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1 C pairs and each having a total length of 15 nucleotide pairs.
2 relationships between individual amino acid--nucleotide pairs.
3 C pairs and each having a total length of 15 nucleotide pairs.
4  between parallel, rather than antiparallel, nucleotide pairs.
5 uplex and flipping out two damage-containing 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                   Extension from the correct nucleotide pair (C) was not observed, but the primer wit
18 and the geometrical parameters indicate that nucleotide pairs closer to the orientation needed for ph
19                           We identify the 14-nucleotide-pair DNA sequence recognized by Wor1, charact
20  coupling to the chemical energy (as well as nucleotide pairing energies) for molecular motors.
21 ws that Rad4 flips out both 6-4PP-containing nucleotide pairs, forming an 'open' conformation.
22    (ii) Determinations of CTP formed and all nucleotide pairs generated during kinetic analysis of CT
23 ibition is the fact that certain synergistic nucleotide pairs give more than additive inhibition.
24 ion is the disruption of a conserved U32.A38 nucleotide pairing in the anticodon stem through inserti
25  in the minor groove and six, seven or eight nucleotide pairs in the major groove.
26 ed from a variety of DNA molecules with five nucleotide pairs in the minor groove and six, seven or e
27 the predicted thermodynamic stability of the nucleotide pairs in these positions.
28 NA molecules; a major groove separation of 9 nucleotide pairs is possible at low concentrations.
29 ases are identified that copy a non-standard nucleotide pair joined by a hydrogen bonding pattern dif
30                         The circular, 17,443 nucleotide-pair mitochondrial (mt) DNA molecule of the s
31         A heteroplasmic G-to-A transition at nucleotide pair (np) 14459 within the mitochondrial DNA
32 n the number of Cs in a poly C track between nucleotide pairs (nps) 301 and 309.
33                                       A 2500-nucleotide pair (ntp) sequence of F-type mitochondrial (
34                                     The 3231-nucleotide-pair (ntp) sequence of one end of one of the
35  plus the lack of significant deviations for nucleotide pairs on other length scales up to 20 codons
36                                       The yC nucleotide (paired opposite G) was destabilizing by a sm
37 enzymatic removal of natural and non-natural nucleotides paired opposite a thymine dimer through exon
38 imination based on frequencies of individual nucleotide pairs or gaps (i.e., of possible alignment co
39          These results explain the conserved nucleotide-pairing patterns in animal miRNA target sites
40         The 8-arm junction is stable with 16 nucleotide pairs per arm, but the 12-arm junction has be
41 he 12-arm junction has been stabilized by 24 nucleotide pairs per arm.
42 r groove separations of six, seven, or eight nucleotide pairs produce stable PX DNA molecules; a majo
43 izes the rates of hybridization of GC and AT nucleotide pairs, reduced the bias against sequences wit
44 re used to determine the minimum, contiguous nucleotide pairing required between an siRNA and a targe
45 re favorable interaction with an IE-specific nucleotide pair(s) than it does with the corresponding O
46  a favorable interaction with an OE-specific nucleotide pair(s), while Pro47 may cause a more favorab
47 n it does with the corresponding OE-specific nucleotide pair(s).
48 reactions of complex I, using four different nucleotide pairs to encompass a range of reaction rates.
49 EGIS) add independently replicable unnatural nucleotide pairs to the natural G:C and A:T/U pairs foun
50 s between target nucleotides t10 and t11-the nucleotides paired to piRNA guide positions g10 and g11-
51  to unstacking and extrusion of the 6-4PP:AA nucleotide pairs towards the major groove.
52 gnificant structural adjustments between the nucleotide pairs usually are needed for crosslinking.
53 en used together and depend on the number of nucleotides paired when attacking gyrase A mRNA.
54 s 427-580) bound to DNA containing an abasic nucleotide paired with guanine, providing a glimpse of t
55 ly to work with natural enzymes if the added nucleotides pair with geometries that are similar to tho
56 ive constraints on adjacent first and second nucleotide pairs within codons.
57 olves additive contributions from successive nucleotide pairs within the target sequence.