High-frequency generation of viable mice from engineered bi-maternal embryos-Reference-Cited by-同舟云学术

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High-frequency generation of viable mice from engineered bi-maternal embryos

Published:2007-08-19 Issue:9 Volume:25 Page:1045-1050
ISSN:1087-0156
Container-title:Nature Biotechnology
language:en
Short-container-title:Nat Biotechnol

Author:

Kawahara Manabu,Wu Qiong,Takahashi Nozomi,Morita Shinnosuke,Yamada Kaori,Ito Mitsuteru,Ferguson-Smith Anne C,Kono Tomohiro

Publisher

Springer Science and Business Media LLC

Subject

Biomedical Engineering,Molecular Medicine,Applied Microbiology and Biotechnology,Bioengineering,Biotechnology

Link

http://www.nature.com/articles/nbt1331.pdf

Reference24 articles.

1. Surani, M.A., Barton, S.C. & Norris, M.L. Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis. Nature 308, 548–550 (1984).

2. McGrath, J. & Solter, D. Completion of mouse embryogenesis requires both the maternal and paternal genomes. Cell 37, 179–183 (1984).

3. Kono, T., Obata, Y., Yoshimzu, T., Nakahara, T. & Carroll, J. Epigenetic modifications during oocyte growth correlates with extended parthenogenetic development in the mouse. Nat. Genet. 13, 91–94 (1996).

4. Obata, Y. et al. Disruption of primary imprinting during oocyte growth leads to the modified expression of imprinted genes during embryogenesis. Development 125, 1553–1560 (1998).

5. Obata, Y. & Kono, T. Maternal primary imprinting is established at a specific time for each gene throughout oocyte growth. J. Biol. Chem. 277, 5285–5289 (2002).

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