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The ability of NAC to cross the blood brain barrier has been questioned, an important consideration for use in neurodegenerative diseases
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Since the binding of SNIP1 to the wild-type and mutated (Thr358A and Thr369A) SF3B1 proteins remained equal, this indicates that the other P-Thr residues in SF3B1 can compensate for the loss of P-Thr358 and P-Thr369 (Supplementary Fig
