140 research outputs found
Implementing and Characterizing Real-time Broadband RFI Excision for the GMRT Wideband Backend
The Giant Metrewave Radio Telescope (GMRT) is being upgraded to increase the
receiver sensitivity. This makes the receiver more susceptible to man-made
Radio Frequency Interference (RFI). To improve the receiver performance in
presence of RFI, real-time RFI excision (filtering) is incorporated in the GMRT
wideband backend (GWB). The RFI filtering system is implemented on FPGA and
CPU-GPU platforms to detect and remove broadband and narrowband RFI. The RFI is
detected using a threshold-based technique where the threshold is computed
using Median Absolute Deviation (MAD) estimator. The filtering is carried out
by replacing the RFI samples by either noise samples or constant value or
threshold. This paper describes the status of the real-time broadband RFI
excision system in the wideband receiver chain of the upgraded GMRT (uGMRT).
The test methodology for carrying out various tests to demonstrate the
performance of broadband RFI excision at the system level and on radio
astronomical imaging experiments are also described.Comment: 7 pages, 7 figure
Tunable Oscillations in the Purkinje Neuron
In this paper, we study the dynamics of slow oscillations in Purkinje neurons
in vitro, and derive a strong association with a forced parametric oscillator
model. We demonstrate the precise rhythmicity of the oscillations in Purkinje
neurons, as well as a dynamic tunability of this oscillation using a
photo-switchable compound. We show that this slow oscillation can be induced in
every Purkinje neuron, having periods ranging between 10-25 seconds. Starting
from a Hodgkin-Huxley model, we also demonstrate that this oscillation can be
externally modulated, and that the neurons will return to their intrinsic
firing frequency after the forced oscillation is concluded. These results
signify an additional functional role of tunable oscillations within the
cerebellum, as well as a dynamic control of a time scale in the brain in the
range of seconds.Comment: 12 pages, 5 figure
Primary fallopian tube carcinoma: review of MR imaging findings
Objectives To review the epidemiological and clinical features of primary fallopian tube carcinoma (PFTC), and to illustrate the spectrum of MRI findings, with pathological confirmation. Methods This article reviews the relevant literature on the epidemiological, clinical, and imaging features of primary fallopian tube carcinoma, with pathological confirmation, using illustrations from the authors' teaching files. Results Primary fallopian tube carcinoma came under focus over the last few years due to its possible role on the pathogenesis of high-grade serous epithelial ovarian and peritoneal cancers. Typical symptoms, together with the presence of some of the most characteristic MRI signs, such as a "sausage-shaped" pelvic mass, hydrosalpinx, and hydrometra, may signal the presence of primary fallopian cancer, and allow the radiologist to report it as a differential diagnosis. Conclusions Primary fallopian tube carcinoma has a constellation of clinical symptoms and magnetic resonance imaging features, which may be diagnostic. Although these findings are not present together in the majority of cases, radiologists who are aware of them may include the diagnosis of primary fallopian tube cancer in their report more frequently and with more confidence. Teaching Points PFTC may be more frequent than previously thought PFTC has specific clinical and MRI characteristics Knowledge of typical PFTC signs enables its inclusion in the differential diagnosis PFTC is currently staged under the 2013 FIGO system PFTC is staged collectively with ovarian and peritoneal neoplasmsinfo:eu-repo/remantics/publishedVersio
Comparative Dissolution Profile Study Of Aciclovir In Solid Dosage Formulations
This study compares the in vitro efficacy of two distinct brands of acyclovir tablets with the same strength—ACYPROVE-200 (Aciclovir Tablet IP) and ZOVIRAX TABLETS (Aciclovir Tablet IP200MG).Friability, hardness, thickness, solubility, and weight fluctuation tests are only a few of the many comparisons. The most crucial test that enables us to ascertain the precise concentration of the active ingredient (acyclovir) in every capsule and the quantity of medication discharged from these formulations is the dissolution test.Because of its great solubility and limited permeability, the medication aciclovir is categorized as Class III in the BCS classification.Dissolution tests were conducted in acid medium, pH 4.5 buffer medium, and pH 6.8 buffer medium in this study. The dissolution rate is determined by measuring the amount of medication released at intervals of 10, 15, and 30 minutes. The results also show the similarity and difference between the two products.The study concludes that there is a range of 0–15 and 50–100 for the Difference factor (f1) and Similarity factor (f2) between "ACYPROVE-200 (Aciclovir Tablet IP) and ZOVIRAX TABLETS (Aciclovir Tablet IP200MG).
Fast imaging employing steady-state acquisition (FIESTA) MRI to investigate cerebrospinal fluid (CSF) within dural reflections of posterior fossa cranial nerves
: There is no consensus approach to covering skull base meningeal reflections-and cerebrospinal fluid (CSF) therein-of the posterior fossa cranial nerves (CNs VII-XII) when planning radiotherapy (RT) for medulloblastoma and ependymoma. We sought to determine whether MRI and specifically fast imaging employing steady-state acquisition (FIESTA) sequences can answer this anatomical question and guide RT planning.
: 96 posterior fossa FIESTA sequences were reviewed. Following exclusions, measurements were made on the following scans for each foramen respectively (left, right); internal acoustic meatus (IAM) (86, 84), jugular foramen (JF) (83, 85) and hypoglossal canal (HC) (42, 45). A protocol describes measurement procedure. Two observers measured distances for five cases and agreement was assessed. One observer measured all the remaining cases.
: IAM and JF measurement interobserver variability was compared. Mean measurement difference between observers was -0.275 mm (standard deviation 0.557). IAM and JF measurements were normally distributed. Mean IAM distance was 12.2 mm [95% confidence interval (CI) 8.8-15.6]; JF was 7.3 mm (95% CI 4.0-10.6). The HC was difficult to visualize on many images and data followed a bimodal distribution.
: Dural reflections of posterior fossa CNs are well demonstrated by FIESTA MRI. Measuring CSF extension into these structures is feasible and robust; mean CSF extension into IAM and JF was measured. We plan further work to assess coverage of these structures with photon and proton RT plans.
: We have described CSF extension beyond the internal table of the skull into the IAM, JF and HC. Oncologists planning RT for patients with medulloblastoma and ependymoma may use these data to guide contouring.DJN is currently funded by Addenbrooke's Charitable Trust with future funding from Cancer Research UK via the Cambridge Cancer Centre
Microbial community composition of deep-sea corals from the Red Sea provides insight into functional adaption to a unique environment
Microbes associated with deep-sea corals remain poorly studied. The lack of symbiotic algae suggests that associated microbes may play a fundamental role in maintaining a viable coral host via acquisition and recycling of nutrients. Here we employed 16 S rRNA gene sequencing to study bacterial communities of three deep-sea scleractinian corals from the Red Sea, Dendrophyllia sp., Eguchipsammia fistula, and Rhizotrochus typus. We found diverse, species-specific microbiomes, distinct from the surrounding seawater. Microbiomes were comprised of few abundant bacteria, which constituted the majority of sequences (up to 58% depending on the coral species). In addition, we found a high diversity of rare bacteria (taxa at 90% of all bacteria). Interestingly, we identified anaerobic bacteria, potentially providing metabolic functions at low oxygen conditions, as well as bacteria harboring the potential to degrade crude oil components. Considering the presence of oil and gas fields in the Red Sea, these bacteria may unlock this carbon source for the coral host. In conclusion, the prevailing environmental conditions of the deep Red Sea (>20 °C, <2 mg oxygen L−1) may require distinct functional adaptations, and our data suggest that bacterial communities may contribute to coral functioning in this challenging environment.This work was supported from baseline funds to CRV and under the Center Competitive Funding
(CCF) Program FCC/1/1973-18-01 by the King Abdullah University of Science and Technology (KAUST)
Results of a single-arm pilot study of 32P microparticles in unresectable locally advanced pancreatic adenocarcinoma with gemcitabine/nab-paclitaxel or FOLFIRINOX chemotherapy.
BACKGROUND: Unresectable locally advanced pancreatic cancer (LAPC) is generally managed with chemotherapy or chemoradiotherapy, but prognosis is poor with a median survival of ∼13 months (or up to 19 months in some studies). We assessed a novel brachytherapy device, using phosphorous-32 (32P) microparticles, combined with standard-of-care chemotherapy. PATIENTS AND METHODS: In this international, multicentre, single-arm, open-label pilot study, adult patients with histologically or cytologically proven unresectable LAPC received 32P microparticles, via endoscopic ultrasound-guided fine-needle implantation, planned for week 4 of 5-fluorouracil, leucovorin, irinotecan and oxaliplatin (FOLFIRINOX) or gemcitabine/nab-paclitaxel chemotherapy, per investigator's choice. The primary endpoint was safety and tolerability measured using Common Terminology Criteria for Adverse Events version 4.0. The lead efficacy endpoint was local disease control rate at 16 weeks. RESULTS: Fifty patients were enrolled and received chemotherapy [intention-to-treat (ITT) population]. Forty-two patients received 32P microparticle implantation [per protocol (PP) population]. A total of 1102 treatment-emergent adverse events (TEAEs) were reported in the ITT/safety population (956 PP), of which 167 (139 PP) were grade ≥3. In the PP population, 41 TEAEs in 16 (38.1%) patients were possibly or probably related to 32P microparticles or implantation procedure, including 8 grade ≥3 in 3 (7.1%) patients, compared with 609 TEAEs in 42 (100%) patients attributed to chemotherapy, including 67 grade ≥3 in 28 patients (66.7%). The local disease control rate at 16 weeks was 82.0% (95% confidence interval: 68.6% to 90.9%) (ITT) and 90.5% (95% confidence interval: 77.4% to 97.3%) (PP). Tumour volume, carbohydrate antigen 19-9 levels, and metabolic tumour response at week 12 improved significantly. Ten patients (20.0% ITT; 23.8% PP) had surgical resection and median overall survival was 15.2 and 15.5 months for ITT and PP populations, respectively. CONCLUSIONS: Endoscopic ultrasound-guided 32P microparticle implantation has an acceptable safety profile. This study also suggests clinically relevant benefits of combining 32P microparticles with standard-of-care systemic chemotherapy for patients with unresectable LAPC
Serum NT-pro BNP estimation for diagnosis of cardiac diseases in dogs withand without Holter Electrocardiographic arrhythmias
The study was conducted with an objective torule out the dogs presented with a complaint of
clinical signs suggestive of cardiac disease. A total of 14 animals were chosenfor theassessment of
serum NT-pro BNP level. The animals were grouped into to group 1 with Holterelectrocardiographic
arrhythmias and group 2 without Holterelectrocardiographic arrhythmias. Group 1 showed
significant increase in the NT-pro BNP levels in contrast to the control and group 2 animals. NT-pro
BNP estimation in screening of dogs suspected for cardiac sickness was found to be reliable step
when done concurrently withother diagnostic tests
Imaging response assessment for CNS germ cell tumours: consensus recommendations from the European Society for Paediatric Oncology Brain Tumour Group and North American Children's Oncology Group
Homogeneous and common objective disease assessments and standardised response criteria are important for better international clinical trials for CNS germ cell tumours. Currently, European protocols differ from those of North America (the USA and Canada) in terms of criteria to assess radiological disease response. An international working group of the European Society for Paediatric Oncology Brain Tumour Group and North American Children's Oncology Group was therefore established to review existing literature and current practices, identify major challenges regarding imaging assessment, and develop consensus recommendations for imaging response assessment for patients with CNS germ cell tumours. New clinical imaging standards were defined for the most common sites of CNS germ cell tumour and for the definition of locoregional extension. These new standards will allow the evaluation of response to therapy in patients with CNS germ cell tumours to be more consistent, and facilitate direct comparison of treatment outcomes across international studies
Isolation and characterization of a novel 2-sec-butylphenol-degrading bacterium Pseudomonas sp. strain MS-1
A novel bacterium capable of utilizing 2-sec-butylphenol as the sole carbon and energy source, Pseudomonas sp. strain MS-1, was isolated from freshwater sediment. Within 30 h, strain MS-1 completely degraded 1.5 mM 2-sec-butylphenol in basal salt medium, with concomitant cell growth. A pathway for the metabolism of 2-sec-butylphenol by strain MS-1 was proposed on the basis of the identification of 3 internal metabolites—3-sec-butylcatechol, 2-hydroxy-6-oxo-7-methylnona-2,4-dienoic acid, and 2-methylbutyric acid—by gas chromatography-mass spectrometry analysis. Strain MS-1 degraded 2-sec-butylphenol through 3-sec-butylcatechol along a meta-cleavage pathway. Degradation experiments with various alkylphenols showed that the degradability of alkylphenols by strain MS-1 depended strongly on the position (ortho ≫ meta = para) of the alkyl substitute, and that strain MS-1 could degrade 2-alkylphenols with various sized and branched alkyl chain (o-cresol, 2-ethylphenol, 2-n-propylphenol, 2-isopropylphenol, 2-sec-butylphenol, and 2-tert-butylphenol), as well as a dialkylphenol (namely, 6-tert-butyl-m-cresol)
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