ライフサイエンスコーパス: be processed for

1 Cry recordings were processed for 118 neonates, and 65 neonates were in

2 cancer patients were enrolled and 1001 swabs were processed for 16S rRNA gene PCR and sequencing.

3 Comorbidity in HIV infection (COCOMO) study were processed for 16S rRNA sequencing and ImP measured

4 e distal colon to the lumbar DRG, where they were processed for 5-HT(3) receptor-like immunoreactivit

5 attern unconventional substrates that cannot be processed for a variety of reasons, such as incompati

6 human immunodeficiency virus (HIV) infection was processed for a radiolabeled white blood cell study

7 Retina and vitreous from some animals were processed for adenosine diphosphatase (ADPase) flat

8 Choroids were processed for alkaline phosphatase flat-embedding.

9 On PN30, brains were processed for anterograde horseradish peroxidase (H

10 uggest that herpes simplex tegument proteins are processed for antigen presentation in vivo and are p

11 respond strongly or weakly to photoperiod), were processed for autoradiography using the radioligand

12 Specimens were processed for avidin-biotin permanent labeling, and

13 Mycobacterium tuberculosis clinical isolates were processed for BMD and whole genome sequencing.

14 The brains were processed for both immunocytochemistry and autoradi

15 e mandibular teeth and supporting structures were processed for both light microscopic examination an

16 Lymphocyte specimens from peripheral blood were processed for BRCA1 and BRCA2 by complete sequencin

17 2, the animals were perfused, and the brains were processed for c-fos immunocytochemistry.

18 T(3)-T(4) spinal cord of Sprague-Dawley rats were processed for c-fos immunohistochemistry following

19 Brains were processed for c-fos immunoreactivity, and neural ne

20 t a cue-primed reinstatement test and brains were processed for c-fos mRNA expression.

21 Brains were processed for c-Fos-like immunoreactivity (FLI).

22 Alternate brain sections were processed for CCK and preproenkephalin (PPE) mRNA i

23 The normal KL protein products are processed for cell surface expression, where they fo

24 , another MRI study was performed and aortas were processed for cellular composition and gene protein

25 Swabs were processed for Chlamydia trachomatis with a nucleic

26 ections containing the LH, CeA, BNST, and GC were processed for co-localization of FB and FG or GFB a

27 issue obtained 2 h after systemic injections was processed for colocalization of cytoplasmic AVP- and

28 In addition, frozen coronal sections were processed for comparative quantitative autoradiogra

29 Selected eyes were processed for complete histopathologic analysis.

30 These 27 selected eyes were processed for complete histopathologic analysis.

31 Selected eyes were processed for complete histopathologic analysis; so

32 their metabolomic states, contralateral eyes were processed for computational molecular phenotyping.

33 e tissue containing retina, RPE, and choroid was processed for confocal immunofluorescence microscopy

34 All biopsies were processed for conventional histopathologic study, i

35 Explanted hearts were processed for coronary artery histological analysis

36 h pair of biopsies (baseline; 4 or 24 hours) was processed for counts of epidermal CD1a(+) LC; the ot

37 l half of the pons, and every eighth section was processed for CRF immunocytochemistry (rabbit polycl

38 Brain sections were processed for CRH mRNA in situ hybridization.

39 s heat shock protein (HSP):peptide complexes are processed for cross-presentation of HSP-chaperoned p

40 Alternate sections were processed for cytochrome oxidase (CO) and CTB-Au, o

41 Flat-mounts were processed for cytochrome oxidase (CO) to reveal met

42 Sections of the flattened cortex were processed for cytochrome oxidase activity, Nissl su

43 two squirrel monkeys, and three galagos that were processed for cytochrome oxidase, Nissl bodies, or

44 dU and analyzed at different survival times) were processed for DCX, cell proliferation markers (Ki-6

45 Another set of animals was processed for degeneration-induced silver staining,

46 and the calvaria and overlying soft tissues were processed for demineralized histologic analysis.

47 phin (DYN), ENK, and CRF in the LC, sections were processed for detection of DYN and CRF or DYN and E

48 he myenteric and submucosal plexuses and DVC were processed for detection of Fos-like immunoreactivit

49 Embryos were processed for detection of labeled cells.

50 d as C1 cells, the biotinamide-labeled cells were processed for detection of tyrosine hydroxylase.

51 iced 43 days after TBI, and the brain tissue was processed for DiI-labeling fiber and immunohistochem

52 y 216Dx, and positive urine samples in media were processed for direct bacterial identification by ma

53 or left undisturbed and 90 min later brains were processed for double immunohistochemical labeling o

54 brains of AAS and sesame oil-treated animals were processed for double-label immunofluorescence of GA

55 Moreover, we show that these scored data can be processed for downstream analyzes identical to those

56 ons through the rostrocaudal extent of brain were processed for dual immunocytochemical localization

57 nd sham operated (n=3) and normal (n=3) rats were processed for dual label immunohistochemical study

58 The animals were killed and one lung was processed for electron microscopy and morphometry.

59 One week post-surgery, hippocampal tissue was processed for electron microscopy and synapse densit

60 CA1 was processed for electron microscopy and unbiased stere

61 d, and Vibratome sections from pars caudalis were processed for electron microscopy.

62 for treatment of pharmacoresistant seizures were processed for electrophysiological, histological, a

63 l dorsal pons, from colchicine-treated rats, were processed for EM-1 and corticotropin releasing fact

64 of 1171 FF-OCT human cancer biopsies, which were processed for end-to-end completion in 92 h, produc

65 Some retinas were processed for eNOS protein or phosphorylated/total

66 At the end of follow-up, corneal specimens were processed for enumeration of Langerhans cells and h

67 were sacrificed and portions of their livers were processed for examination of microscopic pathology

68 (350-400 degrees C) at which fluoropolymers are processed; for example, at 350 degrees C the half-li

69 ape trials and sections through the striatum were processed for FLI.

70 Fresh-drawn peripheral blood samples were processed for flow cytometric analysis of T-cell po

71 nderwent loud noise stress, and their brains were processed for fluorescent immunohistochemical detec

72 Dorsal root ganglia (T10-S2) were processed for fluorescent immunohistochemistry and

73 The NG and DRG (T5-T13) were processed for fluorescent immunohistochemistry and

74 Brain and lumbosacral spinal cord were processed for Fos immunohistochemistry at 1 h posti

75 rs after inflammation, and brainstem tissues were processed for Fos-Fluorogold double immunocytochemi

76 Excess tissue was processed for gene profiling.

77 vascularization and microglial activation or were processed for genetic and proteomic analysis.

78 serial sagittal sections of embryos (E12-15) were processed for glutamic acid decarboxylase (GAD)-65

79 widespread contamination from lead-rich ore being processed for gold, and environmental management w

80 7 days of withdrawal after which the brains were processed for Golgi-Cox staining and analysis of de

81 ssayed using the forced swim test and brains were processed for Golgi-Cox staining and analyzed for d

82 ks following nicotine administration, brains were processed for Golgi-Cox staining.

83 Upon completion of treatment brains were processed for Golgi-Cox staining.

84 Enucleated eyes were processed for hematoxylin and eosin (H&E) staining.

85 Animals were killed on P-6, and their brains were processed for high-performance liquid chromatograph

86 weeks of age, and their lumbar spinal cords were processed for histo- and immunohistochemistry.

87 Mouse joint cartilage was processed for histologic examination or biochemical

88 Brain tissue was processed for histologic examination.

89 ed without scrape the last week (WW) corneas were processed for histologic analysis and transmission

90 crificed 6 months postloading, and specimens were processed for histologic and histometric analyses.

91 The eyes were processed for histologic evaluation.

92 G recordings were performed, and animal eyes were processed for histologic examination.

93 After MR imaging, transplanted lungs were processed for histologic examination.

94 Eyes were processed for histologic study after functional tes

95 Specimens from 49 cadaveric entheses were processed for histologic study, and all soft tissue

96 Mouse ear pinnae were processed for histologic, transcriptomic, and prote

97 ee weeks after transplantation, spinal cords were processed for histological analysis.

98 Brains of comatose ALF mice were processed for histological and biochemical analyses

99 ls were killed after birth, and their brains were processed for histological and electron microscopic

100 Samples were processed for histological and immunohistochemical

101 Myocardial samples from 2 patients were processed for histological and immunohistochemical

102 Kidneys were processed for histological evaluation, Western blot

103 s, the animals were sacrificed and the teeth were processed for histological evaluation.

104 he second transplant and the heart and liver were processed for histology and cytokine mRNA expressio

105 Biopsies were processed for histology and for human papillomaviru

106 thout anterior or whole pituitary glands and were processed for histology and image analysis.

107 Eyes were processed for histology and immunofluorescence.

108 Brains were processed for histology and immunohistochemistry.

109 Biopsies were processed for histology and RNA extraction.

110 Alternating portions from each SLN were processed for histology and the BLN Assay.

111 Tissues were processed for histology or the isolation of total R

112 Six hours later, the corneas were processed for histology, and TUNEL staining was per

113 Samples were processed for histology, immunohistochemistry, and

114 Tissues and cells were processed for histology, immunohistochemistry, colo

115 All eyes were processed for histology.

116 orneal buttons retrieved during keratoplasty were processed for histology.

117 The right kidneys were processed for histology.

118 ed after 2 weeks and the explanted scaffolds were processed for histology.

119 nd of testing, animals were killed, and eyes were processed for histology.

120 peroxia-injured and room air control animals were processed for histopathologic examination.

121 utopsy from three deceased Covid-19 patients was processed for hyaluronan histochemistry using a dire

122 Mini-BALs were processed for identification, quantitation, and ant

123 Cell lysates were processed for IGFBP-3 ELISA analyses and Western bl

124 Every fourth section through the NTS region was processed for immunocytochemical detection of tyrosi

125 n to fourteen days after recovery, the brain was processed for immunocytochemical identification of c

126 ed with 4% paraformaldehyde and brain tissue was processed for immunocytochemical staining of GABA ne

127 The retinas were processed for immunocytochemical and morphometric a

128 Brain sections were processed for immunocytochemical detection of astro

129 Forebrain sections were processed for immunocytochemical detection of PHA-L

130 fused with fixative 3-5 d later, and tissues were processed for immunocytochemical detection of trans

131 l tissue sections through the caudal medulla were processed for immunocytochemical localization of th

132 Harvested tissue was processed for immunocytochemistry and prepared by ul

133 The brains were processed for immunocytochemistry for Fos, an immed

134 s from 12 SZ, 15 BD, and 15 control subjects were processed for immunocytochemistry for SST and neuro

135 Retinas from RCS and control (RCS-rdy+) rats were processed for immunocytochemistry using antibodies

136 Adult Sprague-Dawley rats were processed for immunocytochemistry with olfactory ma

137 Corneas were processed for immunocytochemistry, and sequential d

138 Pretreatment tumor tissues were processed for immunofluorescence with anti-MRE11 an

139 transcardially perfused and tissue sections were processed for immunogold-silver localization of DOR

140 Adjacent sections were processed for immunohistochemical analysis (as need

141 perfused at 4-h intervals, and their brains were processed for immunohistochemical detection of PER1

142 Samples were processed for immunohistochemical evaluation.

143 Available paraffin-embedded tissue blocks were processed for immunohistochemical staining.

144 g the initial CFA injection, the knee joints were processed for immunohistochemistry analysis using a

145 tinal wholemounts from mice aged 3-11 months were processed for immunohistochemistry and analyzed.

146 Bronchial biopsy specimens were processed for immunohistochemistry and electron mic

147 lysates from embryonic day 16 through adult were processed for immunohistochemistry and immunoblotti

148 viorally (open field test), and their brains were processed for immunohistochemistry and stereology.

149 The heart and spleen were processed for immunohistochemistry cellular analyse

150 Additional mice were processed for immunohistochemistry or Western blot

151 fter CNV was induced, eyes of recipient mice were processed for immunohistochemistry to detect GFP an

152 sus monkeys, and the brains of these animals were processed for immunohistochemistry with an antibody

153 Bronchoscopy samples were processed for immunohistochemistry, and sputum for

154 Additional mice were processed for immunohistochemistry, electron micros

155 ly perfused with fixative, and brain tissues were processed for immunohistochemistry.

156 a neuroanatomical array: rat brain sections were processed for immunohistochemistry/double labeling

157 Human corneas were processed for immunolocalization studies or separat

158 rried out and impression cytologic specimens were processed for immunoperoxidase staining for MMP9 an

159 brains were sliced and sets of SCN sections were processed for immunoreactivity (ir) detecting the F

160 e obtained from 30 donors (ages 16-75 years) was processed for in situ hybridization to detect messen

161 Sections of human OA synovium were processed for in situ hybridization and probed for

162 sections containing the labeled BOTZ neurons were processed for in situ hybridization by using digoxi

163 s of haloperidol-treated and control monkeys were processed for in situ hybridization histochemical a

164 irs of schizophrenic and comparison subjects were processed for in situ hybridization histochemistry

165 Brains were processed for in situ hybridization using specific

166 Serial sections of the umbilical cord vein were processed for in situ hybridization, and immunocyto

167 intervals of 6 hours to 6 weeks, eye tissues were processed for in situ hybridization, Northern blot,

168 used with 4% paraformaldehyde and the brains were processed for in situ hybridization.

169 The brains of these rats were processed for in situ hybridization.

170 At the end of each experiment, hearts were processed for infarct size determination and analys

171 collected from children aged <= 5 years, and were processed for isolation and molecular characterizat

172 Lungs were processed for leukocyte and bacterial counts and cy

173 Tissue was processed for light and electron microscopy and immu

174 and 24 hr, tissue from the injury epicenter was processed for light and electron microscopy, and the

175 d transgenic pigs, newborn to 20 months old, were processed for light and electron microscopic immuno

176 They were processed for light and electron microscopy and ana

177 t the dogs were killed humanely, and corneas were processed for light and electron microscopy and imm

178 entative areas from the macula and periphery were processed for light and electron microscopy.

179 After the recordings, the eyes were processed for light and transmission electron micro

180 The eyes were processed for light microscopy, and seven variables

181 The corneal buttons were processed for light, transmission, and scanning ele

182 e decolorized/matrix removed sample solution was processed for LLME for target analyte's pre-concentr

183 The cell layers were processed for matrix antigen (collagen I, glomerula

184 The hearts were processed for measurements of postmortem LV volume

185 he end of culture, the constructs or pellets were processed for messenger RNA (mRNA) analysis by quan

186 Isolated RNA was processed for microarray analysis using a commercial

187 y into SP and non-SP cells, and purified RNA was processed for microarray analysis with an oligonucle

188 RNA was processed for microarray-based expression profiling.

189 Human, porcine, and mouse tissues and cells were processed for molecular biological, immunohistochem

190 ional measurements, and the contralateral MA was processed for morphologic measurements.

191 Sections of arteries were processed for morphological measurements.

192 Eyes were processed for morphometric analysis and detection o

193 Then, the specimens were processed for morphometric analysis of bone loss, a

194 Specimens from the mandible were processed for morphometric and microcomputed tomogr

195 8 weeks of incubation, MGIT culture aliquots were processed for mSDA analyses.

196 ected to 80% oxygen (24 h), and their brains were processed for myelin basic protein staining.

197 lowing survival times of 7-120 days, animals were processed for NADPH-d histochemistry.

198 Three days later, hippocampal sections were processed for neuronal degeneration using a silver

199 Tissue samples were processed for next generation sequencing, quantitat

200 inflammatory cells synthesize NGF, sections were processed for NGF in situ hybridization and immunoh

201 Alternate sections were processed for Nissl cytoarchitecture or acetylcholi

202 Hippocampal sections were processed for Nissl stain, Prox1-immunocytochemistr

203 ughout the medulla, and every eighth section was processed for NK-1R-LI neurons.

204 sections through the ventromedial shell that were processed for NK1/SP labeling, 46% of the NK1-immun

205 Rat hippocampal sections were processed for NOS immunohistochemistry, photographe

206 Alternate brain sections were processed for OFQ/N or NOP mRNA in situ hybridizati

207 7, 15, 30, and 50 days, maxillary fragments were processed for paraffin embedding or for transmissio

208 ments of maxilla containing the right molars were processed for paraffin embedding.

209 AVFs or contralateral internal jugular veins were processed for PCR, immunofluorescence, immunohistoc

210 Corneas were processed for permeability measurements or f-actin

211 e ventral medulla and single-tissue sections were processed for peroxidase localization of BDA and go

212 Tissue sections through the LC were processed for peroxidase or gold-silver labeling of

213 Protein lysates were processed for phosphoprotein assays and a wound hea

214 Clusters were processed for PKC activity assay 5-120 min after el

215 Adult retinas and optic nerves were processed for plastic-embedded 1-microm sections, a

216 Nasopharyngeal cultures were processed for pneumococcal isolation and serotyping

217 These profiles were processed for predicting genomic similarities with

218 olysosomes and enter the cytosol, where they are processed for presentation by MHC class I molecules

219 sm, a location from which antigenic peptides are processed for presentation to CD8(+) T cells.

220 ted to endosomal compartments where antigens are processed for presentation to class II-restricted T

221 the cytosol of the living cell, where it can be processed for presentation by major histocompatibilit

222 indicating that exogenously delivered Ag can be processed for presentation by MHC class I molecules.

223 n internalize, traffic to the lysosomes, and be processed for presentation by MHC molecules.

224 that prematurely terminated polypeptides can be processed for presentation via the MHC I pathway.

225 proteins conjugated to the tracer particles were processed for presentation by monocytes and could i

226 prior to the pandemic (SARS-CoV-2 negative), were processed for quantification of bioactive lipids an

227 BAL was processed for quantitative cultures, total cell coun

228 After 3 weeks, lung tissue was processed for quantitative image analysis of smooth

229 ated 20 min after infusion onset, and brains were processed for quantitative autoradiography.

230 e examined up to 6 weeks after SCI and cords were processed for quantitative histopathological analys

231 onal sections through the dorsal hippocampus were processed for quantitative peroxidase immunohistoch

232 Tissues from the right hemisphere were processed for quantitative RT-PCR analysis of BDNF

233 Maxillary gingival tissues were processed for real-time polymerase chain reaction (

234 Muller cells lysates were processed for real-time polymerase chain reaction t

235 s were euthanized, and both carotid arteries were processed for real-time reverse transcription-polym

236 plasmic production suggests that they should be processed for recognition by CTLs.

237 Cells were processed for reduced glutathione (GSH) measurement

238 The solutions of peroxynitrite are processed for removal of IPA and isoamyl alcohol by

239 eaction in which double-strand breaks in DNA are processed for repair by homologous recombination.

240 The eyes were processed for retinal morphology.

241 ents, placental specimens collected at birth were processed for RNA sequencing.

242 NA collected from these treatment conditions were processed for RNAseq.

243 llowing the Spalteholtz method and the other was processed for routine histologic examination.

244 One joint was processed for routine histological analysis.

245 The remaining blocks were processed for routine histologic examination.

246 he mice were killed, and their external ears were processed for routine histology and immunohistochem

247 Left eyes were processed for routine histology.

248 quantitative bacteriology; selective sutures were processed for scanning electron microscopy (SEM).

249 ings of long-finned pilot whales in Scotland were processed for scanning electron microscopy observat

250 At day 10, specimens were processed for scanning electron microscopy.

251 After 1, 2, 3, or 6 days in culture, tongues were processed for scanning electron or light microscopy

252 uch localization is consistent with myocilin being processed for secretion but is also consistent wit

253 At euthanasia, tissues were processed for semiquantitative histopathology or qu

254 d of less than 30 in the diagnostic PCR test were processed for sequencing.

255 Retinal tissue from an adult macaque was processed for serial block-face scanning electron mi

256 Trigeminal ganglion tissue sections were processed for single or double immunohistochemistry

257 wley rats at postnatal days 1, 6, 12, and 18 were processed for single- and double-label immunocytoch

258 Mouse lacrimal glands were processed for single- and double-label indirect imm

259 Mouse LGs were processed for single- and double-labeled indirect i

260 Mouse PPG and lacrimal glands were processed for single- and double-labeled indirect i

261 t, after a short-term infection (5 h), cells were processed for single-cell cloning and analyzed for

262 Six adult human corneas were processed for single-cell RNAseq and 16 cell cluste

263 C samples and 10 matched normal lung samples was processed for small RNA species and profiled on MirV

264 -DOPA for 1, 5, or 10 d, and striatal nuclei were processed for snRNA-seq.

265 Adjacent sections were processed for somatostatin immunoreactivity or Timm

266 A selection of cases (n=18) was processed for spatial transcriptomics analysis.

267 To assess tumor burden, sections were processed for standard hematoxylin-eosin (H&E) stai

268 After NLM examination, specimens were processed for standard paraffin-embedded histology

269 ak of developmental apoptosis in the retina, were processed for TdT-dUTP terminal nick-end labeling (

270 us of the nucleus tractus solitarius (dlNTS) was processed for the histochemical visualization of tra

271 injected into these neurons, and the tissue was processed for the visualization of HRP and biotinami

272 Tissues were processed for the analysis of differentially expres

273 ucleus basalis magnocellularis, and striatum were processed for the combined immunocytochemical detec

274 Additional sections were processed for the concurrent demonstration of two o

275 s from 2 demented and 4 nondemented subjects were processed for the demonstration of Abeta immunoreac

276 were killed, and alternate cortical sections were processed for the demonstration of BDA or CO.

277 F mRNA, and tissues from the left hemisphere were processed for the detection and quantification of B

278 AEC) DNA could be identified from cards that were processed for the evaluation of fecal occult blood.

279 y capsules for 5 d, after which their brains were processed for the immunocytochemical detection of P

280 Brains and orbital tissues were processed for the immunohistochemical detection of

281 Alternate histological sections were processed for the visualization of somatostatin and

282 Brainstem and spinal cord sections were processed for tracers transported by cutaneous affe

283 After 1,2, and 4 weeks, eyes were processed for transmission electron microscopy (TEM

284 of the optic disc, using a 2-mm trephine and were processed for transmission electron microscopy (TEM

285 libitum for 6 and 9 wk or pair-fed for 9 wk were processed for transmission electron microscopy.

286 as from cases that mandated conversion to PK were processed for transmission electron microscopy.

287 Equivalent rats were processed for transmission EM.

288 l putamen and substantia nigra pars compacta were processed for tyrosine hydroxylase and dopamine tra

289 crRNAs from the 7 shared CRISPR loci in Pfu are processed for use by all 3 effector complexes, and N

290 rom field-grown, disease-free plants and RNA was processed for use with the full-genome Affymetrix mi

291 ary adenocarcinomas obtained from these rats were processed for vascular density analysis via CD-31 i

292 sulfate, the so-obtained renal ECM scaffolds were processed for vascular imaging, histology, and cell

293 tre sections obtained throughout the medulla were processed for vesicular glutamate transporter-2 (VG

294 (1) generation adults) of EHDV-2 fed females were processed for viral detection through RT-qPCR and p

295 Animal tissues were processed for viral load determination, histopathol

296 d from two captive and four wild populations were processed for virome characterization using both ap

297 mosaic, so that every point in visual space is processed for visual primitives such as contrast and

298 f the experimental sample and how the sample was processed for visualization.

299 Tissues from infant human and rabbit hearts were processed for Western and in vitro kinase analysis.

300 fusion, and control sham operated (n=3) rats were processed for Western blotting to quantify nestin.