ライフサイエンスコーパス: hybridization

1 in Tmem107(-/-) animals as shown by in situ hybridization.

2 piscium sp. type B using fluorescent in situ hybridization.

3 and can result in barriers to interspecific hybridization.

4 ase chain reaction (qRT-PCR) and RNA in situ hybridization.

5 extensively validate the results by in situ hybridization.

6 break the aptamers' secondary structure upon hybridization.

7 bias observed over the generations following hybridization.

8 ng in label-free zeptomolar detection of DNA hybridization.

9 chronic, negative impacts of human-mediated hybridization.

10 zation of miR-218-5p was assessed by in situ hybridization.

11 er for reconstructing phylogeny and studying hybridization.

12 electrode functionalization and on-electrode hybridization.

13 ging and DNA sequential fluorescence in situ hybridization.

14 nd oesophagus of mouse embryos using in situ hybridization.

15 xpected for Yb systems with conventional c-f hybridization.

16 heterotypic cells via sequence-specific DNA hybridization.

17 ncreasing the efficiency and kinetics of DNA hybridization.

18 nanoparticles through sequence-specific DNA hybridization.

19 ted dispersion, or possibly by interspecific hybridization.

20 ase chain reaction followed by type-specific hybridization.

21 nderstanding of the kinetics of nucleic acid hybridization.

22 ntilevers that occur as a consequence of the hybridization.

23 risk, as assessed using fluorescence in situ hybridization.

24 is expression in mechanosensilla via in situ hybridization.

25 ochromosomes and propensity to interspecific hybridization.

26 gametes, a critical barrier to interspecific hybridization.

27 type, cytogenetics, and fluorescence in situ hybridization.

28 C57BL/6J mice by using double-label in situ hybridization.

29 lready available (e.g., fluorescence in situ hybridization, 16-S rRNA gene amplicon sequencing), yet

30 As detected by array comparative genomic hybridization, about one-third of marker chromosomes (18

31 These data suggest that introgressive hybridization accompanied by gross chromosome rearrangem

32 were subjected to array comparative genomic hybridization (aCGH) and/or breakpoint PCR and 64 were c

33 dentified by array-based comparative genomic hybridization (aCGH), the most commonly used technology

34 were validated by array comparative genomic hybridization (aCGH).

35 The hybridization activities of probes were simultaneously m

36 Additionally, hybridization activity profiles sharpen as the spacing b

37 The resulting temperature profiles of hybridization activity show how the stability of hybrids

38 at initial diagnosis by fluorescence in situ hybridization after cell sorting.

39 c groups, with no evidence for introgressive hybridization among any but the most recently derived si

40 Analyses also revealed historical hybridization among lineages, high introgression from Q.

41 Aside from in-plane electronic bonding, the hybridization among out-of-plane boron orbitals is cruci

42 equencing and multiplex fluorescence in situ hybridization analyses mapped the emergence of extra-chr

43 Fluorescence in situ hybridization analyses showed that P. denitrificans was

44 Fluorescence in situ hybridization analysis mapped the EPSPS gene to pericent

45 Pyrosequencing and fluorescence in situ hybridization analysis revealed that denitrifying anaero

46 In situ hybridization analysis revealed that Fusobacterium is pr

47 In situ hybridization analysis, using locked nucleic acid oligo

48 virologic clearance was confirmed by in situ hybridization and a failure of disease to recur after CD

49 anges of the sensor resonance frequency upon hybridization and at varying relative humidity.

50 We identify, by single-molecule in situ hybridization and cell sorting, rare cells positive for

51 Moreover, the hybridization and discrimination efficiency of the chime

52 stably inherited, alterations likely due to hybridization and domestication affect gene expression.

53 -fluorescence in situ hybridization (in situ hybridization and flow cytometry) of primary lymphocytes

54 Double staining using in situ hybridization and immunocytochemistry revealed that BDNF

55 ific RNAseq, nascent RNA-fluorescent in situ hybridization and immunofluorescence), we show here that

56 onal POMC expression in detail using in situ hybridization and immunohistochemical techniques, and re

57 is precursor in A. rubens using mRNA in situ hybridization and immunohistochemistry revealed a widesp

58 rived from this precursor using mRNA in situ hybridization and immunohistochemistry revealed a widesp

59 t the placental level as revealed by in situ hybridization and immunohistochemistry, and is conserved

60 o which phenotypic plasticity, introgressive hybridization and incomplete lineage sorting obscure wel

61 Hybridization and introgression confound chloroplast and

62 c and epigenomic shock that occurs following hybridization and polyploid events and may also contribu

63 High-throughput multiple hybridization and rapid capture strategies using the cur

64 mic and population genomic analyses to study hybridization and reconstruct the evolutionary past of t

65 Cluster analysis, in situ hybridization and RNAi assays indicate that males likely

66 Controlled hybridization and selective breeding have been used for

67 groups that experienced a strong history of hybridization and semi-sexual reproduction.

68 Here, we used multiplexed in situ hybridization and single-cell RNA-Seq in male and female

69 a polysaccharide-rich diet, and (ii) in situ hybridization and spectral imaging analysis methods that

70 Mode hybridization and structural asymmetry allow address-ing

71 Individual RNA molecules are labeled by hybridization and target proteins are concurrently stain

72 By using shorter probes and by performing hybridization and washes at low temperatures, we greatly

73 he p300-bound regulatory landscape following hybridization and whole-genome duplication.

74 -occurrence, mutualism, niche expansion, and hybridization - and rarely decline.

75 of SIV RNA in the brain as shown by in situ hybridization, and generally was observed in animals wit

76 Here we map Armc5 expression by in situ hybridization, and generate Armc5 knockout mice, which a

77 emistry, glutamic acid decarboxylase in situ hybridization, and parvalbumin-immunocytochemistry.

78 m karyotype, DNA index, fluorescence in situ hybridization, and polymerase chain reaction screening f

79 phosphate labeling, RNA fluorescence in situ hybridization, and quantitative reverse transcription po

80 A structure-guided hybridization approach using two privileged substructure

81 obes of relevant electronic states and their hybridization are limited.

82 zation assay, named conditional displacement hybridization assay (CDHA), is described for the concurr

83 proach, the electrochemical steric hindrance hybridization assay (eSHHA) has been introduced for quan

84 A dual hybridization assay quantified aptamer from the epidermi

85 ntitation in crude cell lysate by a CE-based hybridization assay termed direct quantitative analysis

86 A fluorescent microsphere hybridization assay was designed that was capable of det

87 etermining their functionality in a sandwich hybridization assay with enzymatic amplification of the

88 Here, an enzyme-coupled hybridization assay, named conditional displacement hybr

89 eScope-a novel mutation-specific RNA in situ hybridization assay.

90 wn, we employed a peptide-nucleic acid (PNA) hybridization assay.

91 detection schemes, including aptamer labels, hybridization assays, and nucleic acid amplification.

92 olymerase chain reaction (RT-PCR)and in situ hybridization assays, we validated that the Osr2(-/-) em

93 ls, assessed by quantitative PCR and in situ hybridization at 1, 4, 7, and 15 days after the lesion,

94 These hybridization-based approaches cannot be used for high r

95 Here, we report a hybridization-based assay exploiting nucleic acid self-a

96 Nucleic acid hybridization-based lateral flow assay (LFA) holds great

97 Compared with low-coverage RNA-Seq and a hybridization-based targeted RNA-Seq method, cDNA-smMIPs

98 robes increases, indicating more homogeneous hybridization behavior of probes.

99 information on the extent of spin-polarized hybridization between 5f and 6d electronic states by mea

100 Here, we show that hybridization between diploid A. lyrata and A. arenosa c

101 We conclude that hybridization between divergent lineages, when coinciden

102 e net magnetization of BFO to strong orbital hybridization between Fe and Mn across the interfaces.

103 The near-field plasmon hybridization between individual Ag nanodisks and substr

104 ades, it has been assumed that introgressive hybridization between introduced rainbow trout and nativ

105 Hybridization between invasive and native species, a sig

106 selection and introgression via inadvertent hybridization between more and less advanced morphotypes

107 , we evaluate the spatiotemporal dynamics of hybridization between native cutthroat trout and invasiv

108 s of 'contemporary sympatric speciation' via hybridization between octoploid and diploid congeners.

109 The hybridization between PDNA and TDNA was detected by redu

110 We find that the strong hybridization between Ru d and O p states results in a R

111 L emissions (switch "on" state) and with the hybridization between T-rich ssDNA(S1) immobilized on th

112 FeS(111) interfaces, characterized by strong hybridization between the S-p and O-p states of As(OH)3

113 NA-functionalized NPs with no possibility of hybridization between them interact via a strong repulsi

114 Here, we demonstrate that hybridization between two divergent lineages facilitated

115 force the evidence for secondary contact and hybridization between two phylogeographic lineages in th

116 he first time, demonstrates the detection of hybridization both guanine oxidation and indicator reduc

117 between probes or the ionic strength of the hybridization buffer increase.

118 We present here a hybridization capture strategy for purification of unspl

119 zed reporter deposition fluorescence in situ hybridization (CARD-FISH), we show that only four novel

120 ion of target DNA by employing the nonlinear hybridization chain reaction (HCR) amplification.

121 Based on the in situ hybridization colabeling results, we tested the causal r

122 n of cellular HIV Gagpol mRNA by in situ RNA hybridization combined with antibody staining for the HI

123 taining nearly identical free energy for DNA hybridization compared with free DNA.

124 The hybridization condition with a low ionic strength and hi

125 f miRNAs making use of a competitive RNA/RNA hybridization configuration is described in this work.

126 hanced NRIP1 binding to RARalpha RNA in situ hybridization confirmed Nrip1 expression in the developi

127 Whole-mount in situ hybridization confirmed that all 17 selected mRNAs were

128 cluster activation; DNA fluorescence in situ hybridization confirmed that transcriptional activation

129 le to their different extents/frequencies of hybridization, confirmed by our analysis of the single-c

130 and morphological data document that sleeper hybridization conforms to the classic "tension zone" mod

131 any of the hypotheses concerning how and why hybridization contributes to biological diversity curren

132 ver between surface and bulk in the electron hybridization/correlation and we identify a spectroscopi

133 e show here, by means of fluorescent in situ hybridization coupled with tyramide signal amplification

134 In situ hybridization data showed nAChR subunit transcripts in G

135 RNA in situ hybridization detected Adamts17 expression in specific s

136 anese (III) Oxide (Mn2O3) nanofibers for DNA Hybridization detection.

137 that utilizes a series of toehold-triggered hybridization/displacement reactions that are designed t

138 NPs provides the possibility to introduce by hybridization distinct types of bioactive molecules or b

139 t basic mechanisms of evolution, speciation, hybridization, domestication, as well as about the molec

140 carbon atoms undergo changes in bonding and hybridization during a single enzyme-catalyzed cyclizati

141 nts were then tested by fluorescence in situ hybridization during T-cell activation.

142 on the surface, negatively affecting to both hybridization efficiency and surface stability.

143 ling by more directly monitoring the two key hybridization events during the reaction.

144 To ensure that these hybridization events occur, current PCR approaches rely

145 population distinctiveness through separate hybridization events.

146 Fluorescence in situ hybridization experiments showed that micropatterned fib

147 thologs of these genes and performed in situ hybridization, finding that their expression colocalized

148 ell-level studies using fluorescence in situ hybridization (FISH) and growth in microfluidic drops de

149 ene fusion detection is Fluorescence In Situ Hybridization (FISH) and while highly sensitive and spec

150 ances measured using 3D fluorescence in situ hybridization (FISH) experiments.

151 MYC, BCL2, and BCL6 and fluorescence in situ hybridization (FISH) for MYC were performed.

152 used to perform in-line fluorescence in situ hybridization (FISH) of bacterial cells.

153 t mammalian cells using fluorescence in situ hybridization (FISH) probes.

154 tion and replication, a fluorescence in situ hybridization (FISH) protocol was established to detect

155 y, single-molecule mRNA fluorescence in situ hybridization (FISH) reveals that, upon site-specific CT

156 The development of fluorescence in situ hybridization (FISH) technologies enables the quantifica

157 FR CNG was determined by fluorescent in situ hybridization (FISH) using prespecified criteria and EGF

158 Fluorescence in situ hybridization (FISH) will be required to identify HGBL-D

159 recursor-analyzed by RNA fluorescent in situ hybridization (FISH), Northern blots, and RNA sequencing

160 ave developed a fluorescence imaging in situ hybridization (FISH)-based assay for the detection of du

161 gative (HER2-) based on fluorescence in situ hybridization (FISH)-supplemented immunohistochemistry o

162 ging and sequential DNA fluorescence in situ hybridization (FISH).

163 EXCLUSION CRITERIA: fluorescence in situ hybridization, fluorescence imaging for lymph node mappi

164 achieved by evaluating the thermodynamics of hybridization for full-length oligonucleotide-template a

165 r MYC and BCL2, and with fluorescent in situ hybridization for MYC, BCL2, and BCL6 rearrangements.

166 The strong signal of hybridization found by simulations and the D-statistic a

167 facilitated electrochemical detection of DNA hybridization has had an exceptional impact on fields su

168 As fluorescence in situ hybridization has limitations regarding the resolution,

169 Hybridization has played an important role in the evolut

170 n (PCR), real time PCR (RT-PCR) and dot blot hybridization have also been proposed for pathogen ident

171 The down regulation was confirmed by in situ hybridization histochemistry for two strongly down-regul

172 sive mapping of p11 expression using in situ hybridization, immunocytochemistry, and whole-tissue vol

173 ere, we used classical pharmacology, in situ hybridization, immunohistochemistry, and the Daun02 inac

174 ollects and integrates data from RNA in situ hybridization, immunohistochemistry, RT-PCR, northern bl

175 loci by DNA sequential fluorescence in situ hybridization in fixed cells and resolves their identiti

176 ies was also detected by fluorescent in situ hybridization in G. f.

177 ccurrence of and investigate the outcomes of hybridization in plants.

178 omere length using flow-fluorescence in situ hybridization (in situ hybridization and flow cytometry)

179 ite cessation of stocking over 40 years ago, hybridization increased over time at half (50%) of the l

180 zed reporter deposition fluorescence in situ hybridization, indicated that Nitrospinae fix 15 to 45%

181 Hybridization interactions between DNA-functionalized na

182 ple the repulsive forces from the attractive hybridization interactions that are sensitive to the ion

183 Southern hybridization is a convincing and reliable method, but i

184 Hybridization is a key molecular process in biology and

185 By lowering temperature, DNA hybridization is also promoted, allowing the constructio

186 Introgressive hybridization is an important and widespread evolutionar

187 tes, and reproductive isolation arising from hybridization is infrequently demonstrated.

188 sults indicate that the transition state for hybridization is visited before the strands form any sig

189 tmack), a man-made cereal from wheat and rye hybridization, is mainly used as animal feed.

190 tes was detected by a combination of in situ hybridization (ISH), immunofluorescence, and PCR for pos

191 Accurate prediction of hybridization kinetics allows the design of efficient pr

192 In this work, we show that hybridization kinetics can be directly controlled by ele

193 lymerase chain reaction, fluorescent in situ hybridization, lentiviral overexpression, and Luciferase

194 pplicable technique called 'Ligation in situ Hybridization' ('LISH'), which is an alternative methodo

195 Using a new in situ hybridization method that can measure the expression of

196 On array-based comparative genomic hybridization (n = 3), gain of 6p was found in 2 cases a

197 st our model, we designed five different RNA hybridization networks with a linear architecture, and w

198 mRNA in situ hybridization of brain-specific Nav subunits revealed th

199 ntitative viral outgrowth assay, and in situ hybridization of colon tissue-the patient consented to a

200 ously developed a model system that uses the hybridization of complementary DNA strands to model the

201 ion dominance occurs instantly following the hybridization of divergent genomes and significantly inc

202 Moreover, we achieved to detect hybridization of DNA by using the reduction signal of 3-

203 In principle, the specific hybridization of DNA can be used to form a library of in

204 Here, we obtain cavity mediated hybridization of GaAs and J-aggregate excitons in the st

205 odology can be extended for detection of any hybridization of interest by simply adapting an appropri

206 cavity quantum electrodynamics, leads to the hybridization of light and matter excitations.

207 sm in the emission spectra characteristic of hybridization of local and charge transfer excited state

208 ch on the vicariance, secondary contact, and hybridization of marine groups in the northwest Pacific

209 Hybridization of mouse samples to Infinium Human Methyla

210 ochemical indicator, which is able to detect hybridization of probe (single stranded DNA-ssDNA) and h

211 nanopad was utilized as a substrate for the hybridization of probe DNA molecules with the TIRS nanot

212 By means of a formal structural hybridization of the antipsychotic drug aripiprazole and

213 The hybridization of the DNA target with the DNA probes resu

214 which the PEG component interferes with the hybridization of the oligonucleotide remain poorly under

215 d nucleic acid detection schemes rely on the hybridization of the target to surface-bound detection p

216 t in Xenopus laevis, which resulted from the hybridization of two closely related species about 17 mi

217 three-stranded DNAzyme precursor (TSDP), the hybridization of which prevents the DNAzyme from being a

218 , including linker modifications, functional hybridization of ZIFs via the encapsulation of guest spe

219 determine the neurochemistry (using in situ hybridization) of catecholaminergic and noncatecholamine

220 biologic relevance was tested using in situ hybridization on 30 pre-metastatic lesions, showing intr

221 of A tuberculatus using fluorescence in situ hybridization on mitotic metaphase chromosomes and inter

222 The DNA hybridization on the electrode was measured through the

223 formed with immunohistochemistry and in situ hybridization on tissue microarrays for 958 tumors.

224 confirms that AMHB effects outweigh those of hybridization or dipole-dipole interaction.

225 sents a key step towards developing a robust hybridization platform in wheat.Heterosis can rapidly bo

226 eneralized strategy for constructing modular hybridization probes (M-Probes) that overcomes these cha

227 Existing hybridization probes lack the capability to selectively

228 bits improved SNV discrimination rather than hybridization probes relying solely on competition or am

229 study covers all the optimization steps for hybridization procedure and electropolymerization of pyr

230 RNA and enrich coding sequences, subtractive hybridization procedures have become the approach of cho

231 Chiroptera and an ancestral laurasiatherian hybridization process did exhibit some very clear, disti

232 sensor by surface-bound DNA probes through a hybridization process.

233 lation requires the interplay of several RNA hybridization processes, which are expected to be temper

234 nces survive in modern humans due to ancient hybridization, providing an opportunity to assess their

235 ing (WNV) prediction algorithm, in which the hybridization rate constant of an unknown sequence is pr

236 predictive model for accurately determining hybridization rate constants based on sequence informati

237 fects at the nanoscale, (2) a size-dependent hybridization rate of DNA complexes, and (3) electrode m

238 First, we estimated hybridization rates and the direction of gene flow.

239 model in which the rate-limiting step of the hybridization reaction is the alignment of the two stran

240 Sandwich-type hybridization reactions among the FCN-labeled DNA probe,

241 for implementing such networks that exploits hybridization reactions carried out exclusively by multi

242 ion, isothermal amplification, ligation, and hybridization reactions.

243 Our in situ hybridization, real-time quantitative PCR, and stage-spe

244 n of the oxytocin system by qRT-PCR, in situ hybridization, receptor autoradiography ([(125)I]OVTA bi

245 tribe Triticeae have undergone interspecific hybridization, resulting in allopolyploidy; whereas homo

246 n distinct Arachis genotypes, whilst in situ hybridization revealed transcripts in different root tis

247 tein, together with fluorescence in situ RNA hybridization (RNA-FISH) of the intron region of immedia

248 This hybridization-sensing approach adapts in real time to va

249 with previously reported electrochemical DNA hybridization sensors for Dengue virus detection, spanni

250 Whole mount in situ hybridization showed that CrANT is expressed in sperm an

251 matin conformation: qRT-PCR and mRNA in situ hybridization showed that the clustered genes were up-re

252 stinguishable without any overlapping of the hybridization signal - each on one pair of large metacen

253 Based on Bayesian clustering analysis and hybridization simulations, we infer that Spanish teosint

254 ntrast, single-molecule fluorescence in situ hybridization (smFISH) preserves the spatial information

255 res and single-molecule fluorescence in situ hybridization (smFISH) validation.

256 multiplexed single-molecule RNA fluorescence hybridization (smFISH).

257 sing single-molecule RNA fluorescent in situ hybridization (smRNA FISH), we show that egl-1 is transc

258 ants were found to strongly correlate to the hybridization states of the boron orbitals that form the

259 A molecular hybridization strategy was used based on the conformatio

260 Detailed in situ hybridization studies of tip-enriched predictions identi

261 tracing with immunofluorescence and in situ hybridization techniques.

262 In this work, we explore a new hybridization technology using barcoded probes which has

263 By comparison, the hybridization technology was correctly able to detect, t

264 o system uses automated fluorescence in situ hybridization technology with morphokinetic cellular ana

265 ures, however, spatial confinement can cause hybridization that inhibits the robustness of these emer

266 motes mutualist exchange, niche expansion or hybridization, thereby helping species avoid population

267 The most common motifs utilize hybridization to a complementary detection strand couple

268 he present studies used fluorescence in situ hybridization to detect Gad1 and Gad2 mRNA in POMC neuro

269 nt of an electrochemical method based on DNA hybridization to detect HAV.

270 lid fish Astatotilapia burtoni using in situ hybridization to label vesicular glutamate transporters

271 e performed immunohistochemistry and in situ hybridization to localize appetite-stimulating (neuropep

272 c imaging combined with fluorescence in situ hybridization to localize Ca Entotheonella and some of t

273 We used in situ hybridization to measure the colabeling of the activity

274 al. use single molecule fluorescent in situ hybridization to show quantitatively that Ptch receptors

275 lymerase chain reaction (RT-PCR) and in situ hybridization to test if GPR30 is expressed in the brain

276 as by 16S ribosomal RNA fluorescence in situ hybridization, transcriptional analyses, and quantitativ

277 quired for GAS survival in a transposon-site hybridization (TraSH) screen in whole human blood.

278 Fluorescent in situ hybridization was performed to determine the role of MT

279 HER2 statuses (equivocal by IHC and in situ hybridization) was significantly higher in 2014 (four of

280 droplet digital PCR, and fluorescent in situ hybridization, we could demonstrate that HHV-6A/B integr

281 Using fluorescence in situ hybridization, we detected higher Pax3 mRNA+ cell densit

282 arly and late events following interspecific hybridization, we examined the epigenome and the enhance

283 Using comparative genomic hybridization, we found that NCC-derived NBL tumors acqu

284 single-cell RNA-Seq and multiplexed in situ hybridization, we show here that a single marker, Neurom

285 Immunohistochemistry and in situ hybridization were used to determine viral capsid protei

286 egion is characterized by a low frequency of hybridization, where mitochondrial DNA introgression is

287 e learned, we investigate rare cases of song hybridization, where parts of an existing song are splic

288 Natural hybridization, which can be involved in local adaptation

289 Isolated viral RNA was enriched by hybridization with a custom norovirus whole-genome RNA b

290 abilization, cardiac-tissue pretreatment and hybridization with a Cy3-labeled telomeric repeat comple

291 involves cell fixation, permeabilization and hybridization with a set of fluorescently labeled oligon

292 Fluorescence in situ hybridization with a set of wheat cDNAs allowed the macr

293 ce of a DNA microarray chip through specific hybridization with complementary oligonucleotide strands

294 se of the excimer fluorescence for MBs after hybridization with DNA was up to 24-fold.

295 In addition, ssDNA immobilization and hybridization with its complemented strand was shown.

296 omplex demographic processes, in addition to hybridization with other Canis species.

297 noparticles and biomolecules) into ZIFs, and hybridization with polymeric matrices to form mixed matr

298 We used fluorescent in situ hybridization with probes for nascent transcripts to det

299 reat Lakes region and southern Canada, where hybridization with remnant wolf populations was common.

300 RNA heteroduplex structures through specific hybridization with target DNA.