[HTML][HTML] A human iPSC model of Hutchinson Gilford Progeria reveals vascular smooth muscle and mesenchymal stem cell defects

J Zhang, Q Lian, G Zhu, F Zhou, L Sui, C Tan… - Cell stem cell, 2011 - cell.com
The segmental premature aging disease Hutchinson-Gilford Progeria syndrome (HGPS) is
caused by a truncated and farnesylated form of Lamin A called progerin. HGPS affects …

A human iPSC model of Hutchinson Gilford Progeria reveals vascular smooth muscle and mesenchymal stem cell defects

J Zhang, Q Lian, G Zhu, F Zhou, L Sui, C Tan… - Cell Stem Cell, 2011 - hub.hku.hk
The segmental premature aging disease Hutchinson-Gilford Progeria syndrome (HGPS) is
caused by a truncated and farnesylated form of Lamin A called progerin. HGPS affects …

[PDF][PDF] A Human iPSC Model of Hutchinson Gilford Progeria Reveals Vascular Smooth Muscle and Mesenchymal Stem Cell Defects

J Zhang, Q Lian, G Zhu, F Zhou, L Sui, C Tan… - Cell Stem …, 2011 - academia.edu
The segmental premature aging disease Hutchinson-Gilford Progeria syndrome (HGPS) is
caused by a truncated and farnesylated form of Lamin A called progerin. HGPS affects …

A human iPSC model of Hutchinson Gilford Progeria reveals vascular smooth muscle and mesenchymal stem cell defects

J Zhang, Q Lian, G Zhu, F Zhou, L Sui, C Tan… - Cell stem …, 2011 - pubmed.ncbi.nlm.nih.gov
The segmental premature aging disease Hutchinson-Gilford Progeria syndrome (HGPS) is
caused by a truncated and farnesylated form of Lamin A called progerin. HGPS affects …

[引用][C] A Human iPSC Model of Hutchinson Gilford Progeria Reveals Vascular Smooth Muscle and Mesenchymal Stem Cell Defects

J ZHANG, Q LIAN, CL STEWART, A COLMAN… - Cell stem …, 2011 - pascal-francis.inist.fr
A Human iPSC Model of Hutchinson Gilford Progeria Reveals Vascular Smooth Muscle and
Mesenchymal Stem Cell Defects CNRS Inist Pascal-Francis CNRS Pascal and Francis …

[PDF][PDF] A Human iPSC Model of Hutchinson Gilford Progeria Reveals Vascular Smooth Muscle and Mesenchymal Stem Cell Defects

J Zhang, Q Lian, G Zhu, F Zhou, L Sui, C Tan… - Cell Stem Cell, 2011 - core.ac.uk
The segmental premature aging disease Hutchinson-Gilford Progeria syndrome (HGPS) is
caused by a truncated and farnesylated form of Lamin A called progerin. HGPS affects …

A human iPSC model of Hutchinson Gilford Progeria reveals vascular smooth muscle and mesenchymal stem cell defects.

J Zhang, Q Lian, G Zhu, F Zhou, L Sui, C Tan… - Cell Stem …, 2010 - europepmc.org
The segmental premature aging disease Hutchinson-Gilford Progeria syndrome (HGPS) is
caused by a truncated and farnesylated form of Lamin A called progerin. HGPS affects …

[HTML][HTML] A Human iPSC Model of Hutchinson Gilford Progeria Reveals Vascular Smooth Muscle and Mesenchymal Stem Cell Defects

J Zhang, Q Lian, G Zhu, F Zhou, L Sui, C Tan… - Cell Stem Cell, 2011 - cell.com
The segmental premature aging disease Hutchinson-Gilford Progeria syndrome (HGPS) is
caused by a truncated and farnesylated form of Lamin A called progerin. HGPS affects …

[HTML][HTML] A Human iPSC Model of Hutchinson Gilford Progeria Reveals Vascular Smooth Muscle and Mesenchymal Stem Cell Defects

J Zhang, Q Lian, G Zhu, F Zhou, L Sui, C Tan… - Cell Stem Cell, 2011 - Elsevier
The segmental premature aging disease Hutchinson-Gilford Progeria syndrome (HGPS) is
caused by a truncated and farnesylated form of Lamin A called progerin. HGPS affects …

A Human iPSC Model of Hutchinson Gilford Progeria Reveals Vascular Smooth Muscle and Mesenchymal Stem Cell Defects

J Zhang, Q Lian, G Zhu, F Zhou, L Sui, C Tan… - Cell Stem Cell, 2011 - infona.pl
The segmental premature aging disease Hutchinson-Gilford Progeria syndrome (HGPS) is
caused by a truncated and farnesylated form of Lamin A called progerin. HGPS affects …