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

Gilles Ferry

Showing results (21-30 of 76) with videos related to

Pageof 8
Sort By:
The Biochemical Journal|September 24, 2005
Expression of UCP3 in CHO cells does not cause uncoupling, but controls mitochondrial activity in the presence of glucoseJulien Mozo, Gilles Ferry, Aurélie Studeny, et al.
Biochimie|March 20, 2024
Melatonin facts: Melatonin lacks immuno-inflammation boosting capacities at the molecular and cellular levelsJean A Boutin, Valérie Hamon de Almeida, Nathalie Coussay, et al.
Free Radical Research|July 19, 2011
Insights into the redox cycle of human quinone reductase 2Karine Reybier, Pierre Perio, Gilles Ferry, et al.
Protein Science : a Publication of the Protein Society|May 4, 2011
X-ray structural studies of quinone reductase 2 nanomolar range inhibitorsScott D Pegan, Megan Sturdy, Gilles Ferry, et al.
The Journal of Biological Chemistry|February 25, 2003
Post-translational modification of Bid has differential effects on its susceptibility to cleavage by caspase 8 or caspase 3Mauro Degli Esposti, Gilles Ferry, Peggy Masdehors, et al.
Protein Science : a Publication of the Protein Society|July 5, 2012
Mutagenic analysis in a pure molecular system shows that thioredoxin-interacting protein residue Cys247 is necessary and sufficient for a mixed disulfide formation with thioredoxinBenjamin Fould, Véronique Lamamy, Sophie-Penelope Guenin, et al.
European Journal of Medicinal Chemistry|January 1, 2008
Synthesis of potential Rho-kinase inhibitors based on the chemistry of an original heterocycle: 4,4-dimethyl-3,4-dihydro-1H-quinolin-2-oneMarie-Anne Letellier, Jérôme Guillard, Daniel-Henri Caignard, et al.
Acta Crystallographica. Section D, Biological Crystallography|November 22, 2011
The active conformation of human glucokinase is not altered by allosteric activatorsPierre Petit, Mathias Antoine, Gilles Ferry, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|September 29, 2004
Design and synthesis of indole and tetrahydroisoquinoline hydantoin derivatives as human chymase inhibitorsDavid Alagille, Bruno Pfeiffer, Elizabeth Scalbert, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|January 31, 2006
A microplate assay for the screening of ADAMTS-4 inhibitorsMarie Thomas, Massimo Sabatini, Fabrice Bensaude, et al.
Pageof 8

Showing results (21-30 of 76) with videos related to

Sort By:
Pageof 8
The Biochemical Journal|September 24, 2005
Expression of UCP3 in CHO cells does not cause uncoupling, but controls mitochondrial activity in the presence of glucoseJulien Mozo, Gilles Ferry, Aurélie Studeny, et al.
Biochimie|March 20, 2024
Melatonin facts: Melatonin lacks immuno-inflammation boosting capacities at the molecular and cellular levelsJean A Boutin, Valérie Hamon de Almeida, Nathalie Coussay, et al.
Free Radical Research|July 19, 2011
Insights into the redox cycle of human quinone reductase 2Karine Reybier, Pierre Perio, Gilles Ferry, et al.
Protein Science : a Publication of the Protein Society|May 4, 2011
X-ray structural studies of quinone reductase 2 nanomolar range inhibitorsScott D Pegan, Megan Sturdy, Gilles Ferry, et al.
The Journal of Biological Chemistry|February 25, 2003
Post-translational modification of Bid has differential effects on its susceptibility to cleavage by caspase 8 or caspase 3Mauro Degli Esposti, Gilles Ferry, Peggy Masdehors, et al.
Protein Science : a Publication of the Protein Society|July 5, 2012
Mutagenic analysis in a pure molecular system shows that thioredoxin-interacting protein residue Cys247 is necessary and sufficient for a mixed disulfide formation with thioredoxinBenjamin Fould, Véronique Lamamy, Sophie-Penelope Guenin, et al.
European Journal of Medicinal Chemistry|January 1, 2008
Synthesis of potential Rho-kinase inhibitors based on the chemistry of an original heterocycle: 4,4-dimethyl-3,4-dihydro-1H-quinolin-2-oneMarie-Anne Letellier, Jérôme Guillard, Daniel-Henri Caignard, et al.
Acta Crystallographica. Section D, Biological Crystallography|November 22, 2011
The active conformation of human glucokinase is not altered by allosteric activatorsPierre Petit, Mathias Antoine, Gilles Ferry, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|September 29, 2004
Design and synthesis of indole and tetrahydroisoquinoline hydantoin derivatives as human chymase inhibitorsDavid Alagille, Bruno Pfeiffer, Elizabeth Scalbert, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|January 31, 2006
A microplate assay for the screening of ADAMTS-4 inhibitorsMarie Thomas, Massimo Sabatini, Fabrice Bensaude, et al.
Pageof 8