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| 1 | Discovery of phenylaminopyrine derivatives as novel HIV-1 nonnucleoside reverse transcriptase Inhibitors显示文摘 | Junwon Kim and Doohyun Lee | 2012 | ACS Med Chem Lett2012，3，8： | 1 |
| 2 | Analysis of kimchi microflora using denaturing gradient gel electrophoresis显示文摘 | LEE Jungsook HEO Gunyoung LEE Junwon | 2005 | International Journal of Food Microbiology2005，102，2： | 1 |
| 3 | Intrinsic electrochemical activity of Ni in Ni_(3)Sn_(4) anode accommodating high capacity and mechanical stability for fast-charging lithium-ion batteries显示文摘Fast interfacial kinetics derived from bicontinuous three-dimensional(3D)architecture is a strategic feature for achieving fast-charging lithium-ion batteries(LIBs).One of the main reasons is its large active surface and short diffusion path.Yet,understanding of unusual electrochemical properties still remain great challenge due to its complexity.In this study,we proposed a nickel–tin compound(Ni_(3)Sn_(4))supported by 3D Nickel scaffolds as main frame because the Ni_(3)Sn_(4) clearly offers a higher reversible capacity and stable cycling performance than bare tin(Sn).In order to verify the role of Ni,atomic-scale simulation based on density functional theory systematically addressed to the reaction mechanism and structural evolution of Ni_(3)Sn_(4) during the lithiation process.Our findings are that Ni enables Ni_(3)Sn_(4) to possess higher mechanical stability in terms of reactive flow stress,subsequently lead to improve Li storage capability.This study elucidates an understanding of the lithiation mechanism of Ni_(3)Sn_(4) and provides a new perspective for the design of high-capacity and high-power 3D anodes for fast-charging LIBs. | Janghyuk Moon Trung Dinh Hoang Seong Soo Park Seowan Park Dong Young Rhee Junwon Lee Sang A Han Min-Sik Park Jung Ho Kim | 2022 | Journal of Energy Chemistry2022，31，8： | 1 |
| 4 | Silibinin inhibits osteoclast differentiation mediated by TNF family members显示文摘 | Jung Ha Kim Kabsun Kim Hye Mi Jin Insun Song Bang Ung Youn Junwon Lee Nacksung Kim | 2009 | Molecules and Cells2009，，3： | 1 |
| 5 | Experimental demonstration of 50 GHz 2 spaced 422 channel volume holographic demultiplexer显示文摘 | Lee K wonyeon An Junwon Nam Kim | 2002 | Electronics Letters2002，38，14： | 1 |
| 6 | Experimental demonstation of 50 CHz spaced 422 channel volume holographic demultiplexer显示文摘 | Lee K Wonyeon An Junwon Nam Kim | 2002 | Electronics Letters2002，38，14： | 1 |
| 7 | Identification of two HIV inhibitors that also inhibit human RNaseH2显示文摘 | Junghwan Kim Jaewan Yoon MoonKyeong Ju Yunmi Lee Tae-Hee Kim Junwon Kim Peter Sommer Zaesung No Jonathan Cechetto Sung-Jun Han | 2013 | Molecules and Cells2013，，3： | 1 |
| 8 | Enhanced delivery of a low dose of aducanumab via FUS in 5×FAD mice,an AD model显示文摘Background:Aducanumab(Adu),which is a human IgG1 monoclonal antibody that targets oligomer and fibril forms of beta-amyloid,has been reported to reduce amyloid pathology and improve impaired cognition after administration of a high dose(10 mg/kg)of the drug in Alzheimer’s disease(AD)clinical trials.The purpose of this study was to investigate the effects of a lower dose of Adu(3 mg/kg)with enhanced delivery via focused ultrasound(FUS)in an AD mouse model.Methods:The FUS with microbubbles opened the blood-brain barrier(BBB)of the hippocampus for the delivery of Adu.The combined therapy of FUS and Adu was performed three times in total and each treatment was performed biweekly.Y-maze test,Brdu labeling,and immunohistochemical experimental methods were employed in this study.In addition,RNA sequencing and ingenuity pathway analysis were employed to investigate gene expression profiles in the hippocampi of experimental animals.Results:The FUS-mediated BBB opening markedly increased the delivery of Adu into the brain by approximately 8.1 times in the brains.The combined treatment induced significantly less cognitive decline and decreased the level of amyloid plaques in the hippocampi of the 5×FAD mice compared with Adu or FUS alone.Combined treatment with FUS and Adu activated phagocytic microglia and increased the number of astrocytes associated with amyloid plaques in the hippocampi of 5×FAD mice.Furthermore,RNA sequencing identified that 4 enriched canonical pathways including phagosome formation,neuroinflammation signaling,CREB signaling and reelin signaling were altered in the hippocami of 5×FAD mice receiving the combined treatment.Conclusion:In conclusion,the enhanced delivery of a low dose of Adu(3 mg/kg)via FUS decreases amyloid deposits and attenuates cognitive function deficits.FUS-mediated BBB opening increases adult hippocampal neurogenesis as well as drug delivery.We present an AD treatment strategy through the synergistic effect of the combined therapy of FUS and Adu. | Chanho Kong Eun-Jeong Yang Jaewoo Shin Junwon Park Si-Hyun Kim Seong-Wook Park Won Seok Chang Chang-Han Lee Hyunju Kim Hye-Sun Kim Jin Woo Chang | 2022 | Translational Neurodegeneration2022，11，1： | 0 |
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