ライフサイエンスコーパス: microdissect

1 d stromal compartments of 23 ICCs were laser microdissected.

2 mpartments from 23 tumors were laser capture microdissected.

3 mples, either containing >75% tumor cells or microdissected.

4 s aged 52 to 82 years old were laser capture microdissected.

5 10 early adenomas were Feulgen-stained and microdissected.

6 Microdissected adenomas showed multiple fission events,

7 1 expressed sequence tags from laser capture microdissected adult mouse gastric and small intestinal

8 with single-cell RNA sequencing from murine microdissected advanced atherosclerotic lesions with smo

9 s, adenoma, and early and advanced HCCs were microdissected after morphological and immunohistochemic

10 Real-time RT-PCR analysis was applied on microdissected airways.

11 in changes during normal lung development in microdissected alveolar tissue containing only 4,000 cel

12 s representative of the four subclasses were microdissected and allelotyped using genome-wide single

13 ular and extraocular parts of the tumor were microdissected and analyzed separately.

14 lonic adenomas and a hyperplastic polyp were microdissected and characterized for genetic lesions.

15 Individual crypts were microdissected and genotyped; clonal dependency analysis

16 (DMM), and articular cartilage samples were microdissected and subjected to microarray analysis.

17 Different brain regions were microdissected and subjected to real time RT-PCR for neu

18 e centromeric region of the X chromosome was microdissected and the isolated DNA was microcloned.

19 es including epicenter and dorsal column was microdissected and used for further study.

20 The organ of Corti was microdissected, and indirect immunohistochemistry was pe

21 Negative units were laser-capture microdissected, and mutations were identified by polymer

22 ooled sclerae of 3- and 8-week-old mice were microdissected, and total RNA was isolated.

23 ome analyses were performed on laser-capture-microdissected areas of specific epithelial structures f

24 e measured the concentrations of N/OFQ in 47 microdissected areas of the central nervous system of ad

25 Comparison of MLPA data obtained from microdissected areas of the UMs showed heterogeneity in

26 erse transcription-PCR for NKX3.1 mRNA using microdissected atrophy revealed a concordance with prote

27 over, apoptosis gene array screening of K15+ microdissected basal cells demonstrated a dominant trend

28 R-SRF signature is sufficient to distinguish microdissected benign and malignant prostate samples, an

29 iR-182 with mRNA expression in laser-capture microdissected benign prostate epithelium was used to pr

30 tive genomic hybridization (CGH) analyses of microdissected blebs, fluorescence in situ hybridization

31 DNA was extracted from laser microdissected brain material, and HHV-6 genomic sequenc

32 nges in estrogenic signaling capacity within microdissected brain nuclei that are important for socia

33 microarray analysis on highly discrete laser-microdissected brain regions.

34 malin-fixed paraffin-embedded prostates were microdissected by laser-capture microdissection (Arcturu

35 essment of gene expression, on laser capture microdissected c-jun(-/-) mammary epithelium, showed tha

36 s-linking assay and Western blot analysis of microdissected CA1 area of hippocampal slices obtained 1

37 hormone-treated cell lines and laser-capture microdissected cancer tissues.

38 individual lipid droplets containing Mldp in microdissected cardiac muscle fibers.

39 Laser capture microdissected CD68(+) macrophages from atherosclerotic

40 from pools of 500 individually laser-capture microdissected cells of specific germ cell subtypes from

41 e expression profiles of human ameloblastoma microdissected cells were characterized with the purpose

42 By using small pools of microdissected cells, 10cRNA-seq improves technical per-

43 oire of techniques for molecular analysis of microdissected cells, laser microdissection allows host

44 tion procedure enabling RNA sequencing of 10 microdissected cells.

45 ws for the recovery of high-quality RNA from microdissected cells.

46 -molecule genomic data derived from multiple microdissected colorectal cancer glands per tumor, along

47 equencing and gene expression arrays from 95 microdissected control and diseased tubule samples and 5

48 Using microdissected coronary arterial endothelial cells (CAEC

49 We analyzed DNA isolated from 50 microdissected CRC cases, including 35 sporadic and 15 I

50 MP of DNA from microdissected cytology slides and from discarded supern

51 e that mutational profiling (MP) of DNA from microdissected cytology slides and supernatant specimens

52 We used laser-microdissected DA neurons for RNA extraction and next-ge

53 ied by microarray in samples of individually microdissected deep layer 3 pyramidal cells from a subse

54 l and high-throughput transcriptomic data of microdissected dental cells unveils the critical importa

55 Total RNA was isolated from microdissected dentate gyrus and processed for RT-PCR an

56 pilla cells reflected similar differences in microdissected dermal papilla isolated from intact beard

57 To examine these competing hypotheses, we microdissected discrete subregions containing approximat

58 lex signaling pathway were assessed in laser-microdissected DLPFC layer 3 and 5 pyramidal cells and l

59 lex signaling pathway were assessed in laser-microdissected DLPFC layer 3 and 5 pyramidal cells and l

60 We screened 40 laser-microdissected DPC samples and 6 pre-invasive lesions fo

61 has been used to quantify biogenic amines in microdissected Drosophila melanogaster brains and brain

62 Notably, miR-223 expression was lost in microdissected ductal carcinoma in situ (DCIS) from pati

63 LUT3, GLUT4, GK, and SUR1 transcripts in the microdissected DVC, VMH, and LHA from groups of male rat

64 genes that were differentially expressed in microdissected early PanIN lesions (PanIN-1B/2) compared

65 y gene expression profiles were obtained for microdissected embryonic mouse lens at three key develop

66 Using microdissected embryonic tissue from somitic and presomi

67 oneurial endothelial cells and laser-capture microdissected endoneurial microvessels from four cryopr

68 Laser capture microscopy was used to microdissect epithelia from areas of colons that showed

69 quantitative real-time PCR of laser capture microdissected epithelial cells, Her-2 and epidermal gro

70 Lysates prepared from separately microdissected epithelium and stroma were analysed using

71 croarrays to analyze RNA from laser-captured microdissected epithelium and underlying stroma from nor

72 We apply the method to laser-capture-microdissected esophageal adenocarcinoma tissue, reveali

73 ce and copy number analyses of laser capture microdissected fallopian tube lesions (p53 signatures, s

74 T1 mRNA expression is greater (80%) in laser microdissected FC layer I GABAergic neurons than in the

75 anged immunoglobulin genes in the B cells of microdissected follicles revealed clonal amplification,

76 nd rostral ventrolateral medulla (RVLM) were microdissected for gene expression and protein analysis

77 files from whole-thickness and laser-capture microdissected, formalin-fixed, paraffin-embedded tissue

78 enome-wide methylation of DNA extracted from microdissected fresh frozen or formalin-fixed paraffin-e

79 h adjacent normal epithelial cells that were microdissected from 31 prostate cancer specimens using l

80 ections and from two to nine different areas microdissected from 32 FFPE UMs.

81 Individual crypts (range, 8-21 crypts) were microdissected from across 17 lesions from 10 patients.

82 Glomeruli were microdissected from biopsy samples of 20 patients with L

83 Transdifferentiated myocytes from BMSCs were microdissected from cocultures by laser captured microdi

84 of gene expression in large dysplastic cells microdissected from cortical dysplasia surgical specimen

85 inin and parvalbumin interneurons were laser microdissected from dorsolateral prefrontal cortex layer

86 ,000 formalin-fixed, paraffin-embedded cells microdissected from each compartment.

87 n profiling using RNA from 800 to 4400 cells microdissected from ethanol-fixed, paraffin-embedded ute

88 nd normal populations of photoreceptors were microdissected from fresh frozen tissue, RNA was purifie

89 Embryonic day 11.5 metanephroi were microdissected from Hoxb7-green fluorescence protein mic

90 ear using auditory and vestibular endorgans microdissected from human temporal bones obtained at aut

91 nd concentric vascular lesions were serially microdissected from lung explant tissue derived from 7 F

92 Samples were microdissected from mouse embryos at E9-E15 in half-day

93 ics was performed on neurofibrillary tangles microdissected from patients with advanced Alzheimer's d

94 Intrahepatic bile duct units (IBDUs) were microdissected from rat liver then luminal pH was examin

95 RPE sheets were microdissected from rats exposed to NT in drinking water

96 RPE sheets were microdissected from rats exposed to NT in drinking water

97 zen sections, hepatocytes were laser-capture microdissected from several sites within individual CCO-

98 RVs and intact myofibers were laser microdissected from skeletal muscle of 18 sIBM patients

99 g spinal cord glial cells (white matter, WM) microdissected from SMN-deficient SMA mouse model at pre

100 Expression profiling of individual nuclei microdissected from the dorsal thalamus revealed additio

101 In this study, 12 distinct regions were microdissected from the mouse brain and regional changes

102 , we performed microarray analysis on tissue microdissected from the prospective rhombomere 3-5 regio

103 xpression in homogenous populations of cells microdissected from the stratum basale, stratum spinosum

104 ountered when studies are performed on cells microdissected from tissues derived from animal models o

105 te, epithelium and stroma were laser-capture microdissected from ventral, dorsolateral, and anterior

106 l cells from Arabidopsis thaliana were laser-microdissected from whole leaves to generate a focused c

107 T could detect cells with distinct genotypes microdissected from within the same FFPE sample.

108 cases, we found that adjacent laser-capture microdissected G3 and G4 tumors had identical TMPRSS2:ER

109 Both quantitative RT-PCR measurements of microdissected GC cells from tonsils showed that GC cell

110 ctivated cell sorter (FACS)-sorted cells and microdissected GC cells.

111 re compared to those obtained from the laser-microdissected GCL of epileptic patients, identifying se

112 Quantitative PCR of microdissected glands confirmed this trend (P=0.001).

113 Here, we show that data derived from non-microdissected glioblastoma multiforme tumor tissue is e

114 ed a set of 16 promising candidate miRNAs in microdissected glomeruli a confirmation set of 20 human

115 analyzed the expression profile of miRNA in microdissected glomeruli and found that miR-324-3p was t

116 mic analysis performed on laser-captured and microdissected glomeruli and tubulointerstitium identifi

117 sed proteomic analysis of laser-captured and microdissected glomeruli and tubulointerstitium was perf

118 Moreover, microdissected glomeruli from patients with small vessel

119 RNA from microdissected glomeruli of paraffin-embedded tissue was

120 proteoglycans and growth factors from laser-microdissected glomeruli, arterial tunicae mediae, and n

121 bolite analyses, and transcript profiling of microdissected grain tissues.

122 gene expression studies using laser capture microdissected granulomatous lung tissues revealed that

123 ults of fluorescent in situ hybridization of microdissected GRC probes and their sequencing indicate

124 BPA and MBP, and transcriptomic analysis of microdissected heart tissues showed that both chemicals

125 ed by midgut derivatives, long-term-cultured microdissected hepato-biliary-pancreatic organoids devel

126 mic hybridization (aCGH) was performed on 42 microdissected high-grade serous ovarian tumor samples.

127 y, miRNA microarrays were performed on laser-microdissected hippocampal granule cell layer (GCL) and

128 e, a genome-wide transcriptional analysis of microdissected HRS cells compared with other B-cell lymp

129 Here we examined microdissected HRS cells from 29 CHL patients and 5 CHL-

130 lated in HL cell lines, most primary HL, and microdissected HRS cells of 3/5 cases, but not in normal

131 y differentially regulated transcripts in 44 microdissected human kidney samples.

132 Finally, we show in laser capture microdissected human prostate cancer samples and the pro

133 rays using magnetic sorted and laser-capture microdissected human prostate cells with levels of expre

134 As the anagen-to-catagen transformation of microdissected human scalp HFs can be observed in organ

135 M2, M4, and M5 were detected in microdissected immature (postnatal days 10-13) inner hai

136 s, D1, D2, and D5 receptors were detected in microdissected immature (postnatal days 10-13) spiral ga

137 Normal appearing single crypts were laser microdissected in placebo- and sulindac- treated FAP pat

138 (alphaMHC)mCherry(-) (noncardiac) cells from microdissected infarcts within 6 h of infarction underwe

139 -PCR and quantitative real-time PCR of laser microdissected islets for gene expression of proinflamma

140 being recognized preferentially in any of 7 microdissected kidney compartments was also examined.

141 Previous research has used RNA sequencing in microdissected kidney tubules or single cells isolated f

142 tion) and microarray gene expression data of microdissected, laser-captured and FACS-sorted component

143 roteins and phosphoproteins in laser capture microdissected (LCM) primary tumors from a study set of

144 ng optic fissure closure using laser capture microdissected (LCM) tissue from the margins of the fiss

145 n using microarray analysis of laser capture microdissected (LCM) tissues.

146 ne levels were determined in whole and laser microdissected liver tissue by proteome array.

147 s then shown to correlate with that in laser-microdissected lung from the same individuals (Chi2 = 52

148 tissue (MGT), milk somatic cells (SC), laser microdissected mammary epithelial cells (LCMEC), milk fa

149 (hypomethylation) and AIM1 were analyzed in microdissected melanoma PEAT sections.

150 GeneChip analysis of laser-capture-microdissected mesenchymal cells coupled with immunohist

151 ment in neurotransmitter-related pathways in microdissected-migrating nondiabetic and diabetic KCs.

152 The transcriptome of microdissected MIUCB was enriched in genes that drive ep

153 Microdissected mononuclear cells had an activated phenot

154 th spinal cord homogenates and laser capture microdissected motor neurons to determine the mechanisms

155 his, transcriptome analysis of laser capture microdissected Mtgr1(-/-) intestinal crypts revealed Not

156 quantitative RT-PCR studies of laser capture microdissected mucosa and yielded a series of biomarkers

157 erential expression between 31 laser-capture-microdissected nasopharyngeal carcinomas (NPCs) and 10 n

158 ription of murine G3 in specific segments of microdissected nephron, and demonstrated additional G3 e

159 re, through a transcriptome analysis of frog microdissected neural border, we identified an extended

160 he molecules that mediate the transition, we microdissected neuroepithelial cells and compared their

161 Laser microdissected neurons extracted from preplaque amyloid

162 To demonstrate this technique we microdissected neurons from archived tissue blocks of th

163 ss, we examined mRNA levels in laser-capture microdissected neurons from Grade 1 HD caudate compared

164 munohistochemistry, and molecular studies of microdissected neurons.

165 is method we identified over 400 proteins in microdissected neurons; on average 78% that were neurona

166 Transcriptome analyses of laser-capture microdissected nigral dopaminergic neurons in rats and s

167 croarrays, we acquired gene profiles from 32 microdissected non-small-cell lung tumors.

168 ly relevant nuclear genes from laser-capture microdissected non-tangle-bearing neurons from autopsy b

169 Microarray analysis of microdissected noninvasive bronchioloalveolar carcinoma

170 rly PanIN lesions (PanIN-1B/2) compared with microdissected normal duct epithelium.

171 expression in uncultured PBMCs and in laser microdissected normal lung epithelial cells (MNLEC) from

172 d gene expression profiling of laser capture microdissected normal non-neoplastic prostate epithelial

173 Using microdissected, normal human craniofacial structures, we

174 upled with direct amplification of rDNA from microdissected nuclei by polymerase chain reaction, supp

175 Microdissected OHC and DC quantitative reverse transcrip

176 We microdissected omental arterioles from tissue layers not

177 uman prostate cancer specimens laser capture microdissected on the basis of MYC immunohistochemistry,

178 rative profiling of other tissues, including microdissected oocytes and somatic cells, revealed disti

179 ignificantly down-regulated in laser capture microdissected oral cancer epithelia.

180 6 weeks), the same transcripts were found in microdissected organ of Corti and spiral ganglion sample

181 Therefore, we have explored whether microdissected, organ-cultured, human scalp hair follicl

182 ng sophisticated laser capture techniques to microdissect out bulge cells.

183 of proteins from cultured ocular tissues and microdissected outer and inner retinas, as well as from

184 erse transcription (RT)-PCR using a panel of microdissected ovarian tumors.

185 pression and donor/recipient origin in laser-microdissected p53+ tumor cells.

186 oxyphil and chief cells, and laser-captured microdissected PA specimens demonstrate polyclonality in

187 This study, analysing laser microdissected paired benign and malignant prostate epit

188 ctions displaying the most extensive but not microdissected PanIN-2/3 lesions were used in order to o

189 heterozygosity (LOH) maps from laser capture microdissected paraffin-embedded samples using as little

190 ysplasia, high-grade dysplasia, and EA using microdissected paraffin-embedded tissues from 11 patient

191 24 PDAC tumors, including 15 laser-captured microdissected PDAC and 9 patient-derived xenografts, to

192 adenocarcinoma (PDAC) in vivo, a panel of 27 microdissected PDAC specimens were analysed using high-d

193 Genomic DNA samples from laser-capture microdissected PDACs and adjacent PanIN2 and PanIN3 lesi

194 s PDAC xenografts in mice, and laser capture microdissected PDACs from patients (n=91).

195 eam pathways, we performed gene profiling of microdissected pharyngeal arch one (PA1) from Tbx1(+/+)

196 ription factor mRNAs) was assayed in single, microdissected phospho-S6-immunolabeled BCs and GCs as a

197 ication of more than 1000 proteins from each microdissected piece.

198 RNA samples prepared from laser-capture microdissected populations of limbal epithelium were sub

199 Microdissected positive and negative areas from one tumo

200 that are associated with GBC was tested from microdissected preneoplastic lesions using microsatellit

201 Protein analyses of microdissected primary glioma tissue showed up-regulatio

202 We extend these findings to laser-capture microdissected primary Hodgkin Reed-Sternberg cells and

203 ne marrow metastases versus 22 laser capture-microdissected primary prostate cancers was compared usi

204 re protein-coding region of this locus in 30 microdissected prostate adenocarcinomas.

205 ative genomic hybridization of laser-capture microdissected prostate cancer samples spanning stages o

206 strongly with defective LATS2 expression in microdissected prostate cancer tissues.

207 Screening in laser capture microdissected prostate cancer tumors identified miR-182

208 array expression data from 102 laser capture microdissected prostate tissue samples.

209 esults were confirmed in an independent, non-microdissected, publicly available protein data set from

210 Laser capture microdissected pulmonary artery profiles in combination

211 used DNA microarray technology and RNA from microdissected pure epithelial cells to examine changes

212 already apparent in comparing laser-capture microdissected radial and vertical phases of a large pri

213 re we performed microarray analyses in laser microdissected rat ACC after a single or repeated admini

214 es were dramatically enriched in the stained microdissected region of the additional case.

215 nce of corresponding PC molecular species in microdissected regions analyzed by LC/MS/MS.

216 dies recognizing planted antigens from laser-microdissected renal biopsy samples of 20 patients with

217 pecific LacZ expression was also detected in microdissected renal interlobar arteries transduced with

218 ranscriptomic analysis of CCRCCs and matched microdissected renal tubular controls revealed overexpre

219 dentified to a median depth of 8261 genes in microdissected renal tubule samples (105 replicates in t

220 Global miRNA profiling of microdissected renal tubules showed that miRNAs exhibit

221 chemistry and gene analysis of laser capture microdissected retina.

222 ap expression was evaluated in laser-capture microdissected retinal layers of angiogenic lesions and

223 s were analyzed for mRNA using laser capture microdissected RPE cells and by immunohistochemistry for

224 loss of ER-beta expression, was detected in microdissected samples and in cell cultures.

225 erentially expressed genes were confirmed in microdissected samples by real-time quantitative PCR.

226 xpressed significantly in 75% of fresh NSCLC microdissected samples compared to control paired matche

227 Using immunostained, laser capture-microdissected samples from 56 clinical specimens, we de

228 number, with no differences observed in non-microdissected samples.

229 Multi-level and microdissected sampling strikingly reveal that many clon

230 ted panel sequencing including patients with microdissected sarcomatoid and epithelial components.

231 by evaluating the RNA expression profile in microdissected sections using real-time PCR analysis.

232 Using microdissected septal tissue from virgin and age-matched

233 Santa Clara, CA) were used to interrogate 80 microdissected serous LMP tumors and invasive ovarian ma

234 lving CDR3 spectratyping combined with laser microdissected single-cell polymerase chain reaction of

235 uenced transcriptomes of ~100 laser captured microdissected SNpc neurons from each tier from 7 health

236 Here, using laser capture microdissected specimens, we found that the combined hor

237 Microarray analysis of microdissected SPEM lineages induced by DMP-777 showed u

238 progression, we compared gene expression in microdissected squamous epithelial samples from 10 norma

239 mics of exudates, sieve element contents and microdissected stem tissues established that EFP and FP

240 We extracted DNA from laser-microdissected stratum oriens tissue of cornu ammonis 2/

241 Transcriptome profiling of microdissected stromal and epithelial components of high

242 anced high-grade serous ovarian cancer using microdissected stromal ovarian tumour samples and find t

243 Global transcriptional analysis of the microdissected subregions of the hippocampus exposed a C

244 se chain reaction (qRT-PCR) of laser capture microdissected subtissue and fluorescence in situ hybrid

245 hip analyses were performed on laser capture microdissected SV40 TAg-expressing cells in preinvasive

246 Subsequent analyses studied microdissected syncytial cells at 3, 6 and 9 days post i

247 ormulated into mutational load (ML) for each microdissected target analyzed.

248 Using histological features as a guide, we microdissected target cell populations with various hist

249 DNA was extracted from microdissected targets and analyzed for loss of heterozy

250 Microdissected targets histologically classified as inte

251 ML) were defined based on the population of microdissected targets histologically classified as inte

252 All microdissected targets with dysplasia had mutations, wit

253 ated with the histological classification of microdissected targets, with increasingly severe histolo

254 kB and NCAM gene expression in laser capture microdissected taste epithelia were significantly up-reg

255 differentiation of primary MKs and directly microdissected TGCs from embryonic day 9.5 implantation

256 coding VGluT2 or TH in samples of individual microdissected TH immunoreactive (IR) neurons.

257 intraperitoneally within 24 hours of birth, microdissected the gallbladder and extrahepatic bile duc

258 technique for studying this process involves microdissecting the four products (ascospores) of a sing

259 f decade-old materials and exceedingly small microdissected tissue fragments.

260 ped the deletion size of the "second hit" in microdissected tissue from 16 different VHL-associated l

261 DNA was extracted from microdissected tissue obtained from 21 tumors with known

262 Limited total RNA, 100-200 ng, from this microdissected tissue required use of the Atlas SMART tr

263 Qualitative examination of the microdissected tissue revealed that CLANs and CLAN-like

264 Gene analysis was performed on microdissected tissue samples removed from 4-microm thic

265 mens was confirmed by quantitative RT-PCR of microdissected tissue samples.

266 n of GITRL was studied by RT-PCR on RNA from microdissected tissue sections.

267 ng to define large genomic rearrangements in microdissected tissue specimens collected by laser captu

268 lectively isolated tumor cells procured from microdissected tissue specimens.

269 n female VMP were identified with Tag-seq of microdissected tissue, RNA-seq of cell populations, and

270 ptome comparison of FoxJ1-null and wild-type microdissected tissue, we identified candidate genes reg

271 in vivo was confirmed by RT-PCR analysis of microdissected tissue.

272 Thus, our microarray study using microdissected tissues not only provides global informat

273 olymerase chain reaction in whole joints and microdissected tissues of the joint, including the artic

274 qPCR to confirm cell specific expression in microdissected tissues, as well as expression in neonata

275 Using microdissected tissues, we show that TGFBR1*6A is somati

276 yze DNA samples extracted from laser capture microdissected tissues.

277 s fully automated analysis of proteomes from microdissected tissues.

278 Randomly microdissected TRAP(+) OCs from 16 MF patients harbored

279 Analysis of microdissected trophectoderm of the bovine conceptuses r

280 We performed real-time PCR on laser microdissected tubular segments and FACS-sorted renal im

281 -seq datasets from humans and mice and for a microdissected tubule RNA-seq dataset from rat.

282 e) and confirmed as the primary cell type in microdissected tubules and organoids.

283 Using an mRNA microarray on microdissected tubules from a rat model of cyclosporin A

284 ormed whole-exome sequencing analyses of the microdissected tumor and matched nontumor tissues.

285 rom limited numbers of selectively procured, microdissected tumor cells and that two patterns of GBMs

286 -time PCR failed to detect the EBV genome in microdissected tumor cells from any case.

287 how, by phosphoproteomic network analysis of microdissected tumor cells, that interlinked components

288 Transcriptional profiling of microdissected tumor endothelial cells from human ovaria

289 Microdissected tumor epithelium from ER-negative tumors

290 Using DNA from 82 laser-microdissected tumor samples, followed by microsatellite

291 sion of MACC1, Met, and HGF messenger RNA in microdissected tumor tissue and corresponding normal liv

292 allelotyping with microsatellite markers in microdissected tumor tissue from 27 human gastrinomas an

293 ells from fresh specimens were available, 69 microdissected tumors from paraffin tissues, and 10 tumo

294 id-gestation human telencephalon, as well as microdissected upper and deep layers of the prefrontal c

295 esponses were characterized in laser capture microdissected urothelial cells that do or do not contai

296 s, whereas qRT-PCR of RNA from laser capture microdissected ventral horns of normal and wobbler mice

297 multiple library analyses, and 16 had direct microdissected vs. macrodissected replicates.

298 based on accumulation of CD3(+) T cells were microdissected with laser-capture microscopy, and gene t

299 ut microarray analysis of dorsal and ventral microdissected WT retina and found additional photorecep

300 Here, we microdissected Zea mays stomatal complexes and showed th