In amyotrophic lateral sclerosis (ALS) spinal motor neurons (SpMN) progressively degenerate while a subset of cranial motor neurons (CrMN) are spared until late stages of the disease. Using a rapid and efficient protocol to differentiate mouse embryonic stem cells (ESC) to SpMNs and CrMNs. we now report that ESC-derived CrMNs accumulate less human (h)SOD1 and insoluble p62 than SpMNs ... https://olivebookmarks.com/story19598862/seromolecular-study-on-the-prevalence-and-risk-factors-of-toxoplasma-gondii-infection-in-pregnant-women-referred-to-a-gynecology-hospital-in-urmia-northwest-part-of-iran-in-2022