ライフサイエンスコーパス: recombination mechanism

1 IS492 transposition involves a site-specific recombination mechanism.

2 s, an observation inconsistent with a simple recombination mechanism.

3 nerations, and segregated, consistent with a recombination mechanism.

4 some via an integrase-mediated site-specific recombination mechanism.

5 is is proposed that involves a fragmentation-recombination mechanism.

6 d within the specific PAI by a site-specific recombination mechanism.

7 oximately 1 ps suggests a Shockley-Read-Hall recombination mechanism.

8 ppear to utilize an evolutionarily conserved recombination mechanism.

9 site, does not follow any example of a known recombination mechanism.

10 5 bp, providing evidence for a site-specific recombination mechanism.

11 nversion, rather than crossing over, was the recombination mechanism.

12 cific genome target site via a site-specific recombination mechanism.

13 ough template slippage rather than through a recombination mechanism.

14 everal fundamental and novel features of the recombination mechanism.

15 TCR loci, suggesting a general effect on the recombination mechanism.

16 ifies a strong temperature dependent exciton recombination mechanism.

17 mals with respect to telomere regulation and recombination mechanisms.

18 epair, translesion synthesis, and homologous recombination mechanisms.

19 CNV formation through nonallelic homologous recombination mechanisms.

20 facilitates comparative analysis of meiotic recombination mechanisms.

21 key differences between mitotic and meiotic recombination mechanisms.

22 he chromosome as well as to study homologous recombination mechanisms.

23 syndrome and cat-eye syndrome by homologous recombination mechanisms.

24 iving force to acquire and maintain multiple recombination mechanisms.

25 robial and fungal DNA processing enzymes and recombination mechanisms.

26 not known whether NF-kappaB regulates V(D)J recombination mechanisms after RAG-mediated dsDNA breaks

27 The recombination mechanism also differs from the one used b

28 (Saccharomyces cerevisiae) is important for recombination mechanisms and for effects of conversion o

29 he framework of our present understanding of recombination mechanisms and machinery.

30 utations, changes in repetitive DNA systems, recombination mechanisms, and insertion and deletion eve

31 We conclude that when high-frequency recombination mechanisms are blocked, alternative mechan

32 Their recombination mechanisms are distinctly different.

33 patible with known restrictions on the V(D)J recombination mechanism, are infrequent within the endog

34 Isotype switching is the DNA recombination mechanism by which antibody genes diversif

35 ur results have uncovered a novel, RNA-based recombination mechanism by which CSB protects genome sta

36 in telomerase-negative cells, low-frequency recombination mechanisms can avert lethality by elongati

37 organisms and a model for site-specific DNA-recombination mechanisms employed by the lambda-Int supe

38 Here, we present a new two-level recombination mechanism: first, one type of carrier is c

39 Based on these data, we present a recombination mechanism for a eukaryotic DNA virus in wh

40 ing is hypothesized to occur by a homologous recombination mechanism guided by repeat sequences at MD

41 ese cases, the activation of the full VHDHJH recombination mechanism had not occurred.

42 This unexpected recombination mechanism has a much lower energy barrier

43 Recombination mechanisms have been intensely studied in

44 on also creates genetic diversity, and viral recombination mechanisms have important implications for

45 sional models of the complexes, we propose a recombination mechanism in which the synaptic intermedia

46 model for studying intermolecular homologous recombination mechanisms in general in a mammalian syste

47 target site selectivity is useful in probing recombination mechanisms, in studying genome structure a

48 nd have led to new and refined insights into recombination mechanisms, including a detailed understan

49 osomes can be repaired by several homologous recombination mechanisms, including gene conversion and

50 hromatid exchange (SCE) can occur by several recombination mechanisms, including those directly initi

51 and presumably occurs by a conventional DSBR recombination mechanism initiated by cleavage of the rec

52 om two different chromosomes, by a novel RNA recombination mechanism involving trans-splicing of two

53 led at a time, as would be consistent with a recombination mechanism involving two steps of single-st

54 cted heterocyclic systems by a fragmentation-recombination mechanism is described.

55 0.00007) and indicates that the fundamental recombination mechanism is likely to be similar for swit

56 The nature of the recA-independent recombination mechanism is not known but could perhaps r

57 A detailed charge recombination mechanism is presented for organic photovo

58 asion, involving replication directly in the recombination mechanism, is invoked as an alternative.

59 complex disease genes and for investigating recombination mechanisms on the basis of better-quantifi

60 a conventional hydrogen abstraction/hydroxyl recombination mechanism (or its equivalent as a one-step

61 repaired either by one of several homologous recombination mechanisms, or by a number of nonhomologou

62 lf-assembled ribozymes revealed that, of two recombination mechanisms possible for self-assembly, ter

63 In this issue, reveal that different meiotic recombination mechanisms predominate in fission yeast an

64 We have investigated recombination mechanisms promoting the completion of rep

65 ister chromatid exchange, is the predominant recombination mechanism regulating the expansion and con

66 A recombination mechanism responsible for this inversion i

67 demonstrates how unique aspects of mammalian recombination mechanisms shape hotspot evolutionary dyna

68 ucleus, and they have co-opted different DNA recombination mechanisms-some previously unknown.

69 constitutive, recA-independent sister-strand recombination mechanism that allows 9% or more of these

70 ly between the two sites, suggesting a novel recombination mechanism that implicates additional host

71 In these models, the recombination mechanism that inactivates the Pten allele

72 tion of deletion events by an intrachromatid recombination mechanism that is likely to be single-stra

73 This observation is suggestive of a recombination mechanism that operates at centromeres.

74 ogram to compute and visualize site-specific recombination mechanisms that accommodate their experime

75 phage an excellent model to analyze several recombination mechanisms that appear redundant under opt

76 bilized by both homologous and nonhomologous recombination mechanisms, through a telomere-capture eve

77 H replacement provides a unique RAG-mediated recombination mechanism to edit nonfunctional IgH genes

78 endent events that involve a Rad50-dependent recombination mechanism to maintain telomere length.

79 RAD59 gene products in potential cooperative recombination mechanisms used in wild-type cells.

80 Analysis of recombination mechanisms using the current-voltage (J-V)

81 A stepwise dissociation-recombination mechanism was found to be favored.

82 To elucidate SCE recombination mechanisms, we determined whether spontane

83 rather is incorporated into the core of the recombination mechanism, where it is well positioned to

84 However, the exact charge recombination mechanism, whether geminate or nongeminate