Activating the synthesis of progerin, the mutant prelamin A in Hutchinson–Gilford progeria syndrome, with antisense oligonucleotides

Hutchinson–Gilford progeria syndrome (HGPS) is caused by point mutations that increase utilization of an alternate splice donor site in exon 11 of LMNA (the gene encoding lamin C and prelamin A). The alternate splicing reduces transcripts for wild-type prelamin A and increases transcripts for a trun...

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Detalles Bibliográficos
Autores principales: Fong, Loren G., Vickers, Timothy A., Farber, Emily A., Choi, Christine, Yun, Ui Jeong, Hu, Yan, Yang, Shao H., Coffinier, Catherine, Lee, Roger, Yin, Liya, Davies, Brandon S.J., Andres, Douglas A., Spielmann, H. Peter, Bennett, C. Frank, Young, Stephen G.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2694694/
https://www.ncbi.nlm.nih.gov/pubmed/19376814
http://dx.doi.org/10.1093/hmg/ddp184

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