Cargando…
Stochastic Loss of Silencing of the Imprinted Ndn/NDN Allele, in a Mouse Model and Humans with Prader-Willi Syndrome, Has Functional Consequences
Genomic imprinting is a process that causes genes to be expressed from one allele only according to parental origin, the other allele being silent. Diseases can arise when the normally active alleles are not expressed. In this context, low level of expression of the normally silent alleles has been...
Autores principales: | Rieusset, Anne, Schaller, Fabienne, Unmehopa, Unga, Matarazzo, Valery, Watrin, Françoise, Linke, Matthias, Georges, Beatrice, Bischof, Jocelyn, Dijkstra, Femke, Bloemsma, Monique, Corby, Severine, Michel, François J., Wevrick, Rachel, Zechner, Ulrich, Swaab, Dick, Dudley, Keith, Bezin, Laurent, Muscatelli, Françoise |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3764186/ https://www.ncbi.nlm.nih.gov/pubmed/24039599 http://dx.doi.org/10.1371/journal.pgen.1003752 |
Ejemplares similares
-
Context-Aware Naming and Forwarding in NDN-Based VANETs
por: Zafar, Waseeq Ul Islam, et al.
Publicado: (2021) -
Natural breaking of the maternal silence at the mouse and human imprinted Prader-Willi locus: A whisper with functional consequences
por: Matarazzo, Valery, et al.
Publicado: (2013) -
Popularity-Aware Closeness Based Caching in NDN Edge Networks
por: Amadeo, Marica, et al.
Publicado: (2022) -
The Prader-Willi syndrome murine imprinting center is not involved in the spatio-temporal transcriptional regulation of the Necdin gene
por: Watrin, Françoise, et al.
Publicado: (2005) -
Is prone sleeping dangerous for neonates? Polysomnographic characteristics and NDN gene analysis
por: Wong, Shi-Bing, et al.
Publicado: (2019)