C. Elegans worm provides clues to dealing with human disease A step towards understanding cell mutations that result in a variety of human being diseases, particularly in children – – including whatever brings about premature aging and early death – – has been taken by researchers at the Hebrew University of Jerusalem Silberman Institute of Lifestyle Sciences and the John Hopkins University College of Medicine. The researchers have focused their research on a report of induced mutations in the nuclear envelope of cells from the small C read . Elegans worm. Their aim is to thus provide clues towards a better understanding of mutations in proteins of the envelope of the cell nucleus in humans. Related StoriesGriffith University uncovers first 3-D picture of protein linked to cancer spreadRice researchers solve long-position mystery about hemophilia proteinMyriad RBM's DiscoveryMAP platform identifies protein biomarkers associated with CV occasions in diabetes patientsSuch mutations, particularly in lamin proteins A and C, trigger many different diseases, including Hutchison Gilford progeria syndrome.

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