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15篇 您的检索式:作者名="Jinah"
    题名 作者 年代 出处 被引量
1Glutathione suppresses TGF-β-induced PAI-1expression by inhibiting p38and JNK MAPK and the binding of AP-1,SP-1,and Smad to the PAI-1promoter显示文摘Praveen KV Karen EI Jinah C 2007Am J Physiol Lung Cell Mol Physiol2007,293,5:1
2Oxidative stress, endogenous antioxidants, alcohol, and hepatitis C: pathogenic interactions and therapeutic considerations显示文摘Jinah Choi 2012Free Radical Biology and Medicine2012,,7:1
3The Effects of Improvisational Music Therapy on Joint Attention Behaviors in Autistic Children: A Randomized Controlled Study显示文摘Jinah Kim Tony Wigram Christian Gold 2008Journal of Autism and Developmental Disorders2008,,9:1
4DNA methyltransferase 3-like affects promoter methylation of thymineDNA glycosylase independently of DNMT1 and DNMT3B in cancer cells显示文摘Heesun Kim Jinah Park Yeonjoo Jung Sang-Hyun Song Sae-Won Han Do-Youn Oh Seock-Ah Im Yung-Jue Bang Tae-You Kim 2010International Journal of Oncology2010,,6:1
5Effects of alginate hydrogel cross-linking density on mechanical and biological behaviors for tissue engineering显示文摘Jinah J Young J S Hyeon J K 2014Journal of the Mechanical Behavior of Biomedical Materials2014,37,:1
6Dexamethasone transport and ocular delivery from poly (hydroxyethyl methacrylate) gels显示文摘Jinah Kim Anuj Chauhan 2008International Journal of Pharmaceutics2008,353,:1
7Use of vacuum-assisted closure in pediatric open fractures with a focus on the rate of infection 显示文摘Halvorson J Jinah R Kulp B 2011Orthopedics2011,34,7:1
8Induction of incomplete autophagic response by hepatitis C virus via the unfolded protein response显示文摘Donna S Wenling C Jinah C 0,,04:1
9Peroxisome proliferator-activated recepror ligands regulate endothelial membrane superoxide production显示文摘Jinah H Dean J K Bernard L 2005Am J Physiol Cell Physiol2005,288,:1
10Ornamenting 3D printed scaffolds with cell-laid extracellular matrix for bone tissue regeneration 显示文摘Falguni Pati Tae-Ha Song Girdhari Rijal Jinah Jang Sung Won Kim Dong-Woo Cho 2014Biomaterials2014,06,:1
11Age-associated decline in γ-glutamylcysteine synthetase gene expression in rats显示文摘Rui-Ming Liu Jinah Choi 2000Free Radical Biology and Medicine2000,,4:1
12Redox modulation of the hepatitis C virus replication complex is calcium dependent显示文摘Jinah Choi Henry Jay Forman Jing-hsiung Ou Michael M.C. Lai Scott Seronello Anna Nandipati 2006Free Radical Biology and Medicine2006,,9:1
133D cell-printing of gradient multi-tissue interfaces for rotator cuff regeneration显示文摘Owing to the prevalence of rotator cuff(RC)injuries and suboptimal healing outcome,rapid and functional regeneration of the tendon-bone interface(TBI)after RC repair continues to be a major clinical challenge.Given the essential role of the RC in shoulder movement,the engineering of biomimetic multi-tissue constructs presents an opportunity for complex TBI reconstruction after RC repair.Here,we propose a gradient cell-laden multi-tissue construct combined with compositional gradient TBI-specific bioinks via 3D cell-printing technology.In vitro studies demonstrated the capability of a gradient scaffold system in zone-specific inducibility and multi-tissue formation mimicking TBI.The regenerative performance of the gradient scaffold on RC regeneration was determined using a rat RC repair model.In particular,we adopted nondestructive,consecutive,and tissue-targeted near-infrared fluorescence imaging to visualize the direct anatomical change and the intricate RC regeneration progression in real time in vivo.Furthermore,the 3D cell-printed implant promotes effective restoration of shoulder locomotion function and accelerates TBI healing in vivo.In summary,this study identifies the therapeutic contribution of cell-printed constructs towards functional RC regeneration,demonstrating the translational potential of biomimetic gradient constructs for the clinical repair of multi-tissue interfaces.Suhun Chae Uijung Yong Wonbin Park Yoo-mi Choi In-Ho Jeon Homan Kang Jinah Jang Hak Soo Choi Dong-Woo Cho 2023Bioactive Materials2023,,1:0
14Customized 3D-printed occluders enabling the reproduction of consistent and stable heart failure in swine models显示文摘Reproducibility of clinical output is important when investigating therapeutic efficacy in pre-clinical animal studies.Due to its physiological relevance,a swine myocardial infarction(MI)model has been widely used to evaluate the effectiveness of stem cells or tissue-engineered constructs for ischemic heart diseases.Several methods are used to induce MI in the swine model.However,it is difficult,using these approaches,to obtain a similar level of functional outcomes from a group of animals due to interpersonal variation,leading to increased experimental cost.Hence,in order to minimize human intervention,we developed an approach to use a customized occluder that has dimensional similarities with that of the coronary artery of animals in the case of the swine model.We carried out angiography to measure the diameter of the middle left anterior descending artery of each individual animal to fabricate the customized occluder using a 3D-printing system.The fabricated occluder contained a central hole smaller than that of the targeted middle left anterior descending artery to mimic an atherosclerotic coronary artery that has an approximately 20%blocked condition.Interestingly,the 3D-printed occluder can provide continuous blood flow through the central pore,indicating a high survival rate(88%)of up to 28 days post-operation.This method showed the possibility of creating consistent myocardial infarction induction as compared to the conventional representative closed-chest method(50%survival rate),thus highlighting how our method can have a profound effect on accelerating reliable experiments for developing new therapeutic approaches to ischemic heart diseases.Han B.Kim Seungman Jung Hyukjin Park Doo S.Sim Munki Kim Sanskrita Das Youngkeun Ahn Myung H.Jeong Jinah Jang Young J.Hong 2021Bio-Design and Manufacturing2021,4,4:0
15Application of 3D bioprinting in the prevention and the therapy for human diseases显示文摘Rapid development of vaccines and therapeutics is necessary to tackle the emergence of new pathogens and infectious diseases.To speed up the drug discovery process,the conventional development pipeline can be retooled by introducing advanced in vitro models as alternatives to conventional infectious disease models and by employing advanced technology for the production of medicine and cell/drug delivery systems.In this regard,layer-by-layer construction with a 3D bioprinting system or other technologies provides a beneficial method for developing highly biomimetic and reliable in vitro models for infectious disease research.In addition,the high flexibility and versatility of 3D bioprinting offer advantages in the effective production of vaccines,therapeutics,and relevant delivery systems.Herein,we discuss the potential of 3D bioprinting technologies for the control of infectious diseases.We also suggest that 3D bioprinting in infectious disease research and drug development could be a significant platform technology for the rapid and automated production of tissue/organ models and medicines in the near future.Hee-Gyeong Yi Hyeonji Kim Junyoung Kwon Yeong-Jin Choi Jinah Jang Dong-Woo Cho 2021Signal Transduction and Targeted Therapy2021,6,6:0
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