et al.
SLAS Discovery : Advancing Life Sciences R & D|June 22, 2021
Discovery of the SMYD3 Inhibitor BAY-6035 Using Thermal Shift Assay (TSA)-Based High-Throughput ScreeningStefan Gradl, Holger Steuber, Joerg Weiske, et al.
Oncotarget|May 3, 2018
TP-064, a potent and selective small molecule inhibitor of PRMT4 for multiple myelomaKazuhide Nakayama, Magdalena M Szewczyk, Carlo Dela Sena, et al.
Infection and Immunity|September 21, 2022
A Co-Association of Streptococcus mutans and Veillonella parvula/dispar in Root Caries Patients and <i>In Vitro</i> BiofilmsAmber M Abram, Michelle M Szewczyk, Seon G Park, et al.
Journal of Medicinal Chemistry|December 16, 2017
Discovery of Potent and Selective Allosteric Inhibitors of Protein Arginine Methyltransferase 3 (PRMT3)H Ümit Kaniskan, Mohammad S Eram, Kehao Zhao, et al.
RSC Medicinal Chemistry|March 22, 2024
Chemical tools for the Gid4 subunit of the human E3 ligase C-terminal to LisH (CTLH) degradation complexAliakbar Khalili Yazdi, Sumera Perveen, Cheng Dong, et al.
Pageof 16

Showing results (131-140 of 157) with videos related to

Sort By:
Pageof 16
ACS Medicinal Chemistry Letters|July 24, 2018
LLY-283, a Potent and Selective Inhibitor of Arginine Methyltransferase 5, PRMT5, with Antitumor ActivityZahid Q Bonday, Guillermo S Cortez, Michael J Grogan, et al.
Journal of Medicinal Chemistry|February 1, 2021
Discovery of Small-Molecule Antagonists of the PWWP Domain of NSD2Renato Ferreira de Freitas, Yanli Liu, Magdalena M Szewczyk, et al.
Communications Biology|December 9, 2021
Huntingtin structure is orchestrated by HAP40 and shows a polyglutamine expansion-specific interaction with exon 1Rachel J Harding, Justin C Deme, Johannes F Hevler, et al.
Journal of the American Chemical Society|March 28, 2023
Discovery of a Potent and Selective Targeted NSD2 Degrader for the Reduction of H3K36me2Ronan P Hanley, David Y Nie, John R Tabor, et al.
Journal of Medicinal Chemistry|July 27, 2023
Discovery and Characterization of a Chemical Probe Targeting the Zinc-Finger Ubiquitin-Binding Domain of HDAC6Rachel J Harding, Ivan Franzoni, Mandeep K Mann, et al.
SLAS Discovery : Advancing Life Sciences R & D|June 22, 2021
Discovery of the SMYD3 Inhibitor BAY-6035 Using Thermal Shift Assay (TSA)-Based High-Throughput ScreeningStefan Gradl, Holger Steuber, Joerg Weiske, et al.
Oncotarget|May 3, 2018
TP-064, a potent and selective small molecule inhibitor of PRMT4 for multiple myelomaKazuhide Nakayama, Magdalena M Szewczyk, Carlo Dela Sena, et al.
Infection and Immunity|September 21, 2022
A Co-Association of Streptococcus mutans and Veillonella parvula/dispar in Root Caries Patients and <i>In Vitro</i> BiofilmsAmber M Abram, Michelle M Szewczyk, Seon G Park, et al.
Journal of Medicinal Chemistry|December 16, 2017
Discovery of Potent and Selective Allosteric Inhibitors of Protein Arginine Methyltransferase 3 (PRMT3)H Ümit Kaniskan, Mohammad S Eram, Kehao Zhao, et al.
RSC Medicinal Chemistry|March 22, 2024
Chemical tools for the Gid4 subunit of the human E3 ligase C-terminal to LisH (CTLH) degradation complexAliakbar Khalili Yazdi, Sumera Perveen, Cheng Dong, et al.
Pageof 16