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Grafika:Hutchinson-Gilford Progeria Syndrome.png - Wikipedia, wolna encyklopedia

Grafika:Hutchinson-Gilford Progeria Syndrome.png

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Description

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).

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

Date

Published: November 15, 2005

Author

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aktualny20:44, 4 gru 20061 200×968 (1,09 MB)Ayacop ({{Information |Description='''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 )

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