This a model from the article:
A theoretical study on activation of transcription factor modulated by intracellular Ca2+ oscillations.
Zhu CL, Zheng Y, Jia Y
Biophys. Chem.[2007 Aug:129(1):49-55
17560007,
Abstract:
This work presents bo...
Hutchinson Gilford Progeria Syndrome (HGPS) is a rare, sporadic genetic disease caused by mutations in the nuclear lamin A gene. In most cases the mutation creates an efficient donor-splice site that generates an altered transcript encoding a truncated lamin A protein, progerin. In vitro studies ha...
