ライフサイエンスコーパス: in situ hybridization

1 rescent in situ hybridization or chromogenic in situ hybridization).

2 lungs and oesophagus of mouse embryos using in situ hybridization.

3 out using massively multiplexed fluorescence in situ hybridization.

4 NA granules that correlate with fluorescence in situ hybridization.

5 croarray analysis of embryo subdomains using in situ hybridization.

6 in zebrafish was assessed using whole-mount in situ hybridization.

7 Liver biopsy specimens were analyzed by in situ hybridization.

8 pressed genes were analyzed and validated by in situ hybridization.

9 eline cytogenetics according to fluorescence in situ hybridization.

10 genetic risk, as assessed using fluorescence in situ hybridization.

11 f a set of 49 homeobox genes in the MOE with in situ hybridization.

12 tic cluster were confirmed using fluorescent in situ hybridization.

13 lized this expression in mechanosensilla via in situ hybridization.

14 and/or ampl(1q) as assessed by fluorescence in situ hybridization.

15 ally expressed genes using real-time PCR and in situ hybridization.

16 data from The Cancer Genome Atlas and miRNA in situ hybridization.

17 nformatic analysis, together with chromosome in situ hybridization.

18 unophenotype, cytogenetics, and fluorescence in situ hybridization.

19 tages of C57BL/6J mice by using double-label in situ hybridization.

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

21 nt Epulopiscium sp. type B using fluorescent in situ hybridization.

22 polymerase chain reaction (qRT-PCR) and RNA in situ hybridization.

23 sion and extensively validate the results by in situ hybridization.

24 Localization of miR-218-5p was assessed by in situ hybridization.

25 ISPR imaging and DNA sequential fluorescence in situ hybridization.

26 ds in Escherichia coli using RNA fluorescent in-situ hybridization.

27 rs are already available (e.g., fluorescence in situ hybridization, 16-S rRNA gene amplicon sequencin

28 sine kinases and 42 tyrosine phosphatases by in situ hybridization 48 human normal and 24 tumor tissu

29 ties (CA) detected by interphase fluorescent in situ hybridization after CD138 plasma cell purificati

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

31 The in situ hybridization Allen Mouse Brain Atlas was mined

32 e-cell sequencing and multiplex fluorescence in situ hybridization analyses mapped the emergence of e

33 Fluorescence in situ hybridization analyses showed that P. denitrific

34 Fluorescence in situ hybridization analysis mapped the EPSPS gene to

35 Whole-genome sequencing and fluorescence in situ hybridization analysis of two de novo translocat

36 Pyrosequencing and fluorescence in situ hybridization analysis revealed that denitrifyin

37 In situ hybridization analysis revealed that Fusobacteri

38 Fluorescence in situ hybridization analysis showed that all four B-LB

39 With real-time PCR and in situ hybridization analysis, SlPIP2s were considered

40 In situ hybridization analysis, using locked nucleic aci

41 mosomal abnormality detected by fluorescence in situ hybridization analysis.

42 ncident virologic clearance was confirmed by in situ hybridization and a failure of disease to recur

43 al molecular methods, including fluorescence in situ hybridization and array comparative genomic hybr

44 te the complementary utility of fluorescence in situ hybridization and capture sequencing approaches

45 We identify, by single-molecule in situ hybridization and cell sorting, rare cells posit

46 ing flow-fluorescence in situ hybridization (in situ hybridization and flow cytometry) of primary lym

47 ccessfully confirmed by 4C-seq, fluorescence in situ hybridization and Hi-C, as well as coordinated e

48 MGB1 in the host cell cytoplasm, as found by in situ hybridization and IHC, confirmed the virus speci

49 In situ hybridization and immunochemistry double stainin

50 Double staining using in situ hybridization and immunocytochemistry revealed t

51 In situ hybridization and immunofluorescence were perfor

52 ele-specific RNAseq, nascent RNA-fluorescent in situ hybridization and immunofluorescence), we show h

53 non-neuronal POMC expression in detail using in situ hybridization and immunohistochemical techniques

54 Transcriptome and subsequent in situ hybridization and immunohistochemistry analyses

55 tides derived from this precursor using mRNA in situ hybridization and immunohistochemistry revealed

56 from this precursor in A. rubens using mRNA in situ hybridization and immunohistochemistry revealed

57 ressed at the placental level as revealed by in situ hybridization and immunohistochemistry, and is c

58 e present study addresses this issue through in situ hybridization and immunohistochemistry.

59 stages and isolated crypts were analyzed by in situ hybridization and immunohistochemistry.

60 prenatal and postnatal rat tissues by using in situ hybridization and immunohistochemistry.

61 ransection and detected mRNA in axon tips by in situ hybridization and microaspiration of their axopl

62 hermore, we analyzed SMARCB1 by fluorescence in situ hybridization and multiplex ligation-dependent p

63 (ALK) gene rearrangement using fluorescence in situ hybridization and negative for EGFR, ROS1, RET,

64 confirmed this pattern of gene expression by in situ hybridization and observed staining consistent w

65 Cellular miRNA origin was examined by using in situ hybridization and reverse transcriptase quantita

66 Furthermore, RNA in situ hybridization and reverse transcription-polymera

67 markers and COX-2 protein, RNA fluorescence in situ hybridization and RNA immunoprecipitation, the C

68 Cluster analysis, in situ hybridization and RNAi assays indicate that male

69 We validated seven miR-9 pri-miRNAs by in situ hybridization and showed similar expression patt

70 Here, we used multiplexed in situ hybridization and single-cell RNA-Seq in male an

71 ice fed a polysaccharide-rich diet, and (ii) in situ hybridization and spectral imaging analysis meth

72 Fluorescence in situ hybridization and transmission electron microsco

73 inations with each other, as shown by double in situ hybridization and triple immunohistochemistry.

74 chemical perturbation, benchmarking against in situ hybridizations and immunofluorescence staining,

75 w levels of SIV RNA in the brain as shown by in situ hybridization, and generally was observed in ani

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

77 ventional in situ hybridization, chromogenic in situ hybridization, and immunohistochemistry for p16.

78 Here we devise genomics, in situ hybridization, and mouse genetics strategies to

79 nocytochemistry, glutamic acid decarboxylase in situ hybridization, and parvalbumin-immunocytochemist

80 data from karyotype, DNA index, fluorescence in situ hybridization, and polymerase chain reaction scr

81 Transcriptome, in situ hybridization, and proteome analyses demonstrate

82 e 5'-triphosphate labeling, RNA fluorescence in situ hybridization, and quantitative reverse transcri

83 rRNA gene amplicon sequencing, fluorescence in situ hybridization, and targeted metagenome analysis

84 Using a novel in situ hybridization approach, we demonstrated substant

85 Using a quantitative interphase-fluorescence in situ hybridization approach, we previously reported a

86 Using spectral imaging fluorescence in situ hybridization as guided by metagenomic sequence

87 We used a fluorescent in situ hybridization assay to evaluate CD274/PD-L1 and

88 ting BaseScope-a novel mutation-specific RNA in situ hybridization assay.

89 l-time polymerase chain reaction (RT-PCR)and in situ hybridization assays, we validated that the Osr2

90 RNA levels, assessed by quantitative PCR and in situ hybridization at 1, 4, 7, and 15 days after the

91 l improve the performance of a wide range of in situ hybridization-based techniques in both cell cult

92 ining BONCAT with rRNA-targeted fluorescence in situ hybridization (BONCAT-FISH).

93 d catalyzed reporter deposition fluorescence in situ hybridization (CARD-FISH), we show that only fou

94 DNA polymerase chain reaction, conventional in situ hybridization, chromogenic in situ hybridization

95 lls using chromosome-orientation fluorescent in situ hybridization (CO-FISH).

96 Based on the in situ hybridization colabeling results, we tested the

97 By quantitative fluorescent in situ hybridization combined with immunofluorescence t

98 acid enhanced NRIP1 binding to RARalpha RNA in situ hybridization confirmed Nrip1 expression in the

99 Whole-mount in situ hybridization confirmed that all 17 selected mRN

100 RNAscope in situ hybridization confirmed that Grin2a, as well as

101 tabolic cluster activation; DNA fluorescence in situ hybridization confirmed that transcriptional act

102 Fluorescence in Situ Hybridization confirmed the presence of bacteria

103 reveals clusters of co-regulated genes, with in situ hybridization confirming the domain-specific exp

104 tem cells using single-molecule fluorescence in situ hybridization coupled with automated, high-throu

105 We show here, by means of fluorescent in situ hybridization coupled with tyramide signal ampli

106 Integrating our resource with in situ hybridization data from existing databases showe

107 In situ hybridization data showed nAChR subunit transcri

108 nascent RNA sequencing and RNA fluorescence in situ hybridization demonstrate the existence of trans

109 Fluorescence in situ hybridization demonstrated active invasion of th

110 RNA in situ hybridization detected Adamts17 expression in sp

111 Fluorescence in situ hybridization detected APOL1 mRNA in glomeruli (

112 ning events were then tested by fluorescence in situ hybridization during T-cell activation.

113 Fluorescence in situ hybridization experiments showed that micropatte

114 To this end, we performed RNA in situ hybridization experiments, promoter-reporter gen

115 lated orthologs of these genes and performed in situ hybridization, finding that their expression col

116 Single-cell-level studies using fluorescence in situ hybridization (FISH) and growth in microfluidic

117 od for gene fusion detection is Fluorescence In Situ Hybridization (FISH) and while highly sensitive

118 e conformation capture (3C) and fluorescence in situ hybridization (FISH) are two widely used technol

119 rough direct visualization via a fluorescent in situ hybridization (FISH) assay, which can detect tho

120 redictions experimentally by 3D fluorescence in situ hybridization (FISH) experiments and show that a

121 as distances measured using 3D fluorescence in situ hybridization (FISH) experiments.

122 Sperm fluorescence in situ hybridization (FISH) for chromosomes X, Y, and 1

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

124 Fluorescence in situ hybridization (FISH) further confirmed that the

125 Single-molecule mRNA Fluorescence In Situ Hybridization (FISH) has been established as the

126 d immunohistochemistry (IHC) and fluorescent in situ hybridization (FISH) HER2 testing guidelines in

127 Then, postexpansion, fluorescent in situ hybridization (FISH) imaging of RNA can be perfo

128 validate this observation using fluorescence in situ hybridization (FISH) in an additional 87 osteosa

129 ity of immunohistochemistry and fluorescence in situ hybridization (FISH) in distinguishing PNs from

130 lities determined by interphase fluorescence in situ hybridization (FISH) in patients with newly diag

131 Fluorescence in situ hybridization (FISH) is a powerful single-cell t

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

133 nadherent mammalian cells using fluorescence in situ hybridization (FISH) probes.

134 ranscription and replication, a fluorescence in situ hybridization (FISH) protocol was established to

135 tochemical (IHC) analyses, HER2 fluorescence in situ hybridization (FISH) ratio, and copy number resu

136 cordingly, single-molecule mRNA fluorescence in situ hybridization (FISH) reveals that, upon site-spe

137 colaou (Pap) staining and (iii) fluorescence in situ hybridization (FISH) targeting the ALK rearrange

138 The development of fluorescence in situ hybridization (FISH) technologies enables the qu

139 nst the protein LIN28A, and (3) fluorescence in situ hybridization (FISH) testing for the amplificati

140 EGFR CNG was determined by fluorescent in situ hybridization (FISH) using prespecified criteria

141 We performed fluorescence in situ hybridization (FISH) using probes targeting CD27

142 Fluorescence in situ hybridization (FISH) will be required to identif

143 (rRNA) precursor-analyzed by RNA fluorescent in situ hybridization (FISH), Northern blots, and RNA se

144 man colorectal cancer using RNA fluorescence in situ hybridization (FISH), quantitative PCR and immun

145 gy, we have developed a fluorescence imaging in situ hybridization (FISH)-based assay for the detecti

146 A fluorescence in situ hybridization (FISH)-based karyotyping cocktail

147 ) or -negative (HER2-) based on fluorescence in situ hybridization (FISH)-supplemented immunohistoche

148 r 2 gene (HER2) amplification by fluorescent in situ hybridization (FISH).

149 ISPR imaging and sequential DNA fluorescence in situ hybridization (FISH).

150 Spectral karyotyping (SKY) and fluorescent-in-situ hybridization (FISH) demonstrated coordinate loc

151 optimized flow cytometry-based fluorescence in situ hybridization (Flow-FISH) for IFN-gamma to multi

152 EXCLUSION CRITERIA: fluorescence in situ hybridization, fluorescence imaging for lymph no

153 tochemistry were submitted to automated dual in situ hybridization for gene amplification evaluation.

154 earrangements, immunohistochemistry for EBV, in situ hybridization for kappa and lambda light chains,

155 istry for MYC and BCL2, and with fluorescent in situ hybridization for MYC, BCL2, and BCL6 rearrangem

156 In homoploid diploid hybrids, genomic in situ hybridization (GISH) allowed B painting with the

157 As fluorescence in situ hybridization has limitations regarding the reso

158 The down regulation was confirmed by in situ hybridization histochemistry for two strongly do

159 In situ hybridization histochemistry was performed for s

160 RNA fluorescence in situ hybridization identified actively transcribing,

161 rrations detected by interphase fluorescence in situ hybridization (iFISH) of plasma cells are routin

162 Fluorescence in situ hybridization images and metagenome results sugg

163 sion, high-throughput, automated fluorescent in situ hybridization imaging pipeline, for mapping of t

164 omprehensive mapping of p11 expression using in situ hybridization, immunocytochemistry, and whole-ti

165 -nucleotide polymorphism array, fluorescence in situ hybridization, immunohistochemistry and cell-bas

166 Here, we used classical pharmacology, in situ hybridization, immunohistochemistry, and the Dau

167 according to requirements of the following: in situ hybridization, immunohistochemistry, immunofluor

168 s, GXD collects and integrates data from RNA in situ hybridization, immunohistochemistry, RT-PCR, nor

169 by high-throughput quantitative fluorescence in situ hybridization in circulating leukocytes from 1,4

170 N2D mRNA was detected by single-cell PCR and in situ hybridization in diverse interneuron subtypes in

171 es those loci by DNA sequential fluorescence in situ hybridization in fixed cells and resolves their

172 in ovaries was also detected by fluorescent in situ hybridization in G. f.

173 iocyte senescence was assessed by p16(INK4a) in situ hybridization in liver tissue and by senescence-

174 RNA-positive (vRNA+) cells were detected by in situ hybridization in LTs obtained before interruptio

175 reduced miR-26a expression, as determined by in situ hybridization in patient tumors (n=92), is assoc

176 and telomere length using flow-fluorescence in situ hybridization (in situ hybridization and flow cy

177 h catalyzed reporter deposition fluorescence in situ hybridization, indicated that Nitrospinae fix 15

178 We mapped its distribution using in situ hybridization (ISH) and immunohistochemistry (IH

179 further studied with a novel method of mRNA in situ hybridization (ISH) for the detection of transcr

180 use Brain Atlas provides high-resolution 3-D in situ hybridization (ISH) gene expression patterns in

181 NV) and tumour heterogeneity by fluorescence in situ hybridization (ISH) provides additional tissue m

182 p16 immunohistochemical analysis, HPV16 DNA in situ hybridization (ISH), and high-risk HPV E6/E7 mRN

183 p16 immunohistochemical analysis, HPV16 DNA in situ hybridization (ISH), and high-risk HPV E6/E7 mRN

184 lymphocytes was detected by a combination of in situ hybridization (ISH), immunofluorescence, and PCR

185 R2 gene copy number per tumor cell: group 1 (in situ hybridization [ISH]-positive): HER2-to-chromosom

186 Immunohistochemistry, in situ hybridization, laser-assisted microdissection an

187 ption polymerase chain reaction, fluorescent in situ hybridization, lentiviral overexpression, and Lu

188 roadly applicable technique called 'Ligation in situ Hybridization' ('LISH'), which is an alternative

189 ements as probes for multicolor fluorescence in situ hybridization (mcFISH), using an optimized BAC p

190 put of multiplexed error-robust fluorescence in situ hybridization (MERFISH), an image-based approach

191 Using a new in situ hybridization method that can measure the expres

192 Here, we apply a new fluorescence in situ hybridization method that measures allele-specif

193 We describe a fluorescence in situ hybridization method that permits detection of t

194 In situ hybridization methods are used across the biolog

195 o the domestication of 'Miracle-Wheat.' mRNA in situ hybridization, microarray experiments, and indep

196 By in situ hybridization, miR2118 triggers of 21-nt phasiRN

197 Fluorescence in situ hybridization of AAV transgenes was used to iden

198 mRNA in situ hybridization of brain-specific Nav subunits rev

199 nput quantitative viral outgrowth assay, and in situ hybridization of colon tissue-the patient consen

200 FORMED1 (PIN1) auxin transport proteins, and in situ hybridization of leaf developmental transcripts

201 Immunohistochemistry and in situ hybridization of NRG1 and its active receptor Er

202 , the AI with magnetic resonance imaging and in situ hybridization of the immediate early gene zif268

203 Here we determine the neurochemistry (using in situ hybridization) of catecholaminergic and noncatec

204 y quantitative measurements (by fluorescence in situ hybridization) of the joint distributions of mRN

205 Finally, biologic relevance was tested using in situ hybridization on 30 pre-metastatic lesions, show

206 expressed relative to CRH1 and UTS1, we used in situ hybridization on brain tissue from spotted gar (

207 Here we use multicolour fluorescence in situ hybridization on brush cytology specimens, from

208 In situ hybridization on inguinal lymph node sections fr

209 genome of A tuberculatus using fluorescence in situ hybridization on mitotic metaphase chromosomes a

210 RNA fluorescence in situ hybridization on primary HL tissues revealed a t

211 was performed with immunohistochemistry and in situ hybridization on tissue microarrays for 958 tumo

212 [IHC]), and gene amplification (fluorescent in situ hybridization or chromogenic in situ hybridizati

213 Double labeling experiments, by either in situ hybridization or immunostaining, demonstrated th

214 In situ hybridization, PCR, and quantitative reverse tra

215 In contrast, in situ hybridization provides the location of gene expr

216 ic glands, and also in normal parathyroid by in situ hybridization, qRT-PCR, and immunohistochemistry

217 lected and analyzed by immunohistochemistry, in situ hybridization, quantitative reverse-transcriptio

218 lyzed using histology, immunohistochemistry, in situ hybridization, radiography, and micro-computed t

219 es and standard antibody and fluorescent DNA in situ hybridization reagents.

220 Our in situ hybridization, real-time quantitative PCR, and s

221 xpression of the oxytocin system by qRT-PCR, in situ hybridization, receptor autoradiography ([(125)I

222 Laser capture microdissection and in situ hybridization revealed a distinct localization o

223 RT-PCR and in situ hybridization revealed CPAMD8 expression in the

224 RNA in situ hybridization revealed expression of the EC cell

225 specific polymerase chain reaction (PCR) and in situ hybridization revealed plentiful mRNA for the lo

226 Further studies using single-molecule RNA in situ hybridization revealed that in fact, replicating

227 In situ hybridization revealed that most neurons in the

228 alysis in distinct Arachis genotypes, whilst in situ hybridization revealed transcripts in different

229 In situ hybridization revealed widespread distribution o

230 stemic localization of all these GT mRNAs by in situ hybridization reveals members with either enrich

231 In situ hybridization reveals photoreceptor and RPE cell

232 ch as conventional karyotyping, fluorescence in situ hybridization, reverse transcription-polymerase

233 anoids were analyzed by immunohistochemical, in situ hybridization, RNA sequence, and chromatin immun

234 In situ hybridization RNAscope assays found higher level

235 Sequential barcoded fluorescent in situ hybridization (seqFISH) allows large numbers of

236 oot defect model, whereas RNA sequencing and in situ hybridization show that the Hh attenuator Hhip i

237 Quantitative polymerase chain reaction and in situ hybridization showed elevated expression of miR-

238 Fluorescence in situ hybridization showed non-weaned rats to harbor s

239 Break-apart fluorescence in situ hybridization showed PRKCA rearrangement, and re

240 Whole mount in situ hybridization showed that CrANT is expressed in

241 In situ hybridization showed that HaEXPB2 transcripts we

242 bosome biogenesis proteins, and fluorescence in situ hybridization showed that MAS2 colocalizes with

243 and chromatin conformation: qRT-PCR and mRNA in situ hybridization showed that the clustered genes we

244 hod is based on single-molecule fluorescence in situ hybridization (smFISH) and quantitative analyses

245 By contrast, single-molecule fluorescence in situ hybridization (smFISH) preserves the spatial inf

246 Single-molecule RNA fluorescence in situ hybridization (smFISH) provides unparalleled res

247 icult to detect single-molecule fluorescence in situ hybridization (smFISH) signals robustly in opaqu

248 ntial rounds of single-molecule fluorescence in situ hybridization (smFISH) to read out these barcode

249 anule cores and single-molecule fluorescence in situ hybridization (smFISH) validation.

250 microscopy and single-molecule fluorescence in situ hybridization (smFISH).

251 ombination with single-molecule fluorescence in situ hybridization (smFISH).

252 rmore, using single-molecule RNA fluorescent in situ hybridization (smRNA FISH), we show that egl-1 i

253 In situ hybridization studies found increased mRNA level

254 beknownst to most researchers, however, Pomc in situ hybridization studies in the rat show specific l

255 Detailed in situ hybridization studies of tip-enriched prediction

256 We used a sensitive in situ hybridization technique to visualize HIV gag-pol

257 de tract tracing with immunofluorescence and in situ hybridization techniques.

258 ate Pheno system uses automated fluorescence in situ hybridization technology with morphokinetic cell

259 in (MICDDRP), which is based on branched DNA in situ hybridization technology.

260 ere length assessment [telomere-fluorescence in situ hybridization (TEL-FISH) coupled with 3D imaging

261 Here, we characterized by in situ hybridization the developmental expression of So

262 ed three-dimensional interphase fluorescence in situ hybridization to decipher spatiotemporal gatheri

263 The present studies used fluorescence in situ hybridization to detect Gad1 and Gad2 mRNA in PO

264 tive polymerase chain reaction combined with in situ hybridization to develop a catalog of nox1, nox2

265 In this study we used in situ hybridization to examine mRNA expression of thre

266 can cichlid fish Astatotilapia burtoni using in situ hybridization to label vesicular glutamate trans

267 terns, we performed immunohistochemistry and in situ hybridization to localize appetite-stimulating (

268 trometric imaging combined with fluorescence in situ hybridization to localize Ca Entotheonella and s

269 We used in situ hybridization to measure the colabeling of the a

270 Using fluorescent in situ hybridization to monitor segment 7 mRNA localiza

271 olphe et al. use single molecule fluorescent in situ hybridization to show quantitatively that Ptch r

272 Here we used in situ hybridization to specifically examine LGR5 mRNA

273 ption polymerase chain reaction (RT-PCR) and in situ hybridization to test if GPR30 is expressed in t

274 e-cell amplicon sequencing, and fluorescence in situ hybridization, to show that individual cells of

275 as well as by 16S ribosomal RNA fluorescence in situ hybridization, transcriptional analyses, and qua

276 positive OPC (by p16 immunohistochemistry or in situ hybridization) treated at our institution from J

277 Using in situ hybridization, UCN3 mRNA was found to be express

278 ed using immunofluorescence and fluorescence in situ hybridization using a specific 16S ribosomal RNA

279 al CT, we performed multi-color fluorescence in situ hybridization using six probes extending across

280 oci and dual viral and cellular fluorescence in situ hybridization (viral FISH) analysis of environme

281 he enrolled patients were assessed, and CSF1 in situ hybridization was performed to confirm the mecha

282 Fluorescent in situ hybridization was performed to determine the rol

283 Next, fluorescence in situ hybridization was performed to visualize L. majo

284 tch in AA transmitter phenotype, fluorescent in situ hybridization was used to detect vGlut2 and Gad

285 resolved HER2 statuses (equivocal by IHC and in situ hybridization) was significantly higher in 2014

286 -eGFP-IRES-CreERT2/Rosa26-TdTomato mice) and in situ hybridization, we analyzed gastric stem cell res

287 (qPCR), droplet digital PCR, and fluorescent in situ hybridization, we could demonstrate that HHV-6A/

288 t cycle manipulations, hormone implants, and in situ hybridization, we demonstrate in a nocturnally b

289 Using a novel sensitive RNAscope in situ hybridization, we detected CB2R mRNA expression

290 Using fluorescence in situ hybridization, we detected higher Pax3 mRNA+ cel

291 Using high-resolution multiplex in situ hybridization, we determined that brain pericyte

292 Using in situ hybridization, we examined temporal and spatial

293 Here, using intracellular labeling and in situ hybridization, we investigated the detailed morp

294 Using single-molecule fluorescence in situ hybridization, we measured transcript numbers of

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

296 Immunohistochemistry and in situ hybridization were used to determine viral capsi

297 Fluorescence in situ hybridization with a set of wheat cDNAs allowed

298 classifier were analyzed using fluorescence in situ hybridization with BCL2, BCL6, MYC, immunoglobul

299 pling multiplex single molecule fluorescence in situ hybridization with machine learning algorithm ba

300 We used fluorescent in situ hybridization with probes for nascent transcript