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We found that phosphorylation of the S114 priming residue altered the nucleocytoplasmic distribution of NHR-49 and was necessary for subsequent phosphorylation of adjacent residues by recombinant KIN-19 (Figs
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After RNA isolation from lymphocytes, isolated variable domain of heavy-chain-only antibody (VHH)-coding regions were amplified and cloned into phagemids to generate immune libraries followed by phage display 24
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