A ceRNA approach may unveil unexpected contributors to deletion syndromes, the model of 5q- syndrome

In genomic deletions, gene haploinsufficiency might directly configure a specific disease phenotype. Nevertheless, in some cases no functional association can be identified between haploinsufficient genes and the deletion-associated phenotype. Transcripts can act as microRNA sponges. The reduction o...

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Detalles Bibliográficos
Autores principales: Arancio, Walter, Genovese, Swonild Ilenia, Bongiovanni, Lucia, Tripodo, Claudio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Research Perspective
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4671954/
https://www.ncbi.nlm.nih.gov/pubmed/26682279

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4671954/
https://www.ncbi.nlm.nih.gov/pubmed/26682279

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