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101.
The classical Voronoi identity $$\Delta (x) = - \frac{2}{\pi }\sum\limits_{n = 1}^\infty {d(n)} \left( {\frac{x}{n}} \right)^{1/2} \left( {K_1 (4\pi \sqrt {xn} ) + \frac{\pi }{2}Y_1 (4\pi \sqrt {xn} )} \right)$$ is proved in a relatively simple way by the use of the Laplace transform. Here Δ(x) denotes the error term in the Dirichlet divisor problem, d(n) is the number of divisors of n and K_1, Y_1 are the Bessel functions. The method of proof may be used to yield other identities similar to Voronoi's.  相似文献   
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Full length v-SNARE protein in lipid vesicles when exposed to t-SNARE-reconstituted lipid membrane results in the self-assembly of a t-/v-SNARE complex in a ring pattern, forming pores, and establishing continuity between the opposing bilayers. It is known that smaller vesicles fuse more efficiently than larger ones, and hence the curvature of secretory vesicles may dictate the potency and efficacy of their fusion at the cell plasma membrane. The diameter of t- and v-SNARE vesicles may, therefore, reflect the size of the t-/v-SNARE complex formed. In the present study, this hypothesis was tested, and results from the study demonstrate that the size of the t-/v-SNARE complex is directly proportional to the vesicle diameter (R2 = 0.9725).  相似文献   
105.
Ab initio calculations on fluoroethane reactions with the hydroxyl radical have been carried out at different levels of theory. The convergence of reaction barriers and reaction enthalpies has been systematically investigated with respect to the size and quality of the basis set and the treatment of correlation energy. The G2 and MP2 barrier heights and reaction enthalpies show the best agreement with the experimental data. The split valence basis sets of triple-zeta quality supplemented by diffuse and polarization functions are necessary to reproduce experimental values for barrier heights and reaction enthalpies at the MP2 level of theory. The full counterpoise correction was used to calculate the basis set superposition error for several standard basis sets, including polarization and diffuse functions. The smallest counterpoise corrections are associated with basis sets that contain polarization and diffuse functions, the diffuse functions being the most effective in reducing BSSE. However, in our case, the uncorrected barrier heights are in better agreement with experimental results than the counterpoise-corrected data. Thus, at the MP2 level of theory, which seems to be dictated for larger electronic systems of chemical interest, the optimal approach is to increase the basis set to the maximum size affordable and to use results without counterpoise corrections for the calculation of reaction barriers. A viable alternative is the use of G2 theory because its results for the barrier heights and reaction enthalpies are in excellent agreement with the experimental data. © 1997 John Wiley & Sons, Inc. J Comput Chem 18: 1190–1199  相似文献   
106.
Cells have evolved elaborate mechanisms to regulate DNA replication machinery and cell cycles in response to DNA damage and replication stress in order to prevent genomic instability and cancer. The E3 ubiquitin ligase SCFDia2 in S. cerevisiae is involved in the DNA replication and DNA damage stress response, but its effect on cell growth is still unclear. Here, we demonstrate that the absence of Dia2 prolongs the cell cycle by extending both S- and G2/M-phases while, at the same time, activating the S-phase checkpoint. In these conditions, Ctf4—an essential DNA replication protein and substrate of Dia2—prolongs its binding to the chromatin during the extended S- and G2/M-phases. Notably, the prolonged cell cycle when Dia2 is absent is accompanied by a marked increase in cell size. We found that while both DNA replication inhibition and an absence of Dia2 exerts effects on cell cycle duration and cell size, Dia2 deficiency leads to a much more profound increase in cell size and a substantially lesser effect on cell cycle duration compared to DNA replication inhibition. Our results suggest that the increased cell size in dia2∆ involves a complex mechanism in which the prolonged cell cycle is one of the driving forces.  相似文献   
107.
The greatest Serbian mathematician, Jovan Karamata (1902–1967), gained worldwide fame working on problems related to theorems of a Tauberian nature. His simple and elegant 1930 proof of the Hardy–Littlewood theorem found its place in the well-known monographs by Titchmarsh, Knopp, Doetsch, Widder, Hardy and Favard. It is less known that the method used in this proof was mentioned for the first time at a conference of the Academy of Natural Sciences of the Serbian Royal Academy of Sciences in Belgrade in 1929, where Karamata introduced the notion of majorizability as a new condition of convergence for Abel summable series. This fact holds the key to a historical insight into Karamata’s famous proof of the Hardy–Littlewood theorem.  相似文献   
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It is not completely unreasonable to expect that a computable function bounding the number of Pachner moves needed to change any triangulation of a given 3-manifold into any other triangulation of the same 3-manifold exists. In this paper we describe a procedure yielding an explicit formula for such a function if the 3-manifold in question is a Seifert fibred space.Revised version: 5 March 2004  相似文献   
110.
Mass spectrometry has been applied in order to study the main fragmentation routes of some 4-pyrimidene carboxylic acids. Differences in fragmentation were caused by the nature of the substituent in position 2 of the pyrimidine ring, while the methyl group in position 1, 3 or 6 did not influence the fragmentation route.  相似文献   
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