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Qing Ye

Researcher at University of Zurich

Publications -  13
Citations -  942

Qing Ye is an academic researcher from University of Zurich. The author has contributed to research in topics: Tissue engineering & Cell culture. The author has an hindex of 10, co-authored 13 publications receiving 906 citations.

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Fibrin gel as a three dimensional matrix in cardiovascular tissue engineering

TL;DR: A three-dimensional fibrin gel structure can serve as a useful scaffold for tissue engineering with controlled degradation, excellent seeding effects and good tissue development.
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Tissue engineering in cardiovascular surgery: MTT, a rapid and reliable quantitative method to assess the optimal human cell seeding on polymeric meshes

TL;DR: It is feasible to use human aortic myofibroblasts to develop a new functional tissue in vitro and twenty-four hours is an optimal seeding interval for seeding human aORTic my ofibro Blasts on PGA scaffolds and MTT test is a rapid and reliable quantitative method to assess the optimal human cell seeding on polymeric meshes.
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Operative Results of "Repair" of Ventricular Septal Rupture After Acute Myocardial Infarction

TL;DR: Patch closure of the ventricular septal rupture, remodeling of the left ventricle to improve stroke volume and reduce wall stress, and selective myocardial revascularization provided acceptable results.
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Frequency of collateral blood flow in the infarct-related coronary artery in rupture of the ventricular septum after acute myocardial infarction

TL;DR: Patients with postinfarction ventricular septal rupture have poor residual or collateral blood flow in the infarct artery and do not benefit from ischemic preconditioning, suggesting that rupture of the ventricular Septum occurs on an unprotected and unprepared myocardium.
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Tissue engineering in cardiovascular surgery: new approach to develop completely human autologous tissue

TL;DR: Improved cell culture technique may render human aortic myofibroblasts to a native tissue-like structure and a three-dimensional completely autologous human tissue may be further developed on the base of this structure with no show toxic degradation or inflammatory reactions.