Ankyrin G overexpression in Hutchinson-Gilford progeria syndrome fibroblasts identified through biological filtering of expression profiles [PDF]
Jian Wang+7 more
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Nesprin-2 giant safeguards nuclear envelope architecture in LMNA S143F progeria cells [PDF]
Sebastian Kandert+12 more
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Progeria is a rare genetic disease with striking features that resemble accelerated aging. The inheritance pattern, paternal age effect, and lack of consanguinity argue that it is due to a sporadic dominant mutation. We have observed elevated levels of hyaluronic acid (HA) excretion in progeria patients.
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Phenotype and Course of Hutchinson–Gilford Progeria Syndrome [PDF]
Melissa A. Merideth+24 more
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Severe Mandibuloacral Dysplasia-Associated Lipodystrophy and Progeria in a Young Girl with a Novel Homozygous Arg527Cys LMNA Mutation [PDF]
Anil K. Agarwal+3 more
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Increasing the length of progerin's isoprenyl anchor does not worsen bone disease or survival in mice with Hutchinson-Gilford progeria syndrome [PDF]
Brandon S.J. Davies+10 more
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Highlights of the 2007 Progeria Research Foundation Scientific Workshop: Progress in Translational Science [PDF]
L. B. Gordon+2 more
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Assessing the efficacy of protein farnesyltransferase inhibitors in mouse models of progeria [PDF]
Shao H. Yang+5 more
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