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1.
The interaction between gene activation and cellular activity has recently emerged as a critical aspect of brain behavior, but the dynamics of networks incorporating these interactions are poorly understood. An interesting phenomena arises when the genetic activation oscillates endogenously and a network of such cells synchronize to a coherent rhythm, such as is the case with the suprachiasmatic nucleus. To explain this synchronization, we propose a model in which a mRNA/protein expression cycle drives neurons electrical activity, and synaptic activation shifts the phase of the protein rhythm. Using lattice networks, we demonstrate that these interactions are sufficient to generate coherent oscillation. © 2006 Wiley Periodicals, Inc. Complexity 12: 67–72, 2006 相似文献
2.
An optimization approach for planning daily drayage operations 总被引:1,自引:0,他引:1
Yetkin Ileri Mokhtar Bazaraa Ted Gifford George Nemhauser Joel Sokol Erick Wikum 《Central European Journal of Operations Research》2006,14(2):141-156
Daily drayage operations involve moving loaded or empty equipment between customer locations and rail ramps. Our goal is to
minimize the cost of daily drayage operations in a region on a given day. Drayage orders are generally pickup and delivery
requests with time windows. The repositioning of empty equipment may also be required in order to facilitate loaded movements.
The drayage orders are satisfied by a heterogeneous fleet of drivers. Driver routes must satisfy various operational constraints.
We present an optimization methodology for finding cost-effective schedules for regional daily drayage operations. The core
of the formulation is a set partitioning model whose columns represent routes. Routes are added to the formulation by column
generation. We present numerical results for real-world data which demonstrate that our methodology produces low cost solutions
in a reasonably short time. 相似文献
3.
H. Postma J. D. Bowman C. D. Bowman J. E. Bush P. P. J. Delheij C. M. Frankle C. R. Gould D. G. Haase J. Knudson G. E. Mitchell S. Penttilä N. R. Roberson S. J. Seestrom J. J. Szymansky S. H. Yoo V. W. Yuan X. Zhu 《Hyperfine Interactions》1992,75(1-4):153-163
Parity violation effects have been studied at 40 neutron p-wave resonances of the even-even nuclei238U and232Th. Of these 11 show parity violation effects larger than 2 standard deviations, making parity violation a rather common phenomenon.
Parity mixing up to 10% has been found. The root-mean squared matrix elements for parity violation derived from these resonances
are M=0.58 (+0.50/-0.25) meV for238U, respectively 1.39 (+0.35/-0.38) meV for232Th. 相似文献
4.
5.
6.
V. A. Glushkov I. V. Mashevskaya V. I. Sokol E. V. Feshina O. A. Maiorova 《Chemistry of Heterocyclic Compounds》1997,33(7):783-788
The reaction of arylhydrazides of -alkyl--chlorocarboxylic acids with thiocyanate ions gave intermediate thiocyanates which rearranged to isothiocyanates on heating and the latter cyclized to 5,5-dialkyl-3-arylamino-2-thiohydantoins.Institute of Technical Chemistry, Urals Branch, Russian Academy of Sciences, Perm' 614000. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 898–903, July, 1997. 相似文献
7.
L. V. Baikalova V. I. Sokol I. A. Zyryanova I. V. Fedyanin V. N. Khrustalev E. A. Zel’bst O. A. Tarasova V. S. Sergienko B. A. Trofimov 《Russian Journal of General Chemistry》2006,76(5):791-797
The crystal and molecular structures of bis(1-isopropenylimidazole)dichlorocobalt (C12H16Cl2·N4Co) [R 0.036 (R W 0.089) for 3229 unique reflections with I > 2σ(I)] and tetra(1-vinylimidazole)dichlorocobalt (C20H24Cl2N8Co) [R 0.031 (R W 0.072) for 1863 unique reflections with I > 2σ(I)] were determined. In these molecular complexes, the monodentate terminal 1-alkenylimidazole ligands coordinate to the metal via a “pyridine” nitrogen atom. In C12H16Cl2N4Co, the Co atom has a distorted tetrahedral 2N,2Cl coordination. The coordination polyhedron of cobalt in C20H24Cl2N8Co is a strongly elongated 4N,2Cl octahedron. The Co-N and Co-Cl bonds [Co-N 2.015(2) and 2.032(4) Å; Co-Cl 2.229(2) Å] in the tetrahedral complex C12H16Cl2N4Co are shorter than those in the octahedral complex C20H24Cl2N8Co [Co-N 2.134(2) and 2.157(2) Å; Co-Cl 2.518(1) Å]. In the structures of both complexes there are short contacts involving the Cl atoms. 相似文献
8.
Davydov V. V. Al-Salekh O. A. Mercur'eva N. Yu. Ryabov M. A. Sokol V. I. Sergienko V. S. Shklyaev Yu. V. 《Russian Journal of Coordination Chemistry》2003,29(1):16-21
Twenty new complexes were synthesized by reacting Co(II), Cu(II), Zn, Cr(III), Fe(III), Cd and Ag salts with 3,3-dimethyl-1-(3-methylpyrazole-5-onilidene-4)-1,2,3,4-tetrahydroisoquinoline (L1), spiro{cyclohexane-1,3"-[1-(1-phenyl-3-methylpyrazole-5-onilidene-4)-1,2,3,4-tetrahydroisoquinoline]} (L2), and 3,3-dimethyl-1-(1-phenyl-3-methylpyrazole-5-onilidene-4)-1,2,3,4-tetrahydroisoquinoline (L3). These compounds were studied by IR and electronic absorption spectroscopy. The type of coordination of their ligands was discussed on the basis of the results obtained and X-ray diffraction data for L3 and [CuL2
2 Cl2] · 2L2 obtained previously. 相似文献
9.
V. I. Sokol L. V. Baikalova E. S. Domnina M. A. Porai-Koshits 《Russian Chemical Bulletin》1992,41(6):1076-1079
The crystal and molecular structures of 1,1-divinyl-2,2-biimidazolyl (L) were determined by x-ray crystallographic analysis. It was established that the molecule of L has crystallographic symmetry 2 and a cisoid conformation with an angle of rotation of 128° between the imidazole rings. The length of the C2-C2 bond is increased to 1.485(11) Å compared with the length of the analogous bond in unsubstituted 2,2-biimidazolyl (1.423 Å). Localization of the N=C multiple bond is observed [1.297(9) Å]. The other N-C bonds of the ring are almost equalized (1.374 Å) and are close to the standard values for bonds of the C
sp
2-N type in imidazoles. The angle between the plane of the heterocycle and the plane passing through the atoms of the vinyl group amounts to 7°.N. S. Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, 117907 Moscow. Irkutsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, 664033 Irkutsk. Translated fromIzvestiya Akademii Nauk, Seriya Khimicheskaya, No. 6, pp. 1376–1380, June, 1992. 相似文献
10.
V. V. Davydov V. L. Sokol E. V. Balebanova Yu. V. Shklyaev S. V. Sergeev V. A. Nikanorov B. E. Zaitsev M. A. Porai-Koshits 《Russian Chemical Bulletin》1993,42(2):288-294
3,3-Dimethyl- and 3-methyl-1-(4,4-dimethyl-2,6-dioxocyclohex-1-yl)-3,4-dihydroisoquinolines have been synthesized. Crystal and molecular structures of the 3,3-dimethyl derivative have been determined. In the crystalline state this compound exists as a tautomeric form where a hydrogen atom is located at the N atom of the dihydroisoquinoline fragment of the molecule. The tautomeric equilibrium does not shift noticeably in solutions, as shown by IR, UV, and NMR spectroscopy.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 331–336, February, 1993. 相似文献