Hutchinson-Gilford progeria syndrome alters the endothelial genetic response to laminar shear stress
<h4>Introduction</h4>Hutchinson-Gilford Progeria Syndrome (HGPS) is a fatal, accelerated-aging disease caused by a mutation in the nuclear envelope protein Lamin A. The resulting mutant protein, progerin, accumulates on the nuclear envelope, causing nuclear blebbing, altered gene …
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