Variation in gene expression and aberrantly regulated chromosome regions in cloned mice
Biology of Reproduction, ISSN: 0006-3363, Vol: 73, Issue: 6, Page: 1302-1311
2005
- 52Citations
- 25Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations52
- Citation Indexes52
- 52
- CrossRef42
- Captures25
- Readers25
- 25
Article Description
DNA microarray analysis was used to determine the precise genome-wide gene expression profiles of somatic cloned mice derived from Sertoli and cumulus cells. It demonstrated unexpectedly large epigenetic diversity in neonatal cloned mice, despite their normal appearance and genetic identity. In three neonatal tissues of the cloned mice, the expression of 9-40% of the genes examined was more than two times higher or lower in donor cell-dependent or -independent manners compared with normal controls. Relatively few (0.4-4%) of the genes exhibited up- or downregulation in the same manner in both types of clone. A cluster analysis of the variation in gene expression led to the identification of several chromosome regions in which gene expression was aberrantly controlled in the somatic clones. These results provide a more complete understanding of how somatic clones differ from each other and from normal individuals produced by sexual reproduction and indicate the significant difficulties that face the application of somatic cloning in regenerative medicine. © 2005 by the Society for the Study of Reproduction, Inc.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=28144458322&origin=inward; http://dx.doi.org/10.1095/biolreprod.105.044958; http://www.ncbi.nlm.nih.gov/pubmed/16120825; https://academic.oup.com/biolreprod/article-lookup/doi/10.1095/biolreprod.105.044958; https://dx.doi.org/10.1095/biolreprod.105.044958; https://academic.oup.com/biolreprod/article-abstract/73/6/1302/2667079?redirectedFrom=fulltext
Oxford University Press (OUP)
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