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R Neubig

Showing results (41-50 of 257) with videos related to

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Molecular Pharmacology|January 16, 2007
N-terminal residues control proteasomal degradation of RGS2, RGS4, and RGS5 in human embryonic kidney 293 cellsJohannes Bodenstein, Roger K Sunahara, Richard R Neubig
Progress in Molecular Biology and Translational Science|August 10, 2010
Regulators of G protein signaling proteins as targets for drug discoveryBenita Sjögren, Levi L Blazer, Richard R Neubig
Molecular Pharmacology|December 29, 2006
The highly conserved DRY motif of class A G protein-coupled receptors: beyond the ground stateG Enrico Rovati, Valérie Capra, Richard R Neubig
Trends in Pharmacological Sciences|March 1, 1996
alpha 2-Adrenoceptors take centre stage at Nashville meetingR M Graham, R Neubig, K R Lynch
The Journal of Biological Chemistry|December 2, 2000
Walker A lysine mutations of TAP1 and TAP2 interfere with peptide translocation but not peptide bindingP E Lapinski, R R Neubig, M Raghavan
Journal of Medicinal Chemistry|July 1, 1987
Radioiodinated p-iodoclonidine: a high-affinity probe for the alpha 2-adrenergic receptorM Van Dort, R Neubig, R E Counsell
The Journal of Pharmacology and Experimental Therapeutics|December 1, 1994
The novel alpha-2 adrenergic radioligand [3H]-MK912 is alpha-2C selective among human alpha-2A, alpha-2B and alpha-2C adrenoceptorsS Uhlén, A C Porter, R R Neubig
Journal of Biomolecular Screening|June 18, 2009
Polyplexed flow cytometry protein interaction assay: a novel high-throughput screening paradigm for RGS protein inhibitorsDavid L Roman, Shodai Ota, Richard R Neubig
The Journal of Pharmacology and Experimental Therapeutics|July 20, 2000
Agonist-directed trafficking of porcine alpha(2A)-adrenergic receptor signaling in Chinese hamster ovary cells: l-isoproterenol selectively activates G(s)C B Brink, S M Wade, R R Neubig
FEBS Letters|December 5, 1994
Rapid kinetics of G protein subunit association: a rate-limiting conformational change?R R Neubig, M P Connolly, A E Remmers
Pageof 26

Showing results (41-50 of 257) with videos related to

Sort By:
Pageof 26
Molecular Pharmacology|January 16, 2007
N-terminal residues control proteasomal degradation of RGS2, RGS4, and RGS5 in human embryonic kidney 293 cellsJohannes Bodenstein, Roger K Sunahara, Richard R Neubig
Progress in Molecular Biology and Translational Science|August 10, 2010
Regulators of G protein signaling proteins as targets for drug discoveryBenita Sjögren, Levi L Blazer, Richard R Neubig
Molecular Pharmacology|December 29, 2006
The highly conserved DRY motif of class A G protein-coupled receptors: beyond the ground stateG Enrico Rovati, Valérie Capra, Richard R Neubig
Trends in Pharmacological Sciences|March 1, 1996
alpha 2-Adrenoceptors take centre stage at Nashville meetingR M Graham, R Neubig, K R Lynch
The Journal of Biological Chemistry|December 2, 2000
Walker A lysine mutations of TAP1 and TAP2 interfere with peptide translocation but not peptide bindingP E Lapinski, R R Neubig, M Raghavan
Journal of Medicinal Chemistry|July 1, 1987
Radioiodinated p-iodoclonidine: a high-affinity probe for the alpha 2-adrenergic receptorM Van Dort, R Neubig, R E Counsell
The Journal of Pharmacology and Experimental Therapeutics|December 1, 1994
The novel alpha-2 adrenergic radioligand [3H]-MK912 is alpha-2C selective among human alpha-2A, alpha-2B and alpha-2C adrenoceptorsS Uhlén, A C Porter, R R Neubig
Journal of Biomolecular Screening|June 18, 2009
Polyplexed flow cytometry protein interaction assay: a novel high-throughput screening paradigm for RGS protein inhibitorsDavid L Roman, Shodai Ota, Richard R Neubig
The Journal of Pharmacology and Experimental Therapeutics|July 20, 2000
Agonist-directed trafficking of porcine alpha(2A)-adrenergic receptor signaling in Chinese hamster ovary cells: l-isoproterenol selectively activates G(s)C B Brink, S M Wade, R R Neubig
FEBS Letters|December 5, 1994
Rapid kinetics of G protein subunit association: a rate-limiting conformational change?R R Neubig, M P Connolly, A E Remmers
Pageof 26