Tet1 is dispensable for maintaining pluripotency and its loss is compatible with embryonic and postnatal development. [electronic resource]
Producer: 20120315Description: 166-75 p. digitalISSN:- 1875-9777
- 5-Methylcytosine -- analogs & derivatives
- Animals
- Animals, Newborn
- Body Size
- Cytosine -- analogs & derivatives
- DNA Methylation -- genetics
- DNA-Binding Proteins -- deficiency
- Embryo, Mammalian -- metabolism
- Embryonic Development -- genetics
- Embryonic Stem Cells -- cytology
- Female
- Fertility
- Gene Expression Regulation, Developmental
- Gene Knockout Techniques
- Genetic Complementation Test
- Mice
- Mice, Inbred C57BL
- Pluripotent Stem Cells -- cytology
- Proto-Oncogene Proteins -- deficiency
- Tetraploidy
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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