265 research outputs found

    Wireless Throughput and Energy Efficiency under QoS Constraints

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    Mobile data traffic has experienced unprecedented growth recently and is predicted to grow even further over the coming years. As one of the main driving forces behind this growth, wireless transmission of multimedia content has significantly increased in volume and is expected to be the dominant traffic in data communications. Such wireless multimedia traffic requires certain quality-of-service (QoS) guarantees. With these motivations, in the first part of the thesis, throughput and energy efficiency in fading channels are studied in the presence of randomly arriving data and statistical queueing constraints. In particular, Markovian arrival models including discrete-time Markov, Markov fluid, and Markov-modulated Poisson sources are considered, and maximum average arrival rates in the presence of statistical queueing constraints are characterized. Furthermore, energy efficiency is analyzed by determining the minimum energy per bit and wideband slope in the low signal-to-noise ratio (SNR) regime. Following this analysis, energy-efficient power adaptation policies in fading channels are studied when data arrivals are modeled as Markovian processes and statistical QoS constraints are imposed. After formulating energy efficiency (EE) as maximum throughput normalized by the total power consumption, optimal power control policies that maximize EE are obtained for different source models. Next, throughput and energy efficiency of secure wireless transmission of delay sensitive data generated by random sources are investigated. A fading broadcast model in which the transmitter sends confidential and common messages to two receivers is considered. It is assumed that the common and confidential data, generated from Markovian sources, is stored in buffers prior to transmission, and the transmitter operates under constraints on buffer/delay violation probability. Under such statistical QoS constraints, the throughput is determined. In particular, secrecy capacity is used to describe the service rate of buffers containing confidential messages. Moreover, energy efficiency is studied in the low signal-to-noise (SNR) regime. In the final part of the thesis, throughput and energy efficiency are addressed considering the multiuser channel models. Five different channel models, namely, multiple access, broadcast, interference, relay and cognitive radio channels, are considered. In particular, throughput regions of multiple-access fading channels are characterized when multiple users, experiencing random data arrivals, transmit to a common receiver under statistical QoS constraints. Throughput regions of fading broadcast channels with random data arrivals in the presence of QoS requirements are studied when power control is employed at the transmitter. It is assumed that superposition coding with power control is performed at the transmitter with interference cancellation at the receivers. Optimal power control policies that maximize the weighted combination of the average arrival rates are investigated in the two-user case. Energy efficiency in two-user fading interference channels is studied when the transmitters are operating subject to QoS constraints. Specifically, energy efficiency is characterized by determining the corresponding minimum energy per bit requirements and wideband slope regions. Furthermore, transmission over a half-duplex relay channel with secrecy and QoS constraints is studied. Secrecy throughput is derived for the half duplex two-hop fading relay system operating in the presence of an eavesdropper. Fundamental limits on the energy efficiency of cognitive radio transmissions are analyzed in the presence of statistical quality of service (QoS) constraints. Minimum energy per bit and wideband slope expressions are obtained in order to identify the performance limits in terms of energy efficiency

    Clinical importance of serum and pleural fluid prominin-1 and hypoxia-inducible factor-1α concentration in the evaluation of lymph node involvement in patients with malignant pleural effusion

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    IntroductionMalignant pleural effusion (MPE) and lymph node metastasis (LNM) presence are poor prognostic factors that have importance for cancer patients. The study objective was to determine whether hypoxia-inducible factor-1α (HIF-1α) and prominin-1 (CD133) in pleural fluid (P) and serum (S) could be used as biomarkers for diagnosis of lymph node involvement in patients with MPE. Materials and methodsFifty-six patients with MPE and 30 healthy control subjects were included. Computerized tomography (CT) and positron emission tomography (PET) were used to diagnose pleural effusion. Patients with malignant cells in pleural fluid cytological examination were included in the MPE group. Thirty-five patients with lymph node metastases on CT were included in the LNM-positive MPE group. Serum and pleural fluid HIF-1α and CD-133 concentrations were measured manually via enzyme-linked immunosorbent assay (ELISA). ResultsSerum concentrations of HIF-1α and CD133 were higher in MPE patients. It was found that CD133/HIF-1α (S) ratio was higher in the malignant patient group with positive lymph node involvement than in the negative group, while concentrations of HIF-1α (P) were lower. Pleural fluid HIF-1α and CD133/HIF-1α (S) ratio had sufficient performance in diagnosing lymphatic metastases in patients with MPE (AUC = 0.90 and 0.83, respectively). ConclusionsIn conclusion, serum HIF-1α and CD133 concentrations were higher in patients with MPE, consistent with our hypothesis. Concentrations of HIF-1α (P) and CD133/HIF-1α (S) ratio can be used as biomarkers in diagnosing lymph node involvement in MPE patients, according to this experiment

    Investigation of Poison Gland of Sphex flavipennis Fabrius, 1793 Hymenoptera: Sphecidae : Morphology and Ultrastructure

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    T he structure of poison gland of Sphex flavipennis was investigated by using, scannig electron microscopy and transmission electron microscopy. Poison apparatus consists of poison gland, poison sac, Dufour’s gland and poison needle. Poison is produced in a gland consisting of two ramified glandular tubules terminating in a common sac. Each tubule is 6-8 mm in length and approximately 90 μm in diameter. These tubules are lined with the secretory cells and duct cells. The secretory cells have a well-developed secretory unit which is open to the lumen of tubules. In addition, there are free ribosomes, large secretory vesicle and a few mitochondria in the cells. Apical surface of cells are lined by irregular microvilli. Glandular tubules go into pear-like sac. Apical surface of the cells in the poison sac are lined cuticle. Outer surface of poison sac is surrounded muscle fibril and connective tissue. Lumen side of glandular tubules and poison sac are surrounded with monolayer epithelial cell

    Proton density fat fraction: magnetic resonance imaging applications beyond the liver

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    Magnetic resonance imaging-proton density fat fraction (MRI-PDFF) is an emerging quantitative imaging biomarker that accurately measures the fat fraction of tissue by correcting factors influencing magnetic resonance signal intensity. Beyond fat quantification, it also measures R2* which is a direct measure of iron concentration. The utilization of MRI-PDFF in liver diseases is well established. In the present review, we focused on applications of MRI-PDFF in different body areas including pancreas, bone, muscle, spleen, testis, visceral, and subcutaneous adipose tissue. Future studies can enable tracking of quantitative fat fraction changes in different organs simultaneously, which can be critical in understanding fat metabolism

    Antimicrobial resistance among migrants in Europe: a systematic review and meta-analysis

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    BACKGROUND: Rates of antimicrobial resistance (AMR) are rising globally and there is concern that increased migration is contributing to the burden of antibiotic resistance in Europe. However, the effect of migration on the burden of AMR in Europe has not yet been comprehensively examined. Therefore, we did a systematic review and meta-analysis to identify and synthesise data for AMR carriage or infection in migrants to Europe to examine differences in patterns of AMR across migrant groups and in different settings. METHODS: For this systematic review and meta-analysis, we searched MEDLINE, Embase, PubMed, and Scopus with no language restrictions from Jan 1, 2000, to Jan 18, 2017, for primary data from observational studies reporting antibacterial resistance in common bacterial pathogens among migrants to 21 European Union-15 and European Economic Area countries. To be eligible for inclusion, studies had to report data on carriage or infection with laboratory-confirmed antibiotic-resistant organisms in migrant populations. We extracted data from eligible studies and assessed quality using piloted, standardised forms. We did not examine drug resistance in tuberculosis and excluded articles solely reporting on this parameter. We also excluded articles in which migrant status was determined by ethnicity, country of birth of participants' parents, or was not defined, and articles in which data were not disaggregated by migrant status. Outcomes were carriage of or infection with antibiotic-resistant organisms. We used random-effects models to calculate the pooled prevalence of each outcome. The study protocol is registered with PROSPERO, number CRD42016043681. FINDINGS: We identified 2274 articles, of which 23 observational studies reporting on antibiotic resistance in 2319 migrants were included. The pooled prevalence of any AMR carriage or AMR infection in migrants was 25·4% (95% CI 19·1-31·8; I2 =98%), including meticillin-resistant Staphylococcus aureus (7·8%, 4·8-10·7; I2 =92%) and antibiotic-resistant Gram-negative bacteria (27·2%, 17·6-36·8; I2 =94%). The pooled prevalence of any AMR carriage or infection was higher in refugees and asylum seekers (33·0%, 18·3-47·6; I2 =98%) than in other migrant groups (6·6%, 1·8-11·3; I2 =92%). The pooled prevalence of antibiotic-resistant organisms was slightly higher in high-migrant community settings (33·1%, 11·1-55·1; I2 =96%) than in migrants in hospitals (24·3%, 16·1-32·6; I2 =98%). We did not find evidence of high rates of transmission of AMR from migrant to host populations. INTERPRETATION: Migrants are exposed to conditions favouring the emergence of drug resistance during transit and in host countries in Europe. Increased antibiotic resistance among refugees and asylum seekers and in high-migrant community settings (such as refugee camps and detention facilities) highlights the need for improved living conditions, access to health care, and initiatives to facilitate detection of and appropriate high-quality treatment for antibiotic-resistant infections during transit and in host countries. Protocols for the prevention and control of infection and for antibiotic surveillance need to be integrated in all aspects of health care, which should be accessible for all migrant groups, and should target determinants of AMR before, during, and after migration. FUNDING: UK National Institute for Health Research Imperial Biomedical Research Centre, Imperial College Healthcare Charity, the Wellcome Trust, and UK National Institute for Health Research Health Protection Research Unit in Healthcare-associated Infections and Antimictobial Resistance at Imperial College London
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