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The prevalence of loss of imprinting of H19 and IGF2 at birth
Imprinted genes are monoallelically expressed according to the parent of origin and are critical for proper placental and embryonic development. Disruption of methylation patterns at imprinted loci resulting in loss of imprinting (LOI) may lead to serious imprinting disorders (e.g., Beckwith-Wiedema...
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| Hauptverfasser: | , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Federation of American Societies for Experimental Biology
2013
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3714582/ https://ncbi.nlm.nih.gov/pubmed/23620526 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1096/fj.12-225284 |
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