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The Global ETD Search service is a free service for researchers
to find electronic theses and dissertations. This service is
provided by the
Networked Digital Library of Theses and Dissertations.
Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
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Showing 221 to 230 of 10149 (0.047 seconds)| 221 |
Heterogeneity in the thermally induced triplet quenching of multitryptophan globular proteinsDomanus, Jerry January 1978 (has links)
No description available.
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| 222 |
Studies on proteins of bovine skeletal muscle during aging.Legore, Audley. January 1967 (has links)
No description available.
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| 223 |
Models of the stability of proteinsDias, Cristiano L. January 2007 (has links)
No description available.
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| 224 |
Room temperature phosphorescence and the dynamic aspects of protein structureSaviotti, Maria Laura January 1975 (has links)
No description available.
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| 225 |
Studies on some intermediate reactions in bacterial protein synthesis /Bernlohr, Robert William January 1958 (has links)
No description available.
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| 226 |
An investigation of the later stages in protein synthesis /Lingrel, Jerry B. January 1960 (has links)
No description available.
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| 227 |
Infrared studies of metal proteins /Yen, Lei January 1971 (has links)
No description available.
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| 228 |
The influence of pH, temperature, and proteins on the electrophoretic, thermal, textural, and elastic properties of model meat analogs /Rizvi, Syed S. H. January 1976 (has links)
No description available.
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| 229 |
Some studies of functional properties and characteristics of soybean leaf proteins /Ali, Mohammed Hasan January 1978 (has links)
No description available.
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Biochemical properties of caldesmon.Abougou, Jean-Claude January 1988 (has links)
An attempt to develop a short and reliable method of caldesmon purification led to the development of three procedures of caldesmon purification. The first method was seldom used because of its low yield and the lack of caldesmon endogenous kinase activity. However, it allowed us to purify MLCK (myosin light chain kinase). The second and third methods gave respectively, a caldesmon sample with and without kinase activity. We were able to localize the endogenous kinase in the 0-30% ammonium sulfate precipitated DEAE pellet but we were unsuccessful at purifying the kinase to homogeneity. We found that caldesmon can also be phosphorylated by rat brain Ca²⁺-calmodulin-dependent kinase II at sites identical to those of caldesmon endogenous kinase but different to those of kinase C. In addition, caldesmon and its endogenous kinase are two different proteins. Furthermore, our study of caldesmon inhibition of actomyosin ATPase activity showed that further research needs to be done to refute F-actin bundling process as a possible cause of caldesmon inhibition of actomyosin ATPase activity. In addition, our studies of caldesmon inhibition of HMM and S-1 ATPase activity suggest that S-2 might be partially involved in the inhibition mechanism. Finally, caldesmon did not affect the 6S-10S transition of myosin conformation and since caldesmon cannot compete against higher affinity calmodulin-binding protein such as MLCK thus, the flip-flop theory is untenable.
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