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1 otated, and their expression associated with tissue type.
2 entrations varying with macrophyte taxon and tissue type.
3 on-cancerous cells originating from the same tissue type.
4 e of power delivery, number of antennas, and tissue type.
5 ence and strength of regulation depending on tissue type.
6  even when these cancers arise from the same tissue type.
7 he remarkable characteristics of this unique tissue type.
8  even when these cancers arise from the same tissue type.
9  together, with similar results between each tissue type.
10 n levels in thousands of cells from the same tissue type.
11 t significant marker for resistance based on tissue type.
12 de of PI3K pathway activation rather than by tissue type.
13 uclei was dependent on fiber orientation and tissue type.
14 e shape/magnitude of the XRD spectra and the tissue type.
15 as a function of both developmental time and tissue type.
16 arization markers (CD80 or HLA-DR) on either tissue type.
17 nment have wide ranging effects on resultant tissue type.
18 ccurrence networks were constructed for each tissue type.
19 semblance in the ERalpha patterns of the two tissue types.
20 its regulation can vary substantially across tissue types.
21 and profile ILCs across healthy and inflamed tissue types.
22 a close association in contrast to benign LN tissue types.
23 fy molecular features discriminating between tissue types.
24 its action on macrophages and other cell and tissue types.
25 determine which gene is affected in specific tissue types.
26 n level of lncRNA or mRNA differs in the two tissue types.
27 tures to differentiate between normal breast tissue types.
28 ks (GRNs) are highly dynamic among different tissue types.
29 erize lncRNAs conserved in other species and tissue types.
30  and the kinetic parameter values of 3 tumor tissue types.
31 to generate CRC models for 75 human cell and tissue types.
32 are differentially expressed between cell or tissue types.
33  containing samples from two or more cell or tissue types.
34 varies from days to years across species and tissue types.
35  functional implications in distinct cell or tissue types.
36 had a significant strong correlation for all tissue types.
37 onstrating applicability for a wide range of tissue types.
38 implicated in self-renewal in several normal tissue types.
39 ortunity to study cis-mediation across human tissue types.
40 omponents and cellulose differed among plant tissue types.
41 interest (VOIs) in CT datasets for different tissue types.
42 ng samples (RNA-seq) from 13 different human tissue types.
43 as demonstrated by applications to different tissue types.
44 SI mass spectra of pathologically determined tissue types.
45 cers millions of times more often than other tissue types.
46 gle miRNA gene often differ between cell and tissue types.
47 rtex, and were expressed in diverse cell and tissue types.
48 nhanced biochemical distinction of different tissue types.
49  numerous biological processes in almost all tissue types.
50 lities were detected by contrasts in various tissue types.
51 ining shoot and root meristems and all basic tissue types.
52 s, multiple ionization sources, and multiple tissue types.
53 could be easily adapted for use on different tissue types.
54  change in expression levels among different tissue types.
55 nome-wide TFNs in 41 distinct human cell and tissue types.
56 h a limited cell population and inaccessible tissue types.
57 oughout the mouse genome in diverse cell and tissue types.
58 on of enhancers across a variety of cell and tissue types.
59 d required for normal development of various tissue types.
60 equire independent modifications to multiple tissue types.
61 ncompassing over 1000 samples from different tissue types.
62 g data sets across 30 diverse human cell and tissue types.
63 position of polyA sites in three human adult tissue types.
64  there is a considerable overlap between the tissue types.
65 tines are tubular organs composed of several tissue types.
66 s physiological defects in specific cell and tissue types.
67 accurately distinguished the age of multiple tissue types.
68 re highly sequestered among the various seed tissue types.
69 ted with gene expression changes in specific tissue types.
70  and the kinetic parameter values of 3 tumor tissue types.
71 works as a result of signaling between these tissue types.
72 xample, other species or additional cell and tissue types.
73 dictive of cis-eQTL SNVs across a variety of tissue types.
74 of cis-hubs and trans-eQTL regulation across tissue types.
75 ing simulations of clinically relevant tumor tissue types.
76 al altered pathways shared among NATs across tissue types.
77 an atlas of 2,534,123 enhancers for 105 cell/tissue types.
78 n, and inflammation in a variety of cell and tissues types.
79   How do signaling pathways specify distinct tissue types?
80                                      In many tissues, type 4 NADPH oxidase is induced upon ischemia o
81 1 genes and the corresponding proteins in 14 tissue types across nearly 200 samples.
82 ii) effects of parasites infecting different tissue types (across guild).
83 sion of aging genes across a large number of tissue types also points to a high level of connectivity
84  differences in disease status, sex, cell or tissue type, ancestry, genetic background, experimental
85 m20 to other splicing factors that vary with tissue type and developmental age.
86 sis of the transcriptome data indicated that tissue type and protein kinase expression had large infl
87 sociated with a specific time of expression, tissue type and subcellular compartment.
88 between 5 and 25 mum thick, depending on the tissue type and the analyte(s) of interest.
89 ncer genes, gene amplification and deletion, tissue type and transcriptional data.
90                                              Tissue type and tumor localization did not affect repeat
91 bitor-1 (PAI-1) is the main inhibitor of the tissue type and urokinase type plasminogen activators.
92  ENCODE/Roadmap consortium covering 127 cell/tissue types and 8 major epigenomic marks.
93 ferentiation and classification of different tissue types and contrast agents can be extremely challe
94 are distributed throughout a wide variety of tissue types and detect extracellular ATP as a danger si
95 of transcript variants across different cell/tissue types and disease conditions.
96 arly-stage fruit development with five fruit tissue types and five developmental stages from floral a
97 ally more robust across a range of different tissue types and for realistic noise levels.
98  enriched for histone mark peaks in relevant tissue types and gene promoter regions.
99 pid adaptation of these viruses to different tissue types and host cells.
100 ors are expressed in virtually all cells and tissue types and mediate an astonishing array of biologi
101 enotypic similarity between related cell and tissue types and reveal molecular basis for their simila
102 t both the clear differences between the two tissue types and the important role that composition and
103 ive differences in the complexome in various tissue types and under various conditions.
104 all RNA sequencing data sets from four human tissue types and were able to classify six different typ
105 ne-like fragments on Bs are transcribed in a tissue-type and genotype-specific manner.
106 re observed using this approach according to tissue type, and a tissue recognition system using multi
107 ng a range of processes, (non)photosynthetic tissue types, and cell cultures.
108 fection rates, virus replication in multiple tissue types, and earlier mortality.
109 LOCK is shown to work reasonably well across tissue types, and often with only small degradation acro
110 ween cells of different cell stage, cell and tissue types, and organisms.
111 , each mammal favors the same mt-tRNA in all tissue types, and strikingly, when steady-state levels o
112 rsensitive sites (DHSs) in 45 mouse cell and tissue types, and systematically compared these with hum
113 superior performance across diverse cell and tissue types, and the enhancer locations are significant
114                                However, many tissue types are difficult to access and are not collect
115                                     Multiple tissue types are discussed that utilize the insulin-rela
116 ple, whole-body imaging where a diversity of tissue types are present, this variation across tissue t
117 lel; compare gene expression among different tissue types as well as between normal and cancer cells;
118  discernible and consistent across all human tissue types assessed, whereas long intergenic ncRNAs, s
119 te steadily over time in all of the assessed tissue types, at a rate of approximately 40 novel mutati
120 ancies appear to be restricted to either (1) tissue types bearing the same molecular defect that unde
121 ticle surrounding the body and heterogeneous tissue types beneath the cuticle.
122  140 benign tissue samples representing nine tissue-types (bladder, breast, liver, lung, prostate, st
123 ed to be constitutively expressed throughout tissue types but recent studies have shown they vary wit
124 ental changes vary considerably according to tissue type, but molecular analyses at an organ-wide lev
125 egment anatomical features and differentiate tissue types, but existing approaches are both CPU and m
126 actility in smooth muscle and other cell and tissue types, but the mechanisms by which Paks regulate
127 ing with the values from regular tissue, the tissue type can be determined quickly and accurately.
128     The variation in the makeup of different tissue types can result in significant differences in an
129        This method is generalizable to other tissue types, cancers, and organisms, and this new infor
130 nting of the mouse genome across 25 cell and tissue types, collectively defining approximately 8.6 mi
131 issue microarrays consisting of samples of 7 tissue types (columnar cell metaplasia, Barrett esophagu
132        Difficulty in differentiating between tissue types commonly results in the requirement for add
133 across developmental trajectories of several tissue types consistent with known biology and find a no
134 The ability to reliably annotate loci across tissue types demonstrates the potential of CoRAL to char
135 cies with different roles that are cell- and tissue-type dependent.
136                The mass spectral data reveal tissue type-dependent lipid profiles which are consisten
137  show that in GDM-associated defect on IR is tissue type-dependent.
138 dence, or p110beta, which would suggest that tissue type determines isoform dependence.
139 rnative splicing is strongly associated with tissue type, developmental stage, and stress condition.
140 stimate the differential network between two tissue types directly without inferring the network for
141 cancer cell lines reflecting the genomic and tissue-type diversity of human cancers, to systematicall
142 though pathologic methods exist to determine tissue type during surgery, these methods can compromise
143 roup, n = 13 for each posterior group) for 2 tissue types (enamel and dentine).
144  had a higher rate of false negatives in all tissue types, especially for the ear notch samples (miss
145 eplicate across studies despite variation in tissue type, ethnicity and analytic approaches.
146 sses: within tissue type exclusivity, across tissue type exclusivity and between tissue type exclusiv
147 exclusivity into three basic classes: within tissue type exclusivity, across tissue type exclusivity
148 , across tissue type exclusivity and between tissue type exclusivity.
149                         However, both normal tissue types exhibited significant positive correlations
150 y data to supplement consultation with local tissue typing experts.
151 funNorm method, and introducing cell-type or tissue-type flexibility.
152  and tissue-specific RNA expression in eight tissue types for six primate species.
153  consistent lipidomic profiles of individual tissue types found within LNs.
154 cted transcriptome data in a wide variety of tissue types from post-mortem donors.
155 ce of TSSs for numerous human and mouse cell/tissue types from within R, greatly increasing the acces
156 covered, considering the number of patterned tissue types generated during development.
157                                         Some tissue types give rise to human cancers millions of time
158 n-GTEx studies, the accessibility of certain tissue types greatly limits the feasibility and scale of
159                             Metadata such as tissue type, growth conditions and developmental stage w
160 ability of the same protein across different tissue types, i.e., across-tissues variability.
161 eractions among parasites infecting a single tissue type in determining infection patterns.
162 olyps based on the REIMS fingerprint of each tissue type in vivo.
163 derlying substrate, is one of the four major tissue types in adult organisms.
164 ene expression profiles across six different tissue types in domesticated tomato (Solanum lycopersicu
165 imately 8 million records, covering 102 cell/tissue types in five organisms.
166 d identical distribution patterns as per the tissue types in matched IHC images.
167 mating the mixing proportions of distinctive tissue types in next-generation sequencing data.
168 Depression and Anxiety (NESDA), and multiple tissue types in the Genotype-Tissue Expression (GTEx) co
169         By analyzing data from nine selected tissue types in the GTEx pilot project, we demonstrated
170  purification of nuclei from defined cell or tissue types in vertebrate embryos using INTACT (isolati
171 eriments were then replicated using multiple tissue types in which the analyte's MS signal was monito
172 rnal standards compensate for differences in tissue types in, for example, whole-body imaging, a set
173 ss spectrometry imaging to identify discrete tissue-types in the seed in which these non-native fatty
174 ressed in distinct cellular compartments, or tissue types, in which they are believed to execute dist
175 -hypersensitive sites was also found in many tissue types, including brain tissue.
176 a cytoprotectant and gasotransmitter in many tissue types, including mediating vascular tone in blood
177 ls representing a variety of different human tissue types, including non-transformed cells (cardiomyo
178  diverse native grasses, colonizing multiple tissue types, including seeds, leaves and inflorescence
179 r the functions of a broad range of cell and tissue types, including sensory and central neurons, and
180 ound batteries enriched in specific cell and tissue types, indicating that the approach can be used t
181 re compromised by the deletion regardless of tissue type, insulator function is only disrupted in tis
182 nated growth and development of the multiple tissue types involved in the functional regeneration of
183 whether the variation observed in one of the tissue types is representative of other sources or wheth
184 ureus to adapt to different host species and tissue types is strongly influenced by the acquisition o
185 l tissues revealed that species, rather than tissue type, is the primary determinant of editing level
186 Our protocol, which may be suitable for many tissue types, is so far the only working ChIP system for
187 ng multiple parameters like genes, diseases, tissue types, keywords and associated publications in or
188 3 loci were enriched for genes, pathways and tissue types known to be involved in growth and together
189 ng, a set of tissue homogenates of different tissue types (lung, liver, kidney, heart, and brain) fro
190 s in various biological processes, including tissue type maintenance and determining the general feat
191 rimary murine mucosal-type MC and connective tissue-type MC released phenotypically different EV popu
192 eomic analysis of CD63(+) EV from connective tissue-type MC unveiled an abundance of MC-specific prot
193 embrane phenotype similar to i.p. connective tissue-type MC, but were smaller and hypogranular by flo
194 pression is variable in human cell lines and tissue types, mechanisms underlying SAMHD1 gene regulati
195                                      In many tissue types, metastasis is fueled by the epithelial-to-
196 nt levels of noise and used to calculate the tissue-type misclassification errors of spectral cluster
197 -photon imaging to identify distinct adipose tissue types, monitor their functional state, and charac
198 nomic activity patterns in cancer and normal tissue types more accurately than alternative methods, b
199 fy proteins from specific locations in three tissue types; ocular lens, brain, and kidney.
200 al classification method, we showed that the tissue type of a sample can be successfully predicted ba
201 rate RNA-seq data from more than 40 cell and tissue types of four mammalian species to identify sets
202 rent spectroscopic features for the two main tissue types of healthy and adenoma.
203 ction of individual cell lines and different tissue types of origin.
204 2684 predicted motifs classified the cell or tissue types of the datasets with an accuracy of 81.29%.
205 on of lipid metabolism between the different tissue types of the seed.
206 emporal aspects of processes such as cell or tissue type or developmental stage.
207 ing methods estimate GRN for a specific cell/tissue type or in a tissue-naive way, or do not specific
208 nesis on profiles was much less than that of tissue type or light and most differences were explicabl
209 es, including substrates not present in most tissue types or cell lines.
210  show alternating dominance across different tissue types or variation in the degree of bias in diffe
211 gnificant interactions between wear type and tissue type ( P = 0.0157 and P = 0.0003, respectively) a
212                              Across cell and tissue types, paused genes (pausing index > 2) comprise
213 ts function as an inhibitor of urokinase and tissue-type plasminogen activator (PA), PA inhibitor-1 (
214      National guidelines endorse recombinant tissue-type plasminogen activator (r-tPA) in eligible pa
215 n this study, we demonstrate that VDAC binds tissue-type plasminogen activator (t-PA) on human neurob
216 is has been dominated by the experience with tissue-type plasminogen activator (t-PA), which proved l
217 dy, we demonstrate that GRP78 also binds the tissue-type plasminogen activator (t-PA), which results
218 l analysis of fibrinolysis after recombinant tissue-type plasminogen activator (tPA) administration r
219 ing further reduction in treatment times for tissue-type plasminogen activator (tPA) administration.
220 e hypothesis, namely, that marked release of tissue-type plasminogen activator (tPA) followed by dela
221 al trials suggest the benefit of intravenous tissue-type plasminogen activator (tPA) in acute ischemi
222 functioning as an activator of fibrinolysis, tissue-type plasminogen activator (tPA) interacts with n
223                                              Tissue-type plasminogen activator (tPA) is known to prom
224                                              Tissue-type plasminogen activator (tPA) is the major int
225                                              Tissue-type plasminogen activator (tPA), a protease up-r
226 dard thrombolytic treatment with recombinant tissue-type plasminogen activator (tPA).
227 namic transfection of a plasmid encoding for tissue-type plasminogen activator (tPA).
228 ith bleeding complications after intravenous tissue-type plasminogen activator administration to pati
229 ndard of care: intravenous thrombolysis with tissue-type plasminogen activator and endovascular treat
230  levels) and the fibrinolytic system (plasma tissue-type plasminogen activator and plasminogen activa
231 t amorphous protein aggregates interact with tissue-type plasminogen activator and plasminogen, via a
232 low-dose (25 mg), slow infusion (6 hours) of tissue-type plasminogen activator for the treatment of p
233 nd more eligible patients to be treated with tissue-type plasminogen activator if onset is </=2 hours
234  1, 2010 and March 31, 2015 and who received tissue-type plasminogen activator in the emergency depar
235 10 patients with IS treated with intravenous tissue-type plasminogen activator in the Get With The Gu
236 ng patients with IS treated with intravenous tissue-type plasminogen activator is associated with hig
237 ents with acute ischemic stroke treated with tissue-type plasminogen activator is associated with imp
238                Intravenous thrombolysis with tissue-type plasminogen activator remains the mainstay o
239 ve thrombosis model) followed by recombinant tissue-type plasminogen activator treatment (10 mg/kg, I
240                             The mean dose of tissue-type plasminogen activator used was 48.7+/-29.5 m
241                       Between 2004 and 2012, tissue-type plasminogen activator was administered to 24
242                   Low-dose, slow infusion of tissue-type plasminogen activator with repeated doses as
243               Intravenous rt-PA (recombinant tissue-type plasminogen activator) is effective in impro
244 solve thrombi acutely and r-tPA (recombinant tissue-type plasminogen activator) therapy may be requir
245 <60 minutes in >50% of patients treated with tissue-type plasminogen activator), and (5) face-to-face
246  The LRP1 agonists, alpha2-macroglobulin and tissue-type plasminogen activator, attenuated expression
247  conventional approaches such as recombinant tissue-type plasminogen activator, direct thrombin inhib
248  ligands, including alpha2-macroglobulin and tissue-type plasminogen activator, failed to cause LRP1
249 n plasma of pregnant women inhibits FXIa and tissue-type plasminogen activator-induced clot fibrinoly
250 hy confirmed clot dissolution in recombinant tissue-type plasminogen activator-treated animals, but e
251 here were 15 191 of 44 410 (34%) intravenous tissue-type plasminogen activator-treated IS patients wi
252  of the thrombus was detected in recombinant tissue-type plasminogen activator-treated rats but not i
253  accomplished in the context of the multiple tissue types present within a developing organ remains u
254 g gene expression by both cancer subtype and tissue type, providing clinicians more refined tools to
255 n of sense/antisense pair expressions across tissue types revealed lineage-specific, ubiquitous and c
256 atin-state maps for islets and other diverse tissue types revealed that cis-eQTLs for islet-specific
257  RNAs, and other noncoding RNAs across three tissue types (siliques, seedling shoots, and roots) and
258 availability of Cre mouse lines with cell or tissue type-specific expression of Cre recombinase.
259        Furthermore, we constructed cancer or tissue type-specific, gene co-expression based protein i
260 etal proteins, whose expression is cell- and tissue type-specific.
261 al and post-transcriptional regulation shape tissue-type-specific proteomes, but their relative contr
262 f post-transcriptional regulation to shaping tissue-type-specific proteomes.
263  group-wise comparative analyses across sex, tissue type, state and developmental age.
264  cycle and the oscillating species vary with tissue type suggesting that perhaps a much larger fracti
265 ls in erythroid cells than any other cell or tissue type, suggesting that Setd8 has an erythroid-cell
266 es were conditional upon the environment and tissue type, suggesting that these TFs may allow the pla
267 induced apoptosis of tumor cells of multiple tissue types, supporting its role as a broad bona fide t
268  transcriptome profiling of specific cell or tissue types that are isolated from tomato using laser m
269 ors and that a variety of factors, including tissue type, the underlying cancer genetics, the tumor m
270                             Depending on the tissue type, the Wnt pathway can promote stem cell self-
271  rate of scaffold degradation depends on the tissue type to be regenerated, next-generation scaffolds
272 ) data from 376 cancer samples covering nine tissue types to comprehensively characterize the landsca
273 tor (WNT-974) on the regeneration of several tissue types to identify potentially unwanted chemical e
274  DNA methylation in a wide range of cell and tissue types to identify putative regulatory elements.
275 overns the sensitivity of specific cells and tissue types to ribosomal protein mutations.
276 nteractome of lamin A/C in multiple cell and tissue types under various treatment conditions.
277 ers were well conserved across many cell and tissue types, unique differences in certain cells and ti
278                                  For a given tissue type, variable cancer risk between individuals is
279 n mean value of the measured metric for each tissue type was used in the analysis.
280 APA; the significance of differences between tissue types was assessed by an appropriately designed p
281 e the potential interactions between the two tissue types, we analyzed epithelial-specific beta-caten
282  that are unmethylated in 11 different fetal tissue types, we show that increases in DNA methylation
283 g of carbohydrates and lignin within a plant tissue type were generally the same, regardless of funga
284               In this study, various ovarian tissue types were analysed by DESI-MSI and co-registered
285                    Congener profiles of five tissue types were dominated by PCB 28/31 and higher-chlo
286                                              Tissue types were identified and segmented from clinical
287  with the alpha (BK)-subunit in almost every tissue type where they are found.
288 hin 0.3-1.3 y of formation, depending on the tissue type, whereas tissues older than ca. 1955 have hi
289 d with variation of BBB opening in different tissue types, which is not typically observed in small a
290 the nucleus exacerbates toxicity in multiple tissue types, while confining HDL2-Q138 to the cytoplasm
291 ake Huron, Lake Michigan, or Lake Superior), tissue type (whole fish or eggs), and contaminant type (
292 el to reflect diverse biological systems and tissue types will further improve our understanding of a
293 assignment of a majority of them to specific tissue types will inform future studies of this newly di
294 sue types are present, this variation across tissue types will therefore add to the overall uncertain
295 netic load depended on both the drug and the tissue type with 10 tissues being particularly vulnerabl
296                     Organs are composites of tissue types with diverse developmental origins, and the
297 idopsis embryo establishes polarity and main tissue types with the first five rounds of cell division
298 he DT and AT networks were distinct for each tissue type, with no microbial relationships maintained
299  well versus existing methods in classifying tissue types within a single dataset, and that GRAPE ach
300 erent lipid compositions between the various tissue types within the seed.

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