ライフサイエンスコーパス: recombination reaction

1 unction, which determines the outcome of the recombination reaction.

2 ls, allowing assessment of the site-specific recombination reaction.

3 earize the minus strand via a non-homologous recombination reaction.

4 mutants to specific transition steps in the recombination reaction.

5 sing of the broken ends may occur during the recombination reaction.

6 ing non-random usage of DNA substrate in the recombination reaction.

7 mplicated in initiating the last step of the recombination reaction.

8 regulating and executing a site-specific DNA recombination reaction.

9 uring the DNA end joining phase of the V(D)J recombination reaction.

10 uctural properties of an intermediate in the recombination reaction.

11 nsert them into a plasmid vector in a single recombination reaction.

12 combinant DNA molecules in a single in vitro recombination reaction.

13 st two mechanisms are involved in the charge recombination reaction.

14 r DNA cleavage limit the overall rate of the recombination reaction.

15 patterns associated with this site-specific recombination reaction.

16 or before the DNA cleavage step of the V(D)J recombination reaction.

17 intermediate conformations during the V(D)J recombination reaction.

18 matrix element, V, for the subsequent charge recombination reaction.

19 ive of whether conditions support a complete recombination reaction.

20 s a role for this protein in specialized DNA recombination reactions.

21 s thus an energetic barrier to inappropriate recombination reactions.

22 lexes by means of conservative site-specific recombination reactions.

23 d commandeering cellular proteins to promote recombination reactions.

24 r-complete inhibition of unproductive charge recombination reactions.

25 cation apparatus and is capable of mediating recombination reactions.

26 22 share similarities in their site-specific recombination reactions.

27 tein filament, the catalytic intermediate in recombination reactions.

28 ed for both the charge separation and charge recombination reactions.

29 t with tryptophan oxidation mediating charge recombination reactions.

30 key catalytic intermediate in Rad51-mediated recombination reactions.

31 ad52 and XPF/ERCC1 in a number of homologous recombination reactions.

32 We term this early precursor in the V(D)J recombination reaction a "stable cleavage complex."

33 ide a strong indication that in the complete recombination reaction a restacking of helices occurs be

34 In a subsequent site-specific recombination reaction, a gene of interest can be integr

35 In our PSII-inspired complex, the recombination reaction activation energy is <2 kcal mol(

36 estriction on the rate of the spin-selective recombination reaction also means that the detrimental e

37 gions of RAGs are sufficient to catalyze the recombination reaction, although with lower joining effi

38 of a "core" domain that is required for the recombination reaction and a C-terminal nonessential or

39 protein, although dispensable for the basic recombination reaction and for Ig heavy chain DH to JH j

40 eview our current understanding of the V(D)J recombination reaction and how it is regulated during ly

41 he molecular mechanism and regulation of the recombination reaction and illustrates a design by which

42 The recombination reaction and newly generated genome may re

43 ng of the catalytic residues involved in the recombination reaction and that their positions differ i

44 position pathway resembles that of the V(D)J recombination reaction and the mechanism of hAT and Tran

45 wn spectroscopy (CRDS) in monitoring radical recombination reactions and associated magnetic field ef

46 in both the efficiency and rate of in vitro recombination reactions and offers an explanation for st

47 -junction) is both a central intermediate of recombination reactions and, in some cases, a controllin

48 gion plays a critical regulatory role in the recombination reaction, and mutations in this region hav

49 Finally, we found that in vitro Cre recombination reactions are much more stringent for eval

50 e presented that not one but several on-step recombination reactions are responsible for dinitrogen f

51 plicating a defect in the early steps of the recombination reaction as the basis of the clinical phen

52 bution from the acceptor side in the form of recombination reactions as well as from the donor side o

53 gration reaction, and perhaps other cellular recombination reactions as well.

54 imurium stimulates several site-specific DNA recombination reactions, as well as transcription of a n

55 ociation inhibit the efficiency of the V(D)J recombination reaction at the endogenous immunoglobulin

56 o distinct classes based on the stage in the recombination reaction at which they are blocked.

57 r on dye aggregation on the TiO2 surface and recombination reactions at TiO2/dye/electrolyte interfac

58 ent after photobleaching of rhodopsin is the recombination reaction between its apoprotein opsin and

59 bute this maximum to either elimination of a recombination reaction between the redox-active tyrosine

60 as determined by analysis of the kinetics of recombination reactions between P700+ and reduced accept

61 specific RNA target requires two homologous recombination reactions between plasmids and phages in b

62 that is not strictly required for the basic recombination reaction but helps to regulate recombinati

63 Blocking an early stage of the recombination reaction by disruption of XRCC3 not only s

64 In the absence of mediators, ssb inhibits recombination reactions by competing with recombinase fo

65 rified Srs2 strongly inhibits Rad51-mediated recombination reactions by disrupting the Rad51-ssDNA pr

66 ins allowed tracking of second-order heme CO recombination reactions by transient absorbance.

67 Several steps of the V(D)J recombination reaction can be reconstituted in vitro wit

68 n and T-cell receptor (TCR) genes, the V(D)J recombination reaction can in principle generate three t

69 sequence homology and in some cases aberrant recombination reactions can be detected using such micro

70 difference of barrier heights in these three recombination reactions can be rationalized in terms of

71 either of the two coding ends in these V(D)J recombination reactions can recombine with either of the

72 Recombination reactions carried out in vitro are accompa

73 The simplest recombination reaction catalyzed by Int does not require

74 The normal recombination reaction catalyzed by the Flp (pronounced

75 For the site-specific recombination reactions catalyzed by the bacteriophage l

76 catalytic quantity of Srs2 to Rad51-mediated recombination reactions causes severe inhibition of thes

77 ed for diversity generation through frequent recombination reactions creates a situation where the HJ

78 an effect of the metal binding on the charge recombination reaction D+*QAQB-* --> DQAQB suggests that

79 units were able to participate in a complete recombination reaction, demonstrating that the interacti

80 Here, we report a robust recombination reaction employing oligonucleotide substra

81 hat confer directionality upon site-specific recombination reactions encoded by plasmids, transposons

82 acteriophage lambda lysogen, a site-specific recombination reaction excises the phage genome from the

83 Here we describe defined in vitro recombination reactions for both phiRv1 integrase-mediat

84 Here we reconstitute the complete V(D)J recombination reaction in a cell-free system.

85 intermediates of the G1 phase-specific V(D)J recombination reaction in progenitor lymphocytes.

86 mbination proteins, catalyzes the homologous recombination reaction in the context of a helical prote

87 n DNA invertase promotes a site-specific DNA recombination reaction in the Salmonella chromosome.

88 tigate the mechanistic properties of the Hin recombination reaction in vivo, we have analysed the top

89 challenge phages through a single homologous recombination reaction in vivo.

90 dissecting the role of hRad51 and hRad54 in recombination reactions in human cells.

91 g DNA double-strand breaks and enhancing DNA recombination reactions in maize cells.

92 Using TFM-FRET, we observed individual recombination reactions in real time and analyzed their

93 This process requires a series of recombination reactions in which the internal guide sequ

94 oxP substrate reveals an intermediate in the recombination reaction, in which a Cre molecule has clea

95 otide excision repair and homology-dependent recombination reactions, including DNA single strand ann

96 in the region of the FRT site (following the recombination reaction) indicated that a precise rearran

97 gnal ends, these nonhairpin coding-end V(D)J recombination reaction intermediates have 3' overhanging

98 Recombination reactions involve particular geometric and

99 A fundamental step in site-specific recombination reactions involves the formation of proper

100 of the E2A proteins is rate limiting for the recombination reaction involving these Vdelta regions.

101 1, 1-2 and 2-3 bp of branch migration during recombination reactions involving 6, 7 and 8 bp spacers,

102 The mechanism of the ClO recombination reaction is also discussed, and the result

103 p1-dependent, pre-SC transition early in the recombination reaction is an essential component of meio

104 The recombination reaction is catalyzed by four monomers of

105 The V(D)J recombination reaction is composed of multiple nucleolyt

106 c analysis shows that directionality of this recombination reaction is conferred by the irreversibili

107 as, so far, been very low because the charge recombination reaction is faster than the catalytic four

108 bination complex and/or mediate a controlled recombination reaction is impaired.

109 An obligatory step in the recombination reaction is the association, or synapsis,

110 A hierarchy of isotopically substituted recombination reactions is formulated for production of

111 akes the reaction unique among site-specific recombination reactions is that the first step, XerD-med

112 the case and that RAD18 plays a role in the recombination reaction itself.

113 m component gene segments by a site-specific recombination reaction known as V(D)J recombination.

114 h inhibit different steps in a site-specific recombination reaction mediated by the bacteriophage lam

115 The site-specific recombination reaction mediated by the Flp recombinase o

116 s are central intermediates in site-specific recombination reactions mediated by tyrosine recombinase

117 ental data on the kinetics and regulation of recombination reactions mediated by varphiC31 integrase

118 The site-specific V(D)J recombination reaction necessary to assemble the genes c

119 during lymphoid development by a specialized recombination reaction normally observed only in cells o

120 This integrase-mediated site-specific recombination reaction occurs between the phage attP sit

121 o new insights into the unwanted interfacial recombination reaction of the injected electrons with th

122 The geminate ligand recombination reactions of photolyzed carbonmonoxyhemogl

123 itro; nevertheless, many failed to mediate a recombination reaction on supercoiled plasmid in vivo or

124 Recombination reactions or deprotonations of the radical

125 n vivo the role of Mu B in the two different recombination reactions performed by phage Mu: non-repli

126 The recombination reaction proceeds by sequential sets of ge

127 The V(D)J recombination reaction proceeds through RSS recognition

128 Traditionally, recombination reactions promoted by RecA-like proteins i

129 quences of the change in effective radiative recombination reaction rate coefficients produced by int

130 arge recombination is mainly governed by the recombination reaction rate constant and the charge dens

131 t which RipX and CodV catalyze site-specific recombination reactions required for normal chromosome p

132 products of integrase-mediated site-specific recombination reactions results in a single recombinase

133 mpletely randomized arm in a functional loxP recombination reaction revealed that only three wild-typ

134 Thus, the overall charge-recombination reaction seems to involve a concerted prot

135 dy provides important insight into the V(D)J recombination reaction, specifically that significant in

136 logenetically, and mechanistically different recombination reactions, such as V(D)J recombination and

137 nase variants were found to be active in all recombination reactions tested: excision, integration, a

138 /RAG2 endonuclease (RAG) initiates the V(D)J recombination reaction that assembles immunoglobulin hea

139 ombinase family, it catalyses an integrative recombination reaction that occurs by a different crosso

140 recombination (CSR) is a region-specific DNA recombination reaction that replaces one immunoglobulin

141 he Hin recombinase catalyzes a site-specific recombination reaction that results in the reversible in

142 Depending on the type of recombination reaction that takes place, intermediates m

143 lled the bloodstream VSG expression site, or recombination reactions that move silent VSGs or VSG cop

144 led the creation of molecular models for the recombination reactions that result in pilin antigenic v

145 g P680(*+), the relay is thought to mitigate recombination reactions, thereby ensuring a high quantum

146 lates to individual biochemical steps in the recombination reaction these mutants, R123Q, T124I, and

147 These can undergo a second recombination reaction to generate odd-noded knots.

148 erD, allowing both intra- and intermolecular recombination reactions to go to completion.

149 etic fields (not exceeding 46 mT) on radical recombination reactions to investigate protein-substrate

150 The highly directional and tightly regulated recombination reaction used to site-specifically excise

151 mplications on the role of ICP8 in mediating recombination reactions using viral transcripts.

152 in developing lymphocytes by a site-specific recombination reaction, V(D)J recombination.

153 donor, reduced bacteriopheophytin acceptor) recombination reaction was measured in a series of react

154 ility to participate in a full site-specific recombination reaction was reduced only slightly.

155 atches on the kinetics of the RecA-catalyzed recombination reaction, we used assays based upon fluore

156 Hin recombinase on the DNA for a step in the recombination reaction which occurs either at and/or pri

157 This process is executed by the V(D)J recombination reaction, which can be divided into DNA cl

158 of the signal and coding joints in the V(D)J recombination reaction, which is necessary for productio

159 It shows that synapsis is a slow step in the recombination reaction, while subsequent strand exchange

160 day junction recombination intermediates and recombination reactions with chimeric recombinases, to i

161 gene, pilE, which result from nonreciprocal recombination reactions with numerous silent loci, pilS.

162 rather dimers stemming from radical-radical recombination reactions, with p-isotoluene as a clear ex