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红细胞酶缺乏症:从遗传基础到基因转移

Red cell enzyme deficiencies: from genetic basis to gene transfer.

作者信息

Mason P J

机构信息

Department of Haematology, Royal Postgraduate Medical School, Hammersmith Hospital, London, United Kingdom.

出版信息

Semin Hematol. 1998 Apr;35(2):126-35.

PMID:9565155
Abstract

Features of some of the more common erythrocyte enzyme deficiencies that may be relevant to possible future attempts to correct the deficiencies by gene transfer approaches are considered. The last few years have seen rapid progress in our understanding of the molecular basis of these diseases and the regulation of the genes underlying these deficiencies is now coming into focus. Animal models for some of the conditions are available and others can be produced by homologous recombination techniques. Although considerable improvements in gene transfer vectors and protocols are required, this research may lead eventually to gene replacement therapy for these severe conditions.

摘要

本文考虑了一些较为常见的红细胞酶缺乏症的特征,这些特征可能与未来通过基因转移方法纠正这些缺乏症的尝试相关。在过去几年中,我们对这些疾病的分子基础的理解取得了迅速进展,这些缺乏症背后基因的调控现在正成为焦点。某些病症的动物模型已经存在,其他模型可以通过同源重组技术产生。尽管基因转移载体和方案仍需大幅改进,但这项研究最终可能会为这些严重病症带来基因替代疗法。

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