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1 le in homologous recombination by activating RAD51 recombinase.
2 ated DNA synthesis from a D-loop made by the Rad51 recombinase.
3 trolled by the DNA damage checkpoint and the Rad51 recombinase.
4 s recombination (HR), where it regulates the RAD51 recombinase.
5 sis of DNA double strand break repair by the Rad51 recombinase.
6 s recombination requires the function of the RAD51 recombinase.
7 ng domain (N-DBD) stimulates the function of RAD51 recombinase.
8 duct and examining its interactions with the Rad51 recombinase.
9 gle-stranded DNA and (ii) stimulation of the RAD51 recombinase.
10 d repair, presumably in conjunction with the Rad51 recombinase.
11 shown here to promote D-loop formation with Rad51 recombinase.
12 ed Pir51, that strongly interacts with human Rad51 recombinase.
13 n vivo, HsRad54 protein interacts with human Rad51 recombinase.
14 the beta-isoform of BCCIP in relation to the RAD51 recombinase.
15 erlapping chromosomal foci with the DMC1 and RAD51 recombinases.
16 es of both the bacterial RecA and eukaryotic Rad51 recombinases.
18 Thus, Rad52 functions as a co-factor for the Rad51 recombinase, acting specifically to overcome the a
19 trated that Y54 phosphorylation enhances the RAD51 recombinase activity by at least two different mec
20 tivity of UAF1 is indispensable for enhanced RAD51 recombinase activity within the context of the UAF
23 , XRCC2, and XRCC3) that share homology with RAD51 recombinase and are known as the RAD51 paralogs ar
24 and the functional interactions of PCNA with Rad51 recombinase and DNA polymerase (Pol) delta, Pol et
25 s to demonstrate that human RECQL5 binds the Rad51 recombinase and inhibits Rad51-mediated D-loop for
26 s at DNA damage sites concomitantly with the RAD51 recombinase and is retained after RAD51 disassembl
27 function through interactions with the human Rad51 recombinase and play a crucial role in the homolog
28 rtantly, Rdh54 physically interacts with the Rad51 recombinase and promotes D-loop formation by the l
30 Moreover, we find that poleta interacts with RAD51 recombinase and RAD51 stimulates poleta-mediated D
31 BRCA2 protein interacts directly with the RAD51 recombinase and regulates recombination-mediated D
32 oreover, Rad52 physically interacts with the Rad51 recombinase and serves as a mediator in the Rad51-
33 avelled, in that key HR proteins such as the RAD51 recombinase and the tumour suppressors BRCA1 and B
34 al accessory protein that interacts with the RAD51 recombinase and this interaction fluctuates during
36 4 (PTD4)], inhibited subnuclear assembly of RAD51 recombinase, and sensitized Chinese hamster ovary
38 des the major sites for interaction with the RAD51 recombinase, and uses the MaxEnt and HBond splicin
39 recombination (HR) reactions mediated by the RAD51 recombinase are essential for DNA and replication
40 tional repair of double-stranded DNA breaks, RAD51 recombinase assembles as a nucleoprotein filament
43 ite their requirement for stable assembly of RAD51 recombinase at DNA damage sites, these proteins ar
45 n cancer cells, phosphorylates the essential Rad51 recombinase at serine 14 (S14) during the cell cyc
47 sDNA from replication protein A (RPA) to the RAD51 recombinase during DNA break and replication fork
51 s recombination relies on the formation of a Rad51 recombinase filament that forms on single-stranded
52 log complex Rad55-Rad57 promotes assembly of Rad51 recombinase filament through transient interaction
60 attributed to its role as a mediator of the RAD51 recombinase in HR repair of programmed DNA double-
61 cancer suppressor protein BRCA2 controls the RAD51 recombinase in reactions that lead to homologous D
66 Homologous recombination catalyzed by the RAD51 recombinase is essential for maintaining genome in
68 elicase activity and the ability to displace Rad51 recombinase, it was unclear which functions were r
69 -ABL1 (nonmutated and T315I mutant) promoted RAD51 recombinase-mediated unfaithful homeologous recomb
70 is a distinctive activity of Rad52; neither Rad51 recombinase nor the yeast Rad52 paralog Rad59 has
71 logous recombination (HR) is the assembly of Rad51 recombinase on single-strand DNA (ssDNA), forming
72 s homologous recombination by nucleating the Rad51 recombinase onto replication protein A-coated sing
76 e are two BIR pathways, one dependent on the Rad51 recombinase protein and one Rad51 independent; the
77 ess to identify the times for the loading of Rad51 recombinase protein onto the DSB ends at MAT, the
79 anemia complementation group D2 (FANCD2) and RAD51 recombinase (RAD51) were transiently up-regulated
81 WRN helicase-interacting protein 1 (WRNIP1), RAD51 recombinase (RAD51), and BRCA2 DNA repair associat
83 is analysis between mutants defining Rrp1/2, Rad51 (recombinase), Swi5 and Rad57 (HR-mediators) plus
84 ns multiple copies of a motif that binds the Rad51 recombinase (the BRC repeat), and the C terminus c
88 e for Mek1 in inhibiting the activity of the Rad51 recombinase through phosphorylation of its binding
89 rhangs, which serve as the substrate for the Rad51 recombinase to initiate HR and are refractory to N
90 ase is known to dismantle nucleofilaments of Rad51 recombinase to prevent spurious recombination even
91 nd that it functions in conjunction with the Rad51 recombinase to repair damaged telomeres via the al
92 t replication (RDR), is driven mainly by the Rad51 recombinase, whereas template switching, during th
93 omologous recombination in eukaryotes is the RAD51 recombinase, which forms helical nucleoprotein fil
94 nzymatically by the evolutionarily conserved RAD51 recombinase, which in turn safeguards the specific
95 nctional guide confirms ATP-binding matching RAD51 recombinase, yet highlights distinct CX3 interface