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Effect of Deformation Condition on Axial Compressive Precision Forming Process of Tube with Curling Die
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作者 He YANG and Zhichao SUN College of Materials Science and Engineering, Northwestern Polytechnical University, Xi’an 710072, China 《Journal of Materials Science & Technology》 SCIE EI CAS CSCD 2001年第1期135-136,共2页
The effect of the deformation condition on the axial compressive precision forming process of tube with curling die was investigated by using a rigid-plastic FEM. The results show that the forming accuracy depends mai... The effect of the deformation condition on the axial compressive precision forming process of tube with curling die was investigated by using a rigid-plastic FEM. The results show that the forming accuracy depends mainly on geometric condition rp/d0, little on tube material properties and friction condition; the relative gap △/2rp of double-walled tubes obtained decreases with Increasing rp/d0, and there is a parameter k for a given to/do or rp/t0, when rp/d0 >k, △/2rp< 1, otherwise △/2rp>1. 展开更多
关键词 effect of Deformation Condition on Axial Compressive precision Forming Process of Tube with Curling Die
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Engineering liver disease models in vitro:emerging trends and innovations
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作者 Qi Rao Lei Wang +2 位作者 Frank Tacke Adrien Guillot Nan Ma 《eGastroenterology》 2025年第4期31-44,共14页
In vitro liver disease modelling,a rapidly evolving field,has become a multidimensional endeavour aimed at more precisely and effectively recapitulating the complexity of hepatic pathophysiology.This review systematic... In vitro liver disease modelling,a rapidly evolving field,has become a multidimensional endeavour aimed at more precisely and effectively recapitulating the complexity of hepatic pathophysiology.This review systematically outlines the essential structural and cellular components of the liver as foundational elements for model design.Emphasising pathophysiological states rather than disease hallmarks,we discuss key liver injury paradigms,including hepatic steatosis,drug-induced hepatotoxicity,fibrogenesis,tumourigenesis and cholestatic injury.Each section integrates cellular mechanisms with model development strategies,highlighting advances in co-culture systems,multicellular organoids and liver-on-a-chip platforms.Although challenges persist,emerging platforms are increasingly capable of capturing multicellular crosstalk,structural heterogeneity and injury-response dynamics.Moving forward,model utility will depend not only on structural mimicry but on the ability to produce biologically meaningful outputs under experimentally controlled conditions. 展开更多
关键词 hepatic steatosisdrug induced co culture systems multicellular organoids structural cellular components vitro liver disease modellinga precisely effectively recapitulating complexity hepatic pathophysiologythis vitro liver disease modeling hepatic pathophysiology
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