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Keywords: HGPS
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Journal Articles
J Cell Sci (2014) 127 (8): 1792–1804.
Published: 15 April 2014
...Zi-Jie Chen; Wan-Ping Wang; Yu-Ching Chen; Jing-Ya Wang; Wen-Hsin Lin; Lin-Ai Tai; Gan-Guang Liou; Chung-Shi Yang; Ya-Hui Chi ABSTRACT Hutchinson-Gilford progeria syndrome (HGPS) is a human progeroid disease caused by a point mutation on the LMNA gene. We reported previously that the accumulation...
Includes: Supplementary data
Journal Articles
J Cell Sci (2006) 119 (16): 3265–3272.
Published: 15 August 2006
..., which is defective in two congenital diseases: Hutchinson-Gilford progeria (HGPS) and restrictive dermopathy (RD). These two diseases arise respectively from defects in the prelamin A substrate and the enzyme (ZmpSte24) that processes it. Recent work has shed light on the roles of the lamin proteins...