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

Nicholas D Smith

Showing results (51-60 of 61) with videos related to

Pageof 7
Sort By:
Journal of Medicinal Chemistry|August 9, 2018
Identification of an Orally Bioavailable Chromene-Based Selective Estrogen Receptor Degrader (SERD) That Demonstrates Robust Activity in a Model of Tamoxifen-Resistant Breast CancerJohnny Nagasawa, Steven Govek, Mehmet Kahraman, et al.
Veterinary Immunology and Immunopathology|March 3, 2009
Characterization of alpha(4)beta(1) (CD49d/CD29) on equine leukocytes: potential utility of a potent alpha(4)beta(1) (CD49d/CD29) receptor antagonist in the treatment of equine heaves (recurrent airway obstruction)Kelly M Treonze, Kenneth Alves, Paul Fischer, et al.
Journal of Medicinal Chemistry|April 21, 2009
Discovery of inducible nitric oxide synthase (iNOS) inhibitor development candidate KD7332, part 1: Identification of a novel, potent, and selective series of quinolinone iNOS dimerization inhibitors that are orally active in rodent pain modelsCéline Bonnefous, Joseph E Payne, Jeffrey Roppe, et al.
ACS Medicinal Chemistry Letters|January 19, 2019
Maximizing ER-α Degradation Maximizes Activity in a Tamoxifen-Resistant Breast Cancer Model: Identification of GDC-0927Mehmet Kahraman, Steven P Govek, Johnny Y Nagasawa, et al.
The Journal of Pharmacology and Experimental Therapeutics|November 2, 2010
Pharmacological characterization of KLYP961, a dual inhibitor of inducible and neuronal nitric-oxide synthasesKent T Symons, Phan M Nguyen, Mark E Massari, et al.
Bioorganic & Medicinal Chemistry Letters|October 15, 2015
Optimization of an indazole series of selective estrogen receptor degraders: Tumor regression in a tamoxifen-resistant breast cancer xenograftSteven P Govek, Johnny Y Nagasawa, Karensa L Douglas, et al.
Journal of Medicinal Chemistry|April 17, 2015
Identification of GDC-0810 (ARN-810), an Orally Bioavailable Selective Estrogen Receptor Degrader (SERD) that Demonstrates Robust Activity in Tamoxifen-Resistant Breast Cancer XenograftsAndiliy Lai, Mehmet Kahraman, Steven Govek, et al.
Bioorganic & Medicinal Chemistry Letters|December 28, 2018
Selective estrogen receptor degraders with novel structural motifs induce regression in a tamoxifen-resistant breast cancer xenograftSteven P Govek, Celine Bonnefous, Jackaline D Julien, et al.
Molecular Cancer Therapeutics|May 17, 2008
KD5170, a novel mercaptoketone-based histone deacetylase inhibitor that exhibits broad spectrum antitumor activity in vitro and in vivoChristian A Hassig, Kent T Symons, Xin Guo, et al.
Cancer Research|January 24, 2012
ARN-509: a novel antiandrogen for prostate cancer treatmentNicola J Clegg, John Wongvipat, James D Joseph, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Journal of Medicinal Chemistry|August 9, 2018
Identification of an Orally Bioavailable Chromene-Based Selective Estrogen Receptor Degrader (SERD) That Demonstrates Robust Activity in a Model of Tamoxifen-Resistant Breast CancerJohnny Nagasawa, Steven Govek, Mehmet Kahraman, et al.
Veterinary Immunology and Immunopathology|March 3, 2009
Characterization of alpha(4)beta(1) (CD49d/CD29) on equine leukocytes: potential utility of a potent alpha(4)beta(1) (CD49d/CD29) receptor antagonist in the treatment of equine heaves (recurrent airway obstruction)Kelly M Treonze, Kenneth Alves, Paul Fischer, et al.
Journal of Medicinal Chemistry|April 21, 2009
Discovery of inducible nitric oxide synthase (iNOS) inhibitor development candidate KD7332, part 1: Identification of a novel, potent, and selective series of quinolinone iNOS dimerization inhibitors that are orally active in rodent pain modelsCéline Bonnefous, Joseph E Payne, Jeffrey Roppe, et al.
ACS Medicinal Chemistry Letters|January 19, 2019
Maximizing ER-α Degradation Maximizes Activity in a Tamoxifen-Resistant Breast Cancer Model: Identification of GDC-0927Mehmet Kahraman, Steven P Govek, Johnny Y Nagasawa, et al.
The Journal of Pharmacology and Experimental Therapeutics|November 2, 2010
Pharmacological characterization of KLYP961, a dual inhibitor of inducible and neuronal nitric-oxide synthasesKent T Symons, Phan M Nguyen, Mark E Massari, et al.
Bioorganic & Medicinal Chemistry Letters|October 15, 2015
Optimization of an indazole series of selective estrogen receptor degraders: Tumor regression in a tamoxifen-resistant breast cancer xenograftSteven P Govek, Johnny Y Nagasawa, Karensa L Douglas, et al.
Journal of Medicinal Chemistry|April 17, 2015
Identification of GDC-0810 (ARN-810), an Orally Bioavailable Selective Estrogen Receptor Degrader (SERD) that Demonstrates Robust Activity in Tamoxifen-Resistant Breast Cancer XenograftsAndiliy Lai, Mehmet Kahraman, Steven Govek, et al.
Bioorganic & Medicinal Chemistry Letters|December 28, 2018
Selective estrogen receptor degraders with novel structural motifs induce regression in a tamoxifen-resistant breast cancer xenograftSteven P Govek, Celine Bonnefous, Jackaline D Julien, et al.
Molecular Cancer Therapeutics|May 17, 2008
KD5170, a novel mercaptoketone-based histone deacetylase inhibitor that exhibits broad spectrum antitumor activity in vitro and in vivoChristian A Hassig, Kent T Symons, Xin Guo, et al.
Cancer Research|January 24, 2012
ARN-509: a novel antiandrogen for prostate cancer treatmentNicola J Clegg, John Wongvipat, James D Joseph, et al.
Pageof 7