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1 ression and that they are also intrinsically recombinogenic.
2 , with the former being 10 to 100 times more recombinogenic.
3 5'-nuclease, which permits the generation of recombinogenic 3'-overhanging, single-stranded DNA (ssDN
4 s unaffected, resulting in the production of recombinogenic 3'-terminated ssDNA tails.
5 s of a repeat motif highly homologous to the recombinogenic 76-bp repeat sequences present upstream o
6                         In contrast, 12 base recombinogenic acceptors were utilized poorly and no acc
7 d with DNA duplication initiated by elevated recombinogenic activities in Alu clusters.
8        During HR, BLM has both pro- and anti-recombinogenic activities, either of which may contribut
9                     In budding yeast, Dmc1's recombinogenic activity is controlled by the meiosis-spe
10 ce reporter transgenes, we demonstrate a new recombinogenic activity of AID leading to intra- and int
11 ing that Smc5/6 does not simply restrain the recombinogenic activity of Mph1 via direct binding.
12 gene-containing ecotropic virus demonstrated recombinogenic activity with endogenous FeLV sequences i
13 e that combining RNP delivery with naturally recombinogenic adeno-associated virus (AAV) donor vector
14                                              Recombinogenic Alu sequences bracketed the breakpoints i
15 veillance, transcription-coupled repair, and recombinogenic and meiotic processes.
16 single-stranded gene insertion cassettes are recombinogenic and that these cassettes preferentially t
17            HSV-1 has been shown to be highly recombinogenic, and recombination itself appears to be a
18                   The undesirable mutagenic, recombinogenic, and toxic incorporation of purine base a
19 ls how genomic plasticity within lineages of recombinogenic bacteria can permit adaptation to clinica
20 tanding of diversification and speciation in recombinogenic bacteria.
21 baylyi strain ADP1 is a highly competent and recombinogenic bacterium.
22 ondary structure thus formed and generates a recombinogenic break in the DNA.
23 tream of ScaI cleavage sites, confirming the recombinogenic character of DSBs in mtDNA.
24 mice that could be exploited as an assay for recombinogenic chemicals.
25 s at an early step of recombination in a pro-recombinogenic complex with Rlp1 and Rdl1, two RecA-like
26 Int protomers, within a multiprotein 400-kDa recombinogenic complex, is thought to bind and, with the
27 ducing DNA bends necessary to form an active recombinogenic complex.
28 rdinates Int functions within the multimeric recombinogenic complex.
29 anging Int protomers within the higher-order recombinogenic complex.
30 rm-type sites in integrative versus excisive recombinogenic complexes reflects the regulation of reco
31 tically about the global architecture of the recombinogenic complexes.
32 es and afford a new view of the higher-order recombinogenic complexes.
33 ns that along with Int comprise higher-order recombinogenic complexes.
34 leost fish IgL each contain only two to four recombinogenic components (one to three V, one J) and ex
35                        Here we show that the recombinogenic cores of active hot spots in mice harbor
36 ibution but harbor CO repulsion zones within recombinogenic cores.
37 rotein interactions required for assembly of recombinogenic Cre intasomes.
38  such DNA:RNA hybrids constitute a source of recombinogenic DNA damage taking advantage of Rad51-inde
39 NA hybrids constitute a well-known source of recombinogenic DNA damage.
40 plication fork position and the formation of recombinogenic DNA ends.
41 UMO-PCNA signals for recruitment of the anti-recombinogenic DNA helicase Srs2.
42 lesser extent, srs2, which encode known anti-recombinogenic DNA helicases.
43 idence that marker exchange is stimulated by recombinogenic DNA lesions formed as intermediates in th
44 ry of replicative DNA polymerases results in recombinogenic DNA lesions, presumably double-strand DNA
45                   Topoisomerase IB catalyzes recombinogenic DNA strand transfer reactions in vitro an
46     However, it has also been suggested that recombinogenic DNA:RNA hybrids could be facilitated by t
47                 We show that unscheduled and recombinogenic DNA:RNA hybrids that trigger the SSA even
48 ication efficiencies (>10%) by introducing a recombinogenic double-strand break into the targeted gen
49 y Ref reflects the introduction of directed, recombinogenic double-strand breaks.
50 ms might favor genetic transfer by producing recombinogenic double-stranded DNA ends.
51 iety of cells and cell types by delivering a recombinogenic DSB to the targeted chromosomal locus, us
52        Cleavage of this hairpin results in a recombinogenic DSB.
53  lines will enhance the utility of the hyper-recombinogenic DT40 cell line as a system for the geneti
54 genetic study was undertaken using the hyper-recombinogenic DT40 chicken cell line and a series of mu
55 e from these findings that the mutagenic and recombinogenic effects of msDNAs are due to titrating ou
56 or MutS protein suppresses the mutagenic and recombinogenic effects of msDNAs.
57  targeting vector was constructed with small recombinogenic ends (500 bp) derived from flanking seque
58 ectively cloned by recombination between the recombinogenic ends in the targeting vector and homologo
59  linear DNA containing YAC-specific, unique, recombinogenic ends, thereby ensuring co-integration of
60 lanking the inserts in P1 and PAC vectors as recombinogenic ends.
61 te full-length 3'-UTR reporter constructs by recombinogenic engineering (recombineering) in vivo clon
62                  Greater microcolinearity in recombinogenic (euchromatic) than nonrecombinogenic (het
63 ergoing transformation into yeast are highly recombinogenic, even when diverged.
64  alters the chromosomal architecture in that recombinogenic factors accumulate, fostering large-scale
65 t Rad9 promotes stable annealing between the recombinogenic filament and the donor template in yeast,
66 ombinogenic form of the RecBCD enzyme into a recombinogenic form by causing two distinct enzymatic ch
67                          This important anti-recombinogenic function cannot be performed by Top3beta,
68 Smc5/6 complex can counteract/modulate a pro-recombinogenic function of Mph1 or facilitate the resolu
69                                     The anti-recombinogenic functions of 53BP1 require phosphorylatio
70 elative contributions of these pro- and anti-recombinogenic functions.
71 s RecBCD from a destructive exonuclease to a recombinogenic helicase, we mutated the nuclease catalyt
72  Swi5 and Rad57 (HR-mediators) plus the anti-recombinogenic helicases Srs2 and Rqh1.
73 metabolic burden imposed by the plasmid in a recombinogenic host, rather than to ensure plasmid stabi
74            HSV-1 has been shown to be highly recombinogenic; however, to date, there has been no geno
75 tability yet revealed that this locus may be recombinogenic in a primarily clonal population structur
76            The enzyme-DNA covalent adduct is recombinogenic in cells, because the nicked strand downs
77 ich causes DNA strand breakage and is highly recombinogenic in some model organisms, was tested for i
78 he repeats at the replication fork creates a recombinogenic intermediate that can be differentially p
79 tioning and spatial proximity of potentially recombinogenic intrachromosomal loci.Oncogene advance on
80 he potential of a donor sequence to act as a recombinogenic, invasive end is determined by the stabil
81 sulted in the presence of large and probably recombinogenic LCRs across the region, the creation of t
82  mutation, rfa1-D228Y, causes an increase in recombinogenic lesions as well as the activation of a RA
83  loss of heterozygosity events stemming from recombinogenic lesions on the ribonucleotide-containing
84 ation, suggesting that replication generates recombinogenic lesions.
85 checkpoint mutants suppress the formation of recombinogenic lesions.
86 by the idea that p53 suppresses formation of recombinogenic lesions.
87 ains indicates a persistent albeit decreased recombinogenic lifestyle near the emergence of the MTBC.
88 nsights into the genetic structure of highly recombinogenic loci responsible for combinatorial geneti
89 ic region encoding these proteins revealed a recombinogenic locus with PfRh2a and PfRh2b in a head-to
90 tional allele in which an exon is flanked by recombinogenic loxP sites.
91 ne, suggesting involvement of a common novel recombinogenic mechanism that might also contribute to t
92 PCR to reconstruct missing elements from the recombinogenic middle region of pspB, SP85 was shown to
93 usion events into a distinct group of highly recombinogenic, multireplicon, self-transmissible plasmi
94 ght to have originated in East Africa from a recombinogenic Mycobacterium canettii-like ancestral poo
95 his method exploits the highly efficient and recombinogenic nature of DNA uptake during natural trans
96                 These findings highlight the recombinogenic nature of the MSY, as intrachromosomal NA
97  recombination, and monoadducts were neither recombinogenic nor mutagenic.
98  telomeres after DNA replication, creating a recombinogenic nucleoprotein structure.
99 he recombinase to assemble into higher-order recombinogenic nucleoprotein structures.
100 e tracing of this bacterium and other highly recombinogenic pathogens.
101                                  Linearized, recombinogenic pClasper targeting vector and native geno
102 eral previous studies have indicated a hyper-recombinogenic phenotype in the absence of active PARP1
103 us recombination, in contrast with the hyper-recombinogenic phenotype of yeast SWR1 mutants.
104 cally unstable, exhibiting mutator and hyper-recombinogenic phenotypes.
105  mechanism that might also contribute to the recombinogenic potential of Alu repeats.
106  locus in CHO cells can be used to study the recombinogenic potential of defined DNA sequences.
107                                          The recombinogenic potential of these 50-mers is not parasit
108  by K63-linked polyubiquitylation triggers a recombinogenic process involving template switching.
109                                    The hyper-recombinogenic properties of an E. coli strain in which
110 lity in strand transfer have illuminated the recombinogenic properties of type IB topoisomerases and
111 he BRCA2 C terminus was thought to stabilize recombinogenic RAD51 after the assembly of ATP-extended
112                               Intramolecular recombinogenic recircularization (IRR) of linearized pla
113 Although critically short telomeres are very recombinogenic, recombination among telomeres that have
114  plasmid recombination events in this highly recombinogenic region, even in the absence of viral enzy
115 nation hotspot is located within the 'highly recombinogenic' region of the full-length CaMV RNA that
116 in the large internal repeats, as well as to recombinogenic regions of cellular DNA, such as variable
117 netically dissect and molecularly manipulate recombinogenic regions to test their roles in regulating
118 etained at a higher frequency in the distal, recombinogenic regions.
119 rent Alu elements, combined with a potential recombinogenic role of retrotransposon target-site dupli
120  by ATP hydrolysis, is essential for its pro-recombinogenic role.
121                  Sgs1 has both pro- and anti-recombinogenic roles, and therefore its activity must be
122 he co-location of these genes on a small non-recombinogenic segment simplifies their deployment as a
123 ertheless offers a potential approach to map recombinogenic sequences in BACs and PACs.
124 (TRBP) was found to recognize several G-rich recombinogenic sequences in the EBV genome and in cellul
125                        This gap may act as a recombinogenic signal to initiate cross-link removal.
126                53BP1 limits the formation of recombinogenic single-strand DNA (ssDNA) in BRCA1-defici
127 ation hotspots (5'-GCTGGTGG-3') to produce a recombinogenic single-stranded DNA 3'-end.
128 ent processing of broken DNA ends to produce recombinogenic single-stranded DNA competent for HR.
129                             RecBCD generates recombinogenic single-stranded DNA ends by unwinding DNA
130 ture is the narrow 1.5-2.5-kb width of these recombinogenic sites, these analyses revealed that hot s
131 lly evolving the naturally transformable and recombinogenic species Acinetobacter baylyi with a cockt
132 he genetic macrovariation within a low-level recombinogenic species would accurately be characterized
133 ith PriB being required to limit exposure of recombinogenic ssDNA.
134  these changes is the production of a highly recombinogenic structure known as the presynaptic filame
135 g stop transfer, and can include additional, recombinogenic switches.
136 ase, gammadelta resolvase, form a simplified recombinogenic synaptic complex containing a tetramer of
137                                  To test the recombinogenic systems, we next used the overlapping BAC
138 yeast-bacterial shuttle vector, pClasper, by recombinogenic targeting in yeast.
139 nto a yeast-bacteria shuttle vector by using recombinogenic targeting.
140 m that murine leukemia virus replicative and recombinogenic template switches differ in homology requ
141                             By implying that recombinogenic template switching occurs roughly four ti
142 emplate and primer strand complementarity on recombinogenic template switching.
143 tep process, few seek to exploit the natural recombinogenic tendencies and exponential amplification
144 ipeline showed generally higher abundance in recombinogenic than in nonrecombinogenic regions of the
145 f the proposal that broken DNA ends are more recombinogenic than internal sequences, we have investig
146 tors that make wild-type female meiosis less recombinogenic than male wild-type meiosis do not apply
147 s better guide studies of related genomes in recombinogenic than nonrecombinogenic regions.
148 aking HIV-1 up to an order of magnitude more recombinogenic than recognized previously and demonstrat
149  TMPRSS2-ERG genomic breakpoints, triggering recombinogenic TOP2B-mediated DSBs.
150 te homology facilitates both replicative and recombinogenic transfers, but homology-independent deter
151 ype cells that are normally removed in a non-recombinogenic way, possibly by Rqh1 catalysing their re
152       Plant mitochondrial genomes are highly recombinogenic, with a variety of species-specific direc
153            The plant mitochondrial genome is recombinogenic, with DNA exchange activity controlled to

 
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