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By integrating glutamine restriction with the modulation of tryptophan-derived metabolites, these amino acid-centered strategies provide a comprehensive approach to interrupting pathogenic persistence in AITD

used phenylboronic acid (PBA)-derived LNPs to achieve cell-selective genome editing in sialic acid (SA)-overexpressing cervical cancer cells (Tang et al., 2019)

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To assess whether the statistical power of this MR analysis meets the required threshold, we calculated a power of 0.83, which partially validates the reliability of our study

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Acknowledgements This work was supported by NIH grants R01 DC002368 (P.B-G.), R01 DC011034 (P.B-G.), R01 DC005965 (U.M.) and RO1 DC007704 (U.M.)