11 research outputs found

    The study results of the filtration process in the ground dams body and its chemical effect on piezometers

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    The article describes the definition of filtration flow gradients in the dam's body on the example of the Kattakurgan reservoir, the analysis of the reasons for their change in cross-section. Evaluation of the aggressiveness of the filtration flow in the dam's body plays an important role in ensuring the stability of the reservoir dam and its parts. To assess the aggressiveness of the filtration flow in the dam's body, it is necessary to know the action pattern of the filtration water in the reservoir dam and its effect on the elements of the dam. In addition, the chemical composition of the water in the piezometers was analyzed in the laboratory to determine the aggressive effect of sulfate elements on the piezometers and their corrosion. Measures on the observations of systemic piezometers were also mentioned

    Negatively charged phospholipids stimulate factor XI activation by thrombin

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    Introduction: Coagulation factor XI (FXI) is the zymogen of the serine-protease FXIa, which contributes to thrombin formation by activating factor IX. FXI can be activated by factor XIIa or thrombin, but thrombin-catalysed FXI activation is highly inefficient, unless stimulated by polyanions such as dextran sulphate (DXS) or polyphosphate (PolyP). Aim: To investigate whether negatively charged phospholipids can also enhance thrombin-catalysed FXI activation and to determine the dependence of this reaction on phospholipid concentration and composition, thrombin exosites and ionic strength. Methods: FXI was incubated with thrombin in the absence and presence of DXS, PolyP or phospholipid vesicles, and FXIa generation was followed using a chromogenic substrate. The role of thrombin exosites was probed using specific aptamers. The ionic strength was varied using either sodium chloride (NaCl) or tetrapropylammonium chloride. Results: Similar to DXS and PolyP, phospholipid vesicles with a high percentage of phosphatidic acid or phosphatidylserine enhanced thrombin-catalysed FXI activation by 1–2 orders of magnitude. Moreover, thrombin and FXI bound to negatively charged phospholipids in direct binding assays. Both thrombin exosites contributed to the ability of thrombin to bind to phospholipids and activate FXI, with a predominance of exosite II. Decreasing the ionic strength greatly stimulated FXI activation by thrombin, both in the absence and presence of phospholipids. However, at equal ionic strength, the reaction was more efficient with NaCl than with tetrapropylammonium chloride, suggesting a specific stimulatory effect of Na+. Conclusions: Negatively charged phospholipids, just as DXS and PolyP, stimulate FXI activation by thrombin via a ‘template mechanism’

    The study results of the filtration process in the ground dams body and its chemical effect on piezometers

    No full text
    The article describes the definition of filtration flow gradients in the dam's body on the example of the Kattakurgan reservoir, the analysis of the reasons for their change in cross-section. Evaluation of the aggressiveness of the filtration flow in the dam's body plays an important role in ensuring the stability of the reservoir dam and its parts. To assess the aggressiveness of the filtration flow in the dam's body, it is necessary to know the action pattern of the filtration water in the reservoir dam and its effect on the elements of the dam. In addition, the chemical composition of the water in the piezometers was analyzed in the laboratory to determine the aggressive effect of sulfate elements on the piezometers and their corrosion. Measures on the observations of systemic piezometers were also mentioned

    Genomic structural variants are linked with intellectual disability

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    Mutations in more than 500 genes have been associated with intellectual disability (ID) and related disorders of cognitive function, such as autism and schizophrenia. Here we aimed to unravel the molecular epidemiology of non-specific ID in a genetic isolate using a combination of population and molecular genetic approaches. A large multigenerational pedigree was ascertained within a Dagestan Genetic Heritage research program in a genetic isolate of indigenous ethnics. Clinical characteristics of the affected members were based on combining diagnoses from regional psychiatric hospitals with our own clinical assessment, using a Russian translation of the structured psychiatric interviews, the Diagnostic Interview for Genetic Studies and the Family Interview for Genetic Studies, based on DSM-IV criteria. Weber/CHLC 9.0 STRs set was used for multipoint parametric linkage analyses (Simwalk2.91). Next, we checked CNVs and LOH (based on Affymetrix SNP 5.0 data) in the linked with ID genomic regions with the aim to identify candidate genes associated with mutations in linked regions. The number of statistically significant (p ≤ 0.05) suggestive linkage peaks with 1.3 3 were obtained at 2p25.3-p24.2 under the dominant model, with a peak at 21 cM flanked by loci D2S2976 and D2S2952; at 12q24.22-q24.31 under the recessive model, with a peak at -120 cM flanked by marker D12S2070 and D12S395 and at 22q12.3 under the dominant model, with a peak at 32 cM flanked by marker D22S683 and D22S445. After a set of genes had been designated as possible candidates in these specific chromosomal regions,we conducted an exploratory search for LOH and CNV based on microarray data to detect structural genomic variants within five ID-linked regions with LOD scores between 2.0 and 3.9. In these selected regions we obtained 173 ROH segments and 98 CN segments. Further analysis of region 2p25.3-p24.2 revealed deletions within genes encoding MYTL, SNTG2 and TPO among five of 21 affected cases at 2p25.3-p24.2. In the ID-linked region at 12q24.22-12q24.31 19 out of 21 ID cases carried segmental CNV and 20 of 21 them displayed ROH segments with mean size lengths for ID cases 2512 kb (500-6,472 kb) and for healthy control 682 kb (531-986 kb), including the genes MED13L, HRK, FBXW8, TESC, CDK2AP1 and SBNO1. Seven of 21 affected pedigree members displayed segmental deletions at 22q12.3 that includes the gene LARGE. Eight affected pedigree members carried ROH segments and 6 CN segments at 10p11.23-p11.21 containing the genes ZEB1, c10orf68 and EPC1. Our linkage and structural genomic variation analyses in a remote highland genetic isolate with aggregation of ID demonstrated that even highly isolated single kindred ID has oligo/polygenic pathogenesis. The results obtained implicate 10 genomic regions linked with ID that contain some of previously reported candidate genes, including HRK, FBXW8, TESC, CDK2AP1 and SBNO1 at 12q24 that were shown in recent studies as associated with brain measures derived from MRI scans
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