Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Stephen V Frye

Showing results (51-60 of 126) with videos related to

Pageof 13
Sort By:
Journal of Medicinal Chemistry|October 24, 2023
Fused Tetrahydroquinolines Are Interfering with Your AssayFrances M Bashore, Joel Annor-Gyamfi, Yuhong Du, et al.
Journal of Medicinal Chemistry|July 26, 2011
Optimization of cellular activity of G9a inhibitors 7-aminoalkoxy-quinazolinesFeng Liu, Dalia Barsyte-Lovejoy, Abdellah Allali-Hassani, et al.
Journal of Medicinal Chemistry|March 1, 2013
Exploiting an allosteric binding site of PRMT3 yields potent and selective inhibitorsFeng Liu, Fengling Li, Anqi Ma, et al.
Scientific Reports|April 27, 2019
Discovery of selective activators of PRC2 mutant EED-I363MJunghyun L Suh, Kimberly D Barnash, Tigran M Abramyan, et al.
Plos One|October 27, 2016
MERTK Inhibition Induces Polyploidy and Promotes Cell Death and Cellular Senescence in Glioblastoma MultiformeAlexandra Sufit, Alisa B Lee-Sherick, Deborah DeRyckere, et al.
Nature Communications|May 1, 2019
Canonical PRC1 controls sequence-independent propagation of Polycomb-mediated gene silencingHagar F Moussa, Daniel Bsteh, Ramesh Yelagandula, et al.
European Journal of Medicinal Chemistry|May 26, 2021
UNC5293, a potent, orally available and highly MERTK-selective inhibitorHongchao Zheng, Jichen Zhao, Bing Li, et al.
ACS Combinatorial Science|February 7, 2017
Discovery of Peptidomimetic Ligands of EED as Allosteric Inhibitors of PRC2Kimberly D Barnash, Juliana The, Jacqueline L Norris-Drouin, et al.
The Journal of Clinical Investigation|June 16, 2022
MERTK activation drives osimertinib resistance in EGFR-mutant non-small cell lung cancerDan Yan, Justus M Huelse, Dmitri Kireev, et al.
Journal of Medicinal Chemistry|October 10, 2013
Discovery of an in vivo chemical probe of the lysine methyltransferases G9a and GLPFeng Liu, Dalia Barsyte-Lovejoy, Fengling Li, et al.
Pageof 13

Showing results (51-60 of 126) with videos related to

Sort By:
Pageof 13
Journal of Medicinal Chemistry|October 24, 2023
Fused Tetrahydroquinolines Are Interfering with Your AssayFrances M Bashore, Joel Annor-Gyamfi, Yuhong Du, et al.
Journal of Medicinal Chemistry|July 26, 2011
Optimization of cellular activity of G9a inhibitors 7-aminoalkoxy-quinazolinesFeng Liu, Dalia Barsyte-Lovejoy, Abdellah Allali-Hassani, et al.
Journal of Medicinal Chemistry|March 1, 2013
Exploiting an allosteric binding site of PRMT3 yields potent and selective inhibitorsFeng Liu, Fengling Li, Anqi Ma, et al.
Scientific Reports|April 27, 2019
Discovery of selective activators of PRC2 mutant EED-I363MJunghyun L Suh, Kimberly D Barnash, Tigran M Abramyan, et al.
Plos One|October 27, 2016
MERTK Inhibition Induces Polyploidy and Promotes Cell Death and Cellular Senescence in Glioblastoma MultiformeAlexandra Sufit, Alisa B Lee-Sherick, Deborah DeRyckere, et al.
Nature Communications|May 1, 2019
Canonical PRC1 controls sequence-independent propagation of Polycomb-mediated gene silencingHagar F Moussa, Daniel Bsteh, Ramesh Yelagandula, et al.
European Journal of Medicinal Chemistry|May 26, 2021
UNC5293, a potent, orally available and highly MERTK-selective inhibitorHongchao Zheng, Jichen Zhao, Bing Li, et al.
ACS Combinatorial Science|February 7, 2017
Discovery of Peptidomimetic Ligands of EED as Allosteric Inhibitors of PRC2Kimberly D Barnash, Juliana The, Jacqueline L Norris-Drouin, et al.
The Journal of Clinical Investigation|June 16, 2022
MERTK activation drives osimertinib resistance in EGFR-mutant non-small cell lung cancerDan Yan, Justus M Huelse, Dmitri Kireev, et al.
Journal of Medicinal Chemistry|October 10, 2013
Discovery of an in vivo chemical probe of the lysine methyltransferases G9a and GLPFeng Liu, Dalia Barsyte-Lovejoy, Fengling Li, et al.
Pageof 13