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1 ine deoxyribonucleosides: deoxyadenosine and deoxyinosine.
2 d not only from cordycepin, but also from 3'-deoxyinosine.
3 observed except in the case of a 3'-terminal deoxyinosine.
4 ng deoxyuridine compared with DNA containing deoxyinosine.
5 godeoxyribonucleotide containing 2-fluoro-2'-deoxyinosine.
6 ses acting on RNA (ADAR enzymes) to generate deoxyinosine.
7                                              Deoxyinosine (22), a natural analog which has found exte
8                              Endonuclease V (deoxyinosine 3' endonuclease), the product of the nfi ge
9 and pseudo-Y DNA structures, suggesting that deoxyinosine 3'-endonuclease is a bacterial functional h
10    These biochemical properties suggest that deoxyinosine 3'-endonuclease might be important in the r
11                          Endonuclease V is a deoxyinosine 3'-endonuclease which initiates removal of
12                                              Deoxyinosine 3'-endonuclease, an Escherichia coli repair
13 zyl-3',5'-bis-O-(tert-butyldimethylsilyl)-2'-deoxyinosine (3).
14 uilding block, the O6-(benzotriazol-1-yl)-2'-deoxyinosine 5'-O-DMT 3'-O-phosphoramidite, has been pre
15 amidite monomer of N1-(2,4-dinitrophenyl)-2'-deoxyinosine 9 was prepared from 2'-deoxyinosine in four
16                                  However, 3'-deoxyinosine, a metabolite of cordycepin previously cons
17 ure of the N1-(1-hydroxy-3-buten-2(S)-yl)-2'-deoxyinosine adduct arising from the alkylation of adeni
18                           Rotation of the N1 deoxyinosine adduct into the high syn conformation may f
19 ded a plausible hypothesis as to why this N1 deoxyinosine adduct strongly coded for the incorporation
20 '-deoxynebularine analogues) and C-2 aryl 2'-deoxyinosine analogues can be conveniently prepared via
21 transformed to the desired N1-substituted 2'-deoxyinosine analogues.
22 e that recognizes and cleaves DNA containing deoxyinosine and base mismatches, can cleave heteroduple
23 tially high synthetic utility of 2-chloro-2'-deoxyinosine and in many instances this derivative can s
24 gPNP has kcat values of 54 and 41 s-1 for 2'-deoxyinosine and inosine, its preferred substrates, and
25 containing 2-fluoro-O(6)-trimethylsilylethyl deoxyinosines and the appropriate diamine (ethylenediami
26  in the repair of deaminated deoxyadenosine (deoxyinosine) and abasic sites in DNA, but there was no
27                                     (I is 2'-deoxyinosine), and 5'-...CG*C....
28    Deoxyguanosine is a weaker substrate than deoxyinosine, and DADMe-Immucillin-G is less tightly bou
29 ever, levels of the DNA deamination product, deoxyinosine, and the numbers of apurinic/apyrimidinic (
30 ivity is similar between the double-stranded deoxyinosine- and deoxyxanthosine-containing DNA.
31 The enzyme is also active on single-stranded deoxyinosine- and deoxyxanthosine-containing DNA.
32 e purified from an overproducing strain, the deoxyinosine- and mismatch-specific activities of endonu
33 e V exhibits limited turnover on cleavage of deoxyinosine- and xanthosine-containing DNA.
34 es the conversion of 5'-deoxyadenosine to 5'-deoxyinosine as its major product but will also deaminat
35 ent syntheses of 2-chloro- and 2-tosyloxy-2'-deoxyinosine as their tert-butyldimethylsilyl ethers are
36 CR primers containing mixed-base residues or deoxyinosine at positions of codon degeneracy.
37 edicts that MPG should be able to remove the deoxyinosine base from the DNA strand of RNA-DNA hybrids
38 rms two stable complexes with DNA containing deoxyinosine, but not with DNA containing base mismatche
39 iation, recognition, and dissociation of the deoxyinosine by the endo V, were determined at 5.9, 14.5
40 urine 2'-deoxyribonucleoside and 2-fluoro-2'-deoxyinosine, by the amino triol then yielded diastereom
41                               In addition to deoxyinosine-containing DNA, the enzyme cleaves DNA cont
42  V in a catalytic cycle using a substrate of deoxyinosine-containing single-stranded DNA (ssDNA).
43 des, leading to a mixture of deoxyadenosine, deoxyinosine, cytidine and uridine.
44  BcPh amino tribenzoates with the 2-bromo-2'-deoxyinosine derivative proceeded in comparable yields.
45 nthesized from the O6-(benzotriazol-1-yl)-2'-deoxyinosine derivative.
46 equisite O6-(benzotriazol-1-yl)inosine or 2'-deoxyinosine derivatives.
47 -dihydro-8-oxo-2'-deoxyguanosine (OxodG), 2'-deoxyinosine (dI) and 2'-deoxyguanosine (dG) in otherwis
48 and deoxycytidine (dC) were substituted with deoxyinosine (dI) and 3-(2'-deoxy-beta-D-ribofuranosyl)p
49                                              Deoxyinosine (dI) and deoxyxanthosine (dX) are both form
50 ing 7-deaza-2'-deoxyguanosine (dc(7)G) or 2'-deoxyinosine (dI) in place of dG support oligoribonucleo
51        Replacement of dG at 5'-d(CG) with 2'-deoxyinosine (dI), which lacks the exocyclic C2 amino gr
52 ridine (dU) and 2'-deoxyadenosine (dA) to 2'-deoxyinosine (dI; hypoxanthine).
53 nd two DNA subunits (deoxyadenosine, dA, and deoxyinosine, dI) can be coproduced in the same reaction
54 : 2'-deoxyuridine, 2'-deoxyxanthosine and 2'-deoxyinosine from nitrosative deamination; 8-oxo-2'-deox
55 l endonuclease, which cleaves the 5' side of deoxyinosine, from the hyperthermophilic archaeon, Pyroc
56 bolished in the 5'-...CIG*C...duplex (the 2'-deoxyinosine group, I, lacks this amino group).
57 ic efficiencies: thymidine > deoxyuridine >> deoxyinosine > deoxyguanosine.
58 of structurally disparate lesions, including deoxyinosine (I), which results from the spontaneous oxi
59 donuclease V (endo V) recognizes and cleaves deoxyinosine in deaminated DNA.
60 enyl)-2'-deoxyinosine 9 was prepared from 2'-deoxyinosine in four steps and incorporated into oligome
61 ts that convert A:T pairs into G:C through a deoxyinosine intermediate.
62 e, whereupon the 5'-deoxyribose moiety of 5'-deoxyinosine is further metabolized to deoxyhexoses used
63                                              Deoxyinosine is then converted into abasic sites by a DN
64 ugar-protected or -unprotected inosine or 2'-deoxyinosine nucleosides and 1H-benzotriazol-1-yloxy-tri
65 rates are not affected by bases opposite the deoxyinosine or deoxyxanthosine lesions.
66  (dA) was substituted with adenosine (A), 2'-deoxyinosine, or 2'-deoxyuridine, toxin-dependent signal
67 nd in replication using 7,8-dihydro-8-oxo-2'-deoxyinosine (OxodI).
68                  In contrast, the process of deoxyinosine recognition appeared little affected by the
69  to the 2-fluoro-O(6)-(2-trimethylsilylethyl)deoxyinosine residue of the 12-mer oligonucleotide.
70 oliovirus PCR primers contain mixed-base and deoxyinosine residues to compensate for the high degener
71           The primers contain mixed-base and deoxyinosine residues to compensate for the high rate of
72 l shift (1.3 ppm), indicating that C-6 of 2'-deoxyinosine retains its sp2 hybridization after binding
73 e-ImmH) is a transition-state mimic for a 2'-deoxyinosine ribocation with a fully dissociated N-ribos
74 eater than 20-fold higher for DNA containing deoxyinosine than deoxynebularine or base mismatches.
75 n of dCTP via Hoogsteen-type templating with deoxyinosine, thus generating A-to-G mutations.
76  with half-times ranging from 4 years for 2'-deoxyinosine to 40 years for 2'-deoxycytidine (37 degree
77  was performed to study the conversion of 3'-deoxyinosine to cordycepin 5'-triphosphate in vitro usin
78 ding 2'-deoxyuridine triphosphate (dUTP), 2'-deoxyinosine triphosphate (dITP), and 7-deaza-2'-deoxygu
79 omologs have high specificity for dHAPTP and deoxyinosine triphosphate compared with the four canonic
80  varation, filtering out data collected with deoxyinosine triphosphate during primer extension, gave
81 aminopurine triphosphate (dHAPTP) as well as deoxyinosine triphosphate.
82 otide mutagenesis with reversibly terminated deoxyinosine triphosphates (rtITP).
83 '-bis-O-(tert-butyldimethylsilyl)-2-bromo-2'-deoxyinosine, using a (+/-)-BINAP-Pd complex and Cs2CO3.
84                                           2'-deoxyinosine was converted into an N1-2,4-dinitrophenyl
85 ts yielded a structure in which the modified deoxyinosine was in the high syn conformation about the
86 ne epoxide (BDO), followed by deamination to deoxyinosine, was determined, in the oligodeoxynucleotid
87 osine, formycin A, adenosine, inosine, or 2'-deoxyinosine were determined by x-ray crystallography wi
88 c parameters of the 'universal pairing base' deoxyinosine were determined for the pairs I.C, I.A, I.T
89           Fletcherviruses replace dG with 2'-deoxyinosine, while the firehammerviruses replace dG wit
90 bound inosine in a different way, we labeled deoxyinosine with 13C, excepting an upfield shift of 70-
91 ...CIG*C... sequences, which contain "I" (2'-deoxyinosine), with hydrogen replacing the amino group i