ライフサイエンスコーパス: non-homologous

1 ediction of STAR3D is more accurate for both non-homologous and homologous RNAs than other state-of-t

2 ulatory GTPases, but is atypical in having a non-homologous, C-terminal domain of approximately 20 kD

3 to those observed in Cdk2 KO mice including non-homologous chromosome pairing, unrepaired double-str

4 nto a new region of the same chromosome or a non-homologous chromosome.

5 d chromatin bridges between the telomeres of non-homologous chromosomes in Atrecq4A at metaphase I, i

6 HSCs preferentially undergo non-homologous compared with microhomology-mediated end

7 e, no mechanism able to specifically inhibit non-homologous crossovers has been described in allopoly

8 ene for the main crossover pathway, prevents non-homologous crossovers in allotetraploid Brassica nap

9 We show that non-homologous crossovers originate almost exclusively f

10 romosome segregation requires suppression of non-homologous crossovers while levels of homologous cro

11 Non-homologous DNA appears to divert cells towards error

12 deletion of genomic sequence or insertion of non-homologous DNA at the edited locus in a cell line sp

13 Non-homologous DNA end joining (NHEJ) is the predominant

14 During non-homologous DNA end joining (NHEJ), bringing two brok

15 coni protein D2, ATM protein expression, and non-homologous DNA end joining protein expression and fu

16 2056 phosphorylation, indicative of elevated non-homologous DNA end joining.

17 It is the main nuclease in the non-homologous DNA end-joining pathway (NHEJ).

18 ing site-specific nuclease digestion through non-homologous DNA end-joining, as opposed to single str

19 ndant proteins and test it on a large set of non-homologous domains, as well as on the set of protein

20 ing partners promotes the rapid unbinding of non-homologous dsDNA and drives strand exchange forward

21 Non-homologous dsDNA rapidly unbinds, whereas homologous

22 ce that selection for RPS5 involves multiple non-homologous effectors and multiple pathogen species.

23 Non homologous end joining (NHEJ) is an important proces

24 The non homologous end-joining (NHEJ) pathway of double-stra

25 mosome fusions via the mutagenic alternative non-homologous end joining (A-NHEJ) pathway.

26 Alternative non-homologous end joining (alt-NHEJ) was originally ide

27 iple cell lines, we found that the canonical non-homologous end joining (C-NHEJ) factor XLF promotes

28 mpared to HR, whereas Ku-dependent classical non-homologous end joining (C-NHEJ) has a minimal role t

29 Classic non-homologous end joining (C-NHEJ) is the predominant D

30 ngly none of the components of the canonical non-homologous end joining (C-NHEJ) pathway were identif

31 Canonical non-homologous end joining (c-NHEJ) repairs DNA double-s

32 pair is usually facilitated by the classical non-homologous end joining (C-NHEJ), or homologous recom

33 deletion rearrangement mediated by canonical non-homologous end joining (C-NHEJ).

34 a mutated (ATM); and inhibitors of classical non-homologous end joining (cNHEJ) and alternative end j

35 Classical non-homologous end joining (cNHEJ) and homologous recomb

36 ndependent function for LRF in the classical non-homologous end joining (cNHEJ) pathway of double-str

37 Micro-homology-mediated non-homologous end joining (MMEJ) can also be used but t

38 DNA non-homologous end joining (NHEJ) and homologous recombi

39 ain repair pathways used to resolve DSBs are Non-Homologous End Joining (NHEJ) and Homologous Recombi

40 promotes the two major DSB repair pathways, non-homologous end joining (NHEJ) and homologous recombi

41 ebrafish (Danio rerio) and livestock through non-homologous end joining (NHEJ) and homology-directed

42 trand break repair that buttresses canonical non-homologous end joining (NHEJ) and is manifest in NHE

43 Homology-directed repair and non-homologous end joining (NHEJ) are the two major DSB

44 HD1 is required for DNA damage signaling and non-homologous end joining (NHEJ) at unprotected telomer

45 Finally, I find that all non-homologous end joining (NHEJ) defective cells (wheth

46 XRCC4-like factor (XLF) is a non-homologous end joining (NHEJ) DNA double strand brea

47 The repair of DSBs by non-homologous end joining (NHEJ) has been extensively s

48 Initiation of HR in the G1 phase blocks non-homologous end joining (NHEJ) impairing DSB repair.

49 recognition site in the BRCT domain impairs non-homologous end joining (NHEJ) in cell.

50 DNA double-strand break (DSB) repair by non-homologous end joining (NHEJ) in human cells is init

51 Non-homologous end joining (NHEJ) involves limited proce

52 Non-homologous end joining (NHEJ) is a key cellular proc

53 Non-homologous end joining (NHEJ) is a major DNA double-

54 Non-homologous end joining (NHEJ) is a major pathway to

55 Non-homologous end joining (NHEJ) is critical for the ma

56 Non-homologous end joining (NHEJ) is the main repair pat

57 Non-homologous end joining (NHEJ) is the major model pro

58 Although non-homologous end joining (NHEJ) is the most used DSBs

59 Non-homologous end joining (NHEJ) is the predominant pat

60 m the RAG post-cleavage complex (PCC) to the non-homologous end joining (NHEJ) machinery to promote a

61 capabilities; however, the preponderance of non-homologous end joining (NHEJ) mediated repair events

62 We hypothesize that inhibiting non-homologous end joining (NHEJ) or enhancing homology-

63 and breaks (DSBs) are repaired by either the non-homologous end joining (NHEJ) or homologous recombin

64 regulated process performed predominantly by non-homologous end joining (NHEJ) or homologous recombin

65 implicates breaks followed by repair through non-homologous end joining (NHEJ) or stalled fork repair

66 reaks that can undergo DNA repair either via non-homologous end joining (NHEJ) or, in the presence of

67 se IIIalpha is a component of an alternative non-homologous end joining (NHEJ) pathway for DNA double

68 The non-homologous end joining (NHEJ) pathway is used in div

69 referentially repaired using the error-prone non-homologous end joining (NHEJ) pathway.

70 R) while stymieing repair by the error-prone non-homologous end joining (NHEJ) pathway.

71 Inhibition of Non-Homologous End Joining (NHEJ) repair either pharmaco

72 We studied the impairment of the non-homologous end joining (NHEJ) repair pathway and DNA

73 kinase (DNA-PK) plays a critical role in the non-homologous end joining (NHEJ) repair pathway and the

74 While non-homologous end joining (NHEJ) repair results in vari

75 B-mediated homologous recombination (HR) and non-homologous end joining (NHEJ) repair systems, leadin

76 ught to arise from a moderate attenuation of non-homologous end joining (NHEJ) repair, the role of DE

77 sponses, including checkpoint activation and non-homologous end joining (NHEJ) repair.

78 Non-homologous end joining (NHEJ) repairs DNA double str

79 knockout MEFs exhibited distinct defects in non-homologous end joining (NHEJ) when compared to their

80 Here, we suggest a role of LKB1 in non-homologous end joining (NHEJ), a major DNA double-st

81 nit (DNA-PKcs) plays a key role in mediating non-homologous end joining (NHEJ), a major repair pathwa

82 Non-allelic homologous recombination (NAHR), non-homologous end joining (NHEJ), and microhomology-med

83 for sequence-specific gene knockout through non-homologous end joining (NHEJ), but it remains ineffi

84 ir factors, in particular those required for non-homologous end joining (NHEJ), do not form discrete

85 non-allelic homologous recombination (NAHR), non-homologous end joining (NHEJ), fork stalling and tem

86 hen can become the substrate for error-prone non-homologous end joining (NHEJ), generating mutations

87 xcision repair (NER), mismatch repair (MMR), non-homologous end joining (NHEJ), homologous recombinat

88 Yeast Rap1 protects telomeres from non-homologous end joining (NHEJ), plays important roles

89 common DSB repair mechanism in human cells, non-homologous end joining (NHEJ), rejoins broken DNA en

90 ly detect homology-directed repair (HDR) and non-homologous end joining (NHEJ), respectively.

91 In contrast to non-homologous end joining (NHEJ), TMEJ efficiently repa

92 air by homologous recombination (HR) but not non-homologous end joining (NHEJ), using HeLa cell lines

93 s of either homologous recombination (HR) or non-homologous end joining (NHEJ), whereas SUMO2/3 was r

94 -strand breaks are repaired predominantly by non-homologous end joining (NHEJ), which directly ligate

95 tly reported the involvement of WT TDP-43 in non-homologous end joining (NHEJ)-mediated DSB repair, w

96 e Alb locus in mouse liver is mainly through non-homologous end joining (NHEJ)-mediated knock-in.

97 karyotic cells are predominantly repaired by non-homologous end joining (NHEJ).

98 that support single-strand break repair and non-homologous end joining (NHEJ).

99 ch between homologous recombination (HR) and non-homologous end joining (NHEJ).

100 A repair: homology directed repair (HDR) and non-homologous end joining (NHEJ).

101 nt, while still protecting telomeres against non-homologous end joining (NHEJ).

102 DSBs), thereby influencing the efficiency of non-homologous end joining (NHEJ).

103 . patens mutants for DSB factors involved in non-homologous end joining (NHEJ).

104 switch recombination (CSR), are repaired by non-homologous end joining (NHEJ).

105 factor for DNA double-strand break repair by non-homologous end joining (NHEJ).

106 kinase holoenzyme (DNA-PK) in the process of non-homologous end joining (NHEJ).

107 bition induces a repair defect that involves non-homologous end joining (NHEJ).

108 breaks (DSBs) are predominantly repaired by non-homologous end joining (NHEJ).

109 repair from homologous recombination (HR) to non-homologous end joining (NHEJ).

110 ed through homology-directed repair (HDR) or non-homologous end joining (NHEJ).

111 repair pathways competing with HDR, such as non-homologous end joining (NHEJ).

112 s, homology-directed recombination (HDR) and non-homologous end joining (NHEJ).

113 insights into LINP1's ability to facilitate non-homologous end joining (NHEJ). We characterized LINP

114 t provides DNA ligase activity for classical non-homologous end joining (the predominant DNA double-s

115 that errors in DNA repair pathways, such as non-homologous end joining and homologous recombination,

116 The TRF2-Rap1 complex suppresses non-homologous end joining and interacts with DNAPK-C to

117 e other five types of solid tumors, in which non-homologous end joining and microhomology end joining

118 ted stochastic model of DNA damage repair by non-homologous end joining and of gamma irradiation-indu

119 otein and combined deficiencies in classical non-homologous end joining and p53 predispose to RAG-ini

120 the choice of homologous recombination over non-homologous end joining and potentially other mutagen

121 e found that MMSET is required for efficient non-homologous end joining as well as homologous recombi

122 ssay that is more sensitive than the typical non-homologous end joining assay.

123 RNF168 rescues 53BP1 recruitment involved in non-homologous end joining but not BRCA1 recruitment for

124 the interference of high LET radiation with non-homologous end joining but not homologous recombinat

125 roach to reduce the toxicity associated with non-homologous end joining by promoting the use of homol

126 tivation of the p97-ATX3 complex affects the non-homologous end joining DNA repair pathway and hypers

127 de DNA end binding proteins required for the non-homologous end joining DNA repair pathway, increases

128 end joining (MMEJ) rather than the canonical non-homologous end joining DNA repair pathway.

129 ation (insertion or deletion) by error-prone non-homologous end joining DNA repairing.

130 We found Cas9-gRNA achieved 7-8x higher non-homologous end joining efficiencies (3%) than reTALE

131 fragment at the same time, thereby reducing non-homologous end joining efficiency.

132 t acetylation of H4 regulates binding of the non-homologous end joining factor 53BP1, which engages c

133 G2 shepherd the broken DNA ends to classical non-homologous end joining for proper repair, roles for

134 ting functional redundancy between Rad18 and non-homologous end joining for tolerance of oxidative DN

135 ination (HR) and antagonizes 53BP1-dependent non-homologous end joining in S/G2 phase.

136 Repair of DNA double-strand breaks (DSBs) by non-homologous end joining is critical for neural develo

137 A-dependent protein kinase (DNA-PK)-mediated non-homologous end joining is inhibited.

138 Non-homologous end joining is initiated by the associati

139 repair (HR), while counteracting error-prone non-homologous end joining of DNA double-strand breaks.

140 7 or its adapters impairs Ku80 removal after non-homologous end joining of DSBs.

141 ther demonstrate that the excursions promote non-homologous end joining of dysfunctional telomeres an

142 derived hiPSCs where successful deletion and non-homologous end joining of up to 725 kb reframed the

143 A double-strand breaks can be eliminated via non-homologous end joining or homologous recombination.

144 wed by repair through either the error-prone non-homologous end joining or the homology directed repa

145 s in a G1-like DNA repair mode which favours non-homologous end joining over interchromosomal recombi

146 double-strand DNA break (DSB) repair via the non-homologous end joining pathway, as unrepaired DSBs a

147 DNA-PKcs, which is integral to the non-homologous end joining pathway, thus negatively regu

148 an be further improved by suppression of the non-homologous end joining pathway.

149 uble strand breaks, initiating repair by the non-homologous end joining pathway.

150 B) repair as the underlying mechanism of the non-homologous end joining pathway.

151 proteins of the homologous recombination and non-homologous end joining pathways.

152 led to enhanced phosphorylation of DNA-PK, a non-homologous end joining repair protein, in Hec-108 ce

153 Non-homologous end joining repair-based BCL11A enhancer

154 removal of histone H3 from the genome during non-homologous end joining was promoted by both ATM and

155 EGFR mutation is associated with a defect in non-homologous end joining, a major pathway for DNA doub

156 ecombination, an error-free mechanism, or by non-homologous end joining, a process susceptible to int

157 ctionally contribute to efficient resection, non-homologous end joining, and tolerance to DNA-damagin

158 lta defects in Tel1/ATM kinase signaling and non-homologous end joining, consistent with the role of

159 in vivo genome editing method, combined with non-homologous end joining, enabling permanent chromosom

160 at take part in homologous recombination and non-homologous end joining, respectively, were transcrip

161 A DSB repair by homologous recombination and non-homologous end joining, respectively.

162 In addition to non-homologous end joining, we detect signatures of repl

163 damage-tolerance in G(1) (because of back-up non-homologous end joining-mediated DSB repair), yet Rad

164 gy near the breakpoints resembling repair by non-homologous end joining.

165 ends that are poor substrates for classical non-homologous end joining.

166 sed G overhang levels, and altered levels of non-homologous end joining.

167 repair by both homologous recombination and non-homologous end joining.

168 s of double-strand break repair generated by non-homologous end joining.

169 of chromosomal replication and DSB repair by non-homologous end joining.

170 equent repair by homologous recombination or non-homologous end joining.

171 QLN4 overexpression represses HRR and favors non-homologous end joining.

172 through chromothripsis coupled to classical non-homologous end joining.

173 rimarily function in the DSB repair pathway, non-homologous end joining.

174 epairing double-strand DNA breaks (DSBs) via non-homologous end joining.

175 region of glsA, indicative of Cas9-directed non-homologous end joining.

176 dent on Ku70/80 and LIG4, or the alternative non-homologous end-joining (A-NHEJ), which relies on PAR

177 Classical non-homologous end-joining (C-NHEJ) is the dominant path

178 elomere fusions require either the classical non-homologous end-joining (C-NHEJ) pathway dependent on

179 Besides the KU-dependent classical non-homologous end-joining (C-NHEJ) pathway, an alternat

180 ng mechanisms, the main process is classical non-homologous end-joining (C-NHEJ) which relies on Ku b

181 or critical role in ICL repair was seen for non-homologous end-joining (cku-80) or base excision rep

182 CC4-like factor (XLF) functions in classical non-homologous end-joining (cNHEJ) but is dispensable fo

183 catalytic subunit (DNA-PKcs), is a classical non-homologous end-joining (cNHEJ) factor(1).

184 e repair of DNA double-strand breaks (DSBs): non-homologous end-joining (NHEJ) and homologous recombi

185 Non-homologous end-joining (NHEJ) and homologous recombi

186 ase II (TOP2) are rejoined by TDP2-dependent non-homologous end-joining (NHEJ) but whether this promo

187 TRADD facilitates non-homologous end-joining (NHEJ) by recruiting NHEJ rep

188 to be associated with the components of the non-homologous end-joining (NHEJ) complex and participat

189 rate that combined inactivation of the XRCC4 non-homologous end-joining (NHEJ) DNA repair gene and p5

190 Allele-specific gene disruption induced by non-homologous end-joining (NHEJ) DNA repair offers a po

191 HDR) is limited by the competing error-prone non-homologous end-joining (NHEJ) DNA repair pathway.

192 GE syndrome, as an integral component of the non-homologous end-joining (NHEJ) DSB repair pathway.

193 As the non-homologous end-joining (NHEJ) factor, Ku70/80 (Ku),

194 Non-homologous end-joining (NHEJ) is the most prominent

195 The alternative non-homologous end-joining (NHEJ) machinery facilitates

196 that inactivating terminal components of the non-homologous end-joining (NHEJ) machinery or of the BR

197 the X family that has been implicated in the non-homologous end-joining (NHEJ) pathway during repair

198 The non-homologous end-joining (NHEJ) pathway repairs DNA do

199 roduction of insertion-deletions (INDELs) by non-homologous end-joining (NHEJ) pathway underlies the

200 DNA fragments, which are not repaired by the non-homologous end-joining (NHEJ) pathway.

201 depleting HP1 from cells did not affect the non-homologous end-joining (NHEJ) pathway: instead it el

202 ed via the single-strand annealing (SSA) and non-homologous end-joining (NHEJ) pathways in a manner d

203 Non-homologous end-joining (NHEJ) plays an important rol

204 osomes and generate genome rearrangements by non-homologous end-joining (NHEJ) processes in specializ

205 dation of a novel assay to measure mutagenic non-homologous end-joining (NHEJ) repair in living cells

206 In contrast, alleles created by non-homologous end-joining (NHEJ) repair of double-stran

207 homology directed repair (HDR) and decreased non-homologous end-joining (NHEJ) repair, suggesting tha

208 efficiency, which are typically repaired by non-homologous end-joining (NHEJ) resulting in nonspecif

209 Non-homologous end-joining (NHEJ), a repair process pred

210 n (HR) repair with a concomitant decrease in non-homologous end-joining (NHEJ), accounting for the im

211 e between high-fidelity (HF) and error-prone non-homologous end-joining (NHEJ), as well as between pr

212 syl-DNA phosphodiesterase 2 (TDP2)-dependent non-homologous end-joining (NHEJ), but whether this proc

213 DNA-PKcs; encoded by PRKDC) functions in DNA non-homologous end-joining (NHEJ), the major DNA double

214 ever, mutagenic events caused by error-prone non-homologous end-joining (NHEJ)-mediated repair are in

215 ce between homologous recombination (HR) and non-homologous end-joining (NHEJ)-mediated repair.

216 repaired predominantly in mammalian cells by non-homologous end-joining (NHEJ).

217 tion of DNA end-resection, and DSB repair by non-homologous end-joining (NHEJ).

218 NA damage being channelled through repair by non-homologous end-joining (NHEJ).

219 trand break (DSB) repair pathways, including non-homologous end-joining (NHEJ).

220 )p53(-/-) MEFs, homologous recombination and non-homologous end-joining activities were significantly

221 on are predominantly mediated by alternative non-homologous end-joining activity that may employ eith

222 revious studies have shown that 53BP1 is pro-non-homologous end-joining and anti-HR.

223 timated frequencies of accurate or mutagenic non-homologous end-joining and gene correction by homolo

224 ks between the target sequences, stimulating non-homologous end-joining and homologous recombination.

225 repair occurs in cells fully proficient for non-homologous end-joining and is not compensated by DNA

226 short palindromic repeats (CRISPR)/Cas9 and non-homologous end-joining by deleting the repeat region

227 protein NONO was found to be involved in the non-homologous end-joining DNA repair process and in pol

228 sh that REV7 blocks DSB resection to promote non-homologous end-joining during immunoglobulin class s

229 We find that inversion depends on the non-homologous end-joining enzyme LIG4.

230 e the persistence of random integrations and non-homologous end-joining events.

231 The authors demonstrate that the non-homologous end-joining factor XLF promotes the stabi

232 Hypomorphic mutations in the non-homologous end-joining gene DCLRE1C (encoding ARTEMI

233 e repaired with a high level of precision by non-homologous end-joining in mammalian cells.

234 demonstrate the importance of TDP2-dependent non-homologous end-joining in protecting both gene trans

235 bioluminescence imaging, that the assay for non-homologous end-joining is sensitive, quantitative, r

236 SWI/SNF and RSC enzymes is inhibited by the non-homologous end-joining machinery, and that their rec

237 DSBs are repaired by non-homologous end-joining or homology directed repair (

238 s expressing BCR-ABL1 utilize an alternative non-homologous end-joining pathway (ALT NHEJ) to repair

239 amage response (DDR) and instrumental in the non-homologous end-joining pathway (NHEJ) used to detect

240 rrow failure syndrome) codes for a canonical non-homologous end-joining pathway factor, that the RNA

241 leotides during gap-filling synthesis in the non-homologous end-joining pathway of double-strand brea

242 As a member of the non-homologous end-joining pathway, it is also involved

243 in the proximity of the break were due to a non-homologous end-joining pathway, while larger deletio

244 in E. dermatitidis through disruption of the non-homologous end-joining pathway, with three individua

245 in repairing DNA double-strand breaks by the non-homologous end-joining pathway.

246 This overexpression triggers SSB repair and non-homologous end-joining pathways to increase DNA repa

247 ble-stranded DNA and helps to facilitate the non-homologous end-joining reaction.

248 Wnt signalling enhances non-homologous end-joining repair in CRC, which is media

249 Although DNA non-homologous end-joining repairs most DNA double-stran

250 a novel component regulating the switch from non-homologous end-joining to homologous recombination.

251 double-strand break repair switches from DNA non-homologous end-joining to homologous recombination.

252 ribution of DNA ligase 4-dependent classical non-homologous end-joining to long-range inter-chromosom

253 functions of DNA ligase 1 in replication and non-homologous end-joining uniquely position and capacit

254 e homologous recombination (HR) or mutagenic non-homologous end-joining(1).

255 This result suggests that non-homologous end-joining, even in haploid cells where

256 DNA repair towards faster and more accurate non-homologous end-joining, including in post-mitotic pr

257 breakpoint junctions revealed signatures of non-homologous end-joining, non-allelic homologous recom

258 involved defective base excision repair and non-homologous end-joining, pathways required for repair

259 epaired by homologous recombination (HR) and non-homologous end-joining.

260 pe repair mechanism of hairpin formation and non-homologous end-joining.

261 echanisms, homologous-recombination (HR) and non-homologous-end-joining (NHEJ).

262 nferred when structurally distinct and hence non-homologous enzymes show the ability to catalyze the

263 from head-to-head and head-to-tail oriented "non-homologous" FRT partners are a 4-noded knot and a 5-

264 the other hand, N-glycan structures found on non-homologous glycoproteins do not show significant glo

265 We found several non-homologous human genes containing similar motifs of

266 ) N-linked glycan library and PDB homologous/non-homologous N-glycoprotein sets indicate that GS-alig

267 In contrast, breakpoints associated with non-homologous (NH) mechanisms often have sequence micro

268 n different organs, formed from sequentially non-homologous polypeptide chains and affecting human or

269 large scale, DSB formation is suppressed on non-homologous portions of the sex chromosomes via the D

270 to double-stranded DNA, and a suppression of non-homologous primer annealing and nonspecific amplific

271 chmark sets consisting collectively of 1,153 non-homologous protein targets, where CEthreader detecte

272 he protocol was tested on a large set of 285 non-homologous proteins and generated structural models

273 reconstructions of TCPM mutants in which the non-homologous proteins are individually deleted, we pro

274 The approach was tested on a set of 158 non-homologous proteins collected from the CASP experime

275 Non-homologous proteins in the T4aPM and TCPM are found

276 ket database to predict binding ligand of 75 non-homologous proteins that bind one of seven different

277 othelial cell loss of KRIT1, CCM2 or PDCD10, non-homologous proteins that form an adaptor complex.

278 proteins, such as BigH1, or even unrelated, non-homologous proteins, such as Elba2.

279 separating training and test mutations from non-homologous proteins, which reflects inherent correla

280 ulators share no more sequence identity than non-homologous proteins.

281 sis and robustness tests, we create a set of non-homologous, purely synthetic, minimal promoters for

282 ydrolase family GH30) and then applied it to non-homologous (putative) retaining beta-glucosidases ca

283 dsDNA molecule allows dsDNA to extend along non-homologous Rad51-ssDNA filaments and remain stably b

284 by driving the swift unbinding of dsDNA from non-homologous Rad51-ssDNA filaments, while at the same

285 e normally unstable binding of that dsDNA to non-homologous RecA-ssDNA filaments, whereas pulling on

286 efficiency of both homologous and the other non-homologous recombination, as well as increases sensi

287 d that the relative levels of homologous and non-homologous repair in a given fungal species may play

288 d mechanism involving template switching and non-homologous repair mediates the formation of balanced

289 ts a shift in emphasis for new entries, from non-homologous representatives covering EC reaction spac

290 Conversely, non-homologous RLM domains can converge to catalyze the

291 e same drug (methotrexate) binds to multiple non-homologous RLM drug targets with different topologie

292 itial 8 bp test to rapidly reject almost all non-homologous sequences.

293 Overextended alignments include non-homologous sequences; they occur most frequently bet

294 ce multiple clusters constituting unrelated (non-homologous) sequences.

295 Here we find that non-homologous single-stranded DNA greatly stimulates Ca

296 rison with ssDNA covered with homologous and non-homologous SSBs under mechanical tension.

297 the second end must be processed to remove a non-homologous tail before completing repair by gene con

298 Msh2-Msh3 is also required for 3' non-homologous tail removal (3' NHTR) in double-strand b

299 oupling a microhomology search to removal of non-homologous tails and microhomology-primed synthesis

300 cular dynamics simulations performed on nine non-homologous viral protein structures and from variati