ライフサイエンスコーパス: displacement loop

1 ous plasmid, resulting in the formation of a displacement loop.

2 ptor DNA, consistent with the formation of a displacement loop.

3 ous plasmid, resulting in the formation of a displacement loop.

4 led plasmid, resulting in the formation of a displacement loop.

5 plex plasmid resulting in the formation of a displacement loop.

6 a supercoiled homologous duplex to form a D (displacement)-loop.

7 /cm [Q1-Q3, 1.9-2.7]; P=0.03, torsion-radial displacement loop: 2.7 degrees /mm [Q1-Q3, 2.1-3.6] vers

8 ation of the relative specific activities of displacement loop and nondisplacement loop-containing mi

9 The slope of torsion-radial displacement loop, and its response to exercise, may ser

10 e of the systolic limb of the torsion-radial displacement loop, and the untwist rate were significant

11 r displacement of the invading strand of DNA displacement loops, and 'late' roles, such as dissolutio

12 ions, the percentage of molecules containing displacement loops can be easily and accurately determin

13 c examination for assessing the frequency of displacement loop-containing molecules.

14 The displacement loop (D loop) is a DNA strand invasion prod

15 The displacement loop (D loop) is the product of homology se

16 utations in human cancers are located in the displacement loop (D-loop) and in particular in a polycy

17 , BIR copies the template DNA in a migrating displacement loop (D-loop) and results in conservative i

18 dy, the activities of WRN were examined on a displacement loop (D-loop) DNA substrate that mimics an

19 o, with properties expected for the critical displacement loop (D-loop) intermediates.

20 inhardii has been shown to occur by a double displacement loop (D-loop) mechanism and potentially als

21 r3 helicase activity, proposed to extend the displacement loop (D-loop) recombination intermediate, d

22 oroplast DNA (ctDNA) as a probe, replication displacement loop (D-loop) regions were identified.

23 strand invade a homologous dsDNA to form the displacement loop (D-loop) structure leading to the even

24 A contain a short triple-stranded region, or displacement loop (D-loop), in the major noncoding regio

25 arting at the multiple origins of the strand-displacement loop (D-loop).

26 terminated, defining the 3' boundary of the displacement loop (D-loop).

27 ed processing of recombination-intermediate [displacement loop (D-loop)] substrates.

28 Displacement loops (D-loops) are critical intermediates

29 Displacement loops (D-loops) are pivotal intermediates o

30 Displacement loops (D-loops) are signature intermediates

31 Displacement loops (D-loops) are three-strand intermedia

32 By dissociating precocious DNA displacement loops (D-loops) between sister chromatids,

33 vitro, as evidenced both by the formation of displacement loops (D-loops) in superhelical DNA and by

34 Displacement loops (D-loops) play a pivotal role in HR,

35 ance between stabilization and disruption of displacement loops (D-loops), early HR intermediates tha

36 s nicked recombination intermediates such as displacement loops (D-loops), nicked Holliday junctions,

37 ave investigated whether BLM can disrupt DNA displacement loops (D-loops), which represent the initia

38 steps during DNA repair; DNA end resection, displacement-loop (D-loop) processing, branch migration,

39 and intertwining leads to the formation of a displacement-loop (D-loop).

40 lly distinct, positively supercoiled form of displacement-loop, does not serve as a template for DNA

41 ir is dependent on the formation of a double-displacement loop (double-D-loop), a recombination inter

42 1-RAD54-mediated strand invasion step during displacement loop formation.

43 of donor DNA, synaptic complex assembly, and displacement-loop formation when tested with nucleosome-

44 reate targeted double-strand breaks within a displacement loop formed by RecA.

45 The single-stranded DNA displacement loops formed in urothelial cells during BKP

46 Ref targets displacement loops formed when an oligonucleotide is bou

47 referentially bound to plasmids with a short displacement-loop, in contrast to POLGalpha.

48 Here, we present the cryoEM structure of a displacement loop of human RAD51 that captures the synap

49 cimens) was found in the control region (the displacement loop) of mitochondrial DNA.

50 e mechanism may entail formation of a duplex displacement loop on the nucleosome, facilitating the en

51 crease in 7S DNA molecules, which form short displacement-loops on mitochondrial DNA.

52 n vivo as measured by semiquantitative mtDNA displacement loop PCR.

53 ith at least two breaks localized within the displacement loop region in only one of the two parental

54 NA replication enzyme, and the damage to the displacement loop region of mtDNA (D-loop) were analyzed

55 The systolic slope of the torsion-radial displacement loop relationship decreased with exercise i

56 ickase, cleaving the two target strands of a displacement loop sequentially, (ii) the two strands are

57 shown to cleave the displaced strand of the displacement loop, to partially degrade the 7S-initiatio

58 e 5' end of nascent DNA from the replication displacement loop was identified at position 130,697 for

59 lectively nicks mitochondrial DNA containing displacement loops without nicking supercoiled mitochond