A Tissue Engineered Blood Vessel Model of Hutchinson-Gilford Progeria Syndrome Using Human iPSC-derived Smooth Muscle Cells

Hutchison-Gilford Progeria Syndrome (HGPS) is a rare, accelerated aging disorder caused by nuclear accumulation of progerin, an altered form of the Lamin A gene. The primary cause of death is cardiovascular disease at about 14 years. Loss and dysfunction of smooth muscle cells (SMCs) in the vasculat...

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Detalles Bibliográficos
Autores principales: Atchison, Leigh, Zhang, Haoyue, Cao, Kan, Truskey, George A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557922/
https://www.ncbi.nlm.nih.gov/pubmed/28811655
http://dx.doi.org/10.1038/s41598-017-08632-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557922/
https://www.ncbi.nlm.nih.gov/pubmed/28811655
http://dx.doi.org/10.1038/s41598-017-08632-4

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