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 ylated bases such as N7-methylguanine and N3-methyladenine.
2 nhibitors and with the autophagy inhibitor 3-methyladenine.
3 by 9-methyladenine is 50% stronger than by 7-methyladenine.
4 lear DNA of Tetrahymena are methylated to N6-methyladenine.
5 Alkbh1 encodes a demethylase for N(6)-methyladenine.
6 Tetrahymena thermophila are modified to N 6-methyladenine.
7 triction) recognizes both methylcytosine and methyladenine.
8 ing 3-methylthymidine, 3-methyluracil, and 6-methyladenine.
9 ensitivity to PI3K-class III inhibition by 3-methyladenine.
13 sal of alkylation damage to DNA; primarily 1-methyladenine (1mA) and 3-methylcytosine (3mC) lesions c
14 te and excise N3-methylcytosine (3mC) and N1-methyladenine (1mA), which are also repaired by AlkB-cat
15 nine alkyl derivatives 9-ethyladenine (2), 3-methyladenine (3), 1-methyladenine (4), and N,N-dimethyl
16 we used the stable 3-deaza analog, 3-deaza-3-methyladenine (3-dMeA), which blocks the DNA minor groov
17 rmacological inhibition of autophagy using 3-methyladenine (3-MA) completely suppressed transitory fu
19 nfected cells with the autophagy inhibitor 3-methyladenine (3-MA) markedly reduced the viral titer, a
20 ical or genetic inhibition of autophagy by 3-methyladenine (3-MA) or Beclin-1 small interfering RNA (
21 Autophagy activation was inhibited using 3-methyladenine (3-MA) or siRNA knockdown of Atg5 and the
22 th the phosphoinositide-3 kinase inhibitor 3-methyladenine (3-MA) or were transfected with autophagy-
23 from the combination of 5.Let (or 4) with 3-methyladenine (3-MA) or with curcumin, respectively, rev
25 phagy inhibitors hydroxychloroquine (HCQ), 3-methyladenine (3-MA), and bafilomycin A1 (BafA1) prevent
26 hatidylinositol 3-kinase (PI3K) inhibitor, 3-methyladenine (3-MA), or by depletion of the autophagy-r
29 mal (MG-132 and MG-262) and ALD [NH4Cl and 3-methyladenine (3-MA)] inhibitors to examine their specif
30 as synthesized to preferentially generate N3-methyladenine (3-MeA) adducts which are expected to be c
31 NA glycosylase I (TAG) in complex with its 3-methyladenine (3-MeA) cognate base, and we have used che
33 from the knockout (ko) animals to release 3-methyladenine (3-meA) or 7-methylguanine (7-meG) from 3H
34 beclin-1, or Atg5 or pharmacologically by 3-methyladenine [3-MA] or spautin-1), arguing that NBK/Bik
35 strates (7-methyladenine, 7-methylguanine, 3-methyladenine, 3-methylguanine, purine, 6-chloropurine,
47 including N(7)-methylguanine (7MeG) and N(3)-methyladenine (3MeA), can be induced by environmental me
48 s 9-ethyladenine (2), 3-methyladenine (3), 1-methyladenine (4), and N,N-dimethyladenine (5) have been
49 ucleotides in the DNA template, including N6-methyladenine, 5-methylcytosine and 5-hydroxymethylcytos
51 he bases and their mean amounts (in %) are 2-methyladenine (60.6%), p-cresol (16.3%), adenine (12.5%)
52 the prevalence and significance of DNA N(6)-methyladenine (6mA or m(6)dA) in eukaryotes had been und
53 chlorella viruses contain high levels of N6-methyladenine (6mA) and 5-methylcytosine (5mC), but the
56 A methylation in R-M systems, including N(6)-methyladenine (6mA), 5-methylcytosine (5mC) and N(4)-met
58 ed for a series of AlkA purine substrates (7-methyladenine, 7-methylguanine, 3-methyladenine, 3-methy
59 alkylation and oxidative damage, including 3-methyladenine, 7-methylguanine, hypoxanthine (Hx), and 1
60 f P2Y antagonists related to a 2-chloro-N(6)-methyladenine-9-(2-methylpropyl) scaffold, containing un
61 or cell treatment with autophagy inhibitor 3-methyladenine, a class III PI3K (hVps34) inhibitor, also
62 has defined the biological consequences of 3-methyladenine, a DNA lesion produced by endogenous cellu
66 In addition, it is demonstrated that both N3-methyladenine adduction and cytotoxicity can be inhibite
70 vival of cardiac myocytes was decreased by 3-methyladenine, an inhibitor of autophagy, suggesting tha
72 n-induced neuronal death was attenuated by 3-methyladenine, an inhibitor of autophagy; Atg7 knockdown
73 e for the removal of damaged bases such as 3-methyladenine and 1,N(6)-ethenoadenine from the DNA afte
74 pairs of adenine and thymine, (AT)(-), and 9-methyladenine and 1-methylthymine, (MAMT)(-), have been
77 ntly found to repair cytotoxic DNA lesions 1-methyladenine and 3-methylcytosine by using a novel iron
80 of AlkB enzymes remove methyl groups from 1-methyladenine and 3-methylcytosine in nucleic acids via
81 urified AlkB repairs the cytotoxic lesions 1-methyladenine and 3-methylcytosine in single- and double
82 include 3-methylthymine in DNA, as well as 1-methyladenine and 3-methylcytosine, which all have struc
83 lating agents by repair of the DNA lesions 1-methyladenine and 3-methylcytosine, which are generated
85 h between two DNA fragments carrying both N6-methyladenine and 5-methylcytosine but differing only in
86 o previously described SMRT sequencing of N6-methyladenine and 5-methylcytosine, we show that N4-meth
87 n repair rates of dimethyl sulfate-induced 3-methyladenine and 7-methylguanine adducts were measured
88 yme did not remove alkylated bases such as 3-methyladenine and 7-methylguanine whereas methyl-formami
90 Modeling studies with the cytotoxic lesion 3-methyladenine and accompanying biochemical experiments s
91 goadenylates as long as undecamer, and the 2-methyladenine and adenine derivatives on montmorillonite
94 d (trehalose and Rab1A) or down-regulated (3-methyladenine and ATG5 shRNA) by enhancers or inhibitors
96 d cellular autophagy and was suppressed by 3-methyladenine and bafilomycin A1, by inhibitors of lysos
97 by treatment with the autophagy inhibitor 3-methyladenine and by treatment with the potential therap
98 tization, we used the autophagy inhibitors 3-methyladenine and chloroquine and found that either drug
100 G), which repairs the cytotoxic lesions N(3)-methyladenine and N(7)-methylguanine, may contribute to
102 SMRT) sequencing enables the detection of N6-methyladenine and N4-methylcytosine, two major types of
103 clear relationship between the levels of N3-methyladenine and toxicity in an alkA/tag glycosylase mu
104 tionship between the in vivo formation of N3-methyladenine and toxicity in wild-type and base excisio
106 d in the presence of PI3 kinase inhibitors 3-methyladenine and Wortmannin and also by depletion of At
108 The results demonstrate the importance of 3-methyladenine, and in some cases 3-methylguanine, lesion
110 TMZ-induced lesions (N7-methylguanine and N3-methyladenine) are base excision repair (BER) substrates
112 of MMS-induced alkylation damage, such as N3-methyladenine, as well as bypassing the abasic sites gen
113 ls with a specific inhibitor of autophagy (3-methyladenine) attenuated localization of LC3 to autopha
115 alkylation therapy, by excising cytotoxic N3-methyladenine bases formed by DNA-targeting anticancer c
116 ition of autophagy at an early stage using 3-methyladenine blocked UV-induced autophagic flux in A-T
117 atly alleviated by the autophagy inhibitor 3-methyladenine but not by the proteasome inhibitor N-benz
118 hagy by chemical or genetic means by using 3-methyladenine, chloroquine, a dominant negative form of
119 nhibition of autophagy by pharmacological (3-methyladenine, chloroquine, or bafilomycin A1) or geneti
121 ion of FCVs was significantly inhibited by 3-methyladenine, confirming a role for the autophagic path
125 Here we show that the autophagy inhibitor 3-methyladenine delays neuronal cell loss caused by dysfun
132 lamine or the inhibitor of macroautophagy, 3-methyladenine, did not prevent rapamycin from partially
136 between ERalpha and the DNA repair protein 3-methyladenine DNA glycosylase (MPG) thereby providing a
138 C with increases in the DNA repair enzymes 3-methyladenine DNA glycosylase and apurinic/apyrimidinic
139 We report the crystal structure of human 3-methyladenine DNA glycosylase complexed to a mechanism-b
140 of the DNA with uracil-DNA glycosylase or 3-methyladenine DNA glycosylase failed to reveal additiona
142 excision repair genes (including the MAG1 3-methyladenine DNA glycosylase gene) and a large selectio
145 Here we report the solution structure of 3-methyladenine DNA glycosylase I (TAG) in complex with it
148 DNA glycosylase (AAG) and Escherichia coli 3-methyladenine DNA glycosylase II (AlkA) bind tightly to
153 udy was made possible by the generation of 3-methyladenine DNA glycosylase null mutant cells by targe
155 m DNA suggests an age-dependent decline in 3-methyladenine DNA glycosylase, a BER enzyme responsible
156 se excision-repair enzymes, AAG, the major 3-methyladenine DNA glycosylase, and APE1, the major apuri
158 approximately 0.3 in strains deficient in 3-methyladenine DNA glycosylases I and II, FAPY DNA glycos
162 nofunctional DNA glycosylase AlkA (E. coli 3-methyladenine-DNA glycosylase II) reveals a large hydrop
164 thylpurine-DNA glycosylases (MPG proteins, 3-methyladenine-DNA glycosylases) excise numerous damaged
165 Inhibition of autophagic signaling with 3-methyladenine, dominant-negative Vps34, or Atg7 shRNA re
167 s clearly not essential for AlkB to repair 1-methyladenine effectively, but a nucleotide 5' phosphate
169 ors bafilomycin A1, ammonium chloride, and 3-methyladenine failed to increase ubiquitinated protein l
170 l group from S-adenosyl-l-methionine to N(6)-methyladenine-free lambda DNA and to protect methylated
172 A and U with the phosphate activated with 1-methyladenine generate RNA oligomers containing 40-50 mo
175 omes and lysosomes by temperature block or 3-methyladenine, hampered the conversion of TPP I proenzym
176 ne another and are all below 300 fs, while 7-methyladenine has a significantly longer lifetime (tau =
177 acidities of adenine, 9-ethyladenine, and 3-methyladenine have been investigated for the first time,
178 in vivo repair rates to in vitro rates for 3-methyladenine, however, shows that the rate-limiting ste
180 (TAG) is a DNA repair enzyme that excises 3-methyladenine in DNA and is the smallest member of the h
181 e kinetic parameters for AlkB oxidation of 1-methyladenine in poly(dA), short oligodeoxyribonucleotid
183 The stimulation of oocyte maturation by 1-methyladenine in starfish, and by a steroid in frogs, ha
185 rophages, and inhibition of autophagy with 3-methyladenine increased intracellular accumulation of ch
191 ws that methylation of adenine to form N (6)-methyladenine is a rare but readily detectable modificat
192 that the most commonly written tautomer of 3-methyladenine is not the most stable in the gas phase.
193 demonstrate the cellular toxicity of the N3-methyladenine lesion, and the protective role of base ex
194 unctionality (Me-lex) selectively affords N3-methyladenine lesions in >90% yield relative to the form
198 ent of cells with the autophagy inhibitors 3-methyladenine, LY-294002, or Wortmanin rescued Gn degrad
200 ted bases show high activity in repairing N1-methyladenine (m1A) and N3-methylcytosine (m3C), compara
201 ses are specific to a particular base, the 3-methyladenine (m3A) DNA glycosylases include both highly
203 ompared with the destabilizing effects of N6-methyladenine (m6A) and 5-hydroxymethylcytosine (5hmC) r
204 ed this approach to detect 49,311 putative 6-methyladenine (m6A) residues and 1,407 putative 5-methyl
205 n at N(6) in EA prompted us to evaluate N(6)-methyladenine (m6A), an important epigenetic signal for
206 some (bortezomib), but not macroautophagy (3-methyladenine), markedly increased PNPLA3 levels in WT m
208 complexes formed between adenine (A) or N-6-methyladenine (meA) monomer and deoxythymidylate (dTn) p
210 identified two previously unidentified N(6)-methyladenine motifs and showed that they maintained a c
211 ted nucleobase analogs (N1-methyladenine, N3-methyladenine, N1-methylcytosine, N3-methylcytosine) and
212 resence of methylated nucleobase analogs (N1-methyladenine, N3-methyladenine, N1-methylcytosine, N3-m
214 r, netropsin affects neither the level of N3-methyladenine nor the toxicity of methyl methanesulfonat
216 ition of PKCdelta-facilitated autophagy by 3-methyladenine or Atg5 knock-out renders a greater preval
218 ttenuated when autophagy was suppressed by 3-methyladenine or by small interfering RNA against beclin
219 Pharmacological inhibition of autophagy by 3-methyladenine or chloroquine further exacerbated APAP-in
223 as pretreatment with autophagy inhibitors (3-methyladenine or KU55933) abolished preconditioning-indu
224 ing autophagy by chloroquine, bafilomycin, 3-methyladenine or LC3BsiRNA, significantly blocked penflu
226 Blocking autophagy by treating cells with 3-methyladenine or overexpressing dominant-negative ATG5 a
228 Furthermore, inhibition of autophagy using 3-methyladenine or small interfering RNA specific to VPS34
230 inhibitors of autophagy (bafilomycin A1 or 3-methyladenine) or small interfering RNA (siRNA) against
231 phagic activity by an autophagy inhibitor, 3-methyladenine, or Atg5 small interfering RNA, reduces th
232 s blocked using either chemical inhibitors 3-methyladenine, or by RNA interference knockdown of becli
233 and the 4 analogues that contain the bases-2-methyladenine, p-cresol, adenine, and 2-(methylthio)aden
234 rines such as 8-chlorocaffeine and 8-bromo-9-methyladenine react with [Pt(PPh3)4] under oxidative add
236 f the fluorescence-quenching properties of 1-methyladenine; removal of the alkyl group results in a >
237 human enzymes, ABH2 and ABH3, demethylated 1-methyladenine residues in poly(dA), they were inefficien
238 f the autophagic pathway by treatment with 3-methyladenine restored the bactericidal effects of BMDCs
241 on, we report DA-6mA-seq (DpnI-Assisted N(6)-methylAdenine sequencing), an approach that uses DpnI to
242 port the conclusion that G(i) functions in 1-methyladenine signaling and suggest the possibility of u
243 hod using a new silver cluster probe, termed methyladenine-specific NanoCluster Beacon (maNCB), which
245 3-kinase (PI3K) inhibitors wortmannin and 3-methyladenine, suggesting that it acts through the mamma
246 -induced autophagy using Bafilomycin A1 or 3-methyladenine suppressed viral growth in initial stages;
247 MPG has a role in removing adducts such as 3-methyladenine that block DNA synthesis and there is a po
248 e have likewise measured two acidities for 3-methyladenine, the N10 (347 +/- 4 kcal mol(-)(1)) and th
250 wth arrest by the class III PI3K inhibitor 3-methyladenine was alleviated by essential amino acid sup
251 2 is phosphorylated in vivo in response to 1-methyladenine which precedes MPF activation, making PRK2
252 Inhibition of autophagy by chloroquine and 3-methyladenine worsened renal ischemia/reperfusion injury
253 autophagy, either with the PI3K inhibitors 3-methyladenine, wortmannin, and LY294002 or with small in
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。