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Guo 1,2,3 , (1)Environmental and Occupational Health Sciences Institute, Rutgers, the State University of New Jersey, Piscataway, NJ, (2)Department of Pharmacology and Toxicology, Rutgers, the State University of New Jersey, Piscataway, NJ, (3)Rutgers Center for Lipid Research, Rutgers, the State University of New Jersey, New Brunswick, NJ Background: Farnesoid X Receptor (FXR) has been identified as a therapeutic target for non-alcoholic steatohepatitis (NASH)

Although astrocytes support homeostatic salubrious functions to neurons in a healthy brain, they can also become toxic to neurons in a neurodegenerative brain 1

In contrast, autoimmune glomerulonephritis results from adaptive immune responses targeting specific autoantigens

They are present at varying frequencies and can contribute significantly to the global burden of anaemia via clinically significant homozygous forms and the more common, usually clinically silent carrier forms 243 (Table 3)

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