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Aromatic residues revealed in the fibril surface have actually a rigid band axis but undergo ring flips on a number of time scales from nanoseconds to microseconds. Our method provides direct insight into hydrophobic-core motions, allowing a much better analysis of this conformational heterogeneity created from an NMR architectural ensemble of such amyloid cross-β design. In today's research, the effect of HLA-DPB1 alloimmunity assessed by molecular mismatch algorithms regarding the growth of SSCs in a cohort of

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