Thesis (B.S.)--University of Missouri, School of Mines and Metallurgy, 1910. / The entire thesis text is included in file. Typescript. Illustrated by author. J. J. Bowles determined to be James Joseph Bowles from "Forty-First Annual Catalogue. School of Mines and Metallurgy, University of Missouri". Title from title screen of thesis/dissertation PDF file (viewed February 12, 2009)

Thesis--University of Missouri, School of Mines and Metallurgy, 1893. / The entire thesis text is included in file. Holograph [Handwritten and illustrated in entirety by author]. J. C. Reid determined to be John C. Reid from "1874-1990 MSM-UMR Alumni Directory". Title from title screen of thesis/dissertation PDF file (viewed September 30, 2008)

Thesis (Ph. D.)--University of Michigan, 1920.

Thesis (Ph. D.)--Columbia University, 1942. / Reproduced from type-written copy. Vita. Bibliography: p. [69]-73.

Thesis (B.S.)--University of Missouri, School of Mines and Metallurgy, 1905. / L. H. Hunt determined to be Lamar Horacio Hunt and W. A. Gardiner determined to be William Alexander Gardiner from "Forty-First Annual Catalogue. School of Mines and Metallurgy, University of Missouri". The entire thesis text is included in file. Typescript. Illustrated by authors. Title from title screen of thesis/dissertation PDF file (viewed December 19, 2008)

Thesis (doctoral)--Tübingen, 1981.

Thesis (Ph. D.)--University of Michigan, 1920.

Thesis (B.S.)--University of Missouri, School of Mines and Metallurgy, 1911. / The entire thesis text is included in file. Typescript. Illustrated by authors. Title from title screen of thesis/dissertation PDF file (viewed February 27, 2009) Includes bibliographical references (p. 11).

The involvement of cyanide oxygenase in the metabolism of pyruvate and a-ketoglutarate-cyanohydrin was investigated and shown to occur indirectly by the consumption of free cyanide arising from the cyanohydrins via chemical dissociation. Thus, free cyanide remains the substrate, for which the enzyme displays a remarkably high affinity (Kmapp,4 mM). A model for cyanide utilization is therefore envisioned in which the substrate is initially detoxified by complexation to an appropriate ligand followed by enzymatic oxidation of cyanide arising at sublethal levels via chemical dissociation. Putative cyanide oxygenase in cell extracts consumed both oxygen and NADH in equimolar proportions during cyanide conversion to CO2 and NH3 and existed separately from an unknown heat-stable species responsible for the nonenzymatic cyanide-catalyzed consumption of oxygen. Evidence of cyanide inhibition and nonlinear kinetics between enzyme activity and protein concentration point to a complex mechanism of enzymatic substrate conversion.

Thesis (Ph.D.)--University of Melbourne, Dept. of Earth Sciences, 2001. / Typescript (photocopy). Includes bibliographical references.