Myopia, an increasingly grave public health concern, necessitates the implementation of various techniques for its management. These techniques predominantly comprise the employment of spectacles correction, orthokeratology (ortho-k), and soft bifocal and multifocal lenses. In the present study, a pioneering polish-free ortho-k lens was devised, featuring two reverse lines and three alignment lines, which, respectively, expedite the shaping process and enhance centration. The structural blueprint of the ortho-k lens, along with the simulation of fluorescence staining, was executed employing the FocalPoints software V7.0 (Advance Medical, Milan, Italy). Subsequently, lens aberration elimination was accomplished through ray tracing utilizing ZEMAX software V13.0 (Focus Software, Wixom, MI, USA). The fabrication of the lens was carried out via high-precision lathe turning using the UPC 100 Vision instrument (SCHNEIDER, Ratingen, Germany). The power profile of the ortho-k lens was measured using the CONTEST 2 apparatus (ROTLEX, Omer, Israel). The surface quality was observed under a 200× microscope (ZEISS, Oberkochen, Germany). The fitting of the lens was assessed through the utilization of both Slit-lamp microscopy (MediWorks, Shanghai, China) and Corneal topographer (Medmont E300, Melbourne, VIC, Australia)

A two-stage data envelopment model for evaluating the exchange efficiency of the imports and exports in a railway supply chain network

Strengthening of the barrier function in human telomerase reverse transcription (hTERT) immortalized corneal and conjunctival epithelium by double-stranded RNA

Abstract. Hybrid maize breeding requires constant renewal of the source material. In this regard, broadening of genetic variation in parental lines is one of the primary tasks in heterotic hybrid breeding programs. The use of reverse diploid inbred lines derived from a tetraploid population is considered as an innovative approach to achieve this goal.Results. The investigated material comprised 106 reverse diploid (rediploid) inbred lines originating from diploid plants selected in segregating selfed progenies of triploid populations and consequently subjected to inbreeding, while triploid populations resulted from a cross between plants of a tetraploid population with a broad genetic basis and a diploid line. The use of a system of crosses with 37 sterile testers belonging to different FAO maize maturity groups allowed the evaluation of the rediploid lines’ combining ability and the response to M and C types of CMS. Field tests were conducted in 2019 in the steppe zone of Kabardino-Balkaria. Forty-six lines (43.3%) with the combining ability ranging from ultra-high to good, and 78 lines (73.6%) maintaining the CMS character were identified. Among them, 59 lines (55.7%) were maintainers for the M type CMS, 15 lines (14.1%) for C type CMS, and 4 lines maintained sterility for both CMS types. Sixteen lines (15.1%) restored pollen fertility of the forms with M type CMS, 11 lines (10.4%) were restorers for the C-type and one line turned out to be a universal restorer for both CMS types. Ranking by the “sprout - flowering of ears” interstage period duration showed that most of the lines (66.0%) with the ability to maintain sterility or restore male fertility of M and C CMS types, as well as with the combining ability from ultrahigh to good (32.6%) fell into the group with the flowering period duration of 51-55 days. According to the results of the harvested grain moisture assessment, the hybrids ♀(РГС246с × OL213) × ♂92с5986·2·3, ♀714М × ♂1/67-1 and ♀714М × ♂92н136-4, with the values of 13, 6%, 13.9%, 14.0%, respectively, were identified. The hybrids ♀714М × ♂1/67- 1 and ♀(OL563С × KL1392) × ♂92с0653 2 1 2 were characterized by the maximum value of the selection index, i.e. 5.03 and 5.13, respectively.Conclusions. The results of the studies showed the breeding value of rediploid lines as an initial material for hybrid maize breeding.

Anisotropy and Clausius-Clapeyron relation for forward and reverse stress-induced martensitic transformations in polycrystalline NiTi thin walled tubes

Adults (N = 72) estimated the location of target numbers on number lines that varied in numerical range (i.e., typical range 0-10,000 or atypical range 0-7,000) and spatial orientation (i.e., the 0 endpoint on the left [traditional] or on the right [reversed]). Eye-tracking data were used to assess strategy use. Participants made meaningful first fixations on the line, with fixations occurring around the origin for low target numbers and around the midpoint and endpoint for high target numbers. On traditional direction number lines, participants used left-to-right scanning and showed a leftward bias; these effects were reduced for the reverse direction number lines. Participants made fixations around the midpoint for both ranges but were less accurate when estimating target numbers around the midpoint on the 7,000-range number line. Thus, participants are using the internal benchmark (i.e., midpoint) to guide estimates on atypical range number lines, but they have difficulty calculating the midpoint, leading to less accurate estimates. In summary, both range and direction influenced strategy use and accuracy, suggesting that both numerical and spatial processes influence number line estimation.

Hydrogeochemical Prospecting for evaporate and clay deposits in Harrat ash Shaam basalts, Jordan

Hepatocellular carcinoma (HCC) is one of the most widespread malignant human tumors worldwide. Treatment options include radiotherapy, surgical intervention and chemotherapy; however, drug resistance is an ongoing treatment concern. In the present study, the effects of a microRNA (miR/miRNA), miR-9, on the sensitivity of HCC cell lines to the epidermal growth factor receptor inhibitor, cetuximab, were examined. miR-9 has been proposed to serve a role in tumorigenesis and tumor progression. In the present study, bioinformatics analyses identified the eukaryotic translation initiation factor 5A2 (eIF-5A-2) as a target of miR-9. The expression levels of miR-9 and eIF-5A-2 were examined by reverse transcription-quantitative polymerase chain reaction and HCC cell lines were transfected with miR-9 mimics and inhibitors to determine the effects of the miRNA on cell proliferation and viability. The miR-9 mimic was revealed to significantly increase the sensitivity of epithelial phenotype HCC cells (Hep3B and Huh7) to cetuximab, while the miR-9 inhibitor triggered the opposite effect. There were no significant differences in sensitivity to cetuximab observed in mesenchymal phenotype HCC cells (SNU387 and SNU449). Cells lines displaying high expression levels of eIF-5A-2 were more resistant to cetuximab. Transfection of cells with a miR-9 mimic resulted in downregulation of the expression of eIF-5A-2 mRNA, while an miR-9 inhibitor increased expression. When expression of eIF-5A-2 was knocked down with siRNA, the effects of miR-9 on cetuximab sensitivity were no longer observed. Taken together, these data support a role for miR-9 in enhancing the sensitivity of epithelial phenotype HCC cells to cetuximab through regulation of eIF-5A-2.

Reverse engineering language product lines from existing DSL variants

The exergetic efficiency as a performance evaluation tool in reverse osmosis desalination plants in operation

Although noncancerous immortalized cell lines have been developed by introducing genes into human and murine somatic cells, such cell lines have not been available in large domesticated animals like pigs. For immortalizing porcine cells, primary porcine fetal fibroblasts were isolated and cultured using the human telomerase reverse transcriptase (hTERT) gene. After selecting cells with neomycin for 2 weeks, outgrowing colonized cells were picked up and subcultured for expansion. Immortalized cells were cultured for more than 9 months without changing their doubling time (~24 hours) or their diameter (< 20 µm) while control cells became replicatively senescent during the same period. Even a single cell expanded to confluence in 100 mm dishes. Furthermore, to knockout the CMAH gene, designed plasmids encoding a transcription activator-like effector nuclease (TALENs) pairs were transfected into the immortalized cells. Each single colony was analyzed by the mutation-sensitive T7 endonuclease I assay, fluorescent PCR, and dideoxy sequencing to obtain three independent clonal populations of cells that contained biallelic modifications. One CMAH knockout clone was chosen and used for somatic cell nuclear transfer. Cloned embryos developed to the blastocyst stage. In conclusion, we demonstrated that immortalized porcine fibroblasts were successfully established using the human hTERT gene, and the TALENs enabled biallelic gene disruptions in these immortalized cells.

Undifferentiated nasopharyngeal carcinomas (NPCs) are commonly present with latent EBV infection. However, events regulating EBV infection at early stages of the disease and the role of EBV in disease pathogenesis are largely undefined. Genetic alterations leading to activation of cyclin D1 signaling in premalignant nasopharyngeal epithelial (NPE) cells have been postulated to predispose cells to EBV infection. We previously reported that loss of p16, a negative regulator of cyclin D1 signaling, is a frequent feature of NPC tumors. Here, we report that early premalignant lesions of nasopharyngeal epithelium overexpress cyclin D1. Furthermore, overexpression of cyclin D1 is closely associated with EBV infection. Therefore we investigated the potential role of cyclin D1 overexpression in dysplastic NPE cells in vitro. In human telomerase reverse transcriptase-immortalized NPE cells, overexpression of cyclin D1 or a p16-resistant form of CDK4 (CDK4(R24C)) suppressed differentiation. This suppression may have implications for the close association of EBV infection with undifferentiated NPC. In these in vitro models, we found that cellular growth arrest and senescence occurred in EBV-infected cell populations immediately after infection. Nevertheless, overexpression of cyclin D1 or a p16-resistant form of CDK4 or knockdown of p16 in the human telomerase reverse transcriptase-immortalized NPE cell lines could counteract the EBV-induced growth arrest and senescence. We conclude that dysregulated expression of cyclin D1 in NPE cells may contribute to NPC pathogenesis by enabling persistent infection of EBV.

Human telomerase reverse transcriptase-immortalized porcine monomyeloid cell lines for the production of porcine reproductive and respiratory syndrome virus

An achiral nematic liquid crystal was doped with a small quantity of carbon nanotubes having a net chirality, and the mixture was found to exhibit an average mechanical twist over macroscopic dimensions. The nanotube-induced chiral pitch length P was determined as a function of the average nanotube concentration by measuring the radii of curvature of reverse twist disclination lines in 90° nematic twist cells. The results suggest that the nanotubes’ spatial concentration can vary significantly across the cell and that at high average concentration, the nanotubes undergo aggregation, resulting in an apparent saturation of P−1 at high concentrations. The macroscopic helical twisting power of the nanotubes has been estimated from the results.

BackgroundTransposable Elements (TEs) comprise nearly 45% of the entire genome and are part of sophisticated regulatory network systems that control developmental processes in normal and pathological conditions. The retroviral/retrotransposon gene machinery consists mainly of Long Interspersed Nuclear Elements (LINEs-1) and Human Endogenous Retroviruses (HERVs) that code for their own endogenous reverse transcriptase (RT). Interestingly, RT is typically expressed at high levels in cancer cells. Recent studies report that RT inhibition by non-nucleoside reverse transcriptase inhibitors (NNRTIs) induces growth arrest and cell differentiation in vitro and antagonizes growth of human tumors in animal model. In the present study we analyze the anticancer activity of Abacavir (ABC), a nucleoside reverse transcription inhibitor (NRTI), on PC3 and LNCaP prostate cancer cell lines.Principal FindingsABC significantly reduces cell growth, migration and invasion processes, considerably slows S phase progression, induces senescence and cell death in prostate cancer cells. Consistent with these observations, microarray analysis on PC3 cells shows that ABC induces specific and dose-dependent changes in gene expression, involving multiple cellular pathways. Notably, by quantitative Real-Time PCR we found that LINE-1 ORF1 and ORF2 mRNA levels were significantly up-regulated by ABC treatment.ConclusionsOur results demonstrate the potential of ABC as anticancer agent able to induce antiproliferative activity and trigger senescence in prostate cancer cells. Noteworthy, we show that ABC elicits up-regulation of LINE-1 expression, suggesting the involvement of these elements in the observed cellular modifications.

First year performance review of Magong UF/RO Seawater Desalination Plant

The reverse photoperiod-sensitive genic male sterility (PGMS) and thermo-sensitive genic male sterility (TGMS) lines have an opposite phenotype compared with normal PGMS and TGMS lines widely used by the two-line system in current hybrid rice seed production. Thus, the application of reverse PGMS and TGMS lines can compensate PGMS and TGMS lines in hybrid rice production. YiD1S is a reverse PGMS line, in which pollen fertility is mainly regulated by day-length, but also influenced by temperature. Genetic analysis indicated that male sterility of YiD1S was controlled by two recessive major genes. An F(2) population from a cross between YiD1S and 8528 was developed and used for molecular mapping of the two reverse PGMS genes which were first named rpms1 and rpms2. Both simple sequence repeat (SSR) markers and bulked segregant analysis (BSA) were used in this study. As a result, one reverse PGMS gene (rpms1) was mapped to the interval between SSR markers RM22980 (0.9 cM) and RM23017 (1.8 cM) on chromosome 8. Eight SSR markers, YDS818, RM22984, RM22986, RM22997, YDS816, RM23002, RM339 and YDS810 completely co-segregated with the rpms1 gene. Another reverse PGMS gene (rpms2) was mapped to the interval between SSR markers RM23898 (0.9 cM) and YDS926 (0.9 cM) on chromosome 9. The physical mapping information from publicly available resources shows that the rpms1 and rpms2 loci are located in a region of 998 and 68 kb, respectively. The analysis based on marker genotypes showed that the effect of rpms1 was slightly larger than that of rpms2 and that the two genes interacted in controlling male sterility.

A novel method is described for the measurement of long pitch lengths in chiral nematic liquid crystals using the bowing of reverse twist disclination lines in 90° twisted nematic devices. The method has been used to measure pitch lengths of up to 50 mm, significantly longer than previously possible using existing methods. † The research was performed in part at the Department of Chemistry, The University of York, Heslington, York YO10 5DD, UK.

Vascular access recirculation (R) is a well-known cause of decreased dialysis dose. In this paper a new easy protocol for R detection in pre-dialysis derived from the classic Glucose Infusion Test (GIT) is introduced. The pre-dialysis GIT (GIT-pre) is based on the glucose (5%, 10 ml) bolus injection directly into the venous needle and on a simultaneous withdrawal from the arterial needle. If the glucose value increases during the glucose bolus, R is present. This new protocol was validated on 29 chronic haemodialysis patients (20 AVFs, 7 CVCs, 2 PTFE grafts), comparing the glucose increase with the classic GIT during dialysis. Only one CVC had R with the blood lines in the normal position (deltaglu = 465 mg/dl with GIT-pre and a deltaglu = 186 mg/dl, R = 9.3% with classic GIT) while in the reverse blood line position, all CVCs showed a significant glucose increase (mean GIT-pre deltaglu = 195 mg/dl; mean GIT deltaglu = 140 mg/dl corresponding to a R = 8%). There were 5 AVFs with true R (correct blood lines position) clearly identified by both methods (mean values deltaglu = 316 mg/dl with GIT-pre and a deltaglu = 390 mg/dl, R = 19.5% with classic GIT). Preliminary results show good reliability of the new protocol in identifying VA R caused either by failing VA with stenosis or by reverse blood lines position. The GIT-pre is a simpler application of the classic GIT useful for testing new VA, new needle positions or CVC performance before starting dialysis. A simpler R test could increase the frequency of the measurements and consequently the power of R in early detection of VA problems.

The behavior of the interface and the lateral to longitudinal stain ratio due to the stress-induced martensitic transformation (SIMT) were investigated in the regions of superelasticity (SE) and shape memory effect (SME) in a TiNi shape-memory alloy wire through the tensile test. The interface between a parent phase and a martensitic phase which appears due to SIMT during the loading process and its reverse transformation during unloading starts at both ends in the gripping parts of a wire and propagates towards the central part. When the two interfaces meet, SIMT completes.