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Such methods can more accurately confirm the precise location of YTHDF1 binding to SLC7A5 mRNA and the specific m6A-modified sites, thereby providing deeper insights into the molecular details of how YTHDF1 recognizes and regulates SLC7A5 translation

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In fact, LRRK2 gene mutation (G2019S mutation) is known to cause the majority of autosomal dominant familial forms of PD and some of the sporadic cases (Rui et al

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Vandoorne, T., De Bock, K