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Description
Cytoskeletal remodeling is an early manifestation of podocyte injury in DKD
Wilson disease: Copper everywhere Wilson disease is caused by mutation of the ATP7B gene, which results in impaired copper excretion and accumulation of toxic levels of copper in many organs principally the liver, brain, and eye
A structural model for GroEL-polypeptide recognition
It also plays an essential role in the glutathione antioxidant cycle and is required to regenerate reduced glutathione
