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Jacqueline L Norris

Showing results (11-20 of 47) with videos related to

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Biorxiv : the Preprint Server for Biology|March 10, 2025
Open-Source DNA-Encoded Library Package for Design, Decoding and Analysis: DELiJames Wellnitz, Brandon Novy, Travis Maxfield, et al.
Journal of Medicinal Chemistry|September 12, 2025
Development of Next Generation Cell-Permeable Peptide Inhibitors for the Oncological Target MAGE-A4Jiwoong Lim, Lilly F Chiou, Brandon Novy, et al.
Cell Chemical Biology|December 14, 2019
Degradation of Polycomb Repressive Complex 2 with an EED-Targeted Bivalent Chemical DegraderFrances Potjewyd, Anne-Marie W Turner, Joshua Beri, et al.
Journal of Medicinal Chemistry|August 30, 2016
Structure-Activity Relationships and Kinetic Studies of Peptidic Antagonists of CBX ChromodomainsJacob I Stuckey, Catherine Simpson, Jacqueline L Norris-Drouin, et al.
ACS Omega|January 17, 2022
Discovery of Potent Peptidomimetic Antagonists for Heterochromatin Protein 1 Family ProteinsKelsey N Lamb, Sarah N Dishman, Jarod M Waybright, et al.
Journal of Medicinal Chemistry|September 18, 2013
Small-molecule ligands of methyl-lysine binding proteins: optimization of selectivity for L3MBTL3Lindsey I James, Victoria K Korboukh, Liubov Krichevsky, et al.
Medchemcomm|January 28, 2014
The structure-activity relationships of L3MBTL3 inhibitors: flexibility of the dimer interfaceMichelle A Camerino, Nan Zhong, Aiping Dong, et al.
ACS Chemical Biology|August 9, 2023
SETDB1 Triple Tudor Domain Ligand, (<i>R</i>,<i>R</i>)-59, Promotes Methylation of Akt1 in CellsMélanie Uguen, Yu Deng, Fengling Li, et al.
Biorxiv : the Preprint Server for Biology|May 22, 2023
SETDB1 Triple Tudor Domain Ligand, ( <i>R,R</i> )-59, Promotes Methylation of Akt1 in CellsMélanie Uguen, Yu Deng, Fengling Li, et al.
Journal of Medicinal Chemistry|May 6, 2022
Discovery and Structural Basis of the Selectivity of Potent Cyclic Peptide Inhibitors of MAGE-A4Matthew C Fleming, Lilly F Chiou, Percy P Tumbale, et al.
Pageof 5

Showing results (11-20 of 47) with videos related to

Sort By:
Pageof 5
Biorxiv : the Preprint Server for Biology|March 10, 2025
Open-Source DNA-Encoded Library Package for Design, Decoding and Analysis: DELiJames Wellnitz, Brandon Novy, Travis Maxfield, et al.
Journal of Medicinal Chemistry|September 12, 2025
Development of Next Generation Cell-Permeable Peptide Inhibitors for the Oncological Target MAGE-A4Jiwoong Lim, Lilly F Chiou, Brandon Novy, et al.
Cell Chemical Biology|December 14, 2019
Degradation of Polycomb Repressive Complex 2 with an EED-Targeted Bivalent Chemical DegraderFrances Potjewyd, Anne-Marie W Turner, Joshua Beri, et al.
Journal of Medicinal Chemistry|August 30, 2016
Structure-Activity Relationships and Kinetic Studies of Peptidic Antagonists of CBX ChromodomainsJacob I Stuckey, Catherine Simpson, Jacqueline L Norris-Drouin, et al.
ACS Omega|January 17, 2022
Discovery of Potent Peptidomimetic Antagonists for Heterochromatin Protein 1 Family ProteinsKelsey N Lamb, Sarah N Dishman, Jarod M Waybright, et al.
Journal of Medicinal Chemistry|September 18, 2013
Small-molecule ligands of methyl-lysine binding proteins: optimization of selectivity for L3MBTL3Lindsey I James, Victoria K Korboukh, Liubov Krichevsky, et al.
Medchemcomm|January 28, 2014
The structure-activity relationships of L3MBTL3 inhibitors: flexibility of the dimer interfaceMichelle A Camerino, Nan Zhong, Aiping Dong, et al.
ACS Chemical Biology|August 9, 2023
SETDB1 Triple Tudor Domain Ligand, (<i>R</i>,<i>R</i>)-59, Promotes Methylation of Akt1 in CellsMélanie Uguen, Yu Deng, Fengling Li, et al.
Biorxiv : the Preprint Server for Biology|May 22, 2023
SETDB1 Triple Tudor Domain Ligand, ( <i>R,R</i> )-59, Promotes Methylation of Akt1 in CellsMélanie Uguen, Yu Deng, Fengling Li, et al.
Journal of Medicinal Chemistry|May 6, 2022
Discovery and Structural Basis of the Selectivity of Potent Cyclic Peptide Inhibitors of MAGE-A4Matthew C Fleming, Lilly F Chiou, Percy P Tumbale, et al.
Pageof 5