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1  dictated by the proliferative status of the tumor-initiating cell.
2 es are separable based on the lineage of the tumor-initiating cell.
3 odulating the lineage potential of MMTV-Wnt1 tumor initiating cells.
4 t in primary CRC, which potentially includes tumor initiating cells.
5 he elimination of undifferentiated stem-like tumor initiating cells.
6 from noisy expression data of CD44+CD24-/low tumor initiating cells.
7 gene target expression segregate to CD133(+) tumor initiating cells.
8             Tetraspanins mark stem cells and tumor initiating cells.
9 operties of 3T3 fibroblasts and glioblastoma tumor initiating cells.
10 nomic profile of residual, therapy resistant tumor initiating cells.
11 nses to NOTCH3 and expands therapy-resistant tumor-initiating cells.
12 ected strategy of immunotherapy to eradicate tumor-initiating cells.
13 ttributed to the presence of CD44-expressing tumor-initiating cells.
14 t attenuation of tumorigenicity by targeting tumor-initiating cells.
15 ewal is thought to be a critical property of tumor-initiating cells.
16  and also has been linked to the capacity of tumor-initiating cells.
17  and lung metastases are highly enriched for tumor-initiating cells.
18 dentify MELK as a potential target in breast tumor-initiating cells.
19 r eradication of primary tumors derived from tumor-initiating cells.
20 hology, suggesting a mixed-lineage origin of tumor-initiating cells.
21 say, a Lin(-)CD29(H)CD24(H) subpopulation of tumor-initiating cells.
22 gating the normal differentiation program of tumor-initiating cells.
23 sis, providing signals that maintain mammary tumor-initiating cells.
24 d in a decline in kynurenine production from tumor-initiating cells.
25 nt of effective therapeutic agents targeting tumor-initiating cells.
26 ed to be resistant to chemotherapy caused by tumor-initiating cells.
27 t Rspo1 and the Sca1-population, enriched in tumor-initiating cells.
28 emalignant cells and activates quiescence in tumor-initiating cells.
29 oRNA-203 promotes selection and expansion of tumor-initiating cells.
30 ions suggest an active selection process for tumor-initiating cells.
31 ignature similar to that observed for human 'tumor-initiating' cells.
32 flammatory cytokine production, and increase tumor-initiating cell abundance and metastatic progressi
33 the effects of Smoothened antagonists on BCC tumor initiating cell and also suggest that currently av
34 evels results in reduced tumor growth, fewer tumor initiating cells and reduced metastasis within the
35 in turn, regulate the relative proportion of tumor initiating cells and the latency of her-2-driven t
36 the mTORC1 kinase induces differentiation of tumor-initiating cells and allows their subsequent deple
37 at the oncofetal protein 5T4 is expressed on tumor-initiating cells and associated with worse clinica
38 cancer models, we found that TcdBFBD reduces tumor-initiating cells and attenuates growth of basal-li
39 mal transition-driving genes, reminiscent of tumor-initiating cells and claudin-low breast cancer.
40 ed endothelial cells (TDECs) originated from tumor-initiating cells and did not result from cell fusi
41 horylated by a Jak2-mediated pathway only in tumor-initiating cells and in human SHH-type medulloblas
42 to maintain proper exon recognition in brain tumor-initiating cells and may provide new inroads for n
43  at the intersections of stem cell function, tumor-initiating cells and multilineage tumor developmen
44 ms by which RA targets GBM-derived stem-like tumor-initiating cells and novel targets applicable to d
45 how that Fzd7 marks a population of putative tumor-initiating cells and that targeting Fzd7 offers a
46                                     However, tumor-initiating cells and the biological processes that
47  glioblastoma identifies regulators of brain tumor-initiating cells and tumor growth that could serve
48          In this study, the subpopulation of tumor-initiating cells and Wnt signaling pathway activat
49 ined a mixture of red cells (PDGF-expressing/tumor-initiating cells) and green cells (recruited proge
50 iforme (GBM) research is the identity of the tumor-initiating cell, and its contribution to the malig
51 mor cell growth, decreased the proportion of tumor-initiating cells, and decreased tumor formation in
52 resistance, identification of stem cells and tumor-initiating cells, and development of mouse models
53 ) in ovarian cancer cells and ovarian cancer tumor-initiating cells, and that knockdown of SFXN4 inhi
54                            This osteosarcoma tumor-initiating cell appears highly prolific and consti
55 and cell deformability, and demonstrate that tumor-initiating cells are less differentiated in terms
56                                        While tumor-initiating cells are Lgr5(+), most disseminated ca
57                 Cancer stem cells (CSCs), or tumor-initiating cells, are involved in tumor progressio
58 an prospectively identify glioblastoma brain tumor initiating cells as well as human muscle stem cell
59 ng possibility that these cells could be the tumor-initiating cells, as has been suggested for adult
60 pithelial progenitor cell reprogramming into tumor initiating cells at single cell resolution.
61 rowth through the generation or expansion of tumor initiating cells bearing stem-like characteristics
62 onchio-alveolar stem cells (BASCs), putative tumor-initiating cells, both in vitro and in vivo.
63  Breast tumors may derive from self-renewing tumor-initiating cells (BT-ICs), which contribute to tum
64 nd has an important role in regulating brain tumor-initiating cells (BTIC) in GBM.
65 enic signaling by NOTCH is elevated in brain tumor-initiating cells (BTIC) in malignant glioma, but t
66 bolic dysregulation in patient-derived brain tumor-initiating cells (BTIC) to a nexus between MYC and
67 ere elevated in areas infiltrated with brain tumor-initiating cells (BTIC).
68                                        Brain tumor initiating cells (BTICs) co-opt the neuronal high
69 of the endosomal GTPase Rab35 in human brain tumor initiating cells (BTICs) increases glioblastoma gr
70  to tumor progression by enriching for brain tumor initiating cells (BTICs) owing to preferential BTI
71                                        Brain tumor initiating cells (BTICs), also known as cancer ste
72 eractions modulate the galvanotaxis of brain tumor initiating cells (BTICs).
73                                        Brain tumor-initiating cells (BTICs) and orthotopic xenografts
74                           Here we used brain tumor-initiating cells (BTICs) and show that BTICs expre
75                                        Brain tumor-initiating cells (BTICs) drive glioblastoma growth
76 e et al. determined that GSI-resistant brain tumor-initiating cells (BTICs) from GBM express a higher
77                                        Brain tumor-initiating cells (BTICs) have been identified as k
78  both glioma stemlike cells (GSCs) and brain tumor-initiating cells (BTICs) have been implicated in G
79                       In addition, GBM brain tumor-initiating cells (BTICs) increase expression of ca
80 m cell regulatory pathways to maintain brain tumor-initiating cells (BTICs), also known as cancer ste
81  sub-fraction of cancer cells, termed breast tumor-initiating cells (BTICs), that undergo epithelial
82 r cell lines and patient tumor-derived brain tumor-initiating cells (BTICs).
83 rtance of TrkB and TrkC in survival of brain tumor-initiating cells (BTICs).
84 duced tumors contained a large percentage of tumor-initiating cells, but these were reduced significa
85 e tumor growth, angiogenesis, metastasis and tumor-initiating cells by in vivo imaging and provide a
86                           An accumulation of tumor-initiating cells can be found in 2% to 50% of all
87                             The concept that tumor-initiating cells can co-opt the self-renewal progr
88                                       CD133+ tumor-initiating cells can originate from proliferating
89 to the unique properties of iron handling in tumor-initiating cells (cancer stem cells), novel contri
90         Cancer stem cells are proposed to be tumor-initiating cells capable of tumorigenesis, recurre
91                                              Tumor-initiating cells (CD44(+)) have been described for
92 Fbeta drives Notch1-mediated EMT to generate tumor initiating cells characterized by high CD44 expres
93 proposed to be composed of two compartments: tumor-initiating cells characterized by a slow and asymm
94 )CXCR4(+) (CXC receptor 4) colorectal cancer tumor-initiating cells (Co-TICs) and the LN stromal micr
95          Cancer stem cells (CSC; also called tumor-initiating cells) comprise tumor cell subpopulatio
96                 Cancer stem cells (CSCs), or tumor-initiating cells, comprise a subset of tumor cells
97 equired for maintenance of cancer stem cells/tumor-initiating cells (CSCs/TICs), which drive tumorige
98 e showed recently that cancer stem cells, or tumor-initiating cells, derived from human glioblastoma
99                                  Cancer stem/tumor-initiating cells display stress tolerance and meta
100                                              Tumor initiating cells displayed a distinct stem-like st
101 p19(ARF) profoundly influences the nature of tumor-initiating cells during BCR/ABL-mediated leukemoge
102 ell tracking method to follow up the fate of tumor-initiating cells during chemotherapy.
103  lineage-associated OLIG2(+) progenitors are tumor-initiating cells during medulloblastoma tumorigene
104 ations, as well as the CD61(high)CD49f(high) tumor-initiating cell-enriched population.
105 e: Coupling single-cell transcriptomics with tumor-initiating cell enrichment identified IFN response
106                                        These tumor-initiating cells express stem cell markers.
107 tiation in prostate progenitors, presumptive tumor initiating cells for prostate cancer.
108  of cancer.(1-4) The nature and existence of tumor-initiating cells for leukemia and other malignanci
109  xenograft growth assays, we determined that tumor initiating cell frequencies approximate one per 1.
110                 SFX-01 significantly reduced tumor-initiating cell frequency in secondary transplants
111 he growth of a range of tumor types, reduces tumor-initiating cell frequency, and exhibits synergisti
112 bition of SCD1 abrogates chemoresistance and tumor-initiating cell frequency.
113 ink colitis and cancer identifying potential tumor-initiating cells from colitic patients, suggesting
114 d basal-like TNBC tumors in mice and blocked tumor-initiating cell function and macrometastasis.
115 n expression of antigens thought to identify tumor initiating cells, generation of 3D aggregates when
116 novel HSP90 inhibitor, NVP-HSP990, in glioma tumor-initiating cell (GIC) populations, which are stron
117 t brain tumor, harbors a small population of tumor initiating cells (glioblastoma stem cells) that ha
118 rmation and viability of primary human colon tumor-initiating cells harboring mutant KRAS.
119 ther tumor cell holoclones genuinely contain tumor-initiating cells has not been directly addressed.
120                                              Tumor-initiating cells have been suggested to be rare in
121 , the mechanisms that regulate quiescence in tumor-initiating cells have not been analyzed in detail
122 ulations called cancer stem cells (CSCs), or tumor-initiating cells, have been defined in functional
123 astic modulus induced in 3T3 fibroblasts and tumor initiating cells in response to agents that soften
124 ed in airway epithelial repair that may be a tumor-initiating cell in lung cancer and which may be as
125                We explored the nature of the tumor-initiating cell in osteosarcoma, a bone malignancy
126 terogeneity between tumor-initiating and non-tumor-initiating cells in glioblastoma.
127 tify the entire population of epithelial and tumor-initiating cells in human metastatic colon cancer.
128 em cells or intermediate progenitors are the tumor-initiating cells in lola mutants.
129  However, the precise contribution of CD133+ tumor-initiating cells in mediating colon cancer metasta
130  commitment and promotes the accumulation of tumor-initiating cells in pre-neoplastic cells.
131 in signaling can further demarcate high-ALDH tumor-initiating cells in the nondysplastic epithelium o
132 that reparative K14+ progenitor cells may be tumor-initiating cells in this subgroup of smokers with
133 this LEFTY1-BMPR2 interaction is specific to tumor-initiating cells in triple-negative breast cancer
134 erapeutic agents is effective in killing the tumor-initiating cells in vitro and inhibits tumor forma
135 nation in inducing differentiation of breast tumor-initiating cells in vivo Furthermore, gene express
136 astasis, and recurrence, and targeting these tumor-initiating cells is necessary to eradicate tumors.
137    Although the role of CD271 as a marker of tumor-initiating cells is still a matter of debate, its
138 that human malignant glioma tissues and also tumor-initiating cells isolated from fresh human maligna
139 eficiencies) that were derived from CD44(hi) tumor-initiating cells isolated from PCa-20a cells.
140                                          The tumor-initiating cells isolated from these tumors that f
141 CNOT3 expression, as might be expected for a tumor-initiating cell marker.
142 ve and tumorigenic capacities of the mammary tumor-initiating cells (MaTICs) of claudin-low breast ca
143 val in brain tumors and other cancers; thus, tumor initiating cells may extract nutrients with high a
144 in pre-malignant DCIS lesions and that these tumor-initiating cells may determine the phenotype of DC
145 e viability and maintenance of self-renewing tumor-initiating cells may ultimately lead to improved t
146            However, despite the diversity of tumor-initiating cells, most prostate cancer cells expre
147 livary gland imaginal ring, we find that the tumor-initiating cells normally undergo endoreplication
148 nd by increased reliance of cancer cells and tumor-initiating cells on mitochondria, resulting in pot
149 od that enriches cancer stem cells (CSCs) or tumor-initiating cells on the basis of cell adhesion pro
150 renewing, and highly metastatic cells called tumor initiating cells or cancer stem cells (CSCs).
151 for tumor initiation and propagation, termed tumor initiating cells or cancer stem cells (CSCs).
152 y a reservoir of self-renewing cells, termed tumor-initiating cells or cancer stem cells.
153                In SC precursors, which model tumor-initiating cells, pharmacological and genetic inhi
154 n epithelial-to-mesenchymal transition and a tumor initiating cell phenotype, and that it is required
155   PKCiota-ELF3-NOTCH3 signaling controls the tumor-initiating cell phenotype by regulating asymmetric
156 the Lin(-)CD29(H)CD24(H) mouse mammary gland tumor-initiating cell population include those involved
157                 Focusing on one example of a tumor-initiating cell population, we demonstrate that th
158 arker for distinct subsets of chemoresistant tumor-initiating cell populations in diverse human malig
159  to target both established tumor masses and tumor-initiating cell populations.
160 pigenomic profiling revealed that IFE and HF tumor-initiating cells possess distinct chromatin landsc
161 ), consistent with the selective survival of tumor-initiating cells posttreatment.
162 elf-renewal, acting in a small population of tumor-initiating cells present in tumors.
163                                 YAP-mediated tumor initiating cell programs included activation of on
164 r subpopulation, termed cancer stem cells or tumor-initiating cells, promotes therapeutic resistance
165                        The identification of tumor-initiating cells represents a significant challeng
166 uding glioma stem cells (GSC), which are the tumor-initiating cells responsible for treatment failure
167  tumors, which are driven by a component of 'tumor-initiating cells' retaining stem cell properties.
168 enuate cancer stem cell markers, inhibit the tumor-initiating cell's neurosphere-forming capacity, an
169 ddition to angiogenic effects, VEGF promotes tumor-initiating cell self-renewal through VEGFR-2/STAT3
170 rt differential drug sensitivity, indicating tumor-initiating cell states and genetic drivers dictate
171 Here we showed that the basal cell carcinoma tumor-initiating cell surface protein CD200, through ect
172 140/SOX2 pathway critically regulates breast tumor-initiating cell survival, providing a new link bet
173 ribe the isolation and characterization of a tumor-initiating cell (T-IC) subpopulation in primary hu
174 t evidence has demonstrated the existence of tumor-initiating cells (T-ICs) as the culprit for treatm
175 r can arise from a cancer stem cell (CSC), a tumor-initiating cell that has properties similar to tho
176      Human melanomas contain a population of tumor-initiating cells that are able to maintain the gro
177  existence of a small population of CD133(+) tumor-initiating cells that are capable of regenerating
178 own about chromatin mechanisms that regulate tumor-initiating cells that are proposed to be responsib
179 fectively eliminate the subpopulation of GBM tumor-initiating cells that are responsible for relapse.
180 mor growth in vivo, decreasing the number of tumor-initiating cells, thus supporting its pro-oncogeni
181    The effectiveness of CD133NPs in reducing tumor initiating cell (TIC) fraction was investigated us
182 s leads to an induction of a CD24(-)/CD44(+) tumor initiating cell (TIC) population (4) sGRP78(+) bre
183  in pancreatic cancer along with a decreased tumor initiating cell (TIC) population in pancreatic tum
184 tumor sphere formation, a characteristics of tumor initiating cell (TIC).
185                                              Tumor initiating cells (TIC) have been suggested as a me
186 al-mesenchymal transition (EMT), promoting a tumor-initiating cell (TIC) phenotype characterized by i
187 sition reversibly between slow-proliferating tumor-initiating cells (TIC) and their differentiated, f
188                                              Tumor-initiating cells (TIC) are critical yet evasive ta
189                                              Tumor-initiating cells (TIC) are dynamic cancer cell sub
190 y of continuous culture models and human GBM tumor-initiating cells (TIC) in both Boyden chamber and
191           ALDH1(+)CD44(+) cells are putative tumor-initiating cells (TIC) in head and neck squamous c
192 f) receptor 2 (CCR2) decreases the number of tumor-initiating cells (TIC) in pancreatic tumors.
193      Understanding the mechanisms supporting tumor-initiating cells (TIC) is vital to combat advanced
194                                       Breast tumor-initiating cells (TIC) may contribute to tumor pro
195                A tumor cell subpopulation of tumor-initiating cells (TIC) or "cancer stem cells" is a
196  Emerging evidence indicates the presence of tumor-initiating cells (TIC) or cancer stem cells in ost
197                                              Tumor-initiating cells (TIC) perpetuate tumor growth, en
198 ypothesis that HER2/HER3 signaling in breast tumor-initiating cells (TIC) promotes self-renewal and s
199                                              Tumor-initiating cells (TIC) represent cancer stem-like
200 play cellular hierarchies with self-renewing tumor-initiating cells (TIC), also known as cancer stem
201 y organized and driven by a subpopulation of tumor-initiating cells (TIC), or cancer stem cells.
202 P) cells showed up to a 3-fold enrichment of tumor-initiating cells (TIC), suggestive of a sanctuary
203             In examining the role of EGFR in tumor-initiating cells (TIC), we found that EGFR express
204 cancer recurrence is thought to be driven by tumor-initiating cells (TIC).
205 inflammatory markers and spheroid-generating tumor-initiating cells (TIC).
206 ibitors, in particular those that can target tumor-initiating cells (TIC).
207 microenvironment to promote proliferation of tumor initiating cells (TICs) and carcinogenesis.
208                                    Isolating tumor initiating cells (TICs) often requires screening o
209 rogression and relapse is conceivably due to tumor initiating cells (TICs)/cancer stem cells.
210 (RTK)/RAS signaling can lead to outgrowth of tumor-initiating cells (TICs) and drive therapeutic resi
211 ene expression signatures derived from human tumor-initiating cells (TICs) and human mammary stem cel
212 s by activating JAK/STAT signaling in breast tumor-initiating cells (TICs) and promoted TIC self rene
213 east cancer cells bearing characteristics of tumor-initiating cells (TICs) and that strongly associat
214             Targeting the cross-talk between tumor-initiating cells (TICs) and the niche microenviron
215                                              Tumor-initiating cells (TICs) are a sub-population of ce
216                                              Tumor-initiating cells (TICs) are particularly efficient
217                              To determine if tumor-initiating cells (TICs) are present in SCCas, we u
218                                              Tumor-initiating cells (TICs) are thought to be critical
219                               These distinct tumor-initiating cells (TICs) clonally recapitulated the
220 rogression in cancer requires populations of tumor-initiating cells (TICs) endowed with unlimited sel
221                                              Tumor-initiating cells (TICs) have been shown both exper
222  (MECs) to mammary stem cells (MaSCs) and to tumor-initiating cells (TICs) have not been entirely elu
223                            The proportion of tumor-initiating cells (TICs) in the mammary tumors from
224 dentification of therapeutic targets against tumor-initiating cells (TICs) is a priority in the devel
225                                              Tumor-initiating cells (TICs) share features and regulat
226 ucing kinase (NIK), support the expansion of tumor-initiating cells (TICs) that copurify with a CD24(
227 , and treatment resistance is potentiated by tumor-initiating cells (TICs) that thrive under hypoxia.
228  Moreover, GDF15 induces the expansion of MM tumor-initiating cells (TICs), and changes in the serum
229 of cancer in which only a fraction of cells, tumor-initiating cells (TICs), can sustain tumor growth.
230  lentiviral particles, and transduction into tumor-initiating cells (TICs), followed by in vivo trans
231 o has therapeutic implications for targeting tumor-initiating cells (TICs), the tumor stroma, and che
232 oncogene-induced expansion and activities of tumor-initiating cells (TICs), whereas it is largely dis
233 njury and establishes selective pressure for tumor-initiating cells (TICs), which proliferate to form
234 ncer of Zeste Homolog 2 (EZH2) and increased tumor-initiating cells (TICs).
235 ane transport in bulk tumor cells (BTCs) and tumor-initiating cells (TICs).
236 tributed to cancer stem-like cells (CSCs) or tumor-initiating cells (TICs).
237 ssed in and regulates self renewal of breast tumor-initiating cells (TICs).
238 n by a population of stem-like cells, called tumor-initiating cells (TICs).
239 ry significantly stimulates the expansion of tumor-initiating cells (TICs).
240 bserved in a genetic model of ovarian cancer tumor-initiating cells (TICs).
241 ancy-associated traits and the properties of tumor-initiating cells (TICs).
242 as been attributed to expansion of stem-like tumor-initiating cells (TICs).
243  drugs that specifically target glioblastoma tumor-initiating cells (TICs).
244 gulation of CD44, a ubiquitous marker of PCa tumor-initiating cells (TICs)/stem cells.
245 ds on a small subset of tumor cells, called "tumor-initiating cells" (TICs), with SC-like properties.
246  inhibition of SOS1 reduced the frequency of tumor-initiating cells to curb spheroid growth in situ a
247                                              Tumor initiating cell transcriptional programs are conse
248 C receptors by ligands BDNF and NT3 enhances tumor-initiating cell viability through activation of ER
249  that breast cancer is derived from a single tumor-initiating cell with stem-like properties, but the
250                                              Tumor-initiating cells with reprogramming plasticity or
251   Within established GBM, a subpopulation of tumor-initiating cells with stem-like properties (GBM st
252 ver, interaction of accessory cells with the tumor-initiating cell within the microenvironment is oft

 
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