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1 V prefers to select tRNA(Pro), tRNA(Gly), or tRNA(Arg).
2 at of cleavage directed by an intact 5' half tRNAArg.
3 events Can toxicity by hydrolyzing canavanyl-tRNAArg.
4 ssion vector and the dnaY gene which encodes tRNA(Arg)(AGA/AGG) Isolation of the recombinant GP alpha
5 ybrid cell lines containing different mt-Tr (tRNA(Arg)) alleles were generated.
6           Most strikingly, levels of charged tRNAArg and tRNAGln remained unchanged and no ribosome p
7                    The unique recognition of tRNA(Arg) by ATE1 is coordinated through interactions wi
8         In most organisms, Can is ligated to tRNAArg, causing translation of arginine codons with Can
9 taining tRNAs codons read by tRNA(Gln(TTG)), tRNA(Arg(CCG)), and tRNA(Thr(CGT)) These findings collec
10                            A mutation in pre-tRNA(Arg)(CCG) causes yeast cells to be cold-sensitive a
11 mperature, or when Lhp1p is depleted, mature tRNA(Arg)(CCG) is not efficiently aminoacylated.
12 he mutation causes the anticodon stem of pre-tRNA(Arg)(CCG) to misfold into an alternative helix in v
13              A group I intron interrupts the tRNA(Arg)CCU gene of the alpha-purple bacterium Agrobact
14                       Of 10 newly identified tRNA(Arg)CCU genes, we found only two that contained an
15 rium Microcystis aeruginosa and alpha-purple tRNA(Arg)CCU introns suggest that these introns share a
16 restricted and scattered distribution of the tRNA(Arg)CCUg intron among alpha-purple bacteria is cons
17  3' half tRNAArgin the presence of a 7 nt 5' tRNAArg composed only of the acceptor stem region with a
18 a unique and extended loop that wraps around tRNA(Arg), creating extensive contacts with the T-arm of
19 d found single nucleotide mutations of human tRNAArg gene variants enabled differential nonsense supp
20 ophage DNA sequence reconstitutes a complete tRNA(Arg) gene.
21 ce polymorphisms in the mtDNA COIII, ND3 and tRNA(Arg)genes.
22 Three of six arginine codons are read by two tRNA(Arg) isoacceptors in Escherichia coli.
23 and CGA) are decoded by two Escherichia coli tRNA(Arg) isoacceptors.
24 ture that contributes to maintaining arginyl-tRNAArg levels unaffected.
25 or tRNA that represented 5%-18% of the total tRNAArg pool.
26 or 3' tRNase substrates, we tested small pre-tRNA(Arg) substrates lacking the D and anticodon stem-lo
27 ssing the 3' ends of 5S rRNA and the dimeric tRNA(Arg)-tRNA(Asp).
28 ecycline, eliminating the sole gene encoding tRNA(Arg)(UCC), and depletion of translation termination
29   Trm9 methylates the uridine wobble base of tRNAARG(UCU) and tRNAGLU(UUC).
30 antly reduced in the absence of a functional tRNAArg(UCU).
31 alled at AGA codons due to deficiencies in a tRNA(Arg)UCU tRNA and GTPBP2, a mammalian ribosome rescu
32              Here, we focus on a cytoplasmic tRNA(Arg)(UCU) that is expressed specifically in neurons
33                                    Targeting tRNA(Arg)(UCU) with an antisense oligonucleotide replica
34 etermine the cleavage site using various pre-tRNAArg variants and purified pig enzyme.
35 ity of the T stem-loop structures of 3' half tRNAArg variants decreased.
36 onine at threonine codons by the "recruited" tRNAArg was corroborated by in vitro aminoacylation assa
37 drially encoded tRNA arginine (mt-Tr) locus (tRNA(Arg)) was discovered in approximately one-third of
38  was inactivated, was rendered viable when a tRNAArg with a point mutation that changed its anticodon
39   No heptamer-directed cleavage of a 3' half tRNAArg without T stem base pairs was detected.