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1 te diagnostic autopsy and minimally invasive tissue sampling).
2 pectrometry (MS/MS) without manipulating the tissue sample.
3 s the spatial distribution of molecules in a tissue sample.
4 e TME often relies on a small representative tissue sample.
5 s performed on 62 HGT1 and 15 matched normal tissue samples.
6 in response to therapy is difficult in human tissue samples.
7 ondrial protein levels in the isolated tumor tissue samples.
8 essing the biochemical composition of intact tissue samples.
9 iled biochemical characterization of complex tissue samples.
10 nd by immunohistochemical analysis of 64 ICC tissue samples.
11 ite-specific chirality mapping of biological tissue samples.
12 the molecular depth with which IMS can probe tissue samples.
13 N-deleted tumor samples than in normal solid tissue samples.
14 s, including cells, isolated organelles, and tissue samples.
15 metrial glandular and stromal regions within tissue samples.
16  spatially defined chemical information from tissue samples.
17 th immunohistology and expression studies in tissue samples.
18 tment-naive ccRCC and paired normal adjacent tissue samples.
19 and methylmercury, MeHg(I) in water and fish tissue samples.
20 cantly increased on MAIT cells from fibrotic tissue samples.
21  analyses of signaling components in patient tissue samples.
22 pressed with a RPKM greater than 5 in the 22 tissue samples.
23 amples and 144 tumour adjacent normal breast tissue samples.
24  mechanics measurements of moving biological tissue samples.
25 c cancer tissue samples compared with normal tissue samples.
26 umerate immune cell subsets from whole tumor tissue samples.
27 d and 187 down-regulated) were identified in tissue samples.
28 will be useful for studying cell mixtures in tissue samples.
29 ma, cervicovaginal fluid (CVF), and cervical tissue samples.
30 ingle-cell level in different types of human tissue samples.
31 urine model of pulmonary fibrosis and in IPF tissue samples.
32 tomated tracing of multispectral fluorescent tissue samples.
33 n metastatic than in archival primary biopsy tissue samples.
34 rified from threespine stickleback intestine tissue samples.
35 t including 26 tumour and 26 adjacent normal tissue samples.
36 h can be reliably monitored in gynecological tissue samples.
37 ir was assessed by PET and gamma counting of tissue samples.
38 ith high degrees of background, such as some tissue samples.
39 ioneering research tool for imaging of large tissue samples.
40 ific protein complexity in primary cells and tissue samples.
41 hat previously went undetected in bulk brain tissue samples.
42  tissue specimens compared to healthy breast tissue samples.
43 ival formalin-fixed paraffin-embedded (FFPE) tissue samples.
44  suitable for large-scale studies in primary tissue samples.
45 isease states using clinical or animal-model tissue samples.
46 btained from ex-vivo culture of these paired tissue samples.
47 e heterogeneous cellular composition of GTEx tissue samples.
48 This workflow is applicable to both cell and tissue samples.
49 evealed genotype concordance in 33 out of 58 tissue samples.
50  test its performance on heterogeneous human tissue samples.
51 ng, which may be routinely used for cell and tissue samples.
52 on biomarkers and drawbacks of limited human tissue samples.
53 ations can also be estimated from bulk brain tissue samples.
54 c and in situ metabolic profiling in complex tissue samples.
55 ular mutations, which require invasive tumor tissue sampling.
56 le-income countries using minimally invasive tissue sampling.
57 curred in vivo is difficult without invasive tissue sampling.
58 equencing or microarray transcriptomics from tissue samples (4 SB and 2 colonic cohorts; n = 495; n =
59 tocol is demonstrated to work on human brain tissue samples, a source that has proven to be difficult
60 xpression levels and cellular composition of tissue samples across the human body.
61 d the AGR2 protein in cells and in the mouse tissue samples administrated with bortezomib.
62 for N-glycans derived from glycoproteins and tissue samples after chemical derivatization.
63 l microbiota (from fecal or colonic or ileal tissue samples) among patients (adult or pediatric) with
64 dance and the hormone receptor status of the tissue sample, an important factor in the prognosis and
65 suspicious for HER2-positive metastases were tissue sampled and examined by pathologic analysis to do
66 ly label administered GO in Solvable-treated tissue samples and (ii) constructed an automatic sample
67  Upper gastrointestinal adenocarcinoma (UGC) tissue samples and cell models demonstrated significant
68 n a retrospective cohort study, we collected tissue samples and clinical data from 150 BE and 285 EAC
69 of mTOR activation, in three iMCD lymph node tissue samples and controls.
70                       We used choroid plexus tissue samples and CSF from mild cognitive impairment (M
71 ow allow imaging of cleared large biological tissue samples and enable the 3D appreciation of cell an
72  genes HRH1 and NSE/ENO2 in KSHV-infected KS tissue samples and KS visceral tissue microarrays.
73 DNA methylation data for 208 pairs of tumour tissue samples and matched healthy control tissue from C
74 munohistochemistry on paraffin-embedded lung tissue samples and quantified in alveolar and bronchial
75 performed on eight resected brain metastasis tissue samples and revealed B-cell related genes to be h
76 n of formalin fixed paraffin embedded (FFPE) tissue samples and shows a high potential for applicatio
77 ncer, where transcriptomic profiling of bulk tissue samples and single cells are routinely employed.
78 MLM platform that is convenient for standard tissue samples and small intact animals.
79 require needle biopsy for minimally invasive tissue sampling and pathological analysis.
80  this study is the investigate the effect of tissue sampling and preservation on candidate genes incl
81 were detectable in plasma, CVF, and cervical tissue samples, and drug release and plasma drug exposur
82  lymphocyte cytotoxicity across 28 870 human tissue samples, and identified the presence of KLRG1 on
83 o cardiovascular disease using small (<5 mg) tissue samples, and it is applicable to other diseases w
84 ng granulomatous inflammation in one or more tissue samples, and the exclusion of alternative causes
85  by shotgun analyses, crosschecking in brain tissue samples, and verification by targeted proteomic a
86 liopancreatic ductal visualization, targeted tissue sampling, and therapeutic intervention.
87  the bioanalytical chemist working in living tissue samples as well as best practices for mitigating
88 ic particles were found in five out of eight tissue samples associated with ceramic implants.
89 caecum, and sigmoid colon and terminal ileum tissue samples at 22 months.
90 both instrumentation and methodology, MSI of tissue samples at single-cell resolution remains challen
91 [CA](n) sequences from hundreds of low-input tissue samples at up to 14 loci.
92 nital development and used the most relevant tissue sample available to study hypospadias.
93  profiling protocol for tumor-normal matched tissue samples based on low-coverage clinical whole-geno
94 form imaging, which in turn, requires that a tissue sample be disintegrated into a suspension of disp
95 on-level) transcriptome analysis on cortical tissue samples (Brodmann areas 20 and 21) from 86 patien
96 nclude PIWI-associated RNAs, tRFs present in tissue samples but not in cells cultured in vitro, and s
97 ecific plasma cells were detected in patient tissue samples by using mass cytometry.
98                                              Tissue sampling by biopsy may be limited by sampling err
99 nitoring lipid distribution and abundance in tissue samples can lead to major inputs in the understan
100 e cells, has enabled the uniform analysis of tissue samples collected at multiple sites and across ma
101 veraging a unique collection of 186 Atelopus tissue samples collected before and after the Bd outbrea
102 kflows were developed to assess ectocervical tissue samples collected from DMPA users and control sub
103                                        Using tissue samples collected opportunistically from wild emp
104 ne 13), in invasive ductal carcinoma patient tissue samples compared to normal breast tissue.
105 ibed as up-regulated in prostate cancer (PC) tissue samples compared with nonmalignant controls; howe
106 ssion of miR-135b-5p in human gastric cancer tissue samples compared with normal tissue samples.
107                           In most noncleared tissue samples, confocal images can be acquired at no mo
108  from RNA-Seq experiments on a collection of tissue samples, considering only genes whose protein pro
109                                         Four tissue samples containing both cancerous and noncancerou
110 d test the system we used 37424 radiographic tissue samples corresponding to eight different parenchy
111         Its database includes 19,127 patient tissue samples covering more than 50 cancer types and ex
112 cal specimens, cell lysates, and mouse liver tissue samples, demonstrating its highly sensitive and s
113 r detail, the DeepDOF microscope can improve tissue sampling during intraoperative tumor-margin asses
114                                        A new tissue sample embedding and processing method is present
115  over 72X sequencing coverage from low titer tissue samples (equivalent to 28.52 Cq using Li 16 S qPC
116  analysis of high-throughput omics data from tissue samples, estimating and accounting for cell compo
117 eased levels of GPER1 compared with nontumor tissue samples; estrogen promoted proliferation of human
118 permeability of both mouse and human colonic tissue samples ex vivo, using the latest equipment and s
119           We show that the location of human tissue samples extracted along the longitudinal axis of
120  extent and effect of the disease, obtaining tissue samples for diagnosis, planning medical or surgic
121 que to obtain eosinophils from human adipose tissue samples for the purpose of downstream molecular a
122 bility trials with percutaneous image-guided tissue sampling for the identification of breast pCR aft
123             Histopathological examination of tissue sample from colonic ulcer biopsy revealed invasiv
124          Sera, cerebrospinal fluid (CSF) and tissue samples from 100 fatal cases with suspected arbov
125                                              Tissue samples from 115 lesions (from 102 women; average
126 quantifications of 80 small GTPases in brain tissue samples from 15 patients.
127 els were assessed by immunohistochemistry in tissue samples from 151 NSCLC patients who had curative
128  polymerase chain reaction (PCR) analysis of tissue samples from 227 prolactinomas.
129 nducted a retrospective study including lung tissue samples from 24 patients with pulmonary LCDD ((p)
130 708 normal-appearing adjacent-to-tumor (NAT) tissue samples from 27 cancer sites and in 7,149 blood s
131 ptase PCR (RT-PCR) screening revealed that 8 tissue samples from 7 patients out of 103 were positive
132               We apply SpAn to primary tumor tissue samples from a cohort of 432 chemo-naive colorect
133 s data from paired tumor and adjacent benign tissue samples from a cohort of breast cancer patients a
134 ed tissue samples from Syrian hamsters and 4 tissue samples from a NiV-infected African green monkey
135             IFITM3 protein is upregulated in tissue samples from a subset of patients with late-onset
136                            Clinical data and tissue samples from BA infants from the Childhood Liver
137 with B-cell follicles and emphysema, in lung tissue samples from control subjects, and in skin, nasal
138 , endomyocardial biopsies (n=2), and cardiac tissue samples from explanted hearts (n=13).
139    Genome-wide analyses were performed on 13 tissue samples from familial and nonfamilial DGCR8-E518K
140 s, Gln546Lys, His1047Arg, and His1047Leu) in tissue samples from five out of nine patients with GLA.
141                                          All tissue samples from fulminant myocarditis (n=2) and GCM
142 were detected in relevant amounts in cardiac tissue samples from GCM or in blood samples from other t
143 nonfibrotic samples from diseased kidneys or tissue samples from healthy kidneys.
144 orms a protein complex with MCT1 and MCT4 in tissue samples from human breast cancer patients, but no
145    The lipid composition of arteries in lung tissue samples from human PAH and control patients were
146                                              Tissue samples from kidneys with tubulointerstitial fibr
147 th an unbiased proteomics readout to complex tissue samples from model organisms and patient-derived
148        In this study, we used GWAS metadata, tissue samples from pathologically confirmed frontotempo
149  We obtained peripheral blood and intestinal tissue samples from patients with and without IBD and an
150                                        Using tissue samples from patients with autosomal dominant PKD
151 rrelated with tubulointerstitial fibrosis in tissue samples from patients with chronic kidney disease
152  in KRAS or BRAF genes in pathological liver tissue samples from patients with hepatic vascular caver
153 ence in specific taxa in fecal or intestinal tissue samples from patients with IBD vs controls.
154 pared gene expression profiles between liver tissue samples from patients with nonalcoholic steatohep
155                            We obtained liver tissue samples from patients with primary sclerosing cho
156  not feasible, for example when working with tissue samples from patients.
157 duplicated 17-bp promoter was more common in tissue samples from populations of African descendant.
158 emotherapy for each molecular subgroup using tissue samples from PORTEC-3 trial participants.
159 this model generalizes to an external set of tissue samples from prenatal human hippocampi.
160 microbicide Q-Griffithsin (Q-GRFT) in rectal tissue samples from rhesus macaques.
161 nd without HHV-6B plasma viremia, (ii) tumor tissue samples from subjects with large B cell lymphoma
162 ng partial viral genomes from 6 HeV-infected tissue samples from Syrian hamsters and 4 tissue samples
163 und healing" and "neurogenesis") to evaluate tissue samples from the C2-C6 spinal cord 3 days after a
164        We calculate this metric using 11,706 tissue samples from the Genotype Tissue Expression (GTEx
165                Thousands of frozen, archived tissue samples from the human central nervous system (CN
166         Additionally, atrial and ventricular tissue samples from the Myocardial Applied Genomics Netw
167 scriptomic data of TNBC and non-TNBC (NTNBC) tissue samples from the TCGA database, focused on genes
168 ascular lymphocytic infiltration in alveolar tissue samples from transbronchial biopsies (TBBs).
169 on of BOP1 and nucleolar protein 56 in human tissue samples from various stages of CaP progression.
170      Human microbiota were evaluated in lung tissue samples from workers with respiratory symptoms fo
171                                   Sequential tissue sampling from these studies allowed for detailed
172 rmination of contaminants at trace levels in tissue samples has become an unmet need around the globe
173  iPSC findings into clinical aortic aneurysm tissue samples highlights the potential for iPSC-based m
174 in these selected patients when image-guided tissue sampling identifies a breast pCR.
175 irome) genes in 63 tumors and matched normal tissue samples in African Americans and Caucasians.
176     A subset of rinses were then compared to tissue samples in the same patient employing HPViewer to
177 was done in 441 (40%) and minimally invasive tissue sampling in 126 (11%) of the neonatal intensive c
178 s for prognostication has relied upon single-tissue samples, including 2 commercially available multi
179 genomic data sets from primates using frozen tissue samples, including many data sets from our own gr
180 chemistry (IHC) analysis of a panel of human tissue samples, including normal, diseased, and malignan
181 es in the morning compared with nighttime in tissue samples inclusive of the telencephalon and POA, b
182 l angle determination was applied to a human tissue sample investigation for the first time.
183  food product is genuine or counterfeit or a tissue sample is benign or malignant.
184 oach allows to obtain information before the tissue sample is taken, which makes it possible to signi
185                The microscopic assessment of tissue samples is instrumental for the diagnosis and sta
186  accurately quantifying centrosomes in human tissue samples is needed.
187  criterion, the ability to obtain sufficient tissue samples is problematic and requires invasive appr
188  the epigenetic mechanism CpG methylation in tissue samples is to identify regions of concordant diff
189       Quantitative bioanalysis in plasma and tissues samples is required to study the pharmacokinetic
190 onally, the relatively small number of brain tissue samples may have limited our power to detect alte
191                                              Tissue sampling methods were the same for PS and DBT-gui
192 stigated the potential of minimally invasive tissue sampling (MITS) for ascertaining the underlying a
193                Postmortem minimally invasive tissue sampling (MITS) is a potential alternative to the
194                           Minimally invasive tissue sampling (MITS) is a simplified postmortem examin
195  pathologic evaluation of minimally invasive tissue sampling (MITS) specimens, including guidelines f
196 lity surveillance employs minimally invasive tissue sampling (MITS) to gather small samples of body f
197 vestigated the utility of minimally invasive tissue sampling (MITS), placental examination, and clini
198 y surveillance, utilizing minimally invasive tissue sampling (MITS), postmortem laboratory and pathol
199 em diagnostics, including minimally invasive tissue sampling (MITS), were used.
200 le information, including minimally invasive tissue sampling (MITS).
201 sing single-cell-based approaches and unique tissue sampling models.
202                                       Kidney tissue samples obtained from organ donors were analyzed
203 d RNA transcription data from human cortical tissue samples of 233 subjects, and we detected 816 gene
204  of chimeric RNAs in 9495 non-diseased human tissue samples of 53 different tissues from the GTEx pro
205  show, using generalized additive models and tissue samples of 814 U.K.-stranded harbor porpoises col
206 ns, viral sequences were analyzed from brain tissue samples of a single SSPE case and compared with M
207 ition was found between MWF samples and lung tissue samples of case workers compared with control sub
208 xonomic units (OTUs) were not shared between tissue samples of different plant species in both locati
209                                              Tissue samples of EOM and medical records of all partici
210                                              Tissue samples of HIV+ men with anal cancer (n = 26), AI
211 NA-seq analysis of cells isolated from tumor tissue samples of non-small cell lung cancer (NSCLC) pat
212                                 By analyzing tissue samples of patients with breast cancer and type 2
213 ied ACE2 mRNA and protein expression in lung tissue samples of subjects with and without diabetes tha
214 er sample types beyond whole organs, such as tissue samples or isolated cell populations.
215 aining of healthy and diseased human gastric tissue samples paralleled these results.
216  method was evaluated on a cohort of 31 FFPE tissue samples, pursuing a statistical validation approa
217                              Individual fish tissue samples ranged from <LOD to 797.00 ng/g of WW, wh
218 we characterize variability in TLs from 6391 tissue samples, representing >20 tissue types and 952 in
219 formly call somatic mutations from over 7500 tissue samples, representing 36 distinct tissues.
220             Variable cellular composition of tissue samples represents a significant challenge for th
221 ome of E. coli, mouse brain, and mouse liver tissue samples, respectively.
222                     Analyses of human breast tissue samples reveal negative correlations between PAR3
223                                 Results: PCA tissue samples revealed a wide range of PSMA staining in
224  samples and 5 rare normal pediatric pontine tissue samples, revealing clinically relevant functional
225 we examined more than 7,000 oocytes from 160 tissue samples, scoring for the number of foci per cell
226          Whether this is due to fixatives or tissue sampling, selection of gene panels for routine di
227    Principal component analysis (PCA) of the tissue samples showed a clear discrimination among uninf
228                         Analysis of prostate tissue samples showed increased intensity of nuclear EGF
229 tation of ASOs and metabolites in plasma and tissue samples, showing a great potential to replace tra
230 for imaging of O(2) concentration in various tissue samples stained with a nanoparticle based probe,
231 sion and other morphological features of the tissue sample such as position of nuclei and endocrine c
232 cing is becoming more widely available, many tissue samples such as intracranial aneurysms are both f
233 dentification and visualization from complex tissue samples such as mouse brain tissue.
234 ations between the plasma DNA and metastatic tissue samples, suggesting the plasma DNA is highly repr
235 he safety of laboratory personnel who handle tissue samples that harbor pathogens, including those pe
236 s that can be applied to many archived human tissue samples that have been stored long-term.
237  alterations in blood and epididymal adipose tissue samples that were collected from C57BL/6 mice fed
238 f various breast cancer cell lines and human tissue samples, thereby linking alterations in chromatin
239 ast cancer cell-lines and two patient tumour tissue samples through a qPCR instrument and finally pil
240 of chronic periodontitis (CP) using gingival tissue samples through omics-based whole-genome transcri
241 d (3) photocleaving light projected onto the tissue sample to release PC oligonucleotides in any spat
242              DESI-MS was used to analyze 178 tissue samples to determine the molecular signatures of
243 t the importance of assessing intact genital tissue samples to gain insights into HIV susceptibility
244 d organoid cultures, mouse models, and human tissue samples to investigate the biological and molecul
245 ngle-genome and deep sequencing of blood and tissue samples to investigate the mechanisms that sustai
246  reference set for comparisons with diseased tissue samples to map the cellular foundations of pancre
247 ictors use laboratory parameters measured on tissue samples to predict the patient's response to chem
248 CDSeq, that uses only RNA-Seq data from bulk tissue samples to simultaneously estimate both cell-type
249                            For each of these tissue samples, transcriptomic changes induced by the tw
250 nous compounds from a discrete location on a tissue sample using a nano capillary filled with solvent
251 and protein in 68 pairs of adjacent prostate tissue samples using RNA-Seq and SWATH mass spectrometry
252 he analysis of intact proteins directly from tissue samples via mass spectrometry.
253  video imaging obtained immediately prior to tissue sampling via TBB.
254  of proteins from mouse brain and rat kidney tissues sampled via LESA.
255 vity for Gln, thus enabling down-sized brain tissue sample volume procurement for quantification of t
256                                         Each tissue sample was assigned a number between 1 and 130, a
257                                          The tissue sample was raster scanned with TRS to yield a spa
258 rom 804 CC formalin-fixed, paraffin-embedded tissue samples was genotyped with Illumina Immunochip.
259                 The aluminium content of 191 tissue samples was invariably low with over 80% of tissu
260                                 If US-guided tissue sampling was performed, results were obtained fro
261 ed that by capturing these features in fixed tissue samples, we could quantify in situ adaptive immun
262 g the gene expression profiles of 1,038 lung tissue samples, we performed a weighted gene correlation
263        Soil and wheat (Triticum aestivum L.) tissue samples were analyzed to determine the macronutri
264                                              Tissue samples were collected at the end of each study f
265                                      Cardiac tissue samples were collected during the CABG surgery an
266                                              Tissue samples were collected for histopathology and blo
267                                              Tissue samples were collected from anesthetized rats whe
268                                  Ventricular tissue samples were collected from patients at the time
269                                     Cervical tissue samples were collected from women with healthy, h
270                     Hourly blood, urine, and tissue samples were collected.
271 s a lack of spatial resolution as either the tissue samples were homogenized or specific proteins wer
272 orresponding surgically-resected aortic wall tissue samples were obtained and subjected to planar bia
273 erfused in cellular EVLP system for 2 h, and tissue samples were obtained before and after EVLP as we
274                                     Multiple tissue samples were obtained during emergent abdominal s
275 eek, mandibular and cardiac left ventricular tissue samples were obtained following the euthanasia of
276                        Mandibular and kidney tissue samples were obtained following the euthanasia.
277     Paired visceral and subcutaneous adipose tissue samples were obtained from 17 overweight patients
278                                     Gingival tissue samples were obtained from all participants for r
279                            Total grey matter tissue samples were obtained from medial OFC (BA11), lat
280 ic investigations, different category breast tissue samples were obtained in use of surgically remove
281                                              Tissue samples were processed for next generation sequen
282                                              Tissue samples were removed from prefrontal, primary mot
283                        The peri-implant soft tissue samples were retrieved from the sites during sche
284  inclusion and exclusion criteria, and their tissue samples were revisited.
285 ds: Fifty-one human brain and 29 human heart tissue samples were screened for the rs6971 polymorphism
286                                          Bat tissue samples were screened using previously establishe
287                                Subsequently, tissue samples were stained for proteolipid protein (mye
288 e were euthanized during diestrus, and colon tissue samples were subjected to morphological, biochemi
289                      Fasting skeletal muscle tissue samples were taken before and after 5 and 10 wk t
290 V)-mediated gene delivery in mice, and human tissue samples were used to define a regulatory pathway
291 nd remains valid even for irregularly shaped tissue samples when considering only the deformations in
292 tation significantly increased EGF levels in tissue samples, whereas when combined with aromatase inh
293 , genetic biomarker status is confirmed with tissue sampling, which is costly and only available afte
294                 The histological analysis of tissue samples, widely used for disease diagnosis, invol
295  that differentiate between tumor and normal tissue samples with 91% sensitivity (95% Confidence Inte
296 ize N-glycan expression within heterogeneous tissue samples with enhanced sensitivity.
297 estigation at the cell-type level in complex tissue samples with heterogeneous cell-type composition.
298             We also found that normal breast tissue samples with high leptin/adiponectin transcript r
299                           Importantly, mCRPC tissue samples with low AR activity displayed the same a
300 ir corresponding gene expression profiles in tissue samples would enhance understanding of the contri

 
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