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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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Detalhes bibliográficos
Main Authors: Rancourt, Rebecca C., Harris, Holly R., Barault, Ludovic, Michels, Karin B.
Formato: Artigo
Idioma:Inglês
Publicado em: Federation of American Societies for Experimental Biology 2013
Assuntos:
Acesso em linha: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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