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I STEVENSON

Showing results (81-90 of 101) with videos related to

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Chemical Communications (Cambridge, England)|June 10, 2008
Selective turn-on fluorescence detection of cyanide in water using hydrophobic CdSe quantum dotsAngeles Touceda-Varela, Emily I Stevenson, José A Galve-Gasión, et al.
The Journal of Antimicrobial Chemotherapy|November 1, 1989
Clinical and pharmacokinetic aspects of ciprofloxacin in the treatment of acute exacerbations of pseudomonas infection in cystic fibrosis patientsH J Steen, E M Scott, M I Stevenson, et al.
Frontiers in Microbiology|June 5, 2015
Microbial communities of the Lemon Creek Glacier show subtle structural variation yet stable phylogenetic composition over space and timeCody S Sheik, Emily I Stevenson, Paul A Den Uyl, et al.
The Journal of Biological Chemistry|August 15, 1990
Purification of the 5-hydroxytryptamine 5-HT3 receptor from NCB20 cellsR M McKernan, N P Gillard, K Quirk, et al.
The Journal of Organic Chemistry|May 2, 2000
An efficient protocol for the preparation of primary alcohols bearing a beta-chiral center via an oxazolidinone auxiliary mediated resolution, and application to the synthesis of 4,4-disubstituted piperidine substance P antagonistsR T Lewis, T Ladduwahetty, K J Merchant, et al.
Journal of Medicinal Chemistry|March 20, 1992
Novel 5-HT3 antagonists: indol-3-ylspiro(azabicycloalkane-3,5'(4'H)-oxazoles)C J Swain, R Baker, C Kneen, et al.
Proteomics|February 26, 2005
Large-scale evaluation of quantitative reproducibility and proteome coverage using acid cleavable isotope coded affinity tag mass spectrometry for proteomic profilingMark P Molloy, Sam Donohoe, Erin E Brzezinski, et al.
Bioorganic & Medicinal Chemistry Letters|January 2, 2001
2-Aryl tryptamines: selective high-affinity antagonists for the h5-HT2A receptorG I Stevenson, A L Smith, S Lewis, et al.
Bioorganic & Medicinal Chemistry Letters|January 5, 1999
Serine derived NK1 antagonists. 2: A pharmacophore model for arylsulfonamide bindingJ M Elliott, H Broughton, M A Cascieri, et al.
Journal of Medicinal Chemistry|October 29, 1993
3-Acyl-4-hydroxyquinolin-2(1H)-ones. Systemically active anticonvulsants acting by antagonism at the glycine site of the N-methyl-D-aspartate receptor complexM Rowley, P D Leeson, G I Stevenson, et al.
Pageof 11

Showing results (81-90 of 101) with videos related to

Sort By:
Pageof 11
Chemical Communications (Cambridge, England)|June 10, 2008
Selective turn-on fluorescence detection of cyanide in water using hydrophobic CdSe quantum dotsAngeles Touceda-Varela, Emily I Stevenson, José A Galve-Gasión, et al.
The Journal of Antimicrobial Chemotherapy|November 1, 1989
Clinical and pharmacokinetic aspects of ciprofloxacin in the treatment of acute exacerbations of pseudomonas infection in cystic fibrosis patientsH J Steen, E M Scott, M I Stevenson, et al.
Frontiers in Microbiology|June 5, 2015
Microbial communities of the Lemon Creek Glacier show subtle structural variation yet stable phylogenetic composition over space and timeCody S Sheik, Emily I Stevenson, Paul A Den Uyl, et al.
The Journal of Biological Chemistry|August 15, 1990
Purification of the 5-hydroxytryptamine 5-HT3 receptor from NCB20 cellsR M McKernan, N P Gillard, K Quirk, et al.
The Journal of Organic Chemistry|May 2, 2000
An efficient protocol for the preparation of primary alcohols bearing a beta-chiral center via an oxazolidinone auxiliary mediated resolution, and application to the synthesis of 4,4-disubstituted piperidine substance P antagonistsR T Lewis, T Ladduwahetty, K J Merchant, et al.
Journal of Medicinal Chemistry|March 20, 1992
Novel 5-HT3 antagonists: indol-3-ylspiro(azabicycloalkane-3,5'(4'H)-oxazoles)C J Swain, R Baker, C Kneen, et al.
Proteomics|February 26, 2005
Large-scale evaluation of quantitative reproducibility and proteome coverage using acid cleavable isotope coded affinity tag mass spectrometry for proteomic profilingMark P Molloy, Sam Donohoe, Erin E Brzezinski, et al.
Bioorganic & Medicinal Chemistry Letters|January 2, 2001
2-Aryl tryptamines: selective high-affinity antagonists for the h5-HT2A receptorG I Stevenson, A L Smith, S Lewis, et al.
Bioorganic & Medicinal Chemistry Letters|January 5, 1999
Serine derived NK1 antagonists. 2: A pharmacophore model for arylsulfonamide bindingJ M Elliott, H Broughton, M A Cascieri, et al.
Journal of Medicinal Chemistry|October 29, 1993
3-Acyl-4-hydroxyquinolin-2(1H)-ones. Systemically active anticonvulsants acting by antagonism at the glycine site of the N-methyl-D-aspartate receptor complexM Rowley, P D Leeson, G I Stevenson, et al.
Pageof 11