Temsirolimus Partially Rescues the Hutchinson-Gilford Progeria Cellular Phenotype
Author:
Funder
Progeria Research Foundation
Deutsche Forschungsgemeinschaft
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference65 articles.
1. Progeria: a paradigm for translational medicine;LB Gordon;Cell,2014
2. Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome;M Eriksson;Nature,2003
3. Lamin A truncation in Hutchinson-Gilford progeria;A De Sandre-Giovannoli;Science,2003
4. Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome;RD Goldman;Proc Natl Acad Sci U S A,2004
5. Dermal fibroblasts in Hutchinson-Gilford progeria syndrome with the lamin A G608G mutation have dysmorphic nuclei and are hypersensitive to heat stres;M Paradisi;BMC Cell Biol,2005
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