64 research outputs found

    WLAN CSMA/CA Performance in a Bluetooth Interference Environment

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    IEEE 802.11 WLANs and Bluetooth piconets both operate in the 2.4 GHz Industrial Scientific and Medical (ISM) radio band. When operating in close proximity, these two technologies interfere with each other. Current literature suggests that IEEE 802.11 (employing direct sequence spread spectrum technology) is more susceptible to this interference than Bluetooth, which uses frequency hopping spread spectrum technology, resulting in reduced throughput. Current research tends to focus on the issue of packet collisions, and not the fact that IEEE 802.11 may also delay its transmissions while the radio channel is occupied by a Bluetooth signal. This research characterizes previously neglected transmission delay effects. Through analytic modeling and simulation, the impact of this interference is determined to identify all facets of the interference issues. Results show that Bluetooth-induced transmission delays improve network performance in many scenarios. When isolating delay effects, the likelihood that WLAN STA signals collide with each other decreases, causing an overall increase in normalized throughput and decrease in expected delay for many network configurations. As wireless communication technologies become an integral part of national defense, it is imperative to understand every performance characteristic. For instance, if the Air Force uses IEEE 802.11 and wants to incorporate a Bluetooth piconet as well, the impact of concurrent operation should be known beforehand. Since IEEE 802.11 and Bluetooth technologies could become vital for the Air Force to maintain its position of air superiority, all the strengths, weaknesses, and limitations of these systems should be understood

    Principal role of adenylyl cyclase 6 in K+ channel regulation and vasodilator signalling in vascular smooth muscle cells

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    AIMS: Membrane potential is a key determinant of vascular tone and many vasodilators act through the modulation of ion channel currents [e.g. the ATP-sensitive potassium channel (K(ATP))] involved in setting the membrane potential. Adenylyl cyclase (AC) isoenzymes are potentially important intermediaries in such vasodilator signalling pathways. Vascular smooth muscle cells (VSMCs) express multiple AC isoenzymes, but the reason for such redundancy is unknown. We investigated which of these isoenzymes are involved in vasodilator signalling and regulation of vascular ion channels important in modulating membrane potential. METHODS AND RESULTS: AC isoenzymes were selectively depleted (by >75%) by transfection of cultured VSMCs with selective short interfering RNA sequences. AC6 was the predominant isoenzyme involved in vasodilator-mediated cAMP accumulation in VSMCs, accounting for ∌60% of the total response to ÎČ-adrenoceptor (ÎČ-AR) stimulation. AC3 played a minor role in ÎČ-AR signalling, whereas AC5 made no significant contribution. AC6 was also the principal isoenzyme involved in ÎČ-AR-mediated protein kinase A (PKA) signalling (determined using the fluorescent biosensor for PKA activity, AKAR3) and the substantial ÎČ-AR/PKA-dependent enhancement of K(ATP) current. K(ATP) current was shown to play a vital role in setting the resting membrane potential and in mediating the hyperpolarization observed upon ÎČ-AR stimulation. CONCLUSION: AC6, but not the closely related AC5, plays a principal role in vasodilator signalling and regulation of the membrane potential in VSMCs. These findings identify AC6 as a vital component in the vasodilatory apparatus central to the control of blood pressure

    An Evaluation Schema for the Ethical Use of Autonomous Robotic Systems in Security Applications

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    Finishing the euchromatic sequence of the human genome

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    The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∌99% of the euchromatic genome and is accurate to an error rate of ∌1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead

    Omecamtiv mecarbil in chronic heart failure with reduced ejection fraction, GALACTIC‐HF: baseline characteristics and comparison with contemporary clinical trials

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    Aims: The safety and efficacy of the novel selective cardiac myosin activator, omecamtiv mecarbil, in patients with heart failure with reduced ejection fraction (HFrEF) is tested in the Global Approach to Lowering Adverse Cardiac outcomes Through Improving Contractility in Heart Failure (GALACTIC‐HF) trial. Here we describe the baseline characteristics of participants in GALACTIC‐HF and how these compare with other contemporary trials. Methods and Results: Adults with established HFrEF, New York Heart Association functional class (NYHA) ≄ II, EF ≀35%, elevated natriuretic peptides and either current hospitalization for HF or history of hospitalization/ emergency department visit for HF within a year were randomized to either placebo or omecamtiv mecarbil (pharmacokinetic‐guided dosing: 25, 37.5 or 50 mg bid). 8256 patients [male (79%), non‐white (22%), mean age 65 years] were enrolled with a mean EF 27%, ischemic etiology in 54%, NYHA II 53% and III/IV 47%, and median NT‐proBNP 1971 pg/mL. HF therapies at baseline were among the most effectively employed in contemporary HF trials. GALACTIC‐HF randomized patients representative of recent HF registries and trials with substantial numbers of patients also having characteristics understudied in previous trials including more from North America (n = 1386), enrolled as inpatients (n = 2084), systolic blood pressure < 100 mmHg (n = 1127), estimated glomerular filtration rate < 30 mL/min/1.73 m2 (n = 528), and treated with sacubitril‐valsartan at baseline (n = 1594). Conclusions: GALACTIC‐HF enrolled a well‐treated, high‐risk population from both inpatient and outpatient settings, which will provide a definitive evaluation of the efficacy and safety of this novel therapy, as well as informing its potential future implementation

    Wireless Local Area Network Performance in a Bluetooth Interference Environment

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    Since IEEE 802.11 wireless local area networks (WLANs) and Bluetooth (BT) personal area networks both use the 2.4 GHz Industrial, Scientific, and Medical band, interference can occur when these networks are collocated. A WLAN station\u27s clear channel assessment algorithm will declare a channel busy and induce transmission delays when sufficient energy from a BT signal is received. By assuming the BT\u27s frequency hopped spread spectrum signal will not corrupt the direct sequence spread spectrum WLAN transmission, we isolate and characterize transmission delays due solely to BT interference. We develop expressions for throughput, delay, expected backoff interval, expected number of collisions, and other metrics of interest. In situations where numerous collisions occur between WLAN stations, BT-induced transmission delays reduce the probability of expensive WLAN collisions while increasing overall throughput and decreasing delay. An analytic model is developed to predict interference effects and is verified through simulation

    NAFTA and Cross-Border Relations in Niagara, Detroit, and Vancouver

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    International audienceFirst, does free trade, and particularly economicintegration, lead to a process of functional interdependency and to cross-border linkages inNorth America? Second, do politics and institutions mediate this process? Specifically, howdoes the intergovernmental network linking local, regional, provincial/state, and federal institutionsmediate this process and impact local level initiatives? To investigate these questions, this work focuses on cross-border relations in three metropolitanborder areas: the Canadian-American border regions of Niagara-Niagara, Windsor-Detroit, and Vancouver-Seattle. This study takes a Canadian perspective and thus primarilyfocuses on Canada, Ontario, and British Columbia, and on Niagara, Windsor, and Vancouverand their border regions. The findings presented in this paper suggest that economic integrationmay lead to cross-border institution building when borderland communities also share the samevalue system
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