Morning Overview on MSN
Ancient DNA uncovers 12,000-year-old case of rare genetic disorder
A teenager who lived in southern Europe around 12,000 years ago has become the earliest person in history to receive a ...
A McGill-led team of researchers have 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 ...
A McGill-led team of researchers have 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 ...
A new biopharmaceutical company is devoted to developing therapies for rare bone diseases in Montreal. Ocythera was launched ...
Explore the vital role of bone marrow stem cells. Learn how they drive bone remodeling, immunity, and skeletal health in this ...
A new study has unveiled the crucial role of low-density lipoprotein receptor-related protein 1 (LRP1) in skeletal development. Researchers have found that a deficiency of LRP1 in skeletal progenitor ...
Skeletal muscle channelopathies and myotonic disorders constitute a heterogeneous group of neuromuscular conditions caused by mutations that impair the function of ion channels, including sodium and ...
A recent review article in Bone Research examines the role of skeletal interoception in bone health and evaluates biomaterials designed to interact with this system to improve bone regeneration. The ...
Researchers led by the University of Vienna and Liège University Hospital Center have identified genetic variants associated ...
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