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Feng Zhang

Researcher at Fudan University

Publications -  2715
Citations -  225233

Feng Zhang is an academic researcher from Fudan University. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 172, co-authored 1278 publications receiving 181865 citations. Previous affiliations of Feng Zhang include Cincinnati Children's Hospital Medical Center & Nanjing Medical University.

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Intermedin in Paraventricular Nucleus Attenuates Ang II-Induced Sympathoexcitation through the Inhibition of NADPH Oxidase-Dependent ROS Generation in Obese Rats with Hypertension.

TL;DR: Testing the hypothesis that IMD in the PVN can inhibit the generation of ROS caused by Ang II for attenuating sympathetic nerve activity (SNA) and blood pressure (BP) in rats with obesity-related hypertension (OH) indicated that IMd via AM receptors in the MVN attenuates SNA and hypertension, and decreases Ang II-induced enhancement of SNA through the inhibition of NADPH oxidase activity and ERK activation.
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Thermodynamic and exergoeconomic analysis of a novel CO2 based combined cooling, heating and power system

TL;DR: In this paper, a combined cooling, heating and power (CCHP) system consisting of a supercritical carbon dioxide (sCO2) power cycle, a transcritical CO2 power cycle with a carbon dioxide based refrigeration cycle, and a direct heating (DH) system is proposed.
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Genome-wide gene expression analysis suggests an important role of hypoxia in the pathogenesis of endemic osteochondropathy Kashin-Beck disease.

TL;DR: It is suggested that chronic hypoxia-induced mitochondrial damage and apoptosis might play an important role in the pathogenesis of Kashin-Beck Disease.
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CRISPR activation screen identifies BCL-2 proteins and B3GNT2 as drivers of cancer resistance to T cell-mediated cytotoxicity

TL;DR: In this paper , the authors performed a genome-scale CRISPR activation screen for genes that enable human melanoma cells to evade cytotoxic T cell killing, and they found that the genes that enabled resistance to immunotherapy were CD274 (PD-L1), MCL1, JUNB, and B3GNT2.
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Short-term starvation attenuates liver ischemia-reperfusion injury (IRI) by Sirt1-autophagy signaling in mice.

TL;DR: It is found that short-term starvation attenuates liver IRI via the Sirt1-autophagy pathway, and this findings provide a rationale for a novel therapeutic strategy for managing liver I RI.