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</script>doi: 10.1038/ng1253
pmid: 14528307
To address the biological function of RNA interference (RNAi)-related pathways in mammals, we disrupted the gene Dicer1 in mice. Loss of Dicer1 lead to lethality early in development, with Dicer1-null embryos depleted of stem cells. Coupled with our inability to generate viable Dicer1-null embryonic stem (ES) cells, this suggests a role for Dicer, and, by implication, the RNAi machinery, in maintaining the stem cell population during early mouse development.
Mice, Knockout, Ribonuclease III, Stem Cells, Molecular Sequence Data, DEAD-box RNA Helicases, Embryonic and Fetal Development, Mice, Endoribonucleases, Animals, RNA Interference, Amino Acid Sequence, RNA Helicases
Mice, Knockout, Ribonuclease III, Stem Cells, Molecular Sequence Data, DEAD-box RNA Helicases, Embryonic and Fetal Development, Mice, Endoribonucleases, Animals, RNA Interference, Amino Acid Sequence, RNA Helicases
| citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 2K | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 0.1% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 0.1% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 0.1% |
