72 research outputs found

    The Research of Through-casing Resistivity Logging Logging Calibration System Leakage Current Measurement Method

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    This paper introduces the logging principle of through-casing resistivity logging technology, finds a phenomenon that the leakage current measurements are susceptible to sufferring interferences. The through-casing resistivity logging technology in Russia and that of Schlumberger are studied, and the system of through-casing resistivity logging is established to improve the accuracy of calibrating, testing and measuring of the instrument. In this paper, distribution parameters of the form is replaced by the lumped parameter, and precision resistor array simulation in formation leakage current and scale pool simulation in different resistivity of formation are conducted, which make the dynamic range of the simulation in formation resistivity of the medium increase to 1- 300 Ω·m and meet the requirement of through-casing resistivity logging technology measurement range, 1 Ω·m ~ 100 Ω·m. Since the measuring signals of calibration acquisition and processing systems are extremely weak and calculation signals need to tell the nV (nanovolts) level, the high accurate data acquisition system of 24 digits is applied. DOI: http://dx.doi.org/10.11591/telkomnika.v11i12.367

    Generation of an induced pluripotent stem cell lines NSHDMUi001-A from patients with type 2 diabetes

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    Type 2 diabetes mellitus (T2DM) is common in China, and its aetiology and pathogenesis are still unclear. We reprogrammed pEP4EO2SEN2K and pEP4EO2SET2K, pCEP4-M2L was electrotransfected in T2DM patients with pEP4EO2SEN2K, and pCEP4-M2L was electrotransfected in T2DM patients expressing the OCT4, SOX2, NANOG, LIN28, c-MYC, KLF4, and SV40LT transcription factors to obtain induced pluripotent stem cells (iPSCs). The obtained iPSCs have been verified to have pluripotency, normal karyotype and differentiation potential; therefore, these cells can be used in the study of disease pathophysiology and drug development to create new therapeutic targets for T2DM and associated central nervous system damage

    Clonal Dissemination of Multidrug-Resistant and Hypervirulent Klebsiella pneumoniae Clonal Complex in a Chinese Hospital

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    The emergence of high antimicrobial-resistant and hypervirulent Klebsiella pneumoniae (hvKp) clones in clinics has become a cause of concern in recent years. Despite the global spread of the clonal complex (CC) 258, hvKp of other non-CC258 subgroups also emerged. Here, by performing a retrospective study from July 2019 to August 2020 in a Chinese hospital, we obtained 25 K. pneumoniae isolates belonging to CC15. By antimicrobial susceptibility testing and whole genome sequencing and analysis, we obtained the resistant phenotypes and genotypes of these isolates. Twenty-one isolates (84%) were carbapenem-resistant, and eighteen were blaKPC-2 positive. In addition, ten isolates were identified as putative hvKp and seven were carbapenem-resistant hvKp. Nine isolates carried the pLVPK-like virulence plasmid, which contains the fragment including rmpA2, peg-589, iutA, and iucABCD. Another isolate carried iucA. Phylogenetic analysis revealed that the isolates belonged to four lineages, and the putative hvKp isolates were identified in three of these. Two independent sublineages of putative hvKp were caused by the acquisition of pLVPK-like virulence plasmid. Based on comparative genomic analysis, the number of pairwise single nucleotide polymorphisms amongst the four sublineages, Lineage 1a, 1b, 2a, and 2b, were 1–43, 2–13, 129–279, and 3–4, respectively, indicating clonal transmission of Lineage 1a, 1b, and 2b. These results indicate that multiple lineages of CC15 carbapenem-resistant hvKp have emerged in the hospital and caused nosocomial transmission, and that the spreading of virulence plasmids among classic K. pneumoniae subtypes might become more common and happen more easily. These findings highlight the importance of surveillance of local epidemics of non-CC258 subgroups in hospitals

    A hybrid conjugate gradient algorithm for solving relative orientation of big rotation angle stereo pair

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    The fast convergence without initial value dependence is the key of large angle relative directional solution. Therefore, a hybrid conjugate gradient algorithm is proposed in this paper. The concrete process is:â‘  stochastic hill climbing(SHC) algorithm is used to make random disturbance to the given initial value of the relative directional element, and the new value to guarantee the optimization direction is generated; â‘¡ In local optimization, super-linear convergent conjugate gradient method is used to replace the steepest descent method in relative orientation to improve its convergence rate; â‘¢ The global convergence condition is that the calculation error is less than the prescribed limit error. The comparison experiment shows that the method proposed in this paper is independent of initial value, has higher accuracy and fewer iterations

    MicroRNA 107 partly inhibits endothelial progenitor cells differentiation via HIF-1β.

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    Endothelial progenitor cells (EPCs) play an important role in tissue repair after ischemic heart disease. In particular, the recovery of endothelial function is reliant on the ability and rate of EPCs differentiate into mature endothelial cells. The present study evaluated the effect of microRNA 107 (miR-107) on the mechanism of EPCs differentiation. EPCs were isolated from rats' bone marrow and miR-107 expression of EPCs in hypoxic and normoxic conditions were measured by real-time qualitative PCR. CD31 was analyzed by flow cytometry and eNOS was examined by real-time qualitative PCR and western blotting and these were used as markers of EPC differentiation. In order to reveal the mechanism, we used miR107 inhibitor and lentiviral vector expressing a short hairpin RNA (shRNA) that targets miR-107 and hypoxia-inducible factor-1 β (HIF-1β) to alter miR107 and HIF-1β expression. MiR-107 expression were increased in EPCs under hypoxic conditions. Up-regulation of miR-107 partly suppressed the EPCs differentiation induced in hypoxia, while down-regulation of miR-107 promoted EPC differentiation. HIF-1β was the target. This study indicated that miR-107 was up-regulated in hypoxia to prevent EPCs differentiation via its target HIF-1β. The physiological mechanisms of miR-107 must be evaluated if it is to be used as a potential anti-ischemia therapeutic regime
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