Genetics in Disease
Longevity and Age Management
Genetic conditions linked to lung disease
Non-smokers are still at risk of developing chronic obstructive pulmonary disease (COPD) in their 30s, experts warn. ... Continue Reading
New gene discovered that increases diabetes risk
Scientists have identified a gene that increases the risk of type 2 diabetes, and regulates glucose levels. ... Continue Reading
Neurological genetics linked to progression of ALS
Geneticists at the University of Tokyo have shed new light on the genetics of the fatal neurological disease amyotrophic lateral sclerosis (ALS). ... Continue Reading
Biologists determine genetics in neurological disease
Toxic proteins created by faulty RNA have been found to contribute to a range of neurodegenerative disorders in humans. ... Continue Reading
Genetic link to prostate cancer risk identified
A genetic difference could explain why Caucasian men are more likely than Hispanic men to suffer from prostate cancer, a new paper has suggested. ... Continue Reading
Study reveals genetic control of blood proteins
An international team of scientists has discovered the way in which genes control levels of proteins in the blood that can influence the progression of disease. ... Continue Reading
Gene found to increase risk of heart problems
Researchers in London have identified a gene that increases the risk of heart attacks and heart failure. ... Continue Reading
Study links new genetic variations to psoriasis
Researchers at Washington University School of Medicine in St Louis have found seven new sites of DNA variation that increases the risk of psoriasis. ... Continue Reading
Researchers Identify Gene Most Often Responsible For Commonest Form Of Congenital Blindness
Eye Health Month is off to an exciting start, with the recent announcement by MUHC researcher Dr. Robert Koenekoop and his colleagues of a breakthrough discovery in the genetics of childhood blindness. The new study identified the gene most often responsible for LCA (Leber Congenital Amaurosis), the commonest form of congenital blindness. ... Continue Reading
Variation in 3 genes influences risk of age-related macular degeneration
Researchers in Boston have discovered a new common, noncoding variant in the Complement Factor H (CFH) gene that is associated with age-related macular degeneration (AMD), the leading cause of irreversible visual impairment and blindness among persons aged 60 and older. ... Continue Reading
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