267 research outputs found

    Understanding hysteresis in carbon dioxide sorption in porous metal-organic frameworks

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    Two new isostructural microporous coordination frameworks [Mn3(Hpdc)2­(pdc)2] (1) and [Mg3(Hpdc)2­(pdc)2] (2) (pdc2– = pyridine-2,4-dicarboxylate) showing primitive cubic (pcu) topology have been prepared and characterized. The pore aperture of the channels is too narrow for the efficient adsorption of N2; however, both compounds demonstrate substantially higher uptake of CO2 (119.9 mL·g–1 for 1 and 102.5 mL·g–1 for 2 at 195 K, 1 bar). Despite of their structural similarities, 2 shows a typical reversible type I isotherm for adsorption/desorption of CO2, while 1 features a two-step adsorption process with a very broad hysteresis between the adsorption and desorption curves. This behavior can be explained by a combination of density functional theory calculations, sorption, and X-ray diffraction analysis and gives insights into the further development of new sorbents showing adsorption/desorption hysteresis

    SIRT1 Allele Frequencies in Depressed Patients of European Descent in Russia

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    Depressive disorder (DD) is a widespread mental disorder. Although DD is to some extent inherited, the genes contributing to the risk of this disorder and its genetic mechanisms remain poorly understood. A recent large-scale genome-wide association Chinese study revealed a strong association between the SIRT1 gene variants and DD. The aim of this study was to analyze the occurrence of heterozygote carriers and search for rare SNP variants of the SIRT1 gene in a cohort of DD patients as compared with a cohort of randomly selected members of the Russian population. The complete coding sequences of the SIRT1 gene from 1024 DNA samples from the general Russian population and from 244 samples from patients with DD were analyzed using targeted sequencing. Four new genetic variants of the SIRT1 were discovered. While no significant differences in the allele frequencies were found between the DD patients and the general population, differences between the frequencies of homozygote carriers of specific alleles and occurrences of heterozygous were found to be significant for rs2236318 (P < 0.0001), and putatively, rs7896005 (P < 0.05), and rs36107781 (P < 0.05). The study found for the first time that two new SNPs (i.e., 10:69665829 and 10:69665971) along with recently reported ones (rs773025707 and rs34701705), are putatively associated with DD. The revealed DD-associated SIRT1 SNPs might confer susceptibility to this disorder in Russian population of European descent

    Centrality evolution of the charged-particle pseudorapidity density over a broad pseudorapidity range in Pb-Pb collisions at root s(NN)=2.76TeV

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    Palaeozoic orogeneses around the Siberian craton: Structure and evolution of the Patom belt and foredeep

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    International audienceThis paper sheds light on the evolution of the Patom belt. This mountain range draws an arc along the southeastern edge of the Siberian craton. It is supposed to be of Caledonian age and to result from the accretion of microcontinents against the craton, but up to now, its detailed stratigraphic and tectonic history was unclear. A field study allows us to clarify it. The sedimentary record is marked by a slow evolution with stable periods of more than 250 Ma. The observed sedimentary succession confirms the existence of a passive margin setting in the late Riphean (900 Ma), followed during the Vendian (650-600 Ma) by the obduction of the Baikal-Muya ophiolites belt and a foredeep inversion. After that, a Late Cambrian extension occurred, which is first described in this paper. The second collision stage occurred after 385 Ma, in the Late Devonian-Early Carboniferous. Sedimentary and tectonic data are interpreted in the light of the geodynamic evolution of Siberia, which is dominated by continental collages against the Siberian craton. Field data reveal a homogeneous direction of compression from the inner areas to the foreland. Whereas the inner range displays metamorphosed units deformed in the ductile domain, deformation is weaker in the foreland, which developed above the cratonic crust.We relate this high deformation gradient to the presence of the stiff craton which impeded strain propagation. The irregular shape of the craton as well as preexistent basement topography can explain the different tectonic styles observed along the belt

    Ste20-related Protein Kinase LOSK (SLK) Controls Microtubule Radial Array in Interphase

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    Interphase microtubules are organized into a radial array with centrosome in the center. This organization is a subject of cellular regulation that can be driven by protein phosphorylation. Only few protein kinases that regulate microtubule array in interphase cells have been described. Ste20-like protein kinase LOSK (SLK) was identified as a microtubule and centrosome-associated protein. In this study we have shown that the inhibition of LOSK activity by dominant-negative mutant K63R-ΔT or by LOSK depletion with RNAi leads to unfocused microtubule arrangement. Microtubule disorganization is prominent in Vero, CV-1, and CHO-K1 cells but less distinct in HeLa cells. The effect is a result neither of microtubule stabilization nor of centrosome disruption. In cells with suppressed LOSK activity centrosomes are unable to anchor or to cap microtubules, though they keep nucleating microtubules. These centrosomes are depleted of dynactin. Vero cells overexpressing K63R-ΔT have normal dynactin “comets” at microtubule ends and unaltered morphology of Golgi complex but are unable to polarize it at the wound edge. We conclude that protein kinase LOSK is required for radial microtubule organization and for the proper localization of Golgi complex in various cell types
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