Estimating the compressive strength of fly ash added concrete using artificial neural networks

The aim of this study is to develop an artificial intelligence that predicts the compressive strength of fly ash substituted concretes using material mixing ratios. Within the scope of the study, 5 different fly ash mixed concrete samples were estimated. The strength values were estimated using artificial neural networks before the produced samples were subjected to the pressure test. In order to develop the artificial neural network, it is introduced as a dataset of 1030 different mixing ratios consisting of experimental results in the existing literature. In order to estimate the compressive strength, varying ratios of 8 different materials such as water, cement, fly ash entering the mixture are analyzed. As a result of the study, it has been observed that the predictions made using artificial neural networks are very close to the strength values obtained from the experiment

Common Methylenetetrahydrofolate Reductase Polymorphisms (A1298C & C677T) in Ectopic Trophoblasts and Methotrexate Treatment Failure in Tubal Pregnancies

Objectives: The success rate of methotrexate (MTX) therapy varies among tubal ectopic pregnancies. Commonmethylenetetrahydrofolate reductase (MTHFR) polymorphisms (C677T&A1298C) have been suggested to alter MTX effect. This study aimed to assess and compare MTX treatment failure rates with respect to MTHFR polymorphisms in trophoblasts of ectopic tubal pregnancies.Material and methods: A retrospective chart review of tubal ectopic pregnancies was conducted and 34 eligible cases were found. Paraffinized blocks of ectopic trophoblastic tissues were retrieved from the archives of pathology department.Common MTHFR polymorphisms were studied on microdissected trophoblastic tissues. Sixteen cases with history of failed MTX therapy (study group) and 18 control cases were compared for their pertinent clinical characteristics and common MTHFR polymorphisms (C677T&A1298) data.Results: In the study group, there were 8 (50%) C677T single nucleotide polymorphisms (SNP) and 9 (56.7%) A1298C SNP. Polymorphism rates were not found to be different between two groups for neither polymorphism (p > 0.05 for both). Number of compound heterozygotes was 3 (18.7%) in study group and 5 (27.7%) in controls (p = 0.693). In addition, MTHFR polymorphism presence seemed to have no effect on interval serum β-hCG concentration change in MTX-fail group (p=0.693).Conclusions: Our data implied that common MTHFR polymorphisms of ectopic trophoblastic tissue are not associated with MTX failure in patients with tubal pregnancies. Additionally, serum β-hCG concentration changes caused by MTX treatment and studied MTHFR polymorphisms are likely independent

Prevalencija triju virusa medonosne pčele u Turskoj

In this study, 10 worker bees from each of 28 different apiaries were collected (a total of 280 honey bees) from 6 provinces of the Black Sea region in Turkey. These samples were tested by Reverse-Transcriptase PCR (RT-PCR), for three honey bee viruses: acute bee paralysis virus (ABPV), chronic bee paralysis virus (CBPV) and black queen cell virus (BQCV). In addition, the samples were microscopically examined for Varroa destructor. In conclusion, CBPV, BQCV and Varroa destructor were identified in 25%, 21.42% and 53.57% of the bees respectively, but ABPV could not be detected in apiaries. This is the first report of CBPV, BQCV in Turkey.Prikupljeno je po 10 radilica s 28 različitih pčelinjaka u šest provincija na području oko Crnoga mora u Turskoj. Uzorci su bili pretraženi lančanom reakcijom polimerazom uz prethodnu reverznu transkripciju (RTPCR) na tri virusa medonosne pčele: virus akutne pčelinje paralize, virus kronične pčelinje paralize i virus crnih matičnjaka. Uzorci su povrh toga bili pretraženi na prisutnost parazita Varroa destructor. Virus kronične paralize bio je ustanovljen u 25%, virus crnih matičnjaka u 21,4% i Varroa destructor u 53,57% pčela dok virus akutne pčelinje paralize nije bio dokazan. Ovo je prvi dokaz prisutnosti virusa kronične pčelinje paralize i virusa crnih matičnjaka u Turskoj

Mechanical and radiation attenuation properties of conventional and heavy concrete with diverse aggregate and water/cement ratios

Ovim istraživanjem predstavljaju se rezultati sveobuhvatnog laboratorijskog rada kojemu je cilj ispitati mehanička svojstva i svojstva smanjenja zračenja teških betona u kojima se kao agregat koristio pirit, krom i magnetit te betona normalne težine koji su se proizveli s tri različita vodocementna omjera (v/c = 0,4/0,5/0,6). U laboratoriju su provedena ispitivanja tlačne čvrstoće, brzine prolaska ultrazvuka, eksperimentalni modul elastičnosti te koeficijenta prigušenja mase tih betona. Na temelju provedenih ispitivanja utvrđeno je da betoni normalne težine i teški betoni imaju slično ponašanje u smislu tlačne čvrstoće i modula elastičnosti. U slučaju teških betona (njihovi v/c omjeri povećani su uslijed konstantne količine vode te smanjene količine cementa), gustoća se povećava zbog povećanja količine agregata veće gustoće u odnosu na cement u sastavu betona. To je razlog zašto teški betoni koji su proizvedeni s većim v/c omjerom te koji su manje čvrstoće mogu apsorbirati više rendgenskih zraka. Koeficijenti prigušenja mase konvergiraju pri visokim energetskim razinama kod teških i normalnih betona različitih gustoća.This paper presents the results of comprehensive laboratory work conducted for investigating the mechanical and radiation attenuation characteristics of heavyweight concrete produced with pyrite, chromium, and magnetite aggregates and normal weight concretes produced with three different water/ cement (w/c) ratios. Various experiments were conducted to determine the compressive strengths, ultrasound transmission velocities, experimental elasticity modules, and mass attenuation coefficients of these concretes. Heavy and normal weight concretes exhibited similar behaviour in terms of compressive strength and elasticity modules. In heavyweight concretes, with increased w/c ratios (by keeping the amount of water constant and decreasing the amount of cement), the corresponding density increased due to the increase in the amount of high-density aggregates rather than cement in the composition of concrete. Thus, heavyweight concretes produced with a high w/c ratio and low strength can absorb more X-rays. Mass attenuation coefficients converge in heavy and normal weight concretes with different densities at high energy levels

Investigation and Expression Analysis of R2R3-MYBs and Anthocyanin Biosynthesis-Related Genes during Seed Color Development of Common Bean (Phaseolus vulgaris)

Anthocyanins are responsible for the coloration of common bean seeds, and their accumulation is positively correlated with the expression level of anthocyanin biosynthetic genes. The MBW (MYB-bHLH-WD40) complex is thought to regulate the expression of these genes, and MYB proteins, which are a key factor in activating anthocyanin pathway genes, have been identified in several plants. This study demonstrated gene structures, chromosomal placements, gene duplications of R2R3-MYBs, miRNAs associated with R2R3-MYBs, and the interaction of these genes with other flavonoid regulatory genes. qRT-PCR was used to investigate the role of specific R2R3-MYBs and flavonoid genes in common bean seed color development. As a result of a comprehensive analysis with the help of in silico tools, we identified 160 R2R3-MYB genes in the common bean genome. We divided these genes into 16 classes on the basis of their intron-exon and motif structures. Except for three, the rest of the common bean R2R3-MYB members were distributed to all chromosomes with different densities, primarily located on chromosomes 3 and 8. We identified a total of 44 duplicated gene pairs dispersed across 11 chromosomes and evolved under purifying selection (Ka/Ks  <  1), 19 of which were derived from a whole-genome duplication. Our research uncovered 25 putative repressor PvMYB proteins that contain the EAR motif. Additionally, fifty different cis-regulatory elements regulated by light, stress, and hormone were identified. Within the genome of the common bean, we discovered a total of 36 microRNAs that target a total of 72 R2R3-MYB transcripts. The effect of 16 R2R3-MYB genes and 16 phenylpropanoid pathway genes, selected on the basis of their interaction in the protein-protein interaction map, playing role in the regulation of seed coat color development was evaluated using qRT-PCR in 5 different tissues at different developmental stages. The results revealed that these specific genes have different expression levels during different developmental periods, with higher levels in the pod filling and early pod stages than in the rest of the developmental periods. Furthermore, it was shown that PvTT8 (bHLH), PvTT2 (PvMYB42), PvMYB113, PvTTG1, and PvWD68 genes have effects on the regulation of seed coat color. The findings of this study, which is the first to use whole-genome analysis to identify and characterize the R2R3-MYB genes in common bean, may serve as a reference for future functional research in the legume

Investigation and Expression Analysis of R2R3-MYBs and Anthocyanin Biosynthesis-Related Genes during Seed Color Development of Common Bean (Phaseolus vulgaris)

Anthocyanins are responsible for the coloration of common bean seeds, and their accumulation is positively correlated with the expression level of anthocyanin biosynthetic genes. The MBW (MYB-bHLH-WD40) complex is thought to regulate the expression of these genes, and MYB proteins, which are a key factor in activating anthocyanin pathway genes, have been identified in several plants. This study demonstrated gene structures, chromosomal placements, gene duplications of R2R3-MYBs, miRNAs associated with R2R3-MYBs, and the interaction of these genes with other flavonoid regulatory genes. qRT-PCR was used to investigate the role of specific R2R3-MYBs and flavonoid genes in common bean seed color development. As a result of a comprehensive analysis with the help of in silico tools, we identified 160 R2R3-MYB genes in the common bean genome. We divided these genes into 16 classes on the basis of their intron-exon and motif structures. Except for three, the rest of the common bean R2R3-MYB members were distributed to all chromosomes with different densities, primarily located on chromosomes 3 and 8. We identified a total of 44 duplicated gene pairs dispersed across 11 chromosomes and evolved under purifying selection (Ka/Ks  <  1), 19 of which were derived from a whole-genome duplication. Our research uncovered 25 putative repressor PvMYB proteins that contain the EAR motif. Additionally, fifty different cis-regulatory elements regulated by light, stress, and hormone were identified. Within the genome of the common bean, we discovered a total of 36 microRNAs that target a total of 72 R2R3-MYB transcripts. The effect of 16 R2R3-MYB genes and 16 phenylpropanoid pathway genes, selected on the basis of their interaction in the protein-protein interaction map, playing role in the regulation of seed coat color development was evaluated using qRT-PCR in 5 different tissues at different developmental stages. The results revealed that these specific genes have different expression levels during different developmental periods, with higher levels in the pod filling and early pod stages than in the rest of the developmental periods. Furthermore, it was shown that PvTT8 (bHLH), PvTT2 (PvMYB42), PvMYB113, PvTTG1, and PvWD68 genes have effects on the regulation of seed coat color. The findings of this study, which is the first to use whole-genome analysis to identify and characterize the R2R3-MYB genes in common bean, may serve as a reference for future functional research in the legume

Mortality from gastrointestinal congenital anomalies at 264 hospitals in 74 low-income, middle-income, and high-income countries: a multicentre, international, prospective cohort study

Summary Background Congenital anomalies are the fifth leading cause of mortality in children younger than 5 years globally. Many gastrointestinal congenital anomalies are fatal without timely access to neonatal surgical care, but few studies have been done on these conditions in low-income and middle-income countries (LMICs). We compared outcomes of the seven most common gastrointestinal congenital anomalies in low-income, middle-income, and high-income countries globally, and identified factors associated with mortality. Methods We did a multicentre, international prospective cohort study of patients younger than 16 years, presenting to hospital for the first time with oesophageal atresia, congenital diaphragmatic hernia, intestinal atresia, gastroschisis, exomphalos, anorectal malformation, and Hirschsprung’s disease. Recruitment was of consecutive patients for a minimum of 1 month between October, 2018, and April, 2019. We collected data on patient demographics, clinical status, interventions, and outcomes using the REDCap platform. Patients were followed up for 30 days after primary intervention, or 30 days after admission if they did not receive an intervention. The primary outcome was all-cause, in-hospital mortality for all conditions combined and each condition individually, stratified by country income status. We did a complete case analysis. Findings We included 3849 patients with 3975 study conditions (560 with oesophageal atresia, 448 with congenital diaphragmatic hernia, 681 with intestinal atresia, 453 with gastroschisis, 325 with exomphalos, 991 with anorectal malformation, and 517 with Hirschsprung’s disease) from 264 hospitals (89 in high-income countries, 166 in middleincome countries, and nine in low-income countries) in 74 countries. Of the 3849 patients, 2231 (58·0%) were male. Median gestational age at birth was 38 weeks (IQR 36–39) and median bodyweight at presentation was 2·8 kg (2·3–3·3). Mortality among all patients was 37 (39·8%) of 93 in low-income countries, 583 (20·4%) of 2860 in middle-income countries, and 50 (5·6%) of 896 in high-income countries (p<0·0001 between all country income groups). Gastroschisis had the greatest difference in mortality between country income strata (nine [90·0%] of ten in lowincome countries, 97 [31·9%] of 304 in middle-income countries, and two [1·4%] of 139 in high-income countries; p≤0·0001 between all country income groups). Factors significantly associated with higher mortality for all patients combined included country income status (low-income vs high-income countries, risk ratio 2·78 [95% CI 1·88–4·11], p<0·0001; middle-income vs high-income countries, 2·11 [1·59–2·79], p<0·0001), sepsis at presentation (1·20 [1·04–1·40], p=0·016), higher American Society of Anesthesiologists (ASA) score at primary intervention (ASA 4–5 vs ASA 1–2, 1·82 [1·40–2·35], p<0·0001; ASA 3 vs ASA 1–2, 1·58, [1·30–1·92], p<0·0001]), surgical safety checklist not used (1·39 [1·02–1·90], p=0·035), and ventilation or parenteral nutrition unavailable when needed (ventilation 1·96, [1·41–2·71], p=0·0001; parenteral nutrition 1·35, [1·05–1·74], p=0·018). Administration of parenteral nutrition (0·61, [0·47–0·79], p=0·0002) and use of a peripherally inserted central catheter (0·65 [0·50–0·86], p=0·0024) or percutaneous central line (0·69 [0·48–1·00], p=0·049) were associated with lower mortality. Interpretation Unacceptable differences in mortality exist for gastrointestinal congenital anomalies between lowincome, middle-income, and high-income countries. Improving access to quality neonatal surgical care in LMICs will be vital to achieve Sustainable Development Goal 3.2 of ending preventable deaths in neonates and children younger than 5 years by 2030

Yeni Benzimidazol Türevlerinin Sentezi

Tez (Yüksek lisans) -- Giresun Üniversitesi. Kaynakça var.ıx , 55 s. ; 28 cm.Demirbaş: 0063491