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1 a metastatic niche that captures aggressive circulating tumor cells.
2 ly studied assays, circulating tumor DNA and circulating tumor cells.
3 ent manner, resulting in elevated numbers of circulating tumor cells.
4 were measured in blood, hair follicles, and circulating tumor cells.
5 te cancer, by greatly reducing the number of circulating tumor cells.
6 lls), metastatic prostate cancer lesions and circulating tumor cells.
7 lung but powerfully licenses colonization by circulating tumor cells.
8 c monitoring, most notably in the context of circulating tumor cells.
9 d 19%, respectively, had detectable AR-V7 in circulating tumor cells.
10 of prostate cancer from biopsy specimens and circulating tumor cells.
11 s to anoikis, thereby reducing the number of circulating tumor cells.
12 arkers, single-nucleotide polymorphisms, and circulating tumor cells.
13 changes in tumor burden, than did CA 15-3 or circulating tumor cells.
14 n of tumors and the colonization of lungs by circulating tumor cells.
15 iciently seed metastatic lesions than single circulating tumor cells.
16 n mice, but also to prevent the emergence of circulating tumor cells.
17 S) microfluidic channel for the detection of circulating tumor cells.
18 sociated with invasive cancer phenotypes and circulating tumor cells.
19 heterogeneity in tumors and analyzing single circulating tumor cells.
20 to be a vital trait of cancer cells such as circulating tumor cells, allowing them to undergo revers
22 d dynamic range for routine detection of PCa circulating tumor cells and can be adapted to detect oth
23 analysis in high cellular backgrounds (e.g., circulating tumor cells and fetal cells in maternal bloo
24 carcinoma cells reduced the number of viable circulating tumor cells and inhibited lung metastasis in
25 reduced tumor size as well as the number of circulating tumor cells and metastases in an orthotopic
26 cer following resection, elevated numbers of circulating tumor cells and more spontaneous metastases.
28 mice inhibited extravasation/colonization of circulating tumor cells and significantly reduced metast
29 of commensal homeostasis results in enhanced circulating tumor cells and subsequent dissemination to
30 l assays of drug-target engagement in living circulating tumor cells and therefore have the potential
36 re thus offers a unique route for separating circulating tumor cells, and for label-free cell separat
38 on in the primary tumors, elevated levels of circulating tumor cells, and increased spontaneous metas
40 herringbone patterns suitable for capture of circulating tumor cells are made as a demonstrative appl
42 of metastasis, detection and destruction of circulating tumor cells are vital for impeding metastasi
47 ed with metastases formation and presence of circulating tumor cells before therapy, whereas (iii) th
49 tinuous high-throughput selective capture of circulating tumor cells by dielectrophoresis at arrays o
50 Recent scientific advances in understanding circulating tumor cells, cell-free DNA/RNA, and exosomes
55 Intriguingly, locally disseminated clusters, circulating tumor cell clusters, and lung micrometastase
56 , local dissemination, intravascular emboli, circulating tumor cell clusters, and micrometastases.
58 ine phosphatase level (r = 0.572, P < .001), circulating tumor cell count (r = 0.613, P = .004), and
59 hange in prostate-specific antigen level and circulating tumor cell count (r = 0.63 [95% CI: 0.27, 0.
60 ion with prostate-specific antigen level and circulating tumor cell count were assessed by using Spea
61 ntigen level or a confirmed reduction in the circulating tumor-cell count from 5 or more cells per 7.
62 ored, using individual patient data, week 13 circulating tumor cell (CTC) and prostate-specific antig
63 secondary tumor initiation largely depend on circulating tumor cell (CTC) and vascular endothelial ce
64 Given that previous reports suggested that circulating tumor cell (CTC) AR-V7 detection is a poor p
65 linical benefit from early taxane switch and circulating tumor cell (CTC) biomarkers to interrogate m
66 technique for improving immunoaffinity-based circulating tumor cell (CTC) capture by patterning regio
72 the primary tumor vascular response and the circulating tumor cell (CTC) fraction derived from a tis
73 th PSA > 4.0 ng/mL, safety and tolerability, circulating tumor cell (CTC) levels, and seven plasma IG
74 om primary tumors are believed to facilitate circulating tumor cell (CTC) seeding of distant metastas
75 irculating cancer stem cells (CCSCs), a rare circulating tumor cell (CTC) type, recently arose as a u
77 Such restrictions limit the translation of circulating tumor cell (CTC)-based liquid biopsy assays
79 drug resistance-conferring gene mutations on circulating tumor cells (CTC) and cell-free circulating
82 Most of the current strategies for detecting circulating tumor cells (CTC) are based on the epithelia
84 ss the current and future potential of using circulating tumor cells (CTC) as a biomarker to assess s
87 gital pathology features on 9,225 individual circulating tumor cells (CTC) from 179 unique metastatic
90 specific marker exists for the detection of circulating tumor cells (CTC) from different types of sa
96 are launched into the bloodstream as single circulating tumor cells (CTC) or multicellular CTC clust
98 We sought to develop a biomarker of CIN in circulating tumor cells (CTC) that are more likely to re
99 A method is presented for the detection of circulating tumor cells (CTC) using mass spectrometry (M
102 o the primary tumor, their interactions with circulating tumor cells (CTC) within the bloodstream, an
103 mesenchymal transition (EMT) is prominent in circulating tumor cells (CTC), but how it influences met
104 arly detection of metastasis can be aided by circulating tumor cells (CTC), which also show potential
109 tion of tumor cells in the peripheral blood (circulating tumor cells, CTC) and CSF (cerebrospinal flu
110 spot PIK3CA mutations (E545 K and H1047R) in circulating tumor cells (CTCs) and cell free DNA (cfDNA)
111 terature regarding two potential biomarkers, circulating tumor cells (CTCs) and cell-free DNA (cfDNA)
112 on the molecular information extracted from circulating tumor cells (CTCs) and circulating tumor DNA
113 based biopsies (BBBs), blood is purified for circulating tumor cells (CTCs) and clinical utility is t
114 ssess the prognostic and predictive value of circulating tumor cells (CTCs) and disseminated tumor ce
118 y tumor growth but blocked the production of circulating tumor cells (CTCs) and the formation of lymp
135 cusing microfluidic approaches in retrieving circulating tumor cells (CTCs) at single-cell resolution
138 The methods for isolating rare cells such as circulating tumor cells (CTCs) can be generally classifi
142 en receptor splice variant-7 (AR-V7) mRNA in circulating tumor cells (CTCs) correlated with poor outc
144 Anticancer drug efficacy has been tested on circulating tumor cells (CTCs) derived from patient bloo
148 tivator of NF-kappabeta (RANK) in individual circulating tumor cells (CTCs) from 40 late-stage (III-I
149 tion and rapid molecular characterization of circulating tumor cells (CTCs) from a liquid biopsy coul
150 deaths and it is fueled by the generation of circulating tumor cells (CTCs) from a primary tumor depo
152 ole in human cancer, we characterized EMT in circulating tumor cells (CTCs) from breast cancer patien
153 e biomaterial for the capture and release of circulating tumor cells (CTCs) from cancer patient blood
154 thin the circulatory system, platelets guard circulating tumor cells (CTCs) from immune elimination a
155 ndrogen receptor splice variant 7 (AR-V7) in circulating tumor cells (CTCs) from men with castration-
156 llowed for detection and characterization of circulating tumor cells (CTCs) from patients with cancer
157 enable the detection and isolation of single circulating tumor cells (CTCs) from patients with prosta
159 sitive and high-throughput method to analyze circulating tumor cells (CTCs) from peripheral blood.
160 e examined copy-number aberrations (CNAs) in circulating tumor cells (CTCs) from pretreatment SCLC bl
162 lterations in single primary tumor cells and circulating tumor cells (CTCs) from the same patient.
167 The ability to isolate and analyze rare circulating tumor cells (CTCs) has the potential to furt
171 l as surface marker identification of single circulating tumor cells (CTCs) have been demonstrated.
176 cance of disseminated tumor cells (DTCs) and circulating tumor cells (CTCs) in 1 cohort of patients w
178 quantification and in situ identification of circulating tumor cells (CTCs) in blood are still elusiv
180 e (Fe(3)O(4)) nanoparticles (NPs) to capture circulating tumor cells (CTCs) in blood for head and nec
184 We evaluated the prognostic significance of circulating tumor cells (CTCs) in patients with esophage
185 merase chain reaction (RT-qPCR) detection of circulating tumor cells (CTCs) in patients with melanoma
189 rts that the association of neutrophils with circulating tumor cells (CTCs) in the blood of patients
190 elets have been shown to promote survival of circulating tumor cells (CTCs) in the bloodstream by con
191 tage detection and precise quantification of circulating tumor cells (CTCs) in the peripheral blood o
192 sion persists in metastatic lung nodules and circulating tumor cells (CTCs) in two mouse models of ma
193 R-V7) protein expression and localization on circulating tumor cells (CTCs) is a treatment-specific m
196 port that elevated expression of each GEF in circulating tumor cells (CTCs) isolated from the periphe
199 e metastases is challenging; hence, sampling circulating tumor cells (CTCs) may reveal drug-resistanc
200 h the bloodstream either as single migratory circulating tumor cells (CTCs) or as multicellular group
201 aimed to evaluate the relationships between circulating tumor cells (CTCs) or plasma cell-free DNA (
208 l lines, primary prostate cancer tissues and circulating tumor cells (CTCs) to investigate their role
209 Moreover, uPtDs NPs could target the in vivo circulating tumor cells (CTCs) to suppress TNBC lung met
212 gression-free survival (rPFS) and effects on circulating tumor cells (CTCs), bone biomarkers, serum p
213 A potential solution is to characterize circulating tumor cells (CTCs), but this requires overco
214 opic ultrasound (EUS) to count portal venous circulating tumor cells (CTCs), compared with paired per
216 e of detecting common POC targets, including circulating tumor cells (CTCs), DNA/RNA, and curcumin, a
217 t of an efficient technique for detection of circulating tumor cells (CTCs), due to their significanc
218 nd metastatic disease, through the spread of circulating tumor cells (CTCs), is responsible for the m
219 are often easily accessible in the blood as circulating tumor cells (CTCs), making them ideal target
222 Additionally, deletion of miR-182 decreased circulating tumor cells (CTCs), while overexpression of
223 analysis of cancer cells in blood-so-called circulating tumor cells (CTCs)-may provide unprecedented
224 for detection, isolation, and enrichment of circulating tumor cells (CTCs)-rare cells that enter the
234 MT, however, is not required for metastasis: circulating tumor cells exhibit hybrid epithelial-mesenc
235 of upcoming biomarkers, including microRNA, circulating tumor cells, exosomes, and cell-free DNA, an
236 rker types, including circulating tumor DNA, circulating tumor cells, extracellular vesicles (exosome
237 e analysis of Sur biomarkers in exosomes and circulating tumor cells for a non-invasive liquid biopsy
238 ould be an effective tool to directly target circulating tumor cells for the prevention of prostate c
239 rous devices developed to isolate individual circulating tumor cells from blood, these devices are in
240 or splice variant 7 messenger RNA (AR-V7) in circulating tumor cells from men with advanced prostate
242 n and on-chip phenotypic characterization of circulating tumor cells from peripheral venous blood in
243 se-chain-reaction assay to evaluate AR-V7 in circulating tumor cells from prospectively enrolled pati
245 hly sensitive microfluidic system to capture circulating tumor cells from whole blood of cancer patie
247 CTC transcriptomes, we discovered a unique "circulating tumor cell gene signature" that is distinct
248 tients with informative unfavorable baseline circulating tumor cells >= 5/7.5 mL of blood, 16 (59%) s
251 assay of circulating tumor DNA, CA 15-3, and circulating tumor cells in 30 women with metastatic brea
252 latory shear stress in cellular responses of circulating tumor cells in a physiologically relevant mo
253 In some applications (e.g., working with circulating tumor cells in blood), only a limited number
254 in metastatic capacity and in the number of circulating tumor cells in both the E2F1 and E2F2 knocko
255 label-free identification and measurement of circulating tumor cells in cancer research and disease m
256 y, OGX-427 treatment decreased the number of circulating tumor cells in patients with metastatic cast
257 it of reducing tumor size, PTX increased the circulating tumor cells in the blood and enhanced the me
258 er dormancy is evident from the detection of circulating tumor cells in the blood and tissue-residing
262 novehicle can also effectively eliminate the circulating tumor cells in vivo and inhibit development
263 ADT-sensitivity, and reduces the shedding of circulating tumor cells in vivo with significant shrinka
266 ging of gastrointestinal tract, bladder, and circulating tumor cells (in vivo flow cytometry); and in
267 cells into the mouse leads to the release of circulating tumor cells into the vasculature, which seed
268 scoveries, challenges, and future trends for circulating tumor cell investigations, arguing that the
273 of fluid-based assays, notably, exosomes and circulating tumor cells (liquid biopsy), as tools for fu
275 le of mechanotransduction in cancer, and how circulating tumor cells may be capable of continuously c
276 isrupt the HA machinery of primary tumor and circulating tumor cells may enhance the effectiveness of
281 cific biomolecules, including nucleic acids, circulating tumor cells, proteins, antibodies, and extra
283 ug assays with patient-derived cells such as circulating tumor cells requires manipulating small samp
285 In > 200 cancer cell lines and in primary circulating tumor cells, SETD1A expression correlates wi
286 vestigate small populations of cells such as circulating tumor cells shed from solid tumors and isola
288 nd to move collectively, forming clusters of circulating tumor cells that are key tumor-initiating ag
289 promise as an effective means to neutralize circulating tumor cells that enter blood with the potent
290 al utility of the SNARE with prostate cancer circulating tumor cells to demonstrate its ability to pe
291 ernalization, thus inhibiting the ability of circulating tumor cells to extravasate and colonize, lea
292 ells inhibited extravasation/colonization of circulating tumor cells to the lung and inhibited tumor
293 enrichment and molecular characterization of circulating tumor cells using peripheral venous blood in
294 mic alterations were identified; CA 15-3 and circulating tumor cells were detected in 21 of 27 women
295 s of tumor spread were measured serially and circulating tumor cells were detected via fluorescence m
298 e metastasis by promoting the association of circulating tumor cells with blood cells to augment tumo
299 f the association of androgen receptor-V7 in circulating tumor cells with resistance to enzalutamide