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Raymond C Stevens

Showing results (151-160 of 330) with videos related to

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Angewandte Chemie (International Ed. in English)|November 14, 2006
Time-controlled microfluidic seeding in nL-volume droplets to separate nucleation and growth stages of protein crystallizationCory J Gerdts, Valentina Tereshko, Maneesh K Yadav, et al.
Science (New York, N.Y.)|October 4, 2008
The 2.6 angstrom crystal structure of a human A2A adenosine receptor bound to an antagonistVeli-Pekka Jaakola, Mark T Griffith, Michael A Hanson, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 19, 2015
Single-molecule view of basal activity and activation mechanisms of the G protein-coupled receptor β2ARRajan Lamichhane, Jeffrey J Liu, Goran Pljevaljcic, et al.
Plos One|September 1, 2022
An intensity-based post-processing tool for 3D instance segmentation of organelles in soft X-ray tomogramsAngdi Li, Shuning Zhang, Valentina Loconte, et al.
Genetic Testing|July 14, 2007
Mutations in the regulatory domain of phenylalanine hydroxylase and response to tetrahydrobiopterinLin Wang, Sankar Surendran, Kimberlee Michals-Matalon, et al.
Nature Methods|July 3, 2013
Engineered nanostructured β-sheet peptides protect membrane proteinsHouchao Tao, Sung Chang Lee, Arne Moeller, et al.
Nature Methods|January 22, 2019
An online resource for GPCR structure determination and analysisChristian Munk, Eshita Mutt, Vignir Isberg, et al.
Journal of Molecular Biology|February 9, 2010
A single-domain llama antibody potently inhibits the enzymatic activity of botulinum neurotoxin by binding to the non-catalytic alpha-exosite binding regionJianbo Dong, Aaron A Thompson, Yongfeng Fan, et al.
Journal of Medicinal Chemistry|April 11, 2012
Optimization of adenosine 5'-carboxamide derivatives as adenosine receptor agonists using structure-based ligand design and fragment screeningDilip K Tosh, Khai Phan, Zhan-Guo Gao, et al.
Journal of the American Chemical Society|April 16, 2013
Rational design of fatty acid amide hydrolase inhibitors that act by covalently bonding to two active site residuesKaterina Otrubova, Monica Brown, Michael S McCormick, et al.
Pageof 33

Showing results (151-160 of 330) with videos related to

Sort By:
Pageof 33
Angewandte Chemie (International Ed. in English)|November 14, 2006
Time-controlled microfluidic seeding in nL-volume droplets to separate nucleation and growth stages of protein crystallizationCory J Gerdts, Valentina Tereshko, Maneesh K Yadav, et al.
Science (New York, N.Y.)|October 4, 2008
The 2.6 angstrom crystal structure of a human A2A adenosine receptor bound to an antagonistVeli-Pekka Jaakola, Mark T Griffith, Michael A Hanson, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 19, 2015
Single-molecule view of basal activity and activation mechanisms of the G protein-coupled receptor β2ARRajan Lamichhane, Jeffrey J Liu, Goran Pljevaljcic, et al.
Plos One|September 1, 2022
An intensity-based post-processing tool for 3D instance segmentation of organelles in soft X-ray tomogramsAngdi Li, Shuning Zhang, Valentina Loconte, et al.
Genetic Testing|July 14, 2007
Mutations in the regulatory domain of phenylalanine hydroxylase and response to tetrahydrobiopterinLin Wang, Sankar Surendran, Kimberlee Michals-Matalon, et al.
Nature Methods|July 3, 2013
Engineered nanostructured β-sheet peptides protect membrane proteinsHouchao Tao, Sung Chang Lee, Arne Moeller, et al.
Nature Methods|January 22, 2019
An online resource for GPCR structure determination and analysisChristian Munk, Eshita Mutt, Vignir Isberg, et al.
Journal of Molecular Biology|February 9, 2010
A single-domain llama antibody potently inhibits the enzymatic activity of botulinum neurotoxin by binding to the non-catalytic alpha-exosite binding regionJianbo Dong, Aaron A Thompson, Yongfeng Fan, et al.
Journal of Medicinal Chemistry|April 11, 2012
Optimization of adenosine 5'-carboxamide derivatives as adenosine receptor agonists using structure-based ligand design and fragment screeningDilip K Tosh, Khai Phan, Zhan-Guo Gao, et al.
Journal of the American Chemical Society|April 16, 2013
Rational design of fatty acid amide hydrolase inhibitors that act by covalently bonding to two active site residuesKaterina Otrubova, Monica Brown, Michael S McCormick, et al.
Pageof 33