173 research outputs found
Quaternary TDM-PAM as upgrade path of access PON beyond 10Gb/s
A 20 Gb/s quaternary TDM-PAM passive optical network with chirped and non-linear optical transmitters is experimentally demonstrated. The migration from legacy TDM-PONs and the implications of using available 10 Gb/s components are analyzed. We show that a loss budget of 27.3 dB is compatible together with a packet power ratio of 10 dB between loud and soft optical network units. (c) 2012 Optical Society of Americ
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Endometrial changes in estrogen and progesterone receptor expression during implantation in an oocyte donation program
Implantation is the final and most important stage of embryogenesis and is of paramount importance in achieving a successful pregnancy. Progesterone and estrogen are steroid hormones responsible for the regulation of the implantation window and the current study hypothesised that their receptors may be implicated in women undergoing oocyte donation. A total of 15 women aged 25‑32 years old (mean ± SD, 28.9±2.89) undergoing oocyte donation were recruited into the present study. Participants underwent ovarian stimulation with gonadotrophin‑releasing hormone antagonist and recombinant follicle‑stimulating hormone. Endometrial aspiration biopsy was performed on the day of oocyte retrieval and after 5 days (on days 0 and 5, respectively). Endometrial histology and evaluation of estrogen receptor (ER)α and progesterone receptor (PR)‑B were performed on days 0 and 5. The ER nodal staining percentage on day 0 was age‑associated, with patients aged 30 years exhibiting 90% staining. Pathological staining revealed statistically significant differences between days 0 and 5 following all staining procedures. Wilcoxon signed‑rank test resulted in the following P‑values, for ER (nodes % and stromal %) day 0/5, P=0.0001; for PR (nodes % and stromal %) day 0/5, P=0.0001 and P=0.035, respectively; for ER (grade nodes and stromal %) day 0/5, P=0.0001; and PR (grade nodes and stromal %) day 0/5 P=0.0001 and P=0.016, respectively. Synchronization between blastocyst development and the acquisition of endometrial receptivity is a prerequisite for the success of in vitro fertilisation (IVF). Aside from the recent discovery of molecules that are considered crucial for successful embryo implantation, assessing the functional characteristics of the endometrium may offer unique insights into this process, thus improving IVF results
Electrochemotherapy with bleomycin and cisplatin enhances cytotoxicity in primary and metastatic uveal melanoma cell lines in vitro
Host cell entry mediators implicated in the cellular tropism of SARS‑CoV‑2, the pathophysiology of COVID‑19 and the identification of microRNAs that can modulate the expression of these mediators (Review)
Copyright: © Katopodis et al. The pathophysiology of coronavirus disease 2019 (COVID‑19) is mainly dependent on the underlying mechanisms that mediate the entry of severe acute respiratory syndrome coronavirus 2 (SARS‑CoV‑2) into the host cells of the various human tissues/organs. Recent studies have indicated a higher order of complexity of the mechanisms of infectivity, given that there is a wide‑repertoire of possible cell entry mediators that appear to co‑localise in a cell‑ and tissue‑specific manner. The present study provides an overview of the ‘canonical’ SARS‑CoV‑2 mediators, namely angiotensin converting enzyme 2, transmembrane protease serine 2 and 4, and neuropilin‑1, expanding on the involvement of novel candidates, including glucose‑regulated protein 78, basigin, kidney injury molecule‑1, metabotropic glutamate receptor subtype 2, ADAM metallopeptidase domain 17 (also termed tumour necrosis factor‑α convertase) and Toll‑like receptor 4. Furthermore, emerging data indicate that changes in microRNA (miRNA/miR) expression levels in patients with COVID‑19 are suggestive of further complexity in the regulation of these viral mediators. An in silico analysis revealed 160 candidate miRNAs with potential strong binding capacity in the aforementioned genes. Future studies should concentrate on elucidating the association between the cellular tropism of the SARS‑CoV‑2 cell entry mediators and the mechanisms through which they might affect the clinical outcome. Finally, the clinical utility as a biomarker or therapeutic target of miRNAs in the context of COVID‑19 warrants further investigation
P5: Event-driven Policy Framework for P4-based Traffic Engineering
We present P5, an event-driven policy framework that allows network operators to realize end-to-end policies on top of P4-based data planes in an intuitive and effective manner. We demonstrate how P5 adheres to a service-level agreement (SLA) by applying P4-based traffic engineering with latency constraints
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In silico and in vitro analysis of lncRNA XIST reveals a panel of possible lung cancer regulators and a five-gene diagnostic signature
© 2020 by the authors. Long non-coding RNAs (lncRNAs) perform a wide functional repertoire of roles in cell biology, ranging from RNA editing to gene regulation, as well as tumour genesis and tumour progression. The lncRNA X-inactive specific transcript (XIST) is involved in the aetiopathogenesis of non-small cell lung cancer (NSCLC). However, its role at the molecular level is not fully elucidated. The expression of XIST and co-regulated genes TSIX, hnRNPu, Bcl-2, and BRCA1 analyses in lung cancer (LC) and controls were performed in silico. Differentially expressed genes (DEGs) were determined using RNA-seq in H1975 and A549 NSCLC cell lines following siRNA for XIST. XIST exhibited sexual dimorphism, being up-regulated in females compared to males in both control and LC patient cohorts. RNA-seq revealed 944 and 751 DEGs for A549 and H1975 cell lines, respectively. These DEGs are involved in signal transduction, cell communication, energy pathways, and nucleic acid metabolism. XIST expression associated with TSIX, hnRNPu, Bcl-2, and BRCA1 provided a strong collective feature to discriminate between controls and LC, implying a diagnostic potential. There is a much more complex role for XIST in lung cancer. Further studies should concentrate on sex-specific changes and investigate the signalling pathways of the DEGs following silencing of this lncRNA
Protein expression of transmembrane protease serine 4 in the gastrointestinal tract and in healthy, cancer, and SARS‑CoV‑2 infected lungs
Availability of data and materials:
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.Copyright: © Kerslake et al. In addition to the angiotensin‑converting enzyme 2 (ACE2), a number of host cell entry mediators have been identified for severe acute respiratory syndrome coronavirus‑2 (SARS‑CoV‑2), including transmembrane protease serine 4 (TMPRSS4). The authors have recently demonstrated the upregulation of TMPRSS4 in 11 different cancers, as well as its specific expression within the central nervous system using in silico tools. The present study aimed to expand the initial observations and, using immunohistochemistry, TMPRSS4 protein expression in the gastrointestinal (GI) tract and lungs was further mapped. Immunohistochemistry was performed on tissue arrays and lung tissues of patients with non‑small cell lung cancer with concurrent coronavirus disease 2019 (COVID‑19) infection using TMPRSS4 antibody. The results revealed that TMPRSS4 was abundantly expressed in the oesophagus, stomach, small intestine, jejunum, ileum, colon, liver and pancreas. Moreover, the extensive TMPRSS4 protein expression in the lungs of a deceased patient with COVID‑19 with chronic obstructive pulmonary disease and bronchial carcinoma, as well in the adjacent normal tissue, was demonstrated for the first time, at least to the best of our knowledge. On the whole, the immunohistochemistry data of the present study suggest that TMPRSS4 may be implicated in the broader (pulmonary and extra‑pulmonary) COVID‑19 symptomatology; thus, it may be responsible for the tropism of this coronavirus both in the GI tract and lungs.Cancer Treatment and Research Trust; University Hospitals Coventry and Warwickshire NHS Trust (grant no. 12899)
LogicWiSARD: Memoryless synthesis of weightless neural networks
Weightless neural networks (WNNs) are an alternative pattern recognition technique where RAM nodes function as neurons. As both training and inference require mostly table lookups, few additions, and no multiplications, WNNs are suitable for high-performance and low-power embedded applications. This work introduces a novel approach to implement WiSARD, the leading WNN state-of-the-art architecture, completely eliminating memories and arithmetic circuits and utilizing only logic functions. The approach creates compressed minimized implementations by converting trained WNN nodes from lookup tables to logic functions. The proposed LogicWiSARD is implemented in FPGA and ASIC technologies to illustrate its suitability for edge inference. Experimental results show more than 80% reduction in energy consumption when the proposed LogicWiSARD model is compared with a multilayer perceptron network (MLP) of equivalent accuracy. Compared to previous work on FPGA implementations for WNNs, convolutional neural networks, and binary neural networks, the energy savings of LogicWiSARD range between 32.2% and 99.6%.info:eu-repo/semantics/acceptedVersio
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COVID‑19 and SARS‑CoV‑2 host cell entry mediators: Expression profiling of TMRSS4 in health and disease
Copyright: © Katopodis et al. Severe acute respiratory syndrome (SARS) coronavirus‑2 (SARS‑CoV‑2), the causative viral agent for the ongoing COVID‑19 pandemic, enters its host cells primarily via the binding of the SARS‑CoV‑2 spike (S) proteins to the angiotensin‑converting enzyme 2 (ACE2). A number of other cell entry mediators have also been identified, including neuropilin‑1 (NRP1) and transmembrane protease serine 2 (TMPRSS2). More recently, it has been demonstrated that transmembrane protease serine 4 (TMPRSS4) along with TMPRSS2 activate the SARS‑CoV‑2 S proteins, and enhance the viral infection of human small intestinal enterocytes. To date, a systematic analysis of TMPRSS4 in health and disease is lacking. In the present study, using in silico tools, the gene expression and genetic alteration of TMPRSS4 were analysed across numerous tumours and compared to controls. The observations were also expanded to the level of the central nervous system (CNS). The findings revealed that TMPRSS4 was overexpressed in 11 types of cancer, including lung adenocarcinoma, lung squamous cell carcinoma, cervical squamous cell carcinoma, thyroid carcinoma, ovarian cancer, cancer of the rectum, pancreatic cancer, colon and stomach adenocarcinoma, uterine carcinosarcoma and uterine corpus endometrial carcinoma, whilst it was significantly downregulated in kidney carcinomas, acute myeloid leukaemia, skin cutaneous melanoma and testicular germ cell tumours. Finally, a high TMPRSS4 expression was documented in the olfactory tubercle, paraolfactory gyrus and frontal operculum, all brain regions which are associated with the sense of smell and taste. Collectively, these data suggest that TMPRSS4 may play a role in COVID‑19 symptomatology as another SARS‑CoV‑2 host cell entry mediator responsible for the tropism of this coronavirus both in the periphery and the CNS
Corner and sloped culvert baffles improve the upstream passage of adult European eels (Anguilla anguilla)
Installation of baffles intended to improve fish passage through culverts can reduce discharge capacity and trap debris, increasing flood risk. A sloping upstream face may reduce this risk, but new designs must be tested for fish passage efficiency. The European eel (Anguilla anguilla) is a critically endangered species, yet the suitability of even common baffle types to aid upstream movement has not been tested. This study compared the water depth, velocity, turbulent kinetic energy (TKE), and upstream passage performance of adult yellow-phase eels, between three 6 m long culvert models: smooth and unmodified (control); containing corner baffles (treatment 1); and with prototype sloped baffles installed (treatment 2). Passage of individual fish was assessed during 25 one-hour trials per model. Performance was quantified as entrance efficiency, number of entries per fish, passage efficiency, and overall efficiency. Total and passage delay, and successful passage time were also evaluated. Despite some individuals being able to swim against unexpectedly high water velocities (>1.5 m s?1 for 4 m), passage performance in the control was poor, with an overall efficiency of 28%. Compared to the control, both treatments increased the mean centreline water depth by approximately 0.11 m, created heterogeneous flow conditions with low velocity resting areas, and reduced maximum velocities. As a result, entrance rate and all efficiency parameters were higher for the treatments than for the control (overall efficiency = 84%), despite longer passage delay. The TKE was slightly higher in treatment 2 than 1, but there was no difference in water depth or overall efficiency. The findings show that both corner and sloped baffles can mitigate for impeded upstream adult eel movement. The extent to which the sloping upstream face will improve debris transport should be explored further
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