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Scott C Garman

Showing results (21-30 of 34) with videos related to

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The Biochemical Journal|June 9, 2007
Mutant alpha-galactosidase A enzymes identified in Fabry disease patients with residual enzyme activity: biochemical characterization and restoration of normal intracellular processing by 1-deoxygalactonojirimycinSatoshi Ishii, Hui-Hwa Chang, Kunito Kawasaki, et al.
Nature Chemical Biology|February 21, 2017
Ligand-promoted protein folding by biased kinetic partitioningKaran S Hingorani, Matthew C Metcalf, Derrick T Deming, et al.
The Journal of Biological Chemistry|November 27, 2009
Catalytic mechanism of human alpha-galactosidaseAbigail I Guce, Nathaniel E Clark, Eric N Salgado, et al.
Biochemistry|January 13, 2015
Nickel superoxide dismutase: structural and functional roles of His1 and its H-bonding networkKelly C Ryan, Abigail I Guce, Olivia E Johnson, et al.
Protein Science : a Publication of the Protein Society|April 14, 2020
Characterization of CaMKIIα holoenzyme stabilityAna P Torres-Ocampo, Can Özden, Alexandra Hommer, et al.
Biochemistry|February 3, 2009
Role of conserved tyrosine residues in NiSOD catalysis: a case of convergent evolutionRobert W Herbst, Abigail Guce, Peter A Bryngelson, et al.
The Journal of Clinical Investigation|August 18, 2004
Poor immunogenicity of a self/tumor antigen derives from peptide-MHC-I instability and is independent of toleranceZhiya Yu, Marc R Theoret, Christopher E Touloukian, et al.
Cell Reports|July 13, 2022
CaMKII binds both substrates and activators at the active siteCan Özden, Roman Sloutsky, Tomohiro Mitsugi, et al.
Biorxiv : the Preprint Server for Biology|April 8, 2024
A domain-swapped CaMKII conformation facilitates linker-mediated allosteric regulationBao V Nguyen, Can Özden, Kairong Dong, et al.
Pediatrics|February 17, 2005
Pediatric Fabry diseaseMarkus Ries, Surya Gupta, David F Moore, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
The Biochemical Journal|June 9, 2007
Mutant alpha-galactosidase A enzymes identified in Fabry disease patients with residual enzyme activity: biochemical characterization and restoration of normal intracellular processing by 1-deoxygalactonojirimycinSatoshi Ishii, Hui-Hwa Chang, Kunito Kawasaki, et al.
Nature Chemical Biology|February 21, 2017
Ligand-promoted protein folding by biased kinetic partitioningKaran S Hingorani, Matthew C Metcalf, Derrick T Deming, et al.
The Journal of Biological Chemistry|November 27, 2009
Catalytic mechanism of human alpha-galactosidaseAbigail I Guce, Nathaniel E Clark, Eric N Salgado, et al.
Biochemistry|January 13, 2015
Nickel superoxide dismutase: structural and functional roles of His1 and its H-bonding networkKelly C Ryan, Abigail I Guce, Olivia E Johnson, et al.
Protein Science : a Publication of the Protein Society|April 14, 2020
Characterization of CaMKIIα holoenzyme stabilityAna P Torres-Ocampo, Can Özden, Alexandra Hommer, et al.
Biochemistry|February 3, 2009
Role of conserved tyrosine residues in NiSOD catalysis: a case of convergent evolutionRobert W Herbst, Abigail Guce, Peter A Bryngelson, et al.
The Journal of Clinical Investigation|August 18, 2004
Poor immunogenicity of a self/tumor antigen derives from peptide-MHC-I instability and is independent of toleranceZhiya Yu, Marc R Theoret, Christopher E Touloukian, et al.
Cell Reports|July 13, 2022
CaMKII binds both substrates and activators at the active siteCan Özden, Roman Sloutsky, Tomohiro Mitsugi, et al.
Biorxiv : the Preprint Server for Biology|April 8, 2024
A domain-swapped CaMKII conformation facilitates linker-mediated allosteric regulationBao V Nguyen, Can Özden, Kairong Dong, et al.
Pediatrics|February 17, 2005
Pediatric Fabry diseaseMarkus Ries, Surya Gupta, David F Moore, et al.
Pageof 4