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J K Sanders

Showing results (21-30 of 36) with videos related to

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Journal of Pharmaceutical and Biomedical Analysis|May 1, 1995
NMR study of whole rat bile: the biliary excretion of cefoperazone and benzyl chloride by an isolated perfused rat liverD A Ryan, J K Sanders, G C Curtis, et al.
Biochemistry|August 12, 1986
Formaldehyde metabolism by Escherichia coli. Detection by in vivo 13C NMR spectroscopy of S-(hydroxymethyl)glutathione as a transient intracellular intermediateR P Mason, J K Sanders, A Crawford, et al.
Journal of Pharmaceutical and Biomedical Analysis|May 1, 1995
NMR study of whole rat bile: the biliary excretion of 4-cyano-N,N-dimethyl aniline by an isolated perfused rat liver and a liver in situD A Ryan, J K Sanders, G C Curtis, et al.
Journal of Steroid Biochemistry|July 1, 1983
Recent applications of N.M.R. to the investigation of steroid structuresR D Farrant, D N Kirk, J D Mersh, et al.
FEBS Letters|May 18, 1981
The mode of antibacterial action of some 'masked' formaldehyde compoundsM J Gidley, J K Sanders, E R Myers, et al.
The Journal of Pharmacy and Pharmacology|October 1, 1978
A convenient synthesis of [3H]mepyramine and certain related [3H]antihistaminesD H Marrian, S J Hill, J K Sanders, et al.
Rapid Communications in Mass Spectrometry : RCM|January 7, 2000
Electrospray ionisation Fourier-transform ion cyclotron resonance mass spectrometry of dynamic combinatorial librariesS A Poulsen, P J Gates, G R Cousins, et al.
Biochemistry|June 23, 1981
Acetaldehyde--enkephalins: structure proof and some conformational deductions from one- and two-dimensional proton nuclear magnetic resonance spectraM J Gidley, L D Hall, J K Sanders, et al.
The Biochemical Journal|January 15, 1988
Formaldehyde adducts of glutathione. Structure elucidation by two-dimensional n.m.r. spectroscopy and fast-atom-bombardment tandem mass spectrometryS Naylor, R P Mason, J K Sanders, et al.
Proceedings of the Royal Society of London. Series B, Biological Sciences|December 16, 1975
A pharmacologically active derivative of tetrodotoxinR Y Tsien, D P Green, S R Levinson, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Journal of Pharmaceutical and Biomedical Analysis|May 1, 1995
NMR study of whole rat bile: the biliary excretion of cefoperazone and benzyl chloride by an isolated perfused rat liverD A Ryan, J K Sanders, G C Curtis, et al.
Biochemistry|August 12, 1986
Formaldehyde metabolism by Escherichia coli. Detection by in vivo 13C NMR spectroscopy of S-(hydroxymethyl)glutathione as a transient intracellular intermediateR P Mason, J K Sanders, A Crawford, et al.
Journal of Pharmaceutical and Biomedical Analysis|May 1, 1995
NMR study of whole rat bile: the biliary excretion of 4-cyano-N,N-dimethyl aniline by an isolated perfused rat liver and a liver in situD A Ryan, J K Sanders, G C Curtis, et al.
Journal of Steroid Biochemistry|July 1, 1983
Recent applications of N.M.R. to the investigation of steroid structuresR D Farrant, D N Kirk, J D Mersh, et al.
FEBS Letters|May 18, 1981
The mode of antibacterial action of some 'masked' formaldehyde compoundsM J Gidley, J K Sanders, E R Myers, et al.
The Journal of Pharmacy and Pharmacology|October 1, 1978
A convenient synthesis of [3H]mepyramine and certain related [3H]antihistaminesD H Marrian, S J Hill, J K Sanders, et al.
Rapid Communications in Mass Spectrometry : RCM|January 7, 2000
Electrospray ionisation Fourier-transform ion cyclotron resonance mass spectrometry of dynamic combinatorial librariesS A Poulsen, P J Gates, G R Cousins, et al.
Biochemistry|June 23, 1981
Acetaldehyde--enkephalins: structure proof and some conformational deductions from one- and two-dimensional proton nuclear magnetic resonance spectraM J Gidley, L D Hall, J K Sanders, et al.
The Biochemical Journal|January 15, 1988
Formaldehyde adducts of glutathione. Structure elucidation by two-dimensional n.m.r. spectroscopy and fast-atom-bombardment tandem mass spectrometryS Naylor, R P Mason, J K Sanders, et al.
Proceedings of the Royal Society of London. Series B, Biological Sciences|December 16, 1975
A pharmacologically active derivative of tetrodotoxinR Y Tsien, D P Green, S R Levinson, et al.
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