File:Progeria picture.png

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Summary

Hutchinson-Gilford Progeria Syndrome. HGPS is a childhood disorder caused by mutations in one of the major architectural proteins of the cell nucleus. In HGPS patients the cell nucleus has dramatically aberrant morphology (bottom, right) rather than the uniform shape typically found in healthy individuals (top, right).

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Public Domain

Source:

The Cell Nucleus and Aging: Tantalizing Clues and Hopeful Promises. Scaffidi P, Gordon L, Misteli T. PLoS Biology Vol. 3/11/2005, e395 http://dx.doi.org/10.1371/journal.pbio.0030395

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Date/TimeThumbnailDimensionsUserComment
current05:02, 16 November 2012Thumbnail for version as of 05:02, 16 November 20121,200 × 968 (1.09 MB)NinjaKenHutchinson-Gilford Progeria Syndrome. HGPS is a childhood disorder caused by mutations in one of the major architectural proteins of the cell nucleus. In HGPS patients the cell nucleus has dramatically aberrant morphology (bottom, right) rather than the u

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