Two siblings who have the only known mutations in a key gene anywhere in the world have helped scientists gain new insights that could help progress the search for new treatments in type 1 diabetes.
Siblings with unique genetic change help scientists progress drug search for type 1 diabetes." ScienceDaily. ScienceDaily, 18 April 2024. <www.sciencedaily.comUniversity of Exeter. . Siblings with unique genetic change help scientists progress drug search for type 1 diabetes.
The rare genetic disease cystinosis is caused by mutations in the gene for a protein called cystinosin. A team of scientists has now solved the structure of cystinosin and determined how mutations ... Researchers used advanced three-dimensional mapping techniques at a microscopic level to identify a multitude of genetic variants and corresponding target gene pairings in the pancreas that are ...
Across the world, type 2 diabetes is on the rise. A research group has discovered a new gene that may hold the key to preventing and treating lifestyle related diseases such as type 2 ... An academic has helped draw up a landmark agreement amongst international experts, setting out the world's first standard guidance on how people with diabetes can use modern glucose monitoring ...LIVING & WELL
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