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| 1 | Prevalence and risk factors of hepatitis C and B virus infections in hemodialysis patients and their spouses: A multicenter study in Beijing, China显示文摘 | Yingying Su Ruixue Yan Zhongping Duan Jessie L. Norris Lu Wang Yan Jiang Wenge Xing Yu Chen Yao Xiao Lu Li Jun Tao Ning Wang | 2013 | J Med Virol2013，，3： | 1 |
| 2 | Investigation ongeneration performance for tubular direct methanol fuel cell显示文摘 | Tang Dong Zhang Yang Duan Ruixue | 2011 | Advanced Materials Research2011，，： | 1 |
| 3 | Structural basis of Sphingosine-1-phosphate transport via human SPNS2显示文摘Dear Editor,Sphingosine 1-phosphate(S1P)plays crucial roles in various physiological processes,including immune response,vascular development,and neural system homeostasis1 through activating S1P receptors(S1PRs).Notably,a desirable concentration gradient of S1P which is achieved by S1P transporters,including spinster homolog 2 protein(SPNS2)and MFSD2B that transport S1P from the intracellular side to the extracellular side of cells,2,3 is essential for proper S1P signaling.SPNS2 and MFSD2B belong to the major facilitator superfamily(MFS),and specifically. | Yaning Duan Nancy C.P.Leong Jing Zhao Yu Zhang Dat T.Nguyen Hoa T.T.Ha Na Wang Ruixue Xia Zhenmei Xu Zhengxiong Ma Yu Qian Han Yin Xinyan Zhu Anqi Zhang Changyou Guo Yu Xia Long N.Nguyen Yuanzheng He | 2024 | Cell Research2024，34，2： | 0 |
| 4 | Atomically dispersed Fe sites on hierarchically porous carbon nanoplates for oxygen reduction reaction显示文摘Developing cost-effective,robust and stable non-precious metal catalysts for oxygen reduction reaction(ORR) is of paramount importance for electrochemical energy conversion devices such as fuel cells and metal-air batteries.Although Fe-N-C single atom catalysts(SACs) have been hailed as the most promising candidate due to the optimal binding strength of ORR intermediates on the Fe-N_(4) sites,they suffer from serious mass transport limitations as microporous templates/substrates,i.e.,zeolitic imidazolate frameworks(ZIFs),are usually employed to host the active sites.Motivated by this challenge,we herein develop a hydrogen-bonded organic framework(HOF)-assisted pyrolysis strategy to construct hierarchical micro/mesoporous carbon nanoplates for the deposition of atomically dispersed Fe-N_(4) sites.Such a design is accomplished by employing HOF nanoplates assembled from 2-aminoterephthalic acid(NH_(2)-BDC) and p-phenylenediamine(PDA) as both soft templates and C,N precursors.Benefitting from the structural merits inherited from HOF templates,the optimized catalyst(denoted as Fe-N-C SAC-950) displays outstanding ORR activity with a high half-wave potential of 0.895 V(vs.reversible hydrogen electrode(RHE)) and a small overpotential of 356 mV at 10 mA cm^(-2) for the oxygen evolution reaction(OER).More excitingly,its application potential is further verified by delivering superb rechargeability and cycling stability with a nearly unfading charge-discharge gap of 0.72 V after 160 h.Molecular dynamics(MD) simulations reveal that micro/mesoporous structure is conducive to the rapid mass transfer of O_(2),thus enhancing the ORR performance.In situ Raman results further indicate that the conversion of O_(2) to~*O_(2)-the rate-determining step(RDS) for Fe-N-C SAC-950.This work will provide a versatile strategy to construct single atom catalysts with desirable catalytic properties. | Ruixue Zheng Qinglei Meng Hao Zhang Teng Li Di Yang Li Zhang Xiaolong Jia Changpeng Liu Jianbing Zhu Xiaozheng Duan Meiling Xiao Wei Xing | 2024 | Journal of Energy Chemistry2024，90，3： | 0 |
| 5 | Identification of oleic acid as an endogenous ligand of GPR3显示文摘Although GPR3 plays pivotal roles in both the nervous system and metabolic processes,such as cold-induced thermogenesis,its endogenous ligand remains elusive.Here,by combining structural approach(including cryo-electron microscopy),mass spectrometry analysis,and functional studies,we identify oleic acid(OA)as an endogenous ligand of GPR3.Our study reveals a hydrophobic tunnel within GPR3 that connects the extracellular side of the receptor to the middle of plasma membrane,enabling fatty acids to readily engage the receptor.Functional studies demonstrate that OA triggers downstream Gs signaling,whereas lysophospholipids fail to activate the receptor.Moreover,our research reveals that cold stimulation induces the secretion of OA in mice,subsequently activating Gs/cAMP/PKA signaling in brown adipose tissue.Notably,brown adipose tissues from Gpr3 knockout mice do not respond to OA during cold stimulation,reinforcing the significance of GPR3 in this process.Finally,we propose a“born to be activated and cold to enhance”model for GPR3 activation.Our study provides a starting framework for the understanding of GPR3 signaling in cold-stimulated thermogenesis. | Yangjie Xiong Zhenmei Xu Xinzhi Li Yuqin Wang Jing Zhao Na Wang Yaning Duan Ruixue Xia Zhengbin Han Yu Qian Jiale Liang Anqi Zhang Changyou Guo Asuka Inoue Yu Xia Zheng Chen Yuanzheng He | 2024 | Cell Research2024，34，3： | 0 |
| 6 | Structural basis of omega-3 fatty acid receptor FFAR4 activation and G protein coupling selectivity显示文摘Dear Editor,Omega(w)-3 fatty acids are known to have multiple beneficial effects on health,including anti-inflammation,enhancement of glucose uptake and promotion of brain development.'The effects of w-3 fatty acids are mainly mediated by free fatty acid receptor 4(FFAR4,also known as GPR120),a member of G protein-coupled receptor(GPCR)superfamily.FFAR4 plays crucial roles in main-taining metabolic homeostasis via regulating adipogenesis,insulin sensitivity and inflammation,and is a highly valuable target for treating metabolic diseases such as diabetes.Other FFARs include FFAR1(GPR40)which responds to long-chain FFAs(>12 carbons),and FFAR2(GPR43)and FFAR3(GPR41)that respond to short-chain FFAs(<6 carbons).FFAR4 responds to long-chain FFAs,and a common feature of FFAR4 ligands is the existence of multiple cis double-bonds on the acyl chain of the fatty acids,such as a-linolenic acid(18:3,aLa),stearidonic acid(18:4),eicosapentaenoic acid(20:5,EPA)and docosahexaenoic acid(22:6,DHA).'FFAR4 primarily couples to Gg pathway,but also has been reported to signal through Gs and G. | Han Yin Asuka Inoue Zhengxiong Ma Xinyan Zhu Ruixue Xia Zhenmei Xu Na Wang Yaning Duan Anqi Zhang Changyou Guo Yuanzheng He | 2023 | Cell Research2023，33，8： | 0 |
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