Thesis (M.S.P.H.)--University of Michigan, 1939.

Thesis (M.D.)--University of Pennsylvania, 1807. / Microform version available in the Readex Early American Imprints series.

Thesis (M.D.)--University of Pennsylvania, 1805. / Microform version available in the Readex Early American Imprints series.

Akademisk afhandling--Copenhagen. / Summary also in Danish. "Also published as Supplement no. 44 to Acta dermato-venereo-logica, vol. 41." Bibliography: p. 143-148.

Thesis (M.D.)--Boston University

Increasing the life cycle of critical components is a common goal in many vehicle industries. One of the most common ways to increase the fatigue resistance of fasteners holes is the process of cold expansion. This method introduces a compressive stress field in the region around the hole that slows the propagation of cracks. Determining the life cycle benefits gained from cold expansion is difficult due to the complex nature of the residual stress field. Many groups have attempted to accurately predict how this field is generated and what factors can cause major variations in the resulting stress field. There are still many factors related to the cold expansion process that have not been quantified. By creating a script in the computer language Python it was possible to generate a number of different models quickly and efficiently in the finite element program Abaqus. While not all the models that could be created were initially found to be convergent, the script proved useful in creating a varied number of models to assist in determining which factors were leading to the convergence problems. Confidence in the script's ability to produce accurate models was established by generating models that mirrored the conditions found in other literature, so that a direct comparison of results could be made. For this work two factors were considered for analysis, the effect of starting hole size and multi-layer expansion. The results showed that even within the range of recommended starting hole sizes, a difference in the residual stress field was evident. If the hole was expanded beyond the recommended size a threshold was reached and a severe weakening of the residual stress field was noticed. In the case of two plate expansion, changes in the residual stress field were only observed at the interface region of the plates. For the entrance face of the second plate in the expansion, this change was highly beneficial. The results from the two plate expansion suggest that artificially creating a multi-layer stack-up may be a useful tool to improve the residual stress field at the entrance surface of a plate. / Ph. D.

Thesis (M.S.)--Brigham Young University. Dept. of Exercise Sciences, 2004. / Includes bibliographical references.

Thesis (M. Sc.)--University of Hong Kong, 1978.

The effects of temperature on a 58-kDa phosphoprotein (PP58) have been examined in cell-free extracts of two alfalfa (Medicago sativa L.) cultivars, Apica and Trek. In the extracts prepared without the use of Triton X-100, PP58 is present in a 12,000 x g (P12), 28,000 x g (P28) and 100,000 x g (P100) pellets but is enriched in the P28 fraction. In these fractions PP58 is substantially and equally phosphorylated at both 4° and 24°C. When extracts are prepared in the presence Triton X-100, PP58 is present in the 28,000 x g supernatant (TXS fraction) is extensively dephosphorylated at 24°C but highly phosphorylated at 4°C. The phosphorylation of this protein increased sharply as temperature declined below 12°C, and was 15 times greater at 0° than at 24°C. The phosphorylation level doubled between 12° and 8°C and again between 8° and 4°C. Thus temperature effect is not mediated by Q10 effect. Interestingly, temperature-response curve of PP58 phosphorylation is similar to that of the reported cold-induced calcium influx (Plant Cell 7: 321-331). Labeling reactions carried out in the presence of [gamma-35S]thioATP indicated that low temperature inhibited the dephosphorylation reaction. These results were not mimicked at room temperature by the protein phosphatase 1 and 2A inhibitor okadaic acid. In reactions performed at 4°C, addition of calcium caused a 2-fold increase in the phosphorylation of PP58. A decrease in phosphorylation was observed when equimolar amounts of EGTA were added in the presence of MgCl 2 or MnCl2, but not in the presence of CaCl2, suggesting that this protein is phosphorylated by a calcium-dependent protein kinase. These results are consistent with the suggestion that PP58 and its putative kinase are membrane-localized whereas the putative PP58 phosphatase is a loosely-associated membrane peripheral protein lost to the supernatant during fractionation. We suggest that PP58 could be involved in low te

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