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

Patrick A Riley

Showing results (11-20 of 25) with videos related to

Pageof 3
Sort By:
The Tohoku Journal of Experimental Medicine|July 31, 2007
The mechanism of suicide-inactivation of tyrosinase: a substrate structure investigationEdward J Land, Christopher A Ramsden, Patrick A Riley
Melanoma Research|February 24, 2021
Thirty years of therapeutic innovation in melanoma researchFerdy J Lejeune, Walter J Storkus, Patrick A Riley
Methods in Enzymology|March 25, 2004
Quinone chemistry and melanogenesisEdward J Land, Christopher A Ramsden, Patrick A Riley
Chemical Research in Toxicology|February 11, 2011
Rapid halogen substitution and dibenzodioxin formation during tyrosinase-catalyzed oxidation of 4-halocatecholsMichael R L Stratford, Patrick A Riley, Christopher A Ramsden
Bioorganic & Medicinal Chemistry|January 29, 2013
Mechanistic studies of the inactivation of tyrosinase by resorcinolMichael R L Stratford, Christopher A Ramsden, Patrick A Riley
Organic & Biomolecular Chemistry|August 14, 2009
The influence of catechol structure on the suicide-inactivation of tyrosinaseChristopher A Ramsden, Michael R L Stratford, Patrick A Riley
Bioorganic & Medicinal Chemistry|June 16, 2012
The influence of hydroquinone on tyrosinase kineticsMichael R L Stratford, Christopher A Ramsden, Patrick A Riley
Pigment Cell Research|July 16, 2003
Mechanistic studies of catechol generation from secondary quinone amines relevant to indole formation and tyrosinase activationEdward J Land, Christopher A Ramsden, Patrick A Riley, et al.
Organic & Biomolecular Chemistry|June 25, 2005
Oxidation of N-substituted dopamine derivatives: irreversible formation of a spirocyclic productEdward J Land, Almudena Perona, Christopher A Ramsden, et al.
Organic & Biomolecular Chemistry|February 20, 2009
Dopamine quinone chemistry: a study of the influence of amide, amidine and guanidine substituents [-NH-CX-Y] on the mode of reactionEdward J Land, Almudena Perona, Christopher A Ramsden, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
The Tohoku Journal of Experimental Medicine|July 31, 2007
The mechanism of suicide-inactivation of tyrosinase: a substrate structure investigationEdward J Land, Christopher A Ramsden, Patrick A Riley
Melanoma Research|February 24, 2021
Thirty years of therapeutic innovation in melanoma researchFerdy J Lejeune, Walter J Storkus, Patrick A Riley
Methods in Enzymology|March 25, 2004
Quinone chemistry and melanogenesisEdward J Land, Christopher A Ramsden, Patrick A Riley
Chemical Research in Toxicology|February 11, 2011
Rapid halogen substitution and dibenzodioxin formation during tyrosinase-catalyzed oxidation of 4-halocatecholsMichael R L Stratford, Patrick A Riley, Christopher A Ramsden
Bioorganic & Medicinal Chemistry|January 29, 2013
Mechanistic studies of the inactivation of tyrosinase by resorcinolMichael R L Stratford, Christopher A Ramsden, Patrick A Riley
Organic & Biomolecular Chemistry|August 14, 2009
The influence of catechol structure on the suicide-inactivation of tyrosinaseChristopher A Ramsden, Michael R L Stratford, Patrick A Riley
Bioorganic & Medicinal Chemistry|June 16, 2012
The influence of hydroquinone on tyrosinase kineticsMichael R L Stratford, Christopher A Ramsden, Patrick A Riley
Pigment Cell Research|July 16, 2003
Mechanistic studies of catechol generation from secondary quinone amines relevant to indole formation and tyrosinase activationEdward J Land, Christopher A Ramsden, Patrick A Riley, et al.
Organic & Biomolecular Chemistry|June 25, 2005
Oxidation of N-substituted dopamine derivatives: irreversible formation of a spirocyclic productEdward J Land, Almudena Perona, Christopher A Ramsden, et al.
Organic & Biomolecular Chemistry|February 20, 2009
Dopamine quinone chemistry: a study of the influence of amide, amidine and guanidine substituents [-NH-CX-Y] on the mode of reactionEdward J Land, Almudena Perona, Christopher A Ramsden, et al.
Pageof 3