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1 inal fragment (40 kDa) was found to be fully adenylated.
2 he 3' end were accurately processed and then adenylated.
3 n the nucleoli was found to be processed and adenylated.
4 9/14-kDa proteins, was neither processed nor adenylated.
7 n events in eukaryotic cells can generate 5'-adenylated (5'-AMP) DNA termini that can be removed from
12 ervation indicates that the formation of the adenylated amino acid and its release are the rate-limit
14 n-coding transcripts, Ube3a-ATS was not poly-adenylated and was localized exclusively in the nucleus.
15 that mRNAs entering the editing pathway are adenylated and, therefore, competent for post-editing A/
16 syl-pantetheine conjugate is phosphorylated, adenylated, and phosphorylated once more to generate a f
17 y indicated that the homogeneous protein was adenylated as isolated, and sedimentation velocity exper
19 here find that maternal microRNAs are highly adenylated at their 3' ends in mature oocytes and early
20 N1 also failed to provide excision of the 5'-adenylated BER intermediate in mitochondrial extracts.
21 og N(2)-(carboxymethyl)-l-arginine (CMA) was adenylated by ATP in the crystal and represents a close
22 LF stimulates adenylation of LX complexes de-adenylated by pyrophosphate or following LX decharging d
26 blocked repair intermediates containing a 5'-adenylated-deoxyribose phosphate (5'-AMP-dRP) group.
27 R) intermediates containing the 5'-AMP or 5'-adenylated-deoxyribose phosphate (5'-AMP-dRP) lesions ma
30 simple method of enzymatic synthesis of pre-adenylated DNA linkers/adapters for next-generation sequ
33 at MS2-Xp54 represses the translation of non-adenylated firefly luciferase mRNAs and that mutations i
40 eeds in two steps, including synthesis of an adenylated intermediate followed by biotin transfer to t
45 e explains why nick sensing is restricted to adenylated ligase and why the 5' phosphate is required f
46 lysine residue prevented the formation of an adenylated ligase complex and consequently thwarted liga
47 reaction, the ATP-dependent formation of an adenylated ligase, was studied by measuring the formatio
48 formation of a DNA-bridging intermediate by adenylated LigIII that positions a pair of blunt-ended d
49 in the presence of ATP, suggesting that the adenylated lysine residue is part of the active site for
51 f P. trichocarpa cells, we revealed that the adenylated miRNAs were degraded slower than others witho
52 RNAs, such as housekeeping mRNAs or the poly-adenylated mRNA population, are believed to be distribut
54 te of phosphodiester bond formation at a pre-adenylated nick (step 3 of the ligation pathway) was slo
57 that formation of a phosphodiester at a pre-adenylated nick is subject to a rate limiting step that
58 and Asp65 suppressed ligase binding to a pre-adenylated nick, whereas Asp29, Glu67 and Glu161 mutants
63 e show that Aprataxin acts preferentially on adenylated nicks and double-strand breaks rather than on
64 demonstrate a role for APTX in resolving 5'-adenylated nucleic acid breaks, however, APTX function i
66 d REF/Aly-stabilized transcripts are further adenylated over time, consistent with previous reports l
72 e entire genome can be transcribed into poly-adenylated RNA when viewed at an evolutionary time scale
73 these results indicate that accumulation of adenylated RNA-DNA may contribute to neurological diseas
75 t RNA ligase may act on a specific set of 3'-adenylated RNAs to regulate their processing and downstr
77 he third step (attack of the 3'-OH on the 5'-adenylated strand to form a phosphodiester) by a factor
78 ortant for the attack of the 3'-OH on the 5'-adenylated strand to form a phosphodiester, but dispensa
80 However, the G617I mutant was only weakly adenylated, suggesting that a point mutation in the BRCT
81 placed in the 5'-leader region of capped and adenylated synthetic luciferase RNAs, conferred Arg-spec
85 aracterize the phylogenetic turnover of poly-adenylated transcripts in a comprehensive sampling of ta
86 nd Gtl2 generates alternatively spliced poly-adenylated transcripts lacking a conserved open reading
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