ライフサイエンスコーパス: join

1 ons (indels) via mutagenic nonhomologous end joining.

2 ed DNA repair via microhomology-mediated end joining.

3 n base excision repair and nonhomologous end joining.

4 ints resembling repair by non-homologous end joining.

5 complex (PIC) assembly, to ribosomal subunit joining.

6 's capacity to limit signal (but not coding) joining.

7 required for ATM's capacity to limit signal joining.

8 with a repair bias toward nonhomologous end joining.

9 a5 propeptide have unequal roles in half-mer joining.

10 ed in virtually all steps, including subunit joining.

11 substrates for classical non-homologous end joining.

12 , which typically arise by nonhomologous end joining.

13 erfamily of nucleic acid repair enzymes that join 3'-OH and 5'-PO4 DNA or RNA ends.

14 sheet, forms a genome-delivery apparatus and joins 89 coat protein dimers to form a capsid.

15 g foraging, response to queens attempting to join a colony, circadian patterns of task performance, a

16 Thus, 14 joins a growing list of DprE1 inhibitors that are potent

17 Thus, MARCH8 joins a growing list of host factors attacking HIV-1 Env

18 In the issuance of this statement, ASCO joins a growing number of international organizations by

19 Here, we created a CAR that joins a HER2-binding scFv and an IL13Ralpha2-binding IL-

20 Thus, Hili joins a list of host proteins that inhibit the replicati

21 Importantly, NHEJ instead of alternative end-joining (A-EJ) was revealed as the predominant mechanism

22 the mutagenic alternative non-homologous end joining (A-NHEJ) pathway.

23 or cognitive saccade tasks, but whether this joined activation indexes coordinated activity underlyin

24 reover, Red1 exhibited nonhomologous DNA end-joining activity, thus revealing an unexpected role for

25 utilizes the T4 RNA Ligase 2 to efficiently join adjacent chimeric RNA-DNA probe pairs hybridized in

26 ded connectivity fingerprints and a neighbor-joining algorithm to produce a hierarchical tree with br

27 od with Arithmetic mean (UPGMA) and Neighbor-Joining algorithms.

28 f one T cell receptor beta (TCRbeta) V-to-DJ-joined allele in a functional configuration, while the s

29 By iteratively joining already identified motifs with those patterns, o

30 Alternative end-joining (alt-EJ) repair of DNA double-strand breaks is a

31 gous end joining (C-NHEJ) or alternative end joining (ALT-EJ)], which cause distinct rearrangement ju

32 show that knockdown of alt-nonhomologous end joining (alt-NHEJ) components-XRCC1, LIG3, and PARP1-sup

33 Current methods for constructing amide bonds join amines and carboxylic acids by dehydrative coupling

34 lieves this autoinhibition, enabling MIND to join an assembling kinetochore.

35 e process is a three-component coupling that joins an allylic acetate, and indole and an organo-B(pin

36 a multicomponent alkynyl halo-Prins reaction joins an enyne, a carbonyl derivative, and either a chlo

37 TRUCTURE, Principal Coordinate and Neighbour Joining analysis also revealed that the Sicilian populat

38 ement of liver and pancreas ducts where they join and enter the small intestine.

39 ipants who reported an increased tendency to join and value their social groups exhibited decreased r

40 g mechanisms to exclude competing cells from joining and exploiting their groups.

41 ost-settlement fish behaviours: social group-joining and foraging.

42 urred via both alternative nonhomologous end-joining and homologous recombination pathways.

43 repair pathways, such as non-homologous end joining and homologous recombination, may be important c

44 which suppresses repair by nonhomologous end-joining and homologous recombination.

45 12 bridge plays an important role in subunit joining and in optimizing ribosome functionality.

46 and XLF are both required for efficient end joining and radioresistance in cell-based assays.

47 ne ("HiRise") that can identify poor quality joins and produce accurate, long-range sequence scaffold

48 with the lack of homology between breakpoint joins and the randomness of the order and orientation of

49 nt protein kinase-mediated nonhomologous end-joining, and, when combined with olaparib, caused abunda

50 is required for efficient non-homologous end joining as well as homologous recombination.

51 an improved SFPQ*NONO-dependent in vitro end joining assay.

52 rmine whether larval traits influenced group-joining behaviour.

53 ettlement, but not condition, affected group-joining behaviour; smaller fish were more likely to rema

54 Notably, some philosophers have now also joined biologists in their quest to make sense of the ab

55 rittle Ti-Fe intermetallics which compromise join bonds' mechanical properties.

56 functionally specialized ipsilateral inputs joined broadly distributed contralateral inputs.

57 meters provides a practical viable method to join bulk metallic glasses.

58 guous (1 --> 4)-beta-linked glucose residues joined by (1 --> 3)-beta-linkages.

59 substantial RRE function, provided they are joined by a flexible linker that allows the two domains

60 ein P8 consists of two alpha-helical domains joined by a linker, which allows the trimer to adopt eit

61 ARPin capping repeats were re-designed to be joined by a shared helix in such a way that rigid connec

62 tic polymers in which sugar repeat units are joined by amide linkages.

63 nt size and different anisotropic properties joined by an elastic link and actuated by an external ti

64 ear polysaccharide composed of glucose units joined by beta-(1,3) bonds that possesses unique gelatio

65 Classical non-homologous end-joining (C-NHEJ) is the dominant pathway for DSB repair

66 repair pathways [canonical nonhomologous end joining (C-NHEJ) or alternative end joining (ALT-EJ)], w

67 k repair via the canonical nonhomologous end joining (c-NHEJ) pathway.

68 Canonical non-homologous end joining (c-NHEJ) repairs DNA double-strand breaks (DSBs)

69 ilitated by the classical non-homologous end joining (C-NHEJ), or homologous recombination (HR) pathw

70 wild-type versus classical nonhomologous end-joining (C-NHEJ)-deficient NSPCs reveals that both C-NHE

71 hin S regions by classical nonhomologous end joining (C-NHEJ).

72 is suggests that the financial incentives to join CAR currently exceed the costs.

73 e used in conventional processing such as in joining, casting and injection moulding, in which solidi

74 The interfacial joining characteristics between materials assembled by t

75 n ICL repair was seen for non-homologous end-joining (cku-80) or base excision repair (nth-1, exo-3),

76 Classical non-homologous end joining (cNHEJ) and homologous recombination compete for

77 form when developmental accumulation of WhiB joins constitutive accumulation of WhiA, suggesting that

78 low background, the ligase must efficiently join correctly base-paired substrates, while discriminat

79 We find that Trdd2 joins directly to Trdv, Trdd1, and Trdj segments, wherea

80 are metal-dependent nucleases that break and join DNA for the initiation and completion of conjugativ

81 the PGBD5 transposase domain as well as end-joining DNA repair and induced structural rearrangements

82 und to be involved in the non-homologous end-joining DNA repair process and in poly ADP-ribose polyme

83 junctions are joined via a nonhomologous end joining DNA repair process.

84 play a functional role in nonhomologous end-joining DNA repair.

85 HEJ factors, such as XRCC4, are required for joining DSB intermediates of the G1 phase-specific V(D)J

86 aid of dynactin and an adaptor protein that joins dynein and dynactin into a stable ternary complex.

87 Bicaudal D2 (BICD2) joins dynein with dynactin into a ternary complex (terme

88 The endonuclease Artemis improves joining efficiency by functioning in a complex with DNA-

89 potentially be mediated by either of two end-joining (EJ) repair pathways [canonical nonhomologous en

90 The nanotubes can then join end to end to form stable connections, with unconne

91 must undergo splicing to remove introns and join exons, and splicing elements present a large mutati

92 ingle gene coding, which removes introns and joins exons, and splicing branchpoints are indicators fo

93 emoves non-coding introns from pre-mRNAs and joins exons.

94 regulates binding of the non-homologous end joining factor 53BP1, which engages chromatin through si

95 through antagonism of the nonhomologous end-joining factor 53BP1.

96 Our study addressed this requirement by joining fluorescence-lifetime imaging microscopy/phasor

97 level, social-affective cognitive facet that joins forces with recent developments in the social neur

98 ted to the chemical side of biochemistry and joined Fritz Lipmann's large, hierarchical laboratory to

99 ential usage of few Variable, Diversity, and Joining genes, and skewed length distribution of the TRB

100 was used to knock out, via nonhomologous end-joining genome repair, the 4'OMT2 in opium poppy (Papave

101 fish would forage less and be more likely to join groups, both behaviours that would reduce predation

102 tions in cancer and uses this information to join haplotypes together, thus extending the range of ph

103 (circRNAs) are single-stranded RNAs that are joined head to tail with largely unknown functions.

104 ion thought to facilitate motor readiness to join in during social behavior [9-11].

105 e change in density when monomers covalently join in polymer chains.

106 e, this same group reports reduced desire to join in with the laughter of others-a behavioral profile

107 sets can be more varied, with clusters being joined in some datasets and separated in others.

108 ncy has no impact on V(D)J recombination DSB joining in ATM-deficient pro-B lines.

109 igh level of precision by non-homologous end-joining in mammalian cells.

110 ortance of TDP2-dependent non-homologous end-joining in protecting both gene transcription and genome

111 ally on the transcribed strand from mu-gamma joins, indicating that R-loops limit activation-induced

112 gies that may maximize antiviral pressure by joining innate and engineered T cell responses toward te

113 the synapse, extracted from the tissue, and joined into a form suitable for sequencing.

114 vious studies suggest that rapid 50S subunit joining involves a GTP- and fMet-tRNA(fMet)-dependent "a

115 Subunit joining is controlled by the G-protein eukaryotic transl

116 rdv, Trdd1, and Trdj segments, whereas Trdd1 joining is ordered with joining to Trdd2, a prerequisite

117 air of stalled replication forks and DNA end joining-it fills a unique niche in restoring genomic int

118 sembly from variable (V), diversity (D), and joining (J) subgenic elements (V(D)J recombination).

119 In nonhomologous end joining, Ku loads onto broken DNA via a channel consisti

120 us studies have shown that individuals often join larger groups in response to perceived predation ri

121 f mosaic heterotrimeric G-protein disorders, joining McCune-Albright and Sturge-Weber syndromes.

122 gested fundamental role of nonhomologous end joining mechanism during eccDNA formation.

123 e systematically investigated upon different joining mechanisms using blister tests.

124 l mutation in the microhomology-mediated end-joining (MMEJ) component, polymerase theta/mutagen-sensi

125 Microhomology-mediated end joining (MMEJ), an error-prone pathway for DNA double-st

126 ining (NHEJ), and microhomology-mediated end-joining (MMEJ).

127 ith this modification, Spark SQL serves such joins more than 50x faster than its existing brute force

128 ps), and the gifted postdoctoral fellows who joined my laboratory over four decades form the log of m

129 ns to take public stands on specific issues, join national policy conversations, and express themselv

130 In median-joining networks, we observed a higher frequency of shar

131 ajor DSB repair pathways, non-homologous end joining (NHEJ) and homologous recombination (HR).

132 on of knockout alleles via nonhomologous end joining (NHEJ) and knock-in alleles via homology-directe

133 ology-directed repair and non-homologous end joining (NHEJ) are the two major DSB repair pathways tha

134 ejoined by TDP2-dependent non-homologous end-joining (NHEJ) but whether this promotes or suppresses t

135 TRADD facilitates non-homologous end-joining (NHEJ) by recruiting NHEJ repair factors 53BP1 a

136 ith the components of the non-homologous end-joining (NHEJ) complex and participated in the NHEJ-medi

137 at it is not suppressed by nonhomologous end-joining (NHEJ) components, arguing that nick processing

138 inactivation of the XRCC4 non-homologous end-joining (NHEJ) DNA repair gene and p53 efficiently induc

139 ene disruption induced by non-homologous end-joining (NHEJ) DNA repair offers a potential treatment o

140 pomorphic mutations in the nonhomologous end-joining (NHEJ) DNA repair protein DNA ligase IV (LIG4) l

141 (c)- and alternative (alt)-nonhomologous end joining (NHEJ) during DNA double-strand break (DSB) repa

142 As the non-homologous end-joining (NHEJ) factor, Ku70/80 (Ku), is quickly recruite

143 and break (DSB) repair by non-homologous end joining (NHEJ) in human cells is initiated by Ku heterod

144 Non-homologous end joining (NHEJ) is the main repair pathway for DNA double

145 In humans, nonhomologous DNA end-joining (NHEJ) is the major pathway by which DNA double-

146 Non-homologous end-joining (NHEJ) is the most prominent DNA double strand b

147 Nonhomologous DNA end-joining (NHEJ) is the predominant double-strand break (D

148 thermore, coexpression the nonhomologous end-joining (NHEJ) machinery from the closely related archae

149 ver, the preponderance of non-homologous end joining (NHEJ) mediated repair events over homology dire

150 pothesize that inhibiting non-homologous end joining (NHEJ) or enhancing homology-directed repair (HD

151 re repaired by either the non-homologous end joining (NHEJ) or homologous recombination (HR) pathway.

152 The nonhomologous end-joining (NHEJ) pathway is the primary repair pathway for

153 The non homologous end-joining (NHEJ) pathway of double-strand break (DSB) repa

154 repair by the error-prone non-homologous end joining (NHEJ) pathway.

155 ropriate activation of the nonhomologous end joining (NHEJ) pathway.

156 s recombination (HR) or by nonhomologous end-joining (NHEJ) pathways.

157 genetically eliminating Ku nonhomologous end-joining (NHEJ) protein, indicating that Ctp1-dependent c

158 how that FBXW7 facilitates nonhomologous end-joining (NHEJ) repair and that FBXW7 depletion causes ra

159 ous recombination (HR) and nonhomologous end-joining (NHEJ) repair pathways, with defective localizat

160 tion, proteins involved in nonhomologous end joining (NHEJ) repair restrict amplification of viral DN

161 yme, which are involved in nonhomologous end joining (NHEJ) repair, enhance amplification of viral DN

162 epair (HDR) and decreased non-homologous end-joining (NHEJ) repair, suggesting that Wwox contributes

163 a moderate attenuation of non-homologous end joining (NHEJ) repair, the role of DEK in DNA repair rem

164 Non-homologous end joining (NHEJ) repairs DNA double strand breaks in non-c

165 s a key role in mediating non-homologous end joining (NHEJ), a major repair pathway for DNA double-st

166 a concomitant decrease in non-homologous end-joining (NHEJ), accounting for the improvement in cellul

167 logous recombination (HR), nonhomologous end-joining (NHEJ), and microhomology-mediated end-joining (

168 organisms via error-prone nonhomologous end joining (NHEJ), but the efficiency of precise sequence r

169 terase 2 (TDP2)-dependent non-homologous end-joining (NHEJ), but whether this process suppresses or p

170 ), mismatch repair (MMR), non-homologous end joining (NHEJ), homologous recombination (HR) and inters

171 mechanism in human cells, non-homologous end joining (NHEJ), rejoins broken DNA ends by direct ligati

172 is a central component of nonhomologous end joining (NHEJ), repairing DNA double-strand breaks that

173 ate DSB repair via MMEJ or nonhomologous end-joining (NHEJ).

174 predominantly repaired by non-homologous end joining (NHEJ).

175 e-strand break repair and non-homologous end joining (NHEJ).

176 ued by the inactivation of nonhomologous end joining (NHEJ).

177 nnelled through repair by non-homologous end-joining (NHEJ).

178 d recombination (HDR) and non-homologous end joining (NHEJ).

179 epair pathways, including non-homologous end-joining (NHEJ).

180 events of joining of exons, and 76 events of joining of adjacent genes as a single gene.

181 The liquid-solid joining of BMGs can shed more insights on overcoming the

182 counteracting error-prone non-homologous end joining of DNA double-strand breaks.

183 fecting either IgH germline transcription or joining of DSBs within S regions by classical nonhomolog

184 mpairs Ku80 removal after non-homologous end joining of DSBs.

185 19 novel translational frames, 28 events of joining of exons, and 76 events of joining of adjacent g

186 air, RecA family proteins must promote rapid joining of homologous DNA.

187 f radiation-induced cell killing, reflecting joining of incongruent DNA-ends that alter the genome.

188 he context of deterministic transferring and joining of materials at the microscale where surface adh

189 n through double strand breaks (DSB) and the joining of newly excised transposon ends with target DNA

190 The synthesis, processing, and joining of Okazaki fragments during DNA replication is c

191 NA ligase I that complete the processing and joining of Okazaki fragments, respectively.

192 olves separate transcription of gene pieces, joining of precursor RNAs via trans-splicing, and RNA ed

193 ands A or G and that disulfide bond-mediated joining of strand A to the core strand B cooperatively s

194 Upon joining of the large and small ribosomal subunits, a 100

195 Subsequent joining of the overhand knot end groups by ring-closing

196 However, direct fusion joining of Ti6Al4V to SS316 can cause brittle Ti-Fe inte

197 A method is described for the joining of two alpha-lithiated C(sp(3)) stereocenters ef

198 e successful deletion and non-homologous end joining of up to 725 kb reframed the DMD gene.

199 ch they can undergo Ag-driven activation and join ongoing immunization-induced GC responses.

200 n restart-bypass mechanism terminated by end joining or by microhomology-mediated template switching,

201 generally repaired through nonhomologous end joining or homologous recombination.

202 to allow repair by either nonhomologous end joining or homology-directed repair.

203 enotype, reported herein for the first time, join other complex phospholipid defects that cause leuko

204 be either long reads (longer than 100 bp) or joined paired-end reads.

205 In summary, ALT joins PAN/nut1/T1.1 as a bona fide lncRNA of KSHV with p

206 ble strand break repair by nonhomologous end joining, particularly in nonreplicating cells containing

207 main nuclease in the non-homologous DNA end-joining pathway (NHEJ).

208 -filling synthesis in the non-homologous end-joining pathway of double-strand break repair.

209 The 53BP1-dependent end-joining pathway plays a critical role in double strand b

210 reak (DSB) repair via the non-homologous end joining pathway, as unrepaired DSBs are the primary caus

211 As a member of the non-homologous end-joining pathway, it is also involved in repairing a subs

212 which is integral to the non-homologous end joining pathway, thus negatively regulates ATM activity

213 f the break were due to a non-homologous end-joining pathway, while larger deletions were processed v

214 es that participate in the nonhomologous end-joining pathway.

215 DNA repair proteins in the nonhomologous end-joining pathway.

216 nd breaks by the classical nonhomologous end-joining pathway.

217 reveals that both C-NHEJ and alternative end-joining pathways can generate translocations by joining

218 We used pulsed laser beam welding method to join Pd43Cu27Ni10P20 (at.%) bulk metallic glass and char

219 BldO now joins pleiotropic repressor BldD to exert a multi-layer

220 ange (AAPC) of the trends was evaluated from join-point regression analysis.

221 7Cu28Ni9Al12.3 (at. %), using a liquid-solid joining process.

222 erious single-strand annealing (SSA) and end-joining processes that led to the loss of large chromoso

223 us recombination and other nonhomologous end-joining processes.

224 e the bearing angle, formed between the line joining pursuer and target (called the range vector) and

225 hat arose through microhomology-mediated end joining rather than nonallelic homologous recombination.

226 sphorylation of DNA-PK, a non-homologous end joining repair protein, in Hec-108 cells.

227 tely become substrates for nonhomologous end-joining repair, leading to large-scale genomic rearrange

228 r and, to a lesser extent, nonhomologous end-joining repair.

229 ain-dependent interaction of XRCC1 with APLF joins repair scaffolds that support single-strand break

230 As microhomology-mediated end-joining requires annealing of single-strand DNA ends, we

231 ATM's ability to inhibit VDJ joining requires its enzymatic activity.

232 ologous recombination and non-homologous end joining, respectively, were transcriptionally activated

233 ologous recombination and non-homologous end joining, respectively.

234 ly of the SPN3US head and a likely head-tail joining role for gp64, and its homologs in related phage

235 our failure to develop an efficient barcode joining scheme precludes the widespread application of t

236 nthesis-dependent microhomology-mediated end joining (SD-MMEJ), predicts that differences between DNA

237 and bioorthogonal conjugation reaction that joins semicarbazide to an aryl ketone or aldehyde with a

238 cteristics of a toxin-antitoxin system, thus joining several enigmatic features.

239 L execution engine, that handles efficiently joins that use genomic intervals as keys.

240 uitment of protein bS16, the next protein to join the complex.

241 n which ATP binding allows a Vps4 subunit to join the growing end of the helix and engage the substra

242 At later stages, younger beta-cells join the islet following differentiation from post-embry

243 and a potential network of salt bridges that join the N- and C-terminal poles together.

244 draining secondary lymphoid organs, they may join the ongoing GC response.

245 ies of presymptomatic Alzheimer's disease to join the ongoing prevention trials, for which mAbs conti

246 Thus, preexisting indole levels in the gut join the oocyst dose and immune status as important fact

247 I was fortunate to join the ride when it was a mere carousel of three activ

248 Splicing of their progenitor mRNAs joined the amino termini of these proteins to the NP1 op

249 oter melting, which only occurred when TFB2M joined the complex.

250 g the PASSEL resource), two new members have joined the consortium: MassIVE and jPOST.

251 After traveling the world a bit, Calisher joined the faculty of Colorado State University in 1993,

252 Therefore, ZIKV has joined the group of congenital infections.

253 He joined the National Heart Institute (now the National He

254 Six thousand seven hundred eight individuals joined the organ donor registry (95% confidence interval

255 chromosomal rearrangement formation involves joining the ends from two different chromosomal double-s

256 ion of embryonic myosin in the small muscles joining the neural arches of the spine suggesting that l

257 was a common trunk of segment 2 and 3 ducts joining the segment 4 duct in 67.8% of subjects.

258 n1), ortholog of the metazoan Mis12 complex, joins the centromere-proximal components, Mif2 and COMA,

259 iotherapy or radioimmunotherapy (RIT), which joins the selectivity of antibody targeting with the eff

260 The S4-S5 linker, which joins the voltage sensor and pore domains, plays a criti

261 se activity for classical non-homologous end joining (the predominant DNA double-strand break repair

262 darity and commitment between two adults who join their effort to care for children-is a central cont

263 proteins is a conserved disulfide bond that joins their A and B strands.

264 nd scientists with different backgrounds are joining this field, underscoring the need for unity rega

265 Joining titanium alloy and stainless steel is becoming a

266 e research results are good contributions in joining titanium alloy and stainless steel.

267 NA polymerase theta (Pol theta)-mediated end joining (TMEJ) has been implicated in the repair of chro

268 series comprising a substituted phenyl ring joined to a dimethylpyridone moiety via an amide linkage

269 onjugation systems composed of the IMCpKM101 joined to OMCCs from the A. tumefaciens VirB/VirD4, E. c

270 , in complex with transposon ends covalently joined to target DNA, portrays the transposition machine

271 increasing the rate of 50S ribosomal subunit joining to 30S initiation complexes (ICs) that carry an

272 on landscape by leading to predominant V(D)J joining to a proximal Trdv3 pseudogene that lies just up

273 EJ compensates for loss of nonhomologous end joining to repair rereplication DSBs in a site-specific

274 ments, whereas Trdd1 joining is ordered with joining to Trdd2, a prerequisite for further rearrangeme

275 fungal cells invaded host muscle fibers and joined together to form networks that encircled the musc

276 distant parts of the genome are erroneously joined together.

277 ning pathways can generate translocations by joining TSS-proximal DSBs to DSBs on other chromosomes.

278 This allows us to join two or more DARPins in predefined geometries withou

279 but can contain several misassemblies, which join unlinked regions of the genome.

280 anslational research programmes, but also by joining up with local health and social care services to

281 e address the community and invite others to join us in making a larger impact on undergraduate educa

282 separately processed and, subsequently, were joined using "Low-level" and "Mid-Level" data fusion met

283 d for 40 years that the variable (diversity) joining [V(D)J] recombination-mediated assembly of diver

284 enzyme kinetics of variable, diversity, and joining [V(D)J] recombination.

285 al enzymes for initiating variable-diversity-joining [V(D)J] segment recombination, an essential proc

286 enes [in a process called variable-diversity-joining (VDJ) recombination] and, upon successful rearra

287 nsfer complex (STC) containing catalytically joined vDNA and tDNA.

288 's SH3, SH2, and tyrosine kinase domains are joined via a linker to an F-actin-binding domain (FABD).

289 S-S junctions are joined via a nonhomologous end joining DNA repair proces

290 ion protein of IL2 and its receptor IL2Rbeta joined via a peptide linker (CIRB).

291 ordination based irregular hexagons that are joined via a robust [terpyridine-->Fe(II)<--terpyridine]

292 H3 from the genome during non-homologous end joining was promoted by both ATM and the ATP-dependent n

293 iming of beta7 addition relative to half-mer joining was unclear.

294 mediated (DNA-PK-mediated) nonhomologous end-joining, whereas DNA repair pathways mediated by poly(AD

295 s are resolved to promote long-range DNA end-joining while suppressing genomic instability inherently

296 l detection and resistive pulse sensing will join with other attempts at hybridizing high-throughput

297 rom the quantum-mechanical fluctuation model joined with density functional calculations are within 5

298 C/(12)C, (18)O/(16)O) marker investigations, joined with multivariate statistical analysis, such as P

299 the Ethiopian Public Health Institute (EPHI) joined with the BD-PEPFAR PPP to strengthen laboratory s

300 characteristics of leaf deposited particles, joined with the leaf magnetic content, may successfully