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101.
L. W. Andrews H. Morawitz E. Rupp H. Bauer W. F. Schirmer Karin Thaulow H. Lescoeur E. Biilman F. Lehmann J. Knox P. W. Robertson H. Wastenson G. S. Jamieson F. Utz L. Garnier F. Reinthaler J. A. Muller A. Kolb A. Feldhofen G. Adanti B. Oddo L. Vignon H. R. Procter und R. A. Seymour-Jones 《Fresenius' Journal of Analytical Chemistry》1923,62(10):401-407
Ohne Zusammenfassung 相似文献
102.
E. R. Andrews 《Analytical and bioanalytical chemistry》1917,56(10-11):539-540
103.
L. W. Andrews 《Fresenius' Journal of Analytical Chemistry》1901,40(1):70-72
Ohne Zusammenfassung 相似文献
104.
L. Andrews und J. W. Richards 《Fresenius' Journal of Analytical Chemistry》1899,38(12):796-797
Ohne Zusammenfassung 相似文献
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Summary An approach is described which makes use of X-ray structural data from enzyme-ligand complexes in order to obtain information for application in receptor modelling. The atomic surroundings of five different ligand functional groups were determined for all complex structures recorded in the Brookhaven Protein Data Bank. These atomic surroundings were then superimposed with respect to the atoms of the functional groups of the ligands in order to obtain clouds of neighbouring atoms. General principles were sought to describe the orientiation or favoured position of groups or atoms around those functional groups when bound to a macromolecule. Some simple conclusions and leads for further modelling were thus derived. 相似文献
107.
Differential expression of the skeletal muscle proteome in mdx mice at different ages 总被引:2,自引:0,他引:2
The mdx mouse is the most commonly used animal model for Duchenne muscular dystrophy (DMD), a disease caused by the absence of dystrophin. Although much has been done to elucidate the structure and function of dystrophin and the dystrophin-associated glycoprotein complex (DGC), little is known about the cascade of molecular events triggered by the absence of dystrophin that lead to muscle degeneration. To study the molecular basis of DMD, we decided to systematically study the skeletal muscle proteome in mdx mice at different ages. By using two-dimensional (2-D) gel electrophoresis, we defined changes in the protein expression pattern between mdx and control muscles. Approximately 46 differentially expressed proteins from the cytosolic fraction of mdx hindlimb muscles at three months of age were detected by 2-D gel analysis, of which 24 were identified by matrix assisted laser desorption/ionization- mass spectrometry. Most of the proteins fell into five groups of functionally related proteins. These functional categories are (i) metabolism and energy production, (ii) serine protease inhibitor family, (iii) growth and differentiation, (iv) calcium homeostasis, and (v) cytoskeletal reorganization and biogenesis. The potential roles of the differentially expressed proteins are discussed in the context of the mdx phenotype. Finally, we analyzed alterations of protein expression in mdx mice at one and six months of age to determine how protein expression changes with disease progression. 相似文献
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109.
Ben Andrews 《Journal of the American Mathematical Society》2003,16(2):443-459
A complete classification is given of curves in the plane which contract homothetically when evolved according to a power of their curvature. Applications are given to the limiting behaviour of the flows in various situations.
110.