ライフサイエンスコーパス: nucleotide pair

1 uplex and flipping out two damage-containing nucleotide pairs.

2 C pairs and each having a total length of 15 nucleotide pairs.

3 relationships between individual amino acid--nucleotide pairs.

4 C pairs and each having a total length of 15 nucleotide pairs.

5 between parallel, rather than antiparallel, nucleotide pairs.

6 in the adjacent sequence through alternative nucleotide pairing.

7 logroups sharing an A to G mtDNA mutation at nucleotide pair 10398 had increased mtDNA damage compare

8 m haplogroups lacking the A to G mutation at nucleotide pair 10398.

9 coding region and a polycytosine variant at nucleotide pair 16184-16193 of the control region, as we

10 Contacts with virtually every nucleotide pair account for the evolutionary invariance

11 Furthermore, the spacing between the nucleotide pairs along the helix axis is shorter, sugges

12 de system; a minor groove separation of five nucleotide pairs and major groove separations of six, se

13 o uracil, which can produce mutations of C:G nucleotide pairs, and the mismatch repair protein Msh2 p

14 e substitution rates amongst the 12 possible nucleotide pairs are not homogeneous as they are affecte

15 and T psi C loop sequences, and a mismatched nucleotide pair at the top of the amino-acyl stem.

16 dependent devices are driven by increases in nucleotide pairing at each step in their machine cycles.

17 and the geometrical parameters indicate that nucleotide pairs closer to the orientation needed for ph

18 We identify the 14-nucleotide-pair DNA sequence recognized by Wor1, charact

19 coupling to the chemical energy (as well as nucleotide pairing energies) for molecular motors.

20 (ii) Determinations of CTP formed and all nucleotide pairs generated during kinetic analysis of CT

21 ibition is the fact that certain synergistic nucleotide pairs give more than additive inhibition.

22 in the minor groove and six, seven or eight nucleotide pairs in the major groove.

23 ed from a variety of DNA molecules with five nucleotide pairs in the minor groove and six, seven or e

24 the predicted thermodynamic stability of the nucleotide pairs in these positions.

25 NA molecules; a major groove separation of 9 nucleotide pairs is possible at low concentrations.

26 ases are identified that copy a non-standard nucleotide pair joined by a hydrogen bonding pattern dif

27 The circular, 17,443 nucleotide-pair mitochondrial (mt) DNA molecule of the s

28 A heteroplasmic G-to-A transition at nucleotide pair (np) 14459 within the mitochondrial DNA

29 n the number of Cs in a poly C track between nucleotide pairs (nps) 301 and 309.

30 A 2500-nucleotide pair (ntp) sequence of F-type mitochondrial (

31 The 3231-nucleotide-pair (ntp) sequence of one end of one of the

32 plus the lack of significant deviations for nucleotide pairs on other length scales up to 20 codons

33 The yC nucleotide (paired opposite G) was destabilizing by a sm

34 enzymatic removal of natural and non-natural nucleotides paired opposite a thymine dimer through exon

35 imination based on frequencies of individual nucleotide pairs or gaps (i.e., of possible alignment co

36 These results explain the conserved nucleotide-pairing patterns in animal miRNA target sites

37 The 8-arm junction is stable with 16 nucleotide pairs per arm, but the 12-arm junction has be

38 he 12-arm junction has been stabilized by 24 nucleotide pairs per arm.

39 r groove separations of six, seven, or eight nucleotide pairs produce stable PX DNA molecules; a majo

40 izes the rates of hybridization of GC and AT nucleotide pairs, reduced the bias against sequences wit

41 re used to determine the minimum, contiguous nucleotide pairing required between an siRNA and a targe

42 re favorable interaction with an IE-specific nucleotide pair(s) than it does with the corresponding O

43 a favorable interaction with an OE-specific nucleotide pair(s), while Pro47 may cause a more favorab

44 n it does with the corresponding OE-specific nucleotide pair(s).

45 reactions of complex I, using four different nucleotide pairs to encompass a range of reaction rates.

46 s between target nucleotides t10 and t11-the nucleotides paired to piRNA guide positions g10 and g11-

47 gnificant structural adjustments between the nucleotide pairs usually are needed for crosslinking.

48 en used together and depend on the number of nucleotides paired when attacking gyrase A mRNA.

49 s 427-580) bound to DNA containing an abasic nucleotide paired with guanine, providing a glimpse of t

50 ly to work with natural enzymes if the added nucleotides pair with geometries that are similar to tho

51 ive constraints on adjacent first and second nucleotide pairs within codons.

52 olves additive contributions from successive nucleotide pairs within the target sequence.