Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients

Beckwith-Wiedemann syndrome (BWS) and Silver-Russell syndrome (SRS) are imprinting-related disorders associated with genetic/epigenetic alterations of the 11p15.5 region, which harbours two clusters of imprinted genes (IGs). 11p15.5 IGs are regulated by the methylation status of imprinting control r...

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Detalles Bibliográficos
Autores principales: Rovina, Davide, La Vecchia, Marta, Cortesi, Alice, Fontana, Laura, Pesant, Matthieu, Maitz, Silvia, Tabano, Silvia, Bodega, Beatrice, Miozzo, Monica, Sirchia, Silvia M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7237657/
https://www.ncbi.nlm.nih.gov/pubmed/32427849
http://dx.doi.org/10.1038/s41598-020-65082-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7237657/
https://www.ncbi.nlm.nih.gov/pubmed/32427849
http://dx.doi.org/10.1038/s41598-020-65082-1

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