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Recently, a team of researchers led by Ayhan Yurtsever, Takeshi Fukuma, and Linhao Sun from Kanazawa University, in collaboration with Yuhei Hayamizu at the Institute of Science Tokyo and Mehmet ...
Researchers from the Department of Biology at IISER Pune, in collaboration with teams at University of Toronto and Pontificia ...
Lysosomal Storage Disorders are a rare deadly genetic disorder spreading in India Learn about its causes symptoms ...
Among the hundreds of proteins that are secreted by Legionella pneumophila (the causative agent of Legionnaires’ disease) ...
The molecules that form the foundation of life on Earth are as diverse as they are complex. Among these, carbohydrates play a ...
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AZoLifeSciences on MSNCryo-EM Structures Reveal How IVD Mutations Cause Isovaleric Acidemia ...IVD is a key enzyme in leucine catabolism, catalyzing the conversion of isovaleryl-CoA to 3-methylcrotonyl-CoA.
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News-Medical.Net on MSNStructural insights into IVD enzyme function and isovaleric acidemiaBackground IVD is a key enzyme in leucine catabolism, catalyzing the conversion of isovaleryl-CoA to 3-methylcrotonyl-CoA.
Researchers uncover how key enzymes team up to break down proteins, offering new insight into diseases like Alzheimer’s and certain cancers tied to protein mismanagement.
NPC’s treatment landscape is changing fast, with new FDA approvals and a promising pipeline shaping hope for this ultra-rare ...
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