戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
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.
5                We show that ligases generate adenylated 5' ends containing a ribose characteristic of
6  that produces chemically adducted, toxic 5'-adenylated (5'-AMP) DNA lesions.
7 n events in eukaryotic cells can generate 5'-adenylated (5'-AMP) DNA termini that can be removed from
8                                    While pre-adenylated adapters can be chemically or enzymatically p
9 ofiling assays is adapter ligation using pre-adenylated adapters.
10                          ErEN cleavage of an adenylated alpha-globin 3'UTR was accentuated upon deple
11                                          The adenylated Alu RNA as well as adenylated SRP RNA were bo
12 ervation indicates that the formation of the adenylated amino acid and its release are the rate-limit
13                                              Adenylated and uridylated forms of these RNAs accumulate
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
18 able phosphoramidate-linked analogue of acyl-adenylated aspartic acid.
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
23 oup and then forms a thioester bond with the adenylated C-terminal COOH group of the Ubl.
24 -mitochondrially encoded RNAs over their non-adenylated counterparts.
25 lso bind a second neurokine called pituitary adenylated cyclase-activating polypeptide (PACAP).
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
28 he differences in efficiency of ligating pre-adenylated DNA adapters to RNA 3'-ends.
29 ues 233 to 919) in complex with a nicked, 5' adenylated DNA intermediate.
30  simple method of enzymatic synthesis of pre-adenylated DNA linkers/adapters for next-generation sequ
31 nate with each other in processing of the 5'-adenylated dRP-containing BER intermediate.
32  theta and Ku70) were found to remove the 5'-adenylated-dRP group from the BER intermediate.
33 at MS2-Xp54 represses the translation of non-adenylated firefly luciferase mRNAs and that mutations i
34 horylated single-stranded DNA (ssDNA) to the adenylated form.
35            In vitro transcribed, capped, and adenylated granulocyte-macrophage colony stimulating fac
36 an McC maturation intermediate consisting of adenylated heptapeptide.
37                 While mapping total and poly-adenylated human transcriptomes has now become routine,
38                            DNA LIG k becomes adenylated in reactions with ATP, and the adenylate moie
39 of SRP RNA, is also accurately processed and adenylated in vitro.
40 eeds in two steps, including synthesis of an adenylated intermediate followed by biotin transfer to t
41 to either RNA 3'p or DNA 3'p to generate the adenylated intermediate.
42                  These 3'-terminal phosphate-adenylated intermediates are substrates for deadenylatio
43       The formation of kinetically competent adenylated intermediates was suggested by the observatio
44 also found in a number of proteins that form adenylated intermediates.
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
50 HI4) copurifies with a set of strongly bound adenylated metabolites.
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
53 e deadenylases and repress translation of an adenylated mRNA.
54 te of phosphodiester bond formation at a pre-adenylated nick (step 3 of the ligation pathway) was slo
55 lyzes phosphodiester bond formation at a pre-adenylated nick (step 3).
56                                      When an adenylated nick is encountered by APTX, base pairing at
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
59  effect on phosphodiester formation at a pre-adenylated nick.
60 ed in phosphodiester bond formation at a pre-adenylated nick.
61 ompetent to catalyze strand closure at a pre-adenylated nick.
62 lyzes phosphodiester bond formation at a pre-adenylated nick.
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
65                                          The adenylated or activated biotin functions as the corepres
66 d REF/Aly-stabilized transcripts are further adenylated over time, consistent with previous reports l
67 nicks in double-stranded DNA to produce a 3'-adenylated product.
68 simplifies isolation and purification of the adenylated product.
69 synthetase (hLysRS) by proceeding through an adenylated protein intermediate.
70             Injection of mutant helicases or adenylated reporter mRNA abrogates this association.
71 omoted rapid deadenylation and decay of hypo-adenylated reporter mRNA.
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
74                     APTX efficiently repairs adenylated RNA-DNA, and acting in an RNA-DNA damage resp
75 t RNA ligase may act on a specific set of 3'-adenylated RNAs to regulate their processing and downstr
76            The adenylated Alu RNA as well as adenylated SRP RNA were bound to the SRP 9/14-kDa hetero
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
79 s the primary determinant for recognition of adenylated substrates.
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
82 siae thiazole synthase, was identified as an adenylated thiazole tautomer.
83                                        Fully adenylated TNF-alpha mRNA appeared within 15 min of LPS
84                   Methionine is subsequently adenylated to S-adenosylmethionine (SAM), a cofactor tha
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

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。