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1 ive of whether conditions support a complete recombination reaction.
2 unction, which determines the outcome of the recombination reaction.
3 ls, allowing assessment of the site-specific recombination reaction.
4 earize the minus strand via a non-homologous recombination reaction.
5  mutants to specific transition steps in the recombination reaction.
6 sing of the broken ends may occur during the recombination reaction.
7 ing non-random usage of DNA substrate in the recombination reaction.
8 mplicated in initiating the last step of the 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 regulating and executing a site-specific DNA recombination reaction.
12 ereby facilitating an intramolecular radical recombination reaction.
13 nsert them into a plasmid vector in a single recombination reaction.
14 combinant DNA molecules in a single in vitro recombination reaction.
15 st two mechanisms are involved in the charge recombination reaction.
16 r DNA cleavage limit the overall rate of the recombination reaction.
17  patterns associated with this site-specific recombination reaction.
18 or before the DNA cleavage step of the V(D)J recombination reaction.
19  intermediate conformations during the V(D)J recombination reaction.
20 matrix element, V, for the subsequent charge recombination reaction.
21 s a role for this protein in specialized DNA recombination reactions.
22 s thus an energetic barrier to inappropriate recombination reactions.
23 lexes by means of conservative site-specific recombination reactions.
24 urface is a prerequisite for bimolecular and recombination reactions.
25 es remain low because of uncontrolled charge recombination reactions.
26 d commandeering cellular proteins to promote recombination reactions.
27 cation apparatus and is capable of mediating recombination reactions.
28 r-complete inhibition of unproductive charge recombination reactions.
29 22 share similarities in their site-specific recombination reactions.
30 tein filament, the catalytic intermediate in recombination reactions.
31 ed for both the charge separation and charge recombination reactions.
32 t with tryptophan oxidation mediating charge recombination reactions.
33 key catalytic intermediate in Rad51-mediated recombination reactions.
34 ad52 and XPF/ERCC1 in a number of homologous recombination reactions.
35    We term this early precursor in the V(D)J recombination reaction a "stable cleavage complex."
36 ide a strong indication that in the complete recombination reaction a restacking of helices occurs be
37                In a subsequent site-specific recombination reaction, a gene of interest can be integr
38            In our PSII-inspired complex, the recombination reaction activation energy is <2 kcal mol(
39 estriction on the rate of the spin-selective recombination reaction also means that the detrimental e
40 gions of RAGs are sufficient to catalyze the recombination reaction, although with lower joining effi
41  of a "core" domain that is required for the recombination reaction and a C-terminal nonessential or
42  protein, although dispensable for the basic recombination reaction and for Ig heavy chain DH to JH j
43 eview our current understanding of the V(D)J recombination reaction and how it is regulated during ly
44 he molecular mechanism and regulation of the recombination reaction and illustrates a design by which
45                                          The recombination reaction and newly generated genome may re
46 ng of the catalytic residues involved in the recombination reaction and that their positions differ i
47 position pathway resembles that of the V(D)J recombination reaction and the mechanism of hAT and Tran
48 wn spectroscopy (CRDS) in monitoring radical recombination reactions and associated magnetic field ef
49  of capturing interfacial water dissociation/recombination reactions and electrolytic proton transpor
50  in both the efficiency and rate of in vitro recombination reactions and offers an explanation for st
51 -junction) is both a central intermediate of recombination reactions and, in some cases, a controllin
52 gion plays a critical regulatory role in the recombination reaction, and mutations in this region hav
53          Finally, we found that in vitro Cre recombination reactions are much more stringent for eval
54 e presented that not one but several on-step recombination reactions are responsible for dinitrogen f
55 plicating a defect in the early steps of the recombination reaction as the basis of the clinical phen
56 bution from the acceptor side in the form of recombination reactions as well as from the donor side o
57 gration reaction, and perhaps other cellular recombination reactions as well.
58 imurium stimulates several site-specific DNA recombination reactions, as well as transcription of a n
59 ociation inhibit the efficiency of the V(D)J recombination reaction at the endogenous immunoglobulin
60 o distinct classes based on the stage in the recombination reaction at which they are blocked.
61 r on dye aggregation on the TiO2 surface and recombination reactions at TiO2/dye/electrolyte interfac
62 ent after photobleaching of rhodopsin is the recombination reaction between its apoprotein opsin and
63 bute this maximum to either elimination of a recombination reaction between the redox-active tyrosine
64  encoded enzymes that catalyse site-specific recombination reactions between a short DNA sequence on
65 as determined by analysis of the kinetics of recombination reactions between P700+ and reduced accept
66  specific RNA target requires two homologous recombination reactions between plasmids and phages in b
67  that is not strictly required for the basic recombination reaction but helps to regulate recombinati
68               Blocking an early stage of the recombination reaction by disruption of XRCC3 not only s
69    In the absence of mediators, ssb inhibits recombination reactions by competing with recombinase fo
70 rified Srs2 strongly inhibits Rad51-mediated recombination reactions by disrupting the Rad51-ssDNA pr
71 ins allowed tracking of second-order heme CO recombination reactions by transient absorbance.
72                   Several steps of the V(D)J recombination reaction can be reconstituted in vitro wit
73 n and T-cell receptor (TCR) genes, the V(D)J recombination reaction can in principle generate three t
74 sequence homology and in some cases aberrant recombination reactions can be detected using such micro
75 difference of barrier heights in these three recombination reactions can be rationalized in terms of
76 either of the two coding ends in these V(D)J recombination reactions can recombine with either of the
77                                              Recombination reactions carried out in vitro are accompa
78                                 The simplest recombination reaction catalyzed by Int does not require
79                                   The normal recombination reaction catalyzed by the Flp (pronounced
80                        For the site-specific recombination reactions catalyzed by the bacteriophage l
81 catalytic quantity of Srs2 to Rad51-mediated recombination reactions causes severe inhibition of thes
82 ed for diversity generation through frequent recombination reactions creates a situation where the HJ
83 d donor DNA in three different stages of the recombination reaction cycle.
84 an effect of the metal binding on the charge recombination reaction D+*QAQB-* --> DQAQB suggests that
85 units were able to participate in a complete recombination reaction, demonstrating that the interacti
86                     Here, we report a robust recombination reaction employing oligonucleotide substra
87 hat confer directionality upon site-specific recombination reactions encoded by plasmids, transposons
88 acteriophage lambda lysogen, a site-specific recombination reaction excises the phage genome from the
89            Here we describe defined in vitro recombination reactions for both phiRv1 integrase-mediat
90      Here we reconstitute the complete V(D)J recombination reaction in a cell-free system.
91 intermediates of the G1 phase-specific V(D)J recombination reaction in progenitor lymphocytes.
92 mbination proteins, catalyzes the homologous recombination reaction in the context of a helical prote
93 n DNA invertase promotes a site-specific DNA recombination reaction in the Salmonella chromosome.
94 tigate the mechanistic properties of the Hin recombination reaction in vivo, we have analysed the top
95 challenge phages through a single homologous recombination reaction in vivo.
96  dissecting the role of hRad51 and hRad54 in recombination reactions in human cells.
97 g DNA double-strand breaks and enhancing DNA recombination reactions in maize cells.
98       Using TFM-FRET, we observed individual recombination reactions in real time and analyzed their
99            This process requires a series of recombination reactions in which the internal guide sequ
100 oxP substrate reveals an intermediate in the recombination reaction, in which a Cre molecule has clea
101 otide excision repair and homology-dependent recombination reactions, including DNA single strand ann
102 in the region of the FRT site (following the recombination reaction) indicated that a precise rearran
103 mobile elements exploit FtsK-independent Xer recombination reactions initiated by XerC.
104 gnal ends, these nonhairpin coding-end V(D)J recombination reaction intermediates have 3' overhanging
105                                              Recombination reactions involve particular geometric and
106          A fundamental step in site-specific recombination reactions involves the formation of proper
107 of the E2A proteins is rate limiting for the recombination reaction involving these Vdelta regions.
108 1, 1-2 and 2-3 bp of branch migration during recombination reactions involving 6, 7 and 8 bp spacers,
109                     The mechanism of the ClO recombination reaction is also discussed, and the result
110 p1-dependent, pre-SC transition early in the recombination reaction is an essential component of meio
111                                          The recombination reaction is catalyzed by four monomers of
112                                    The V(D)J recombination reaction is composed of multiple nucleolyt
113 c analysis shows that directionality of this recombination reaction is conferred by the irreversibili
114 as, so far, been very low because the charge recombination reaction is faster than the catalytic four
115 bination complex and/or mediate a controlled recombination reaction is impaired.
116 -strength magnetic fields, provided that the recombination reaction is strongly asymmetric-a scenario
117                    An obligatory step in the recombination reaction is the association, or synapsis,
118      A hierarchy of isotopically substituted recombination reactions is formulated for production of
119 akes the reaction unique among site-specific recombination reactions is that the first step, XerD-med
120  the case and that RAD18 plays a role in the recombination reaction itself.
121 m component gene segments by a site-specific recombination reaction known as V(D)J recombination.
122 h inhibit different steps in a site-specific recombination reaction mediated by the bacteriophage lam
123                            The site-specific recombination reaction mediated by the Flp recombinase o
124 s are central intermediates in site-specific recombination reactions mediated by tyrosine recombinase
125 ental data on the kinetics and regulation of recombination reactions mediated by varphiC31 integrase
126                      The site-specific V(D)J recombination reaction necessary to assemble the genes c
127 during lymphoid development by a specialized recombination reaction normally observed only in cells o
128        This integrase-mediated site-specific recombination reaction occurs between the phage attP sit
129                                          The recombination reaction of phenyl (c-C(6) H(5) ) and benz
130 o new insights into the unwanted interfacial recombination reaction of the injected electrons with th
131                          The geminate ligand recombination reactions of photolyzed carbonmonoxyhemogl
132 itro; nevertheless, many failed to mediate a recombination reaction on supercoiled plasmid in vivo or
133                                              Recombination reactions or deprotonations of the radical
134 n vivo the role of Mu B in the two different recombination reactions performed by phage Mu: non-repli
135                                          The recombination reaction proceeds by sequential sets of ge
136                                    The V(D)J recombination reaction proceeds through RSS recognition
137                               Traditionally, recombination reactions promoted by RecA-like proteins i
138 quences of the change in effective radiative recombination reaction rate coefficients produced by int
139 arge recombination is mainly governed by the recombination reaction rate constant and the charge dens
140 t which RipX and CodV catalyze site-specific recombination reactions required for normal chromosome p
141 products of integrase-mediated site-specific recombination reactions results in a single recombinase
142 mpletely randomized arm in a functional loxP recombination reaction revealed that only three wild-typ
143                     Thus, the overall charge-recombination reaction seems to involve a concerted prot
144 dy provides important insight into the V(D)J recombination reaction, specifically that significant in
145 nate occurred through end-chain scission and recombination reactions, successively yielding PFOS.
146 logenetically, and mechanistically different recombination reactions, such as V(D)J recombination and
147                                    This fast recombination reaction suggests that Cl-containing SO(x)
148 nase variants were found to be active in all recombination reactions tested: excision, integration, a
149 /RAG2 endonuclease (RAG) initiates the V(D)J recombination reaction that assembles immunoglobulin hea
150                 During the site-specific DNA recombination reaction that excises phage lambda from th
151 ombinase family, it catalyses an integrative recombination reaction that occurs by a different crosso
152 recombination (CSR) is a region-specific DNA recombination reaction that replaces one immunoglobulin
153 he Hin recombinase catalyzes a site-specific recombination reaction that results in the reversible in
154                     Depending on the type of recombination reaction that takes place, intermediates m
155 lled the bloodstream VSG expression site, or recombination reactions that move silent VSGs or VSG cop
156 led the creation of molecular models for the recombination reactions that result in pilin antigenic v
157 g P680(*+), the relay is thought to mitigate recombination reactions, thereby ensuring a high quantum
158 lates to individual biochemical steps in the recombination reaction these mutants, R123Q, T124I, and
159                   These can undergo a second recombination reaction to generate odd-noded knots.
160 erD, allowing both intra- and intermolecular recombination reactions to go to completion.
161 etic fields (not exceeding 46 mT) on radical recombination reactions to investigate protein-substrate
162 The highly directional and tightly regulated recombination reaction used to site-specifically excise
163 mplications on the role of ICP8 in mediating recombination reactions using viral transcripts.
164 in developing lymphocytes by a site-specific recombination reaction, V(D)J recombination.
165  donor, reduced bacteriopheophytin acceptor) recombination reaction was measured in a series of react
166 ility to participate in a full site-specific recombination reaction was reduced only slightly.
167 atches on the kinetics of the RecA-catalyzed recombination reaction, we used assays based upon fluore
168 Hin recombinase on the DNA for a step in the recombination reaction which occurs either at and/or pri
169        This process is executed by the V(D)J recombination reaction, which can be divided into DNA cl
170 of the signal and coding joints in the V(D)J recombination reaction, which is necessary for productio
171 It shows that synapsis is a slow step in the recombination reaction, while subsequent strand exchange
172 day junction recombination intermediates and recombination reactions with chimeric recombinases, to i
173  gene, pilE, which result from nonreciprocal recombination reactions with numerous silent loci, pilS.
174  rather dimers stemming from radical-radical recombination reactions, with p-isotoluene as a clear ex

 
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