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Jialin Deng

Researcher at University of Science and Technology of China

Publications -  9
Citations -  25

Jialin Deng is an academic researcher from University of Science and Technology of China. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 1, co-authored 1 publications receiving 3 citations.

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Joint Power Routing and Current Scheduling in Multi-Relay Magnetic MIMO WPT System

TL;DR: This work proposes, design, and implements a multi-relay MIMO MRC-WPT system, and designs an almost optimum joint optimization of power routing and current scheduling method, without relying on any feedback from RX.
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Feruloylated oligosaccharides ameliorate MPTP-induced neurotoxicity in mice by activating ERK/CREB/BDNF/TrkB signalling pathway.

TL;DR: Feruloylated oligosaccharides (FOs) are natural esterification products of ferulic acid and OO and have been shown to contribute to the ensured survival of nigrostriatal dopamine neurons and inhibition of neuroinflammation in Parkinson's disease as discussed by the authors .
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Network pharmacology-based analysis to explore the therapeutic mechanism of Cortex Dictamni on atopic dermatitis.

TL;DR: Cortex Dictamni can improve the symptoms of skin lesions and the degree of inflammation caused by AD, and may inhibit AD through multiple pathways, such as regulating PI3K-AKT and JAK1-STAT3/STAT6 pathways as mentioned in this paper .
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Mag-E4E: Trade Efficiency for Energy in Magnetic MIMO Wireless Power Transfer System

TL;DR: This paper proposes the frequency adjustment based PDL maximization scheme for MIMO MRC-WPT systems, and designs an energy-voltage transform matrix algebra based estimation mechanism to reduce context measurement overhead.
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Dictamnine ameliorates chronic itch in DNFB-induced atopic dermatitis mice via inhibiting MrgprA3.

TL;DR: In this article , the authors used the 2,4-dinitrofluorobenzene (DNFB)-induced atopic dermatitis (AD) mouse model to observe the scratching behavior, inflammatory manifestations, and detect the expression of MrgprA3 and TRPA1 in skin and DRG.