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

Xianming Deng

Showing results (81-90 of 150) with videos related to

Pageof 15
Sort By:
Journal of Medicinal Chemistry|August 14, 2020
Correction to "Synthesis and Structure-Activity Relationships of DCLK1 Kinase Inhibitors Based on a 5,11-Dihydro-6<i>H</i>-benzo[<i>e</i>]pyrimido[5,4-<i>b</i>][1,4]diazepin-6-one Scaffold"Fleur M Ferguson, Yan Liu, Wayne Harshbarger, et al.
The Journal of Biological Chemistry|December 28, 2018
A cell-based high-throughput screening method based on a ubiquitin-reference technique for identifying modulators of E3 ligasesMaoyuan Tian, Taoling Zeng, Mingdong Liu, et al.
Journal of Medicinal Chemistry|June 13, 2020
Synthesis and Structure-Activity Relationships of DCLK1 Kinase Inhibitors Based on a 5,11-Dihydro-6<i>H</i>-benzo[<i>e</i>]pyrimido[5,4-<i>b</i>][1,4]diazepin-6-one ScaffoldFleur M Ferguson, Yan Liu, Wayne Harshbarger, et al.
Science Signaling|October 30, 2014
The kinase ALK stimulates the kinase ERK5 to promote the expression of the oncogene MYCN in neuroblastomaGanesh Umapathy, Abeer El Wakil, Barbara Witek, et al.
Antiviral Research|December 14, 2016
Identification of compounds with anti-human cytomegalovirus activity that inhibit production of IE2 proteinsRooksarr Beelontally, Gavin S Wilkie, Betty Lau, et al.
European Journal of Medicinal Chemistry|September 4, 2020
Discovery of 4-methyl-N-(4-((4-methylpiperazin- 1-yl)methyl)-3-(trifluoromethyl)phenyl)-3-((6-(pyridin-3-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-oxy)benzamide as a potent inhibitor of RET and its gatekeeper mutantXiaoyang Li, Jingyi Su, Yanru Yang, et al.
Chemistry & Biology|April 24, 2012
Small-molecule inhibitors of the c-Fes protein-tyrosine kinaseSabine Hellwig, Chandra V Miduturu, Shigeru Kanda, et al.
Plos One|June 6, 2015
Identification of Novel Small Molecule Inhibitors of Oncogenic RET KinaseMarialuisa Moccia, Qingsong Liu, Teresa Guida, et al.
Journal of Natural Products|September 18, 2015
Aspertetranones A-D, Putative Meroterpenoids from the Marine Algal-Associated Fungus Aspergillus sp. ZL0-1b14Yuezhou Wang, Shuang Qi, Ying Zhan, et al.
Nature Communications|February 27, 2024
Deaggregation of mutant Plasmodium yoelii de-ubiquitinase UBP1 alters MDR1 localization to confer multidrug resistanceRuixue Xu, Lirong Lin, Zhiwei Jiao, et al.
Pageof 15

Showing results (81-90 of 150) with videos related to

Sort By:
Pageof 15
Journal of Medicinal Chemistry|August 14, 2020
Correction to "Synthesis and Structure-Activity Relationships of DCLK1 Kinase Inhibitors Based on a 5,11-Dihydro-6<i>H</i>-benzo[<i>e</i>]pyrimido[5,4-<i>b</i>][1,4]diazepin-6-one Scaffold"Fleur M Ferguson, Yan Liu, Wayne Harshbarger, et al.
The Journal of Biological Chemistry|December 28, 2018
A cell-based high-throughput screening method based on a ubiquitin-reference technique for identifying modulators of E3 ligasesMaoyuan Tian, Taoling Zeng, Mingdong Liu, et al.
Journal of Medicinal Chemistry|June 13, 2020
Synthesis and Structure-Activity Relationships of DCLK1 Kinase Inhibitors Based on a 5,11-Dihydro-6<i>H</i>-benzo[<i>e</i>]pyrimido[5,4-<i>b</i>][1,4]diazepin-6-one ScaffoldFleur M Ferguson, Yan Liu, Wayne Harshbarger, et al.
Science Signaling|October 30, 2014
The kinase ALK stimulates the kinase ERK5 to promote the expression of the oncogene MYCN in neuroblastomaGanesh Umapathy, Abeer El Wakil, Barbara Witek, et al.
Antiviral Research|December 14, 2016
Identification of compounds with anti-human cytomegalovirus activity that inhibit production of IE2 proteinsRooksarr Beelontally, Gavin S Wilkie, Betty Lau, et al.
European Journal of Medicinal Chemistry|September 4, 2020
Discovery of 4-methyl-N-(4-((4-methylpiperazin- 1-yl)methyl)-3-(trifluoromethyl)phenyl)-3-((6-(pyridin-3-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-oxy)benzamide as a potent inhibitor of RET and its gatekeeper mutantXiaoyang Li, Jingyi Su, Yanru Yang, et al.
Chemistry & Biology|April 24, 2012
Small-molecule inhibitors of the c-Fes protein-tyrosine kinaseSabine Hellwig, Chandra V Miduturu, Shigeru Kanda, et al.
Plos One|June 6, 2015
Identification of Novel Small Molecule Inhibitors of Oncogenic RET KinaseMarialuisa Moccia, Qingsong Liu, Teresa Guida, et al.
Journal of Natural Products|September 18, 2015
Aspertetranones A-D, Putative Meroterpenoids from the Marine Algal-Associated Fungus Aspergillus sp. ZL0-1b14Yuezhou Wang, Shuang Qi, Ying Zhan, et al.
Nature Communications|February 27, 2024
Deaggregation of mutant Plasmodium yoelii de-ubiquitinase UBP1 alters MDR1 localization to confer multidrug resistanceRuixue Xu, Lirong Lin, Zhiwei Jiao, et al.
Pageof 15