Adenoviral-mediated serca gene transfer into cardiac myocytes: how much is too much?

Adenoviral-mediated serca gene transfer into cardiac myocytes: how much is too much?
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腺病毒介导的 serca 基因转移至心肌细胞:多少才算太多?

DOI:
10.1161/01.res.88.4.373
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发表时间:
2001
影响因子:
20.1
通讯作者:
Periasamy,M
Periasamy,M
中科院分区:
医学1区
文献类型:
--
作者:
Periasamy,M

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在过去的十年里,腺病毒介导的基因转移到体细胞作为一种可能的治疗方法受到了极大的关注。体细胞基因转移到有丝分裂后细胞(如心肌细胞)提供了一种非常强大的手段来传递目的蛋白,这些目的蛋白要么是功能缺陷的,要么是由于基因表达缺失而丢失的。近年来,心力衰竭的基因治疗获得了相当大的兴趣,这主要是因为载体技术的进步,心脏基因的传递,以及对心力衰竭分子基础的更好理解。1、2
In the last decade, a great deal of attention has been focused on adenoviral-mediated gene transfer into somatic cells as a possible therapeutic approach. Somatic gene transfer into postmitotic cells (such as cardiomyocytes) provides a very powerful means to deliver the protein of interest, which is either functionally defective or missing because of loss of gene expression. In recent years, gene therapy for heart failure has gained considerable interest, mainly because of improvements in vector technology, cardiac gene delivery, and a better understanding of the molecular basis of heart failure. 1, 2
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