Metabolic Enzyme Alterations and Astrocyte Dysfunction in a Murine Model of Alexander Disease With Severe Reactive Gliosis.

Last, in Western blots from human AxD patients and controls, the amount of UGT8 appeared depleted but did not reach statistical significance, perhaps due to low sample number of this rare disease (<1 in 1,000,000 individuals).

also in 111,027 other papers