MeSH tree: A11.284.430.214.190.875.248
A McGill-led team of researchers has made an important discovery shedding light on the genetic basis of a rare skeletal disorder. The study, published in Nature Communications, reveals that a defect in a specific gene (heterozygous ...
Jan 16, 2024
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A research group at the University of Helsinki and its partners have found a promising drug candidate for the treatment of amyotrophic lateral sclerosis (ALS). Cerebral dopamine neurotrophic factor CDNF prolongs the lifespan ...
Sep 22, 2023
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Researchers at the National Heart, Lung, and Blood Institute at NIH, Bethesda, have discovered a potential breakthrough for people with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), marked by extreme exhaustion, ...
Researchers from the University of Seville and the Seville Institute of Biomedicine (IBiS), in collaboration with the University of Cambridge, have identified a new role for one of the genes related to hereditary spastic ...
Mar 27, 2023
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Rendering the invisible visible is among scientists' favorite challenges.
Sep 26, 2022
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Variants of at least 20 different genes have been closely linked to the development of Parkinson's disease, but scientists are still investigating how exactly they cause the severe and incurable motor disorder that afflicts ...
Jul 15, 2022
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Autosomal dominant polycystic kidney disease (ADPKD) is a common genetic condition that can lead to kidney failure and that has no cure. Recent research published in JASN uncovers an over-looked mechanism that likely contributes ...
Jul 12, 2022
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