Increasing the length of progerin’s isoprenyl anchor does not worsen bone disease or survival in mice with Hutchinson-Gilford progeria syndrome

Hutchinson-Gilford progeria syndrome (HGPS) is caused by the synthesis of a truncated prelamin A, commonly called progerin, that contains a carboxyl-terminal farnesyl lipid anchor. The farnesyl lipid anchor helps to target progerin to membrane surfaces at the nuclear rim, where it disrupts the integ...

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Autores principales: Davies, Brandon S. J., Yang, Shao H., Farber, Emily, Lee, Roger, Buck, Suzanne B., Andres, Douglas A., Spielmann, H. Peter, Agnew, Brian J., Tamanoi, Fuyuhiko, Fong, Loren G., Young, Stephen G.
Formato: Artigo
Lenguaje:Inglês
Publicado: American Society for Biochemistry and Molecular Biology 2009
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Articles
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3837462/
https://ncbi.nlm.nih.gov/pubmed/18757838
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1194/jlr.M800424-JLR200
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