ライフサイエンスコーパス: hybridization

1 ll surface through nucleic acid assembly and hybridization.

2 rporates both incomplete lineage sorting and hybridization.

3 subsequently detected by fluorescent in situ hybridization.

4 expression with double fluorescence in situ hybridization.

5 anastomosis and within tumors using in situ hybridization.

6 ouble-label immunohistochemistry and in situ hybridization.

7 s out in having originated through extensive hybridization.

8 entified maxRNAs by RNA fluorescence in situ hybridization.

9 ading, avoiding mutual nonspecific H(1)/H(2) hybridization.

10 e introduced into the sensing system via DNA hybridization.

11 beta-cells and little PCSK2 mRNA by in situ hybridization.

12 er diluted conditions upon sequence-specific hybridization.

13 the apple was mainly driven by interspecific hybridization.

14 een further confirmed by fluorescent in situ hybridization.

15 ied from this assay with whole mount in situ hybridization.

16 ain species boundaries despite high rates of hybridization.

17 goes a two-step activation through crRNA-DNA hybridization.

18 the silicene phases due to the strong Ag-Si hybridization.

19 on could arise from avoidance of maladaptive hybridization.

20 (CNS) of Scyliorhinus canicula using in situ hybridization.

21 sies by immunohistochemistry and in situ RNA hybridization.

22 g of telomeres (ALT) by Fluorescence In Situ Hybridization.

23 oved varieties derived through interspecific hybridizations.

24 ce scanning electron microscopy with in situ hybridization (3D-EMISH) to visualize 3D chromatin foldi

25 ars and find that the current frequencies of hybridization across species pairs contrast with genomic

26 between inbreds and hybrids, suggesting that hybridization affects sRNA expression principally at spe

27 19-nucleotides-long DNA that minimizes self-hybridization, allowing the development of an electroche

28 ostructures beyond what is possible with DNA hybridization alone.

29 ate how new combinations of genes created by hybridization among three species can enhance the potent

30 Through in situ hybridization analyses, we demonstrate that expression o

31 These transitions are induced by polariton hybridization and are controlled by a topological quanti

32 By anatomic tracing, in situ hybridization and channelrhodopsin (ChR2)-assisted circu

33 -complete asymmetry in the directionality of hybridization and decreasing frequencies of later-genera

34 amplification assay based on competitive DNA hybridization and electrochemical detection using eSenso

35 We then use a combination of in situ hybridization and ex vivo two-photon Ca(2+) imaging of t

36 egies and the mechanisms that regulate plant hybridization and gamete fusion.

37 y to explore the immediate changes following hybridization and genome duplication.

38 tomics, single-molecule fluorescence in situ hybridization and high-resolution imaging, can extend th

39 Using in situ hybridization and immunofluorescence techniques, we show

40 By in situ hybridization and immunofluorescence, we showed that Cnr

41 the integration of transcriptomics, in situ hybridization and immunohistochemistry we find evidence

42 d WSe(2) are selected as model materials for hybridization and implemented toward detection of variou

43 s congeners and to evaluate the relevance of hybridization and interspecific gene flow for developing

44 theses regarding phylogenetic relationships, hybridization and introgression, and the biogeographical

45 d was developed by combining oligonucleotide hybridization and LC-MS/MS technologies.

46 ) cytokine levels were determined by DNA-DNA hybridization and multiplexing assays, respectively.

47 Comparative genomic hybridization and next-generation sequencing confirmed t

48 pread implementation of fluorescence in situ hybridization and next-generation sequencing methods in

49 ocess is driven through a combination of DNA hybridization and particle dipolar coupling, a property

50 rect immunofluorescence, fluorescent in situ hybridization and PCR-based investigations.

51 red using flow cytometry, ELISA, RNA in situ hybridization and quantitative real time PCR.

52 rs complete suppression of gRNA:dsDNA-target hybridization and rapid restoration of CRISPR/Cas9 funct

53 spread in birds and strongly associated with hybridization and resource overlap during the breeding s

54 ed a combination of molecular (Southern blot hybridization and reverse-transcription cleaved amplifie

55 embryos, which were subjected to RNA in situ hybridization and RT-qPCR.

56 antibodies), array-based comparative genomic hybridization and targeted next generation sequencing (4

57 foreign genes were quickly eliminated after hybridization and that selection against the minor speci

58 pressed imprinted genes are perturbed during hybridization and that such effects on imprinted genes a

59 R-loops, the byproduct of DNA-RNA hybridization and the displaced single-stranded DNA (ssD

60 Stepwise loss of MSH5B and MSH4D following hybridization and whole-genome duplication may have occu

61 gains identified using fluorescence in situ hybridization and, in particular, next-generation sequen

62 combination of immunohistochemistry, in situ hybridization, and a transgenic reporter assay, our resu

63 n, further confirmed by fluorescence in situ hybridization, and amplified by the MALBAC method before

64 trates extensive interspecific admixture and hybridization, and documents the origin of the highly pr

65 We also used immunohistochemistry, in situ hybridization, and electron microscopy to examine this t

66 ocalization of infection by RNAscope in situ hybridization, and histopathological abnormities by hema

67 odent and primate brains using qPCR, in situ hybridization, and immunocytochemical single and double

68 we then investigate how ancestral variation, hybridization, and independent evolution contributed to

69 ions by phase contrast, fluorescence in situ hybridization, and scanning electron microscopy.

70 nofluorescence staining, fluorescent in situ hybridization, and single-cell sequencing.

71 cer genes by multicolor fluorescence in situ hybridization, and targeted sequence analysis of 563 can

72 ysis, immunohistochemistry, RNAscope in situ hybridization, and transmission electron microscopy show

73 Here, an in situ hybridization approach to generate a single-cell-resolut

74 iants) and cytogenetic (fluorescence in situ hybridization) approaches to study the structure, expres

75 a cooperative supramolecular assembly with a hybridization architecture that enhances the templated r

76 The consequences of hybridization are varied, ranging from the origin of new

77 n probes for large-scale comparative genomic hybridization array processes.

78 citation ratio, being the redshift after the hybridization ascribed to both peaks.

79 In situ hybridization assay of the validated miR was used to ide

80 The capillary electrophoresis (CE)-based hybridization assay proved to be more robust than revers

81 Hybridization assays and enzymatic probing with RNases i

82 In situ hybridization assays detected positive signals of the 2

83 Real-Time PCR and whole mount in situ hybridization assays indicate that prokr1b spatial-tempo

84 The efficacy of fluorescent hybridization assays is often limited by the low signal-

85 tudy, our transcriptome analysis and in situ hybridization assays of maize embryonic leaves suggested

86 e show that the strength and the kinetics of hybridization at large probe density can be improved by

87 calculations shows that electron density and hybridization at the delta position play a dominant role

88 perature on the strength of the post-zygotic hybridization barrier.

89 We developed a high-resolution hybridization-based genotype array coupled with an analy

90 describe the next iteration of ISS, HybISS, hybridization-based in situ sequencing.

91 heat, arising through polyploidization after hybridization between a tetraploid and a diploid species

92 gnatures of the two species may help prevent hybridization between C. marthae and C. subcristatus.

93 logenies across the genome, and evidence for hybridization between divergent lineages.

94 -bipyridine), in a way that preserves strong hybridization between probe and target.

95 Interspecies hybridization between southern platyfish and green sword

96 c evidence is increasingly underpinning that hybridization between taxa is commonplace, challenging o

97 rs and reveal a rich phase space to tune the hybridization between the ferromagnetic order and meron-

98 This is ascribed to the interfacial hybridization between the Ti3d-orbitals of the substrate

99 aled that although it is rare, interfamilial hybridization between the two species is possible but mo

100 f one target RNA can then trigger a cascaded hybridization between these hairpin pairs and thus activ

101 In hybridizations between outbreeding and inbreeding specie

102 Our results support the hypothesis that hybridization can act as a generative force in macroevol

103 Twist-angle-controlled interlayer electronic hybridization can also mix these two types of exciton to

104 Mixing genomes of different species by hybridization can disrupt species-specific genetic inter

105 Our results demonstrate that this improved hybridization capture approach can reveal previously unc

106 s with HBV-related HCC was determined by the Hybridization capture-based next-generation sequencing (

107 sed reporter deposition fluorescence in situ hybridization (CARD-FISH) on >14 500 archaeal and bacter

108 s methods, such as array comparative genomic hybridization (CGH) and whole-genome sequencing (WGS), h

109 ization of metastable DNA hairpins using the hybridization chain reaction (HCR) is reported.

110 in tissues have been developed based on the hybridization chain reaction (HCR).

111 Such oligomerization bested the conventional hybridization chain reaction laddering at both biomechan

112 e of hairpin surface-tethered probes and the hybridization chain reaction was used to amplify the det

113 In situ amplification methods, such as hybridization chain reaction, are valuable tools for map

114 markers, which were visualized in situ using hybridization chain reaction.

115 d on localized surface plasmon resonance and hybridization chain reaction.

116 s for a new barcoding system via sequence-by-hybridization chemistry for improved spatial detection o

117 ploying modern approaches based on molecular hybridization, computational polypharmacology, and machi

118 In situ hybridization confirmed an increase in BDNF expression i

119 tochemical analysis and fluorescence in situ hybridization confirmed the presence of allogeneic parat

120 In situ hybridization confirmed these findings.

121 A long-standing hypothesis suggests that hybridization could deregulate TEs and trigger their acc

122 pendent of the DNA target concentration, the hybridization current (surrogate for detection sensitivi

123 In situ hybridization data localized DCN expression to areas of

124 Genomic outcomes of hybridization depend on selection and recombination in h

125 er or not splice-modulating ASOs also induce hybridization-dependent mis-splicing of unintended targe

126 tructure was proposed and fabricated for DNA hybridization detection.

127 ed with single-molecule fluorescence in situ hybridization directly implicate Y-specific genes that r

128 However, hybridization dynamics vary across all pairs, suggesting

129 By in situ hybridization, each gene responded in different cell sub

130 We emphasize that hybridization effects need to be taken into account to f

131 The mechanism of spatial bias in hybridization efficiency is poorly understood, particula

132 re prone to intra-assay spatial variation in hybridization efficiency.

133 In a comprehensive in situ hybridization effort, we show that the zebra finch vocal

134 tions show that an understanding of both DNA hybridization energetic and magnetic interactions is req

135 However, the small differences in hybridization energy provided by single-base changes mak

136 Binding of a target analyte can disrupt the hybridization equilibrium between the aptamer and the la

137 ased on the photoluminescence of MoS(2), the hybridization events were analyzed for the target (miRNA

138 ed results from IHC and Fluorescence in situ hybridization (FISH) analyses when analyzed with Receive

139 Fluorescent in situ hybridization (FISH) analysis revealed two massively lar

140 Here we used fluorescent in situ hybridization (FISH) and immuno-FISH on metaphase chromo

141 Fluorescence in situ hybridization (FISH) is a powerful method to visualize t

142 Fluorescence in situ hybridization (FISH) is a powerful single-cell technique

143 Background Fluorescence in situ hybridization (FISH) is a standard method for 1p/19q cod

144 > 70% concordance with fluorescence in situ hybridization (FISH) results.

145 We use fluorescence in situ hybridization (FISH) to characterize the endogenous expr

146 ere immunofluorescence, fluorescence in situ hybridization (FISH), micronuclei imaging, and the telom

147 xed with oligopaint DNA-fluorescence in situ hybridization (FISH), RNA-FISH and protein fluorescence,

148 neration sequencing, or fluorescence in situ hybridization (FISH).

149 investigated by means of fluorescent in situ hybridization for 10 different bacterial taxa.

150 luding immunohistochemistry for AVT, in situ hybridization for avt-mRNA, and quantitative PCR.

151 In situ hybridization for miR-517a/c, a C19MC cistron microRNA,

152 novel technology using fluorescence in situ hybridization for rapid species identification (ID) and

153 increased HSPC number as assessed by in situ hybridization for runx1/cmyb and flow cytometry.

154 Vgat) neurons, which we validated by in situ hybridization for Vgat mRNA.

155 , genome duplication following interspecific hybridization) from two now-extinct progenitors.

156 Whether hybridization generates or erodes species diversity has

157 that can support species cohesion even when hybridization has been pervasive throughout the evolutio

158 emical reactions that convert sp(2) to sp(3) hybridization have been demonstrated to be a fascinating

159 ntly, methods for serial fluorescent in situ hybridization have made it possible to measure the three

160 n microbiome mapping by fluorescence in situ hybridization (HiPR-FISH), a versatile technology that u

161 .g. DASH, Depletion of Abundant Sequences by Hybridization), identifying more mutation-positive sampl

162 racing, clonal analysis, multiplexed in situ hybridization, immunostaining, deep confocal imaging, an

163 diversification to test the hypothesis that hybridization impacts the diversification dynamics of sp

164 ngenomic techniques and fluorescence in-situ hybridization in 2 age groups (cutoff age, 18 months) an

165 olymer serves as a steric guide to limit DNA hybridization in a fixed direction, while the DNA serves

166 fluorescent immunohistochemistry and in situ hybridization in combination with whole slide imaging an

167 alization of 18S rRNA by fluorescent in situ hybridization in HEK-293T cells.

168 Most of what is known of contemporary hybridization in nature comes from the study of pairs of

169 genetic consequences of diversification and hybridization in parasitic protozoa.

170 sses, we argue that the transition from mode-hybridization in the strong coupling regime to the dampe

171 the Macrocystis pyrifera x Lessonia spicata hybridization in the wild (Chiloe Island, Southeastern P

172 1377) analyze the fitness consequences of hybridization in toads but do not account for difference

173 leus findings using RNA fluorescence in situ hybridization, in situ sequencing, and computational app

174 Hybridization-interbreeding between species-is generally

175 Interspecific hybridization is a common breeding approach for introduc

176 Peptide hybridization is an effective approach for the design an

177 ing (scRNA-seq) and quantitative RNA in situ hybridization (ISH).

178 miRNAs were validated by qRT-PCR and in situ hybridization (ISH).

179 and suggested the potential for branching at hybridization junctions, all of which were confirmed exp

180 The hybridization LC-MS/MS was considered an improved altern

181 Instead, indirect effects of hybridization like waste of reproductive effort in small

182 d relationship with VEGF pathway via in situ hybridization maps and RNA sequencing data.

183 nts in molecular genetics have revealed that hybridization may be common among plants, animals, and f

184 t match single molecule fluorescence in situ hybridization measurements.

185 ultiplexed error-robust fluorescence in situ hybridization (MERFISH)-based method for genome-scale ch

186 n cancer cells using the fluorescent in situ hybridization method (FISH) and immunohistochemistry (IH

187 lit-FISH, a multiplexed fluorescence in situ hybridization method that leverages a split-probe design

188 in discrete cells was shown through in situ hybridization methods for detecting the viral RNA.

189 Improved in situ hybridization methods for mRNA detection in tissues have

190 imidazole compound which originated from the hybridization of a dimethylphenol benzimidazole series,

191 Hybridization of AuNPs with silica NPs as a material wit

192 he heavy atoms in an analogous manner to the hybridization of C in CH(4) from (2s)(2)(2p)(2) to sp(3)

193 Hybridization of complementary single strands of DNA rep

194 heory calculations suggest Pv can weaken the hybridization of Ni 3d and P 2p orbitals, enrich the ele

195 ry, first introduced nearly 50 y ago, of the hybridization of polar and acoustic modes in quantum par

196 Here we present Hybridization of Probes to RNA for sequencing (HyPR-seq)

197 Hybridization of SICM with coincident characterization t

198 Assembly is via T-junctions formed by hybridization of single-stranded overhangs on the linker

199 gh CT energies are defined by the electronic hybridization of the CT state with local excitations (LE

200 radicals, it is required that the electronic hybridization of the CT states with both the ground and

201 -that is, resonant states resulting from the hybridization of the defect modes and the bulk continuum

202 These findings underscore that hybridization of the emissive state with high-energy sta

203 at occur in these systems are related to the hybridization of the heavy atoms in an analogous manner

204 eled L-Tym by detecting its influence on the hybridization of the labeled complementary strand.

205 Further, hybridization of the surface modes and their evolution w

206 acids and for steric hindrance close to full hybridization of the surface probes.

207 Almost all miRNA sensors utilize cross-hybridization of the target miRNA with a capture probe f

208 Louradour et al. have shown in vitro hybridization of two Leishmania tropica isolates, with t

209 ther quantified using a modified fluorescent hybridization of viral RNA assay.

210 ific splicing enhancers, the substitution or hybridization of which impedes splicing.

211 e we investigated the potential influence of hybridization on the emergence of morphologically and re

212 beta cells were also examined using in situ hybridization on the frozen pancreatic sections.

213 ition, which when bound, altered the DNA-DNA hybridization on the surface, resulting in generation of

214 he epimark in a target DNA, captured through hybridization onto streptavidin-magnetic microbeads (Str

215 o components of the structure and triggering hybridization or dissociation of the overhangs via chang

216 nt evolution than by another process such as hybridization or incomplete lineage sorting.

217 two-dimensional analysis of the kinetics of hybridization, performed at different target concentrati

218 nslational approach and by combining in situ hybridization, primary cell isolation, immunoblotting, q

219 alled 'Vetting & Analysis of RNA for in situ Hybridization probes' (VARNISH) for probe design.

220 nalysis utilizing peptide nucleic acid (PNA) hybridization probes.

221 Moreover, the hybridization process provides an effective strategy aga

222 rs activates the nickase activity, and 28-bp hybridization promotes cleavage of the target strand.

223 rge localization in cuprates and interfacial hybridization provides important clues to their electron

224 rspective, the potential negative effects of hybridization raise concerns on the genetic integrity of

225 strand displacing polymerase enzyme and DNA hybridization reactions for implementing CRNs.

226 re two main approaches based on target/probe hybridization reported in the literature, namely Signal

227 nd are uniquely valuable for advancing plant hybridization, reproductive biology, and polyploid genom

228 g network through chain entanglement and DNA hybridization, resulting in shear-thinning and cyclic st

229 RNAscope in situ hybridization revealed dynamic and special changes of Lr

230 r presence confirmed by fluorescence in situ hybridization, revealed recovery of function of the derm

231 g mates of another species, females increase hybridization's benefits and exert sexual selection acro

232 xchange (SCE) assay with fluorescent in situ hybridization (SCE-FISH).

233 Immunostaining and in situ hybridization show that these cells are concentrated wit

234 Array comparative genomic hybridization showed a 22q11.23 duplication of 1.306 mil

235 Additionally, in situ hybridization showed that DMD messenger RNA primarily lo

236 g fibulin-2 and macrophage CSF1; RNA in situ hybridization showed that expression of these two genes

237 ved early, with a progressive and ubiquitous hybridization signature involving mesenchymal and epithe

238 iplexed single-molecule fluorescence in situ hybridization (smFISH) and measured the expression of IE

239 adapted single molecule fluorescence in situ hybridization (smFISH) for use in the Drosophila wing im

240 ultiplex single-molecule fluorescent in situ hybridization (smFISH) is a powerful method for validati

241 use single-molecule RNA fluorescent in situ hybridization (smFISH) on mouse stem cells derived from

242 ant for single-molecule fluorescence in situ hybridization (smFISH) studies in Caenorhabditis elegans

243 nd single-molecule fluorescence in situ mRNA hybridization (smFISH) studies, we observed that intesti

244 we used single-molecule fluorescence in-situ hybridization (smFISH) to detect alpha-satellite RNA tra

245 tion of single-molecule fluorescence in situ hybridization (smFISH), time-lapse microscopy, and mathe

246 The hybridization specificity afforded by this process furth

247 We therefore developed a strand-specific hybridization (SSH) assay that differentiates between vR

248 fferent temperatures, and the changes in the hybridization state (mainly in the bulk layer) encounter

249 each alkylurea with unit areas of different hybridization states of unified O, N, and C atoms of ami

250 uorescence, electron microscopy, and in situ hybridization studies for SARS-CoV-2 on a subset of samp

251 Hybridization studies show that TMO chimeras consisting

252 Finally, a real-time hybridization study reveals that expanding the effective

253 Interspecific hybridization substantially alters genotypes and phenoty

254 exhibit doping-dependent renormalization and hybridization that are sensitive to the electronic corre

255 Here, we demonstrate by fluorescent in situ hybridization that these inclusions are decorated with A

256 os) for PAINT with LNA-containing oligos for hybridization; therefore, we developed an online tool ca

257 In these systems, antibody probe hybridization to a target protein antigen depends on the

258 Using RNAScope in situ hybridization to characterize activity of different VP c

259 high-throughput screens rely on probe-target hybridization to detect analytes.

260 we utilize multichannel fluorescent in situ hybridization to detect the expression of adrenergic rec

261 uencing coupled with high-resolution in situ hybridization to identify novel transcriptional regulato

262 holinergic gene locus, and then used in situ hybridization to localize mRNA encoding choline acetyltr

263 eotides (ASOs) interact with target RNAs via hybridization to modulate gene expression through differ

264 of MnPO(EP3R) neurons, we first used in situ hybridization to show coexpression of EP3R and the VGluT

265 Finally, we used in situ hybridization to show that sema1a.1 and sema1a.2 express

266 to create and attack bulge-loop regions upon hybridization to target RNA.

267 ally react with each other upon simultaneous hybridization to the same RNA target strand, serving her

268 transcriptional regulators, and used in situ hybridization to validate critical genes and pathways.

269 sors transduce biochemical events (e.g., DNA hybridization) to electrical signals and can be readily

270 By immunohistochemistry, RNAscope in situ hybridization, transmission electron microscopy, and con

271 biochemical techniques, fluorescence in situ hybridization using peptide nucleic acid probes (PNA-FIS

272 Fluorescence in situ hybridization using probes based on oligonucleotides (ol

273 In situ hybridization validated computational predictions of spa

274 ition of a biotinylated-DNA detection probe, hybridization was evidenced using streptavidin-conjugate

275 LFA) serves as a platform for amplification, hybridization, washing, and fluorescent imaging, while m

276 Using chromogenic in situ hybridization we localized aromatase-expressing cells to

277 enches to align DNA-wrapped CNTs through DNA hybridization, we constructed parallel CNT arrays with a

278 With RNAscope in situ hybridization, we demonstrate that key enzymes that synt

279 f geniculate ganglion neurons and by in situ hybridization, we demonstrate that R-spondin-2, the liga

280 f single-cell expression studies and in situ hybridization, we describe that alpha9, but not the alph

281 ic analyses, immunofluorescence, and in situ hybridization, we found that the expression of the orpha

282 etention experiments and multiplexed in situ hybridization, we identify a population of cycling Sox5/

283 Using fluorescent single-molecule in situ hybridization, we showed that distinct NOSs are expresse

284 both chromogenic and single-molecule in situ hybridizations, we validated AKI signatures in multiple

285 ts, and single molecule fluorescence in situ hybridization were performed together with analysis of i

286 ng of hundreds of genomic loci by sequential hybridization, which allows high-resolution conformation

287 species have a long evolutionary history of hybridization, which has phenotypic consequences for ada

288 In situ hybridization with a D3-specific S-35 riboprobe in FAAH

289 oradiography with [H-3]-(+)-PHNO and in situ hybridization with a D3-specific S-35 riboprobe were car

290 Os were extracted from biological samples by hybridization with biotinylated sense-strand oligonucleo

291 CBA achieved high-quality hybridization with collagen, improving mechanical proper

292 oligomers to be retrieved through selective hybridization with complementary, mass-labeled sequences

293 interlayer excitons undergo field-asymmetric hybridization with intralayer K-K excitons.

294 A specific redshift was observed for the hybridization with miRNA21c, but not for the control, de

295 s of adaptive alleles are maintained despite hybridization with non-adapted populations(2-4).

296 genomes to compare contemporary patterns of hybridization with signatures of past introgression acro

297 through an immunoenzymatic process following hybridization with target-specific oligonucleotide captu

298 The typical involvement of oxygen through hybridization with transition metals is discussed, as we

299 Additionally, we combined in situ hybridization with tyrosine hydroxylase (TH) immunochemi

300 screte intermediate, consistent with DNA:RNA hybridization within an initial seed region.