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C Russell Middaugh

Showing results (151-160 of 271) with videos related to

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Biophysical Journal|April 5, 2005
A stopped-flow kinetic study of the assembly of nonviral gene delivery complexesChad S Braun, Mark T Fisher, Donald A Tomalia, et al.
Journal of Pharmaceutical Sciences|December 23, 2004
Structure/function relationships of polyamidoamine/DNA dendrimers as gene delivery vehiclesChad S Braun, Joseph A Vetro, Donald A Tomalia, et al.
Molecular & Cellular Proteomics : MCP|September 20, 2006
A network-based analysis of polyanion-binding proteins utilizing yeast protein arraysNazila Salamat-Miller, Jianwen Fang, Christopher W Seidel, et al.
Nucleosides, Nucleotides & Nucleic Acids|February 26, 2010
Evaluation of NAD(H) analogues as selective inhibitors for Trypanosoma cruzi S-adenosylhomocysteine hydrolaseQing-Shan Li, Sumin Cai, Jianwen Fang, et al.
Biochemistry|April 9, 2008
Comparative kinetics of cofactor association and dissociation for the human and trypanosomal S-adenosylhomocysteine hydrolases. 2. The role of helix 18 stabilityQing-Shan Li, Sumin Cai, Jianwen Fang, et al.
Journal of Pharmaceutical Sciences|January 6, 2010
The effects of substituted cyclodextrins on the colloidal and conformational stability of selected proteinsHardeep S Samra, Feng He, Akhilesh Bhambhani, et al.
Journal of Pharmaceutical Sciences|July 3, 2016
A Micro-Polyethylene Glycol Precipitation Assay as a Relative Solubility Screening Tool for Monoclonal Antibody Design and Formulation DevelopmentVishal M Toprani, Sangeeta B Joshi, Lisa A Kueltzo, et al.
The Journal of Biological Chemistry|November 13, 2002
Structure-function analysis of invasion plasmid antigen C (IpaC) from Shigella flexneriLisa A Kueltzo, John Osiecki, Jeff Barker, et al.
Nucleosides, Nucleotides & Nucleic Acids|February 26, 2010
The rationale for targeting the NAD/NADH cofactor binding site of parasitic S-adenosyl-L-homocysteine hydrolase for the design of anti-parasitic drugsSumin Cai, Qing-Shan Li, Jianwen Fang, et al.
Journal of Pharmaceutical Sciences|July 3, 2017
A Formulation Development Approach to Identify and Select Stable Ultra-High-Concentration Monoclonal Antibody Formulations With Reduced ViscositiesNeal Whitaker, Jian Xiong, Samantha E Pace, et al.
Pageof 28

Showing results (151-160 of 271) with videos related to

Sort By:
Pageof 28
Biophysical Journal|April 5, 2005
A stopped-flow kinetic study of the assembly of nonviral gene delivery complexesChad S Braun, Mark T Fisher, Donald A Tomalia, et al.
Journal of Pharmaceutical Sciences|December 23, 2004
Structure/function relationships of polyamidoamine/DNA dendrimers as gene delivery vehiclesChad S Braun, Joseph A Vetro, Donald A Tomalia, et al.
Molecular & Cellular Proteomics : MCP|September 20, 2006
A network-based analysis of polyanion-binding proteins utilizing yeast protein arraysNazila Salamat-Miller, Jianwen Fang, Christopher W Seidel, et al.
Nucleosides, Nucleotides & Nucleic Acids|February 26, 2010
Evaluation of NAD(H) analogues as selective inhibitors for Trypanosoma cruzi S-adenosylhomocysteine hydrolaseQing-Shan Li, Sumin Cai, Jianwen Fang, et al.
Biochemistry|April 9, 2008
Comparative kinetics of cofactor association and dissociation for the human and trypanosomal S-adenosylhomocysteine hydrolases. 2. The role of helix 18 stabilityQing-Shan Li, Sumin Cai, Jianwen Fang, et al.
Journal of Pharmaceutical Sciences|January 6, 2010
The effects of substituted cyclodextrins on the colloidal and conformational stability of selected proteinsHardeep S Samra, Feng He, Akhilesh Bhambhani, et al.
Journal of Pharmaceutical Sciences|July 3, 2016
A Micro-Polyethylene Glycol Precipitation Assay as a Relative Solubility Screening Tool for Monoclonal Antibody Design and Formulation DevelopmentVishal M Toprani, Sangeeta B Joshi, Lisa A Kueltzo, et al.
The Journal of Biological Chemistry|November 13, 2002
Structure-function analysis of invasion plasmid antigen C (IpaC) from Shigella flexneriLisa A Kueltzo, John Osiecki, Jeff Barker, et al.
Nucleosides, Nucleotides & Nucleic Acids|February 26, 2010
The rationale for targeting the NAD/NADH cofactor binding site of parasitic S-adenosyl-L-homocysteine hydrolase for the design of anti-parasitic drugsSumin Cai, Qing-Shan Li, Jianwen Fang, et al.
Journal of Pharmaceutical Sciences|July 3, 2017
A Formulation Development Approach to Identify and Select Stable Ultra-High-Concentration Monoclonal Antibody Formulations With Reduced ViscositiesNeal Whitaker, Jian Xiong, Samantha E Pace, et al.
Pageof 28