Publications by authors named "Coder J"

Radio spectrum is a scarce resource. To meet demands, new wireless technologies must operate in shared spectrum over unlicensed bands (coexist). We consider coexistence of Long-Term Evolution (LTE) License-Assisted Access (LAA) with incumbent Wi-Fi systems.

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Light-in-flight sensing has emerged as a promising technique in image reconstruction applications at various wavelengths. We report a microwave imaging system that uses an array of transmitters and a single receiver operating in continuous transmit-receive mode. Captures take a few microseconds and the corresponding images cover a spatial range of tens of square meters with spatial resolution of 0.

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This article aims to provide a narrative for addressing wireless coexistence in medical devices to help medical device developers, test engineers, and regulatory affairs personnel throughout the device life cycle. Accordingly, we present a case-study covering the coexistence evaluation process including the risk analysis of the wireless functionality of a hypothetical medical device, determining the corresponding risk category, specification of the device functional wireless performance (FWP), wireless coexistence testing, and measurement of the intended/untended signal ratio. Also, we propose a simple method for translating the test outcome into user recommendations for minimum/maximum separation distances between the device, its intended companion, and the source of unintended signals.

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To improve spectrum sharing between long-term evolution (LTE) license assisted access (LAA) and incumbent systems such as wireless local area networks (WLANs) in unlicensed spectrum, listen before talk (LBT) has been proposed as a candidate for LAA channel access. To allow for a robust spectrum sensing performance, LBT may use a backoff-slot duration that is substantially larger than its WLAN counterpart. There is potential for an unknown backoff slot-jamming (SJ) effect, which may significantly decrease channel access probability (CAP) and throughput of LAA-LBT links.

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Natural killer (NK) cells were identified by their ability to kill target cells without previous sensitization. However, without an antecedent "arming" event, NK cells can recognize, but are not equipped to kill, target cells. How NK cells become armed in vivo in healthy hosts is unclear.

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Improved hepatic microcirculation is one of the postulated mechanisms by which prostaglandin E1 (PGE(1)) could improve liver function in the setting of fulminant hepatic failure or poor allograft function immediately post-transplant. The purpose of this study was to determine whether PGE(1) improves hepatic allograft arterial and portal vein inflow. Fifty patients receiving a primary liver transplant were entered into a prospective randomized double-blind study.

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