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A 50-Year Research Journey-From Laboratory to Clinic -

机译:从实验室到诊所的50年研究历程-

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摘要

Prior important research is not always cited, exemplified by Oswald Avery's pioneering discovery that DNA is the genetic transforming factor; it was not cited by Watson and Crick 10 years later. My first laboratory research (National Institutes of Health 1950 s) resulted in the clinical development of transseptal left heart catheterization. Laboratory studies on cardiac muscle mechanics in normal and failing hearts led to the concept of afterload mismatch with limited preload reserve. At the University of California, San Diego in La Jolla (1968) laboratory experiments on coronary artery reperfusion after sustained coronary occlusion showed salvage of myocardial tissue, a potential treatment for acute myocardial infarction proven in clinical trials of thrombolysis 14 years later. Among 60 trainees who worked with me in La Jolla, one-third were Japanese and some of their important laboratory experiments are briefly recounted, beginning with Sasayama, Tomoike and Shirato in the 1970s. Recently, we developed a method for cardiac gene transfer, and subsequently we showed that gene therapy for the defect in cardiomyopathic hamsters halted the progression of advanced disease. Cardiovascular research and medicine are producing continuing advances in technologies for gene transfer and embryonic stem cell transplantation, targeting of small molecules, and tissue and organ engineering.
机译:奥斯瓦尔德·埃弗里(Oswald Avery)的开创性发现表明DNA是遗传转化因子,这并不总是引用先前的重要研究。十年后,Watson和Crick没有引用它。我的第一个实验室研究(美国国立卫生研究院1950年代)导致经隔隔左心导管的临床发展。对正常心脏和衰竭心脏的心肌力学进行的实验室研究导致了后负荷不匹配且预负荷储备有限的概念。在加利福尼亚大学圣地亚哥分校的拉荷亚(1968)在持续性冠状动脉闭塞后进行冠状动脉再灌注的实验室实验显示,抢救了心肌组织,这是14年后在溶栓治疗的临床试验中证实的治疗急性心肌梗塞的潜在方法。在拉霍亚(La Jolla)与我合作的60名学员中,三分之一是日本人,并简要叙述了他们的一些重要实验室实验,从1970年代的S山,友池和白户开始。最近,我们开发了一种用于心脏基因转移的方法,随后我们证明了针对心肌病仓鼠缺陷的基因治疗阻止了晚期疾病的进展。心血管研究和医学在基因转移和胚胎干细胞移植,靶向小分子以及组织和器官工程的技术方面不断取得进步。

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