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

Julie Grouleff

Showing results (11-20 of 19) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 19 results.
Environmental Health Perspectives|February 20, 2016
In Vitro Effects of the Endocrine Disruptor p,p'-DDT on Human Follitropin ReceptorMathilde Munier, Julie Grouleff, Louis Gourdin, et al.
Journal of the American Chemical Society|March 17, 2011
Trienamines in asymmetric organocatalysis: Diels-Alder and tandem reactionsZhi-Jun Jia, Hao Jiang, Jun-Long Li, et al.
ACS Chemical Neuroscience|July 19, 2016
Interrogating the Molecular Basis for Substrate Recognition in Serotonin and Dopamine Transporters with High-Affinity Substrate-Based Bivalent LigandsJacob Andersen, Lucy Kate Ladefoged, Trine N Bjerre Kristensen, et al.
Nature Communications|May 26, 2016
A conserved leucine occupies the empty substrate site of LeuT in the Na(+)-free return stateLina Malinauskaite, Saida Said, Caglanur Sahin, et al.
Chemical Biology & Drug Design|March 15, 2018
Rational design of isonicotinic acid hydrazide derivatives with antitubercular activity: Machine learning, molecular docking, synthesis and biological testingVasyl Kovalishyn, Julie Grouleff, Ivan Semenyuta, et al.
Journal of Medicinal Chemistry|July 22, 2021
Design, Synthesis, and Characterization of 4-Aminoquinazolines as Potent Inhibitors of the G Protein-Coupled Receptor Kinase 6 (GRK6) for the Treatment of Multiple MyelomaDavid E Uehling, Babu Joseph, Kim Chan Chung, et al.
Journal of Medicinal Chemistry|December 28, 2021
Correction to "Design, Synthesis, and Characterization of 4-Aminoquinazolines as Potent Inhibitors of the G Protein-Coupled Receptor Kinase 6 (GRK6) for the Treatment of Multiple Myeloma"David E Uehling, Babu Joseph, Kim Chan Chung, et al.
European Journal of Medicinal Chemistry|April 5, 2026
Discovery and development of potent and selective dual NUAK/MARK inhibitors as Hippo pathway modulators for the treatment of cancerDavid Smil, Yong Liu, Tao Xin, et al.
Journal of Medicinal Chemistry|January 28, 2022
Phenolic Lipids Derived from Cashew Nut Shell Liquid to Treat Metabolic DiseasesCigdem Sahin, Lilia Magomedova, Thais A M Ferreira, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Environmental Health Perspectives|February 20, 2016
In Vitro Effects of the Endocrine Disruptor p,p'-DDT on Human Follitropin ReceptorMathilde Munier, Julie Grouleff, Louis Gourdin, et al.
Journal of the American Chemical Society|March 17, 2011
Trienamines in asymmetric organocatalysis: Diels-Alder and tandem reactionsZhi-Jun Jia, Hao Jiang, Jun-Long Li, et al.
ACS Chemical Neuroscience|July 19, 2016
Interrogating the Molecular Basis for Substrate Recognition in Serotonin and Dopamine Transporters with High-Affinity Substrate-Based Bivalent LigandsJacob Andersen, Lucy Kate Ladefoged, Trine N Bjerre Kristensen, et al.
Nature Communications|May 26, 2016
A conserved leucine occupies the empty substrate site of LeuT in the Na(+)-free return stateLina Malinauskaite, Saida Said, Caglanur Sahin, et al.
Chemical Biology & Drug Design|March 15, 2018
Rational design of isonicotinic acid hydrazide derivatives with antitubercular activity: Machine learning, molecular docking, synthesis and biological testingVasyl Kovalishyn, Julie Grouleff, Ivan Semenyuta, et al.
Journal of Medicinal Chemistry|July 22, 2021
Design, Synthesis, and Characterization of 4-Aminoquinazolines as Potent Inhibitors of the G Protein-Coupled Receptor Kinase 6 (GRK6) for the Treatment of Multiple MyelomaDavid E Uehling, Babu Joseph, Kim Chan Chung, et al.
Journal of Medicinal Chemistry|December 28, 2021
Correction to "Design, Synthesis, and Characterization of 4-Aminoquinazolines as Potent Inhibitors of the G Protein-Coupled Receptor Kinase 6 (GRK6) for the Treatment of Multiple Myeloma"David E Uehling, Babu Joseph, Kim Chan Chung, et al.
European Journal of Medicinal Chemistry|April 5, 2026
Discovery and development of potent and selective dual NUAK/MARK inhibitors as Hippo pathway modulators for the treatment of cancerDavid Smil, Yong Liu, Tao Xin, et al.
Journal of Medicinal Chemistry|January 28, 2022
Phenolic Lipids Derived from Cashew Nut Shell Liquid to Treat Metabolic DiseasesCigdem Sahin, Lilia Magomedova, Thais A M Ferreira, et al.
Pageof 2