Consistent with the previous identification of ER stress as a hallmark of the MS CNS [16, 36], we detected increased expression of calnexin, BiP/GRP78, GRP94, and the CCAAT/enhancer-binding protein (C/EBP) homologous protein (CHOP) in active, but not chronic lesions (Fig. 1d). This evidence concerns the gene HSP90B1 and myeloid sarcoma.