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We also show that the cross-linking occurs as soon as the AP site arrives to a common favorable position relative to uS3, which is independent on its location in the mRNA. Our findings suggest that the mechanism of stopping translation of damaged mRNAs involving uS3, along with the one mentioned above, could underlie ribosome-associated mRNA quality control.To improve accrual to a randomized clinical trial of double unrelated cord blood (dUC versus HLA-haploidentical bone marrow (haplo-BM) transplantation, patients with less previous
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