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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
21                                         Less circulating tumor cells along with reduction in malignan
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.
27 noikis enables them to disseminate as viable circulating tumor cells and seed distant organs.
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
31 els, ADCC enhancement was crucial to deplete circulating tumor cells and to suppress metastases.
32                                              Circulating tumor cells and tumor-derived RNA in the blo
33 rovements in measurable soft tissue disease, circulating tumor cells, and bone biomarkers.
34 algesic use, measurable soft tissue disease, circulating tumor cells, and bone biomarkers.
35 ctive surveillance have evaluated microRNAs, circulating tumor cells, and exosomes.
36 re thus offers a unique route for separating circulating tumor cells, and for label-free cell separat
37 ormation of ascites, tumor burden over time, circulating tumor cells, and hepatic metastases.
38 on in the primary tumors, elevated levels of circulating tumor cells, and increased spontaneous metas
39 orphological differences among the parental, circulating tumor cells, and lung metastatic cells.
40 herringbone patterns suitable for capture of circulating tumor cells are made as a demonstrative appl
41                                              Circulating tumor cells are tumor-derived pioneers respo
42  of metastasis, detection and destruction of circulating tumor cells are vital for impeding metastasi
43 ing the extravasation process or re-entry of circulating tumor cells at metastatic sites.
44                                              Circulating tumor cell-based AR-V7 detection may serve a
45                               We report that circulating tumor cells become trapped within NETs in vi
46 date by tumor recurrence as a consequence of circulating tumor cells before the surgery.
47 ed with metastases formation and presence of circulating tumor cells before therapy, whereas (iii) th
48  biomarker, expressed on prostate tissue and circulating tumor cells but also found in serum.
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
51 val outcomes was evaluated and compared with circulating tumor cells (CellSearch).
52                                              Circulating tumor cell clusters (CTC clusters) are poten
53                                              Circulating tumor cell clusters (CTC clusters) are prese
54                    This result suggests that circulating tumor cell clusters might be able to better
55 Intriguingly, locally disseminated clusters, circulating tumor cell clusters, and lung micrometastase
56 , local dissemination, intravascular emboli, circulating tumor cell clusters, and micrometastases.
57                    During cancer metastasis, circulating tumor cells constantly experience hemodynami
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
67                                              Circulating tumor cell (CTC) clusters have an enhanced c
68                                              Circulating tumor cell (CTC) detection offers various op
69                                 Conventional circulating tumor cell (CTC) detection strategies rely o
70                                 We evaluated circulating tumor cell (CTC) enumeration as a surrogate
71                                              Circulating tumor cell (CTC) enumeration has not been pr
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
76                                              Circulating tumor cell (CTC)-based liquid biopsies provi
77   Such restrictions limit the translation of circulating tumor cell (CTC)-based liquid biopsy assays
78                  Multicellular aggregates of circulating tumor cells (CTC clusters) are potent initia
79 drug resistance-conferring gene mutations on circulating tumor cells (CTC) and cell-free circulating
80                      The interaction between circulating tumor cells (CTC) and endothelial cells duri
81               This panel was also applied to circulating tumor cells (CTC) and provided evidence that
82 Most of the current strategies for detecting circulating tumor cells (CTC) are based on the epithelia
83                                              Circulating tumor cells (CTC) are shed in peripheral blo
84 ss the current and future potential of using circulating tumor cells (CTC) as a biomarker to assess s
85                                              Circulating tumor cells (CTC) disseminating is an import
86         EGFR expression was also observed in circulating tumor cells (CTC) during prostate cancer met
87 gital pathology features on 9,225 individual circulating tumor cells (CTC) from 179 unique metastatic
88                Molecular characterization of circulating tumor cells (CTC) from blood is technically
89 ), a technique previously used for isolating circulating tumor cells (CTC) from blood.
90  specific marker exists for the detection of circulating tumor cells (CTC) from different types of sa
91             Cancer stem-like cells (CSC) and circulating tumor cells (CTC) have related properties as
92                                              Circulating tumor cells (CTC) in blood are promising new
93                                              Circulating tumor cells (CTC) in the blood are hypothesi
94                                              Circulating tumor cells (CTC) in the peripheral blood co
95                        Blood tests to detect circulating tumor cells (CTC) offer great potential to m
96  are launched into the bloodstream as single circulating tumor cells (CTC) or multicellular CTC clust
97                                              Circulating tumor cells (CTC) released into blood from p
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
100                       Further, both cCAF and circulating tumor cells (CTC) were significantly greater
101                   Here, we evaluated whether circulating tumor cells (CTC) with aberrant ALK-FISH pat
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
105 temic dissemination is most likely caused by circulating tumor cells (CTC).
106 al applications, most recently for isolating circulating tumor cells (CTC).
107 tection of circulating tumor DNA (ctDNA) and circulating tumor cells (CTC).
108 fective metastatic chemoprevention targeting circulating tumor cells (CTC).
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
115                                              Circulating tumor cells (CTCs) and disseminated tumor ce
116              We determined the prevalence of circulating tumor cells (CTCs) and explored their utilit
117                                              Circulating tumor cells (CTCs) and plasma levels of Epst
118 y tumor growth but blocked the production of circulating tumor cells (CTCs) and the formation of lymp
119                                              Circulating tumor cells (CTCs) are a treasure trove of i
120                                              Circulating tumor cells (CTCs) are an important biomarke
121                                              Circulating tumor cells (CTCs) are cancer cells released
122                                              Circulating tumor cells (CTCs) are established cancer bi
123                                              Circulating tumor cells (CTCs) are exfoliated at various
124                                              Circulating tumor cells (CTCs) are important biomarkers
125                                              Circulating tumor cells (CTCs) are important targets for
126                                              Circulating tumor cells (CTCs) are of great interest in
127                                              Circulating tumor cells (CTCs) are of recognized importa
128                                              Circulating tumor cells (CTCs) are phenotypically hetero
129                                              Circulating tumor cells (CTCs) are present at low concen
130                                              Circulating tumor cells (CTCs) are promising biomarkers
131                                              Circulating tumor cells (CTCs) are rare cancer cells tha
132                                              Circulating tumor cells (CTCs) are shed from a solid tum
133                                              Circulating tumor cells (CTCs) are shed into the bloodst
134                                              Circulating tumor cells (CTCs) are shed into the bloodst
135 cusing microfluidic approaches in retrieving circulating tumor cells (CTCs) at single-cell resolution
136                        Molecular analysis of circulating tumor cells (CTCs) at single-cell resolution
137                                 Detection of circulating tumor cells (CTCs) at the time of surgery ma
138 The methods for isolating rare cells such as circulating tumor cells (CTCs) can be generally classifi
139                           Direct analysis of circulating tumor cells (CTCs) can inform on molecular m
140      Characterization of rare, heterogeneous circulating tumor cells (CTCs) can provide insight into
141                                              Circulating tumor cells (CTCs) contain metastatic precur
142 en receptor splice variant-7 (AR-V7) mRNA in circulating tumor cells (CTCs) correlated with poor outc
143                                              Circulating tumor cells (CTCs) derived from a primary tu
144  Anticancer drug efficacy has been tested on circulating tumor cells (CTCs) derived from patient bloo
145                                              Circulating tumor cells (CTCs) detection, enumeration an
146                                              Circulating tumor cells (CTCs) disseminate from the prim
147        We evaluated the prognostic impact of circulating tumor cells (CTCs) for patients with presume
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
151                                 Isolation of circulating tumor cells (CTCs) from blood samples has im
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
158                       Sensitive detection of circulating tumor cells (CTCs) from patients' peripheral
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
161                    Isolation and analysis of circulating tumor cells (CTCs) from the blood of patient
162 lterations in single primary tumor cells and circulating tumor cells (CTCs) from the same patient.
163            The enumeration of EpCAM-positive circulating tumor cells (CTCs) has allowed estimation of
164                  More recently, detection of circulating tumor cells (CTCs) has been considered as an
165                                Evaluation of circulating tumor cells (CTCs) has demonstrated clinical
166                               Enumeration of circulating tumor cells (CTCs) has proved valuable for e
167      The ability to isolate and analyze rare circulating tumor cells (CTCs) has the potential to furt
168                                              Circulating tumor cells (CTCs) have a great potential as
169                                              Circulating tumor cells (CTCs) have become an establishe
170                                 For example, circulating tumor cells (CTCs) have been demonstrated as
171 l as surface marker identification of single circulating tumor cells (CTCs) have been demonstrated.
172                                              Circulating tumor cells (CTCs) have been detected by us
173                                              Circulating tumor cells (CTCs) have been linked to cance
174                                     Although circulating tumor cells (CTCs) have potential as diagnos
175                                              Circulating tumor cells (CTCs) have the potential of bec
176 cance of disseminated tumor cells (DTCs) and circulating tumor cells (CTCs) in 1 cohort of patients w
177                                              Circulating tumor cells (CTCs) in blood are associated w
178 quantification and in situ identification of circulating tumor cells (CTCs) in blood are still elusiv
179                                              Circulating tumor cells (CTCs) in blood can provide valu
180 e (Fe(3)O(4)) nanoparticles (NPs) to capture circulating tumor cells (CTCs) in blood for head and nec
181 sensitive, selective, and rapid detection of circulating tumor cells (CTCs) in blood samples.
182               Presence and frequency of rare circulating tumor cells (CTCs) in bloodstreams of cancer
183          We investigated the relationship of circulating tumor cells (CTCs) in non-small cell lung ca
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
186       Detection and characterization of rare circulating tumor cells (CTCs) in patients' blood is imp
187                We tested the hypothesis that circulating tumor cells (CTCs) in preoperative periphera
188                             The detection of circulating tumor cells (CTCs) in the blood of cancer pa
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
194           The identification and analysis of circulating tumor cells (CTCs) is an important goal for
195                          Magnetic capture of circulating tumor cells (CTCs) is one of the most promis
196 port that elevated expression of each GEF in circulating tumor cells (CTCs) isolated from the periphe
197                The detection and analysis of circulating tumor cells (CTCs) may enable a broad range
198                                              Circulating tumor cells (CTCs) may have utility as surro
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 (
202                                              Circulating tumor cells (CTCs) play a fundamental role i
203                                              Circulating tumor cells (CTCs) provide the capacity for
204                              The analysis of circulating tumor cells (CTCs) provides a means to colle
205                                  Analysis of circulating tumor cells (CTCs) provides real-time measur
206                                              Circulating tumor cells (CTCs) represent a surrogate bio
207                                              Circulating tumor cells (CTCs) shed from solid tumors ca
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
210                                              Circulating tumor cells (CTCs) were detected in the hepa
211                                  We assessed circulating tumor cells (CTCs) with epithelial and mesen
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
215                        We find that cultured circulating tumor cells (CTCs), derived from blood sampl
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
220                Measuring PD-L1 expression in circulating tumor cells (CTCs), may allow real-time moni
221                                              Circulating tumor cells (CTCs), which are prevalent in S
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
225 cancer cells is a new approach for detecting circulating tumor cells (CTCs).
226 gement diagnosis could be performed by using circulating tumor cells (CTCs).
227  for simultaneous isolation and detection of circulating tumor cells (CTCs).
228 el single cell analysis platforms focused on circulating tumor cells (CTCs).
229                                    Increased circulating tumor cells (CTCs; five or more CTCs per 7.5
230            Within an elaborate case study of circulating tumor cells derived from prostate cancer pat
231 were tested for the presence and quantity of circulating tumor cell-derived nucleases.
232 d has been an effective tool to perform rare Circulating Tumor Cells detection.
233                Clinical data on survival and circulating tumor cell DNA (ctDNA) concentrations were u
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
241                        Detection of AR-V7 in circulating tumor cells from patients with castration-re
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
244 te early treatment of metastasis by clearing circulating tumor cells from vasculature.
245 hly sensitive microfluidic system to capture circulating tumor cells from whole blood of cancer patie
246                    Further dissection of the circulating tumor cell gene signature identified signali
247  CTC transcriptomes, we discovered a unique "circulating tumor cell gene signature" that is distinct
248 tients with informative unfavorable baseline circulating tumor cells &gt;= 5/7.5 mL of blood, 16 (59%) s
249 rs such as cancer antigen 15-3 (CA 15-3) and circulating tumor cells have been widely studied.
250             Detection of rare cells, such as circulating tumor cells, have many clinical applications
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
259                                              Circulating tumor cells in the blood of patients are bot
260  and this was associated with a reduction in circulating tumor cells in the E2F2 knockout.
261  markers such as cell-free nucleic acids and circulating tumor cells in the peripheral blood.
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
264 the survival and growth of metastasizing and circulating tumor cells in vivo.
265  specific cells from complex matrices (i.e., circulating tumor cells in whole blood).
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
269        AR-V expression in patient tissues or circulating tumor cells is associated with resistance to
270        A platform for capture and release of circulating tumor cells is demonstrated by utilizing pol
271          Since hematogenous dissemination of circulating tumor cells is the major route of metastasis
272       In studies in vivo, we discovered that circulating tumor cells labeled with the nanohybrids gen
273 of fluid-based assays, notably, exosomes and circulating tumor cells (liquid biopsy), as tools for fu
274 od, 16 (59%) showed conversions to favorable circulating tumor cells &lt; 5.
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
277                   To colonize distant sites, circulating tumor cells must destabilize the endothelial
278                               In this model, circulating tumor cell numbers are significantly reduced
279 on, where active YAP increased the number of circulating tumor cells over time.
280 ng predictor of PFS, even in the presence of circulating tumor cells ( P = .004).
281 cific biomolecules, including nucleic acids, circulating tumor cells, proteins, antibodies, and extra
282                                              Circulating tumor cells provide a source of noninvasivel
283 ug assays with patient-derived cells such as circulating tumor cells requires manipulating small samp
284               Moreover, the observation that circulating tumor cells resemble the parental cell line,
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
287 ovides an important new tool for identifying circulating tumor cell subtypes.
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
296                CA 15-3 levels and numbers of circulating tumor cells were measured at identical time
297                                 Furthermore, circulating tumor cells were significantly reduced in tu
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
300       Moreover, recent analyses suggest that circulating tumor cells within the vasculature often exi

 
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