ライフサイエンスコーパス: be processed for

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

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

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

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

5 Choroids were processed for alkaline phosphatase flat-embedding.

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

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

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

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

10 The brains were processed for both immunocytochemistry and autoradi

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

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

13 2, the animals were perfused, and the brains were processed for c-fos immunocytochemistry.

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

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

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

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

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

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

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

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

22 Selected eyes were processed for complete histopathologic analysis.

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

24 Selected eyes were processed for complete histopathologic analysis; so

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

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

27 All biopsies were processed for conventional histopathologic study, i

28 Explanted hearts were processed for coronary artery histological analysis

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

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

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

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

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

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

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

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

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

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

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

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

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

42 Embryos were processed for detection of labeled cells.

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

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

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

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

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

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

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

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

51 CA1 was processed for electron microscopy and unbiased stere

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

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

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

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

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

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

58 (350-400 degrees C) at which fluoropolymers are processed; for example, at 350 degrees C the half-li

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

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

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

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

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

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

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

66 Excess tissue was processed for gene profiling.

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

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

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

70 7 days of withdrawal after which the brains were processed for Golgi-Cox staining and analysis of de

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

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

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

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

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

76 Mouse joint cartilage was processed for histologic examination or biochemical

77 Brain tissue was processed for histologic examination.

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

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

80 The eyes were processed for histologic evaluation.

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

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

83 Eyes were processed for histologic study after functional tes

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

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

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

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

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

89 Samples were processed for histological and immunohistochemical

90 Kidneys were processed for histological evaluation, Western blot

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

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

93 Biopsies were processed for histology and for human papillomaviru

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

95 Eyes were processed for histology and immunofluorescence.

96 Brains were processed for histology and immunohistochemistry.

97 Biopsies were processed for histology and RNA extraction.

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

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

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

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

102 All eyes were processed for histology.

103 The right kidneys were processed for histology.

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

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

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

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

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

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

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

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

112 The retinas were processed for immunocytochemical and morphometric a

113 Brain sections were processed for immunocytochemical detection of astro

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

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

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

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

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

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

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

121 Corneas were processed for immunocytochemistry, and sequential d

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

123 Adjacent sections were processed for immunohistochemical analysis (as need

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

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

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

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

128 Bronchial biopsy specimens were processed for immunohistochemistry and electron mic

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

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

131 Additional mice were processed for immunohistochemistry or Western blot

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

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

134 Additional mice were processed for immunohistochemistry, electron micros

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

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

137 Human corneas were processed for immunolocalization studies or separat

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

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

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

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

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

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

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

145 Brains were processed for in situ hybridization using specific

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

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

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

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

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

151 Lungs were processed for leukocyte and bacterial counts and cy

152 Tissue was processed for light and electron microscopy and immu

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

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

155 They were processed for light and electron microscopy and ana

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

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

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

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

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

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

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

163 The hearts were processed for measurements of postmortem LV volume

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

165 Isolated RNA was processed for microarray analysis using a commercial

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

167 RNA was processed for microarray-based expression profiling.

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

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

170 Sections of arteries were processed for morphological measurements.

171 Eyes were processed for morphometric analysis and detection o

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

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

174 8 weeks of incubation, MGIT culture aliquots were processed for mSDA analyses.

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

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

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

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

179 Alternate sections were processed for Nissl cytoarchitecture or acetylcholi

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

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

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

183 Rat hippocampal sections were processed for NOS immunohistochemistry, photographe

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

185 7, 15, 30, and 50 days, maxillary fragments were processed for paraffin embedding or for transmissio

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

187 Corneas were processed for permeability measurements or f-actin

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

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

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

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

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

193 These profiles were processed for predicting genomic similarities with

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

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

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

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

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

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

200 BAL was processed for quantitative cultures, total cell coun

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

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

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

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

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

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

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

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

209 Cells were processed for reduced glutathione (GSH) measurement

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

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

212 The eyes were processed for retinal morphology.

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

214 The remaining blocks were processed for routine histologic examination.

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

216 Left eyes were processed for routine histology.

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

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

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

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

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

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

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

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

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

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

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

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

229 Adjacent sections were processed for somatostatin immunoreactivity or Timm

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

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

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

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

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

235 Tissues were processed for the analysis of differentially expres

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

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

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

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

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

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

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

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

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

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

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

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

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

249 Equivalent rats were processed for transmission EM.

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

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

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

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

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

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

256 Animal tissues were processed for viral load determination, histopathol

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

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

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

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