ライフサイエンスコーパス: quadruplet

1 ing tRNA, it influences decoding of the UAGA quadruplet.

2 activated concomitantly by spike triplets or quadruplets.

3 dual log likelihoods of composing amino acid quadruplets.

4 allow decoding of complementary 5'-CAAA(-3') quadruplets.

5 ngletons, 88 of twins, 22 of triplets, 10 of quadruplets, 5 of quintuplets, and 2 of sextuplets.

6 oup of 83 women carrying twins, triplets, or quadruplets (aged 20-46 y) was recruited from 2011 to 20

7 Open time for co-channel quadruplets and quintuplets tends to be relatively long

8 s the codon immediately 5' of the first UAGA quadruplet, and release factor 1 is partially inactivate

9 As part of a study of the potential of quadruplets as codons, the decoding of tandem UAGA quadr

10 plets as codons, the decoding of tandem UAGA quadruplets by an engineered tRNA(Leu) with an eight-bas

11 amino acid into proteins in response to the quadruplet codon, AGGA.

12 dons to all four bases of the complementary, quadruplet codon.

13 frameshift sequence) in the A site, and this quadruplet "codon-anticodon" helix is translocated to th

14 or (YFFS) tRNAs that recognize two different quadruplet codons (CGGG and GGGU) in vivo.

15 ibo-Q1) that efficiently decodes a series of quadruplet codons and the amber codon, providing several

16 ly encoded in response to unique triplet and quadruplet codons including fluorescent, photoreactive a

17 ral amino acids into proteins in response to quadruplet codons, and the creation of an orthogonal tra

18 dology for incorporating UAAs in response to quadruplet codons, but currently, it is mostly limited t

19 As ribo-Q1 independently decodes a series of quadruplet codons, this work provides foundational techn

20 tion of unnatural amino acids in response to quadruplet codons.

21 cused on reassigning termination or decoding quadruplet codons.

22 Each quadruplet composition was characterized by a single des

23 scoring function (log likelihoods of residue quadruplet compositions) is derived by the analysis of a

24 n facilitated by the evolution of orthogonal quadruplet decoding ribosomes and the discovery of mutua

25 nt efforts on genetic code expansion through quadruplet decoding.

26 anslation system that uses amber and evolved quadruplet-decoding transfer RNAs to encode numerous pai

27 etween sequence pairs, but between triplets, quadruplets, etc., is proposed to strengthen the proper

28 ction of interfacial nearest neighbor atomic quadruplets for each complex.

29 ic mutagenesis of both suprabranch guanosine quadruplets (G(4)) revealed a key role of central G resi

30 alators to DNA structure associated with the quadruplet helix and Holliday junction.

31 tity of the codon immediately 5' of the UAGA quadruplet influences the efficiency of quadruplet trans

32 , and we identified two frequently occurring quadruplet marks 'K9me1K23acK27me2K36me2' and 'K9me3K23a

33 plet motif (PQM) and the inverted processing quadruplet motif (iPQM).

34 re than 10 years ago, include the processing quadruplet motif (PQM) and the inverted processing quadr

35 ntation defines all sets of nearest neighbor quadruplets of amino acids.

36 d from medical students while they diagnosed quadruplets of heartbeat cycles.

37 the m1G37 modification in the controversial quadruplet-pairing model of tRNA frameshift suppressors.

38 te of the 4-AzHBA probe was localized to the quadruplet Phe(90)-Met(91)-Val(92)-Phe(93) using ESI LC-

39 genetic code expansion using a non-canonical quadruplet reading frame.

40 epeat, whereas the DM2 expansion is an rCCUG quadruplet repeat.

41 stages of rediploidization were identified: quadruplets retaining their ancestral tetraploid conditi

42 l inactivation of release factor 1, the UAGA quadruplet specifies a leucine residue with an efficienc

43 g their ancestral tetraploid condition, semi-quadruplets still reflecting the ancestral tetraploidy w

44 3' closely matched codon, the efficiency of quadruplet translation at UAGA is reduced.

45 UAGA quadruplet influences the efficiency of quadruplet translation via the properties of its cognate

46 previous model that suppressor tRNAs induce quadruplet translocation now appears incorrect for most,

47 The potential of the quadruplet UAGA in Escherichia coli to specify a single