Latest Mutation Stories
Researchers have discovered a link between nearsightedness and mutations in a gene partially responsible for the regulation of copper and oxygen levels in eye tissues, according to a paper published in Thursday’s edition of the American Journal of Human Genetics.
An international research consortium led by the Universitat Autònoma de Barcelona (UAB), the CIBERER and the University of Wurzburg (Germany) has discovered a gene that can cause three totally different diseases, depending on how it is altered.
Cancer is typically thought to develop after genes gradually mutate over time, finally overwhelming the ability of a cell to control growth.
UAlberta research team uses caffeine and fruit flies to pinpoint genetic pathways that guide DNA repair in cancer cells.
A bizarre twist on the usual way proteins are made may explain mysterious symptoms in the grandparents of some children with mental disabilities.
Research led by a scientist at the University of York has thrown new light on the way breakdowns in the DNA copying process inside cells can contribute to cancer and other diseases.
A study led by St. Jude Children's Research Hospital has discovered mutations in two genes that lead to the death of nerve cells in amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease, and related degenerative diseases.
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