Nuclear genome transfer in human oocytes eliminates mitochondrial DNA variants-Reference-Cited by-同舟云学术

Nuclear genome transfer in human oocytes eliminates mitochondrial DNA variants

Published:2012-12-19 Issue:7434 Volume:493 Page:632-637
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

Paull Daniel,Emmanuele Valentina,Weiss Keren A.,Treff Nathan,Stewart Latoya,Hua Haiqing,Zimmer Matthew,Kahler David J.,Goland Robin S.,Noggle Scott A.,Prosser Robert,Hirano Michio,Sauer Mark V.,Egli Dieter

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/nature11800.pdf

Reference48 articles.

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2. Bolhuis, P. A. et al. Rapid shift in genotype of human mitochondrial DNA in a family with Leber’s hereditary optic neuropathy. Biochem. Biophys. Res. Commun. 170, 994–997 (1990)

3. Cree, L. M. et al. A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes. Nature Genet. 40, 249–254 (2008)

4. Wai, T., Teoli, D. & Shoubridge, E. A. The mitochondrial DNA genetic bottleneck results from replication of a subpopulation of genomes. Nature Genet. 40, 1484–1488 (2008)

5. Steffann, J. et al. Analysis of mtDNA variant segregation during early human embryonic development: a tool for successful NARP preimplantation diagnosis. J. Med. Genet. 43, 244–247 (2006)

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