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The measurement of coupling constants and the use of heteronuclear cross-polarisation in NMR experiments for the study of proteinsRichardson, Julia Margaret January 1993 (has links)
No description available.
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An '8'9Y and '6'3Cu NMR study of some high-Tâ†c superconductorsKontos, Athanasios G. January 1994 (has links)
No description available.
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Imaging pathology in multiple sclerosisLee, Martin A. January 1999 (has links)
No description available.
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An evaluation of Hahnemannian quinquagenimillesimal potencies using nuclear magnetic resonance spectroscopyRoss, Ashley Hilton Adrian January 1997 (has links)
Dissertation submitted in partial compliance with the requirements for the Master's Degree in Technology: Homoeopathy, Technikon Natal, 1997. / The purpose of this investigation was to analyse and compare the Nuclear Magnetic Resonance (NMR) spectra of samples of quinquagenimillesimal (LM) potencies of homoeopathic Sulphur and a lactose-based control produced according to Hahnemann, in order to evaluate homoeopathic medicines thus prepared. It was hypothesised that differences existed in the spectra of respective Sulphur samples, control samples, and between parallel samples of Sulphur and control. It was further hypothesised that these differences correlated proportionately with the degree of potency of samples. The design of the investigation was that of a scientific experiment. Potencies of Sulphur and a lactose-based control were prepared (according to the directions of Hahnemann*) to the LM10 level. LM2, LM6 and LM10 liquid potencies (95% ethanol) of each group were then prepared in =20.8160 ml volumes and despatched for sampling and measurement. NMR spectroscopy was conducted on fifteen (15) samples of each potency. These were prepared in coaxial sample tubes using deuterium oxide (020) as an extemal lock and dioxane as a reference. Samples were drawn and measured in overlapping sequence by the Department of Chemistry, University of Cape Town. The spectrometer em. ployed was a. Varian VXR200 operating at a frequency of 200.057 MHz. Acquisition time for each sample was 3.727 seconds, using a pulse width of 6\xB0. Measurement of each sample was repeated eight times, at a constant temperature of 298.1 K (250. OC) / M
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Dissection of the human low-density lipoprotein receptor structure using NMR spectroscopy /Kurniawan, Nyoman, Dana. January 2002 (has links) (PDF)
Thesis (Ph. D.)--University of Queensland, 2002. / Includes bibliographical references.
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Nuclear magnetic resonance studies on the structure and dynamics of dihydrofolate reductase and its ligandsYang, Qing X. 12 1900 (has links)
No description available.
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Solid-state NMR investigation of structure and dynamics of polyrotaxanesNagapudi, Karthik January 1997 (has links)
No description available.
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Use of Gadolinium reagents in 13C NMR studies /Luke, Barbara J. January 1980 (has links)
Thesis (M.S.)--Rochester Institute of Technology, 1980. / Typescript. Includes bibliographical references.
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Application of biomolecular NMR spectroscopy for protein structure determinationYang, Yinhua, January 2009 (has links)
Thesis (Ph. D.)--University of Hong Kong, 2009. / Includes bibliographical references. Also available in print.
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Part 1. Synthesis of stable-isotope labeled amino acids. Part 2. Synthesis of mechanistic probes of retinoid actionBarnett Derek W. January 2002 (has links)
Thesis (Ph. D.)--Ohio State University, 2002. / Title from first page of PDF file. Document formatted into pages; contains xxiii, 216 p. Includes abstract and vita. Robert W. Curley, College of Pharmacy. Includes bibliographical references (p. 201-216).
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