4.6 Review

Mitochondrial replacement: from basic research to assisted reproductive technology portfolio tool-technicalities and possible risks

期刊

MOLECULAR HUMAN REPRODUCTION
卷 21, 期 1, 页码 3-10

出版社

OXFORD UNIV PRESS
DOI: 10.1093/molehr/gau082

关键词

cytoplasmic transfer; nuclear transfer; mitochondrial disease; mitochondrial DNA; PGD

资金

  1. European Research Council under the European Community [210103]
  2. EU FP7-KBBE-2009-3 Programme [244356]
  3. EU [312097]
  4. FECUND and PRIN MIUR founding [2009JE3CHM]
  5. project MIUR FIRB CNR 'GenHome'
  6. Bank Foundation Tercas (Teramo, Italy)
  7. Auckland Medical Research Foundation
  8. Nurture Foundation
  9. Maurice and Phyllis Paykel Trust
  10. Fertility Associates

向作者/读者索取更多资源

Mitochondrial DNA(mtDNA) mutations are a relatively common cause of progressive disorders that can be severe or even life-threatening. There is currently no cure for these disorders; therefore recent research has been focused on attempting to prevent the transmission of these maternally inherited mutations. Here we highlight the challenges of understanding the transmission of mtDNA diseases, discuss current genetic management options and explore the use of germ-line reconstruction technologies to prevent mtDNA diseases. In particular we discuss their potential, indications, limitations and possible safety concerns.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据