(Medical Xpress)—Researchers at The University of Manchester and King's College London, funded by Arthritis Research UK, have developed a new method to identify people that are at a very high-risk of developing rheumatoid ...
Sep 20, 2013
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A genetic mutation, known as GBA, that leads to early onset of Parkinson's disease and severe cognitive impairment (in about 4 to 7 percent of all patients with the disease) also alters how specific lipids, ceramides and ...
Sep 18, 2013
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Why some people are troubled by cold sores while others are not has finally been explained by scientists.
Sep 16, 2013
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Japanese researchers have identified a mutation associated with a higher incidence of lung cancer in Japanese women who do not smoke, but better survival in lung cancer patients. In a study published today in the journal ...
Sep 11, 2013
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Johns Hopkins scientists have identified a molecular marker called "Mig 6" that appears to accurately predict longer survival—up to two years—among patients prescribed two of the most widely used drugs in a class of anticancer ...
Sep 5, 2013
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Forensic DNA-based familial search methods may mistakenly identify individuals in a database as siblings or parents of an unknown perpetrator, when in fact they are distant relatives, according to research published August ...
Aug 14, 2013
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A new strategy that cripples the ability of the dengue virus to escape the host immune system has been discovered by A*STAR's Singapore Immunology Network (SIgN). This breakthrough strategy opens a door of hope to what may ...
Aug 13, 2013
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While it is well known that there is a strong genetic basis to both diabetes and obesity, and that they are linked, Australian researchers say that there are many rare genetic variants involved, which will pose a significant ...
Aug 7, 2013
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Complex genetic interaction between the mosquito and the virus that causes dengue fever lie at the spread of this dangerous disease, a study by French and Thai scientists said Thursday.
Jul 31, 2013
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(Medical Xpress)—A University of Alberta researcher has pinpointed a mutation that brings the medical community another step closer to treating those who suffer from a fatal type of muscular dystrophy.
Jul 30, 2013
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