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1 We found that it induces reversion of epithelial to mesenchymal transition.
2 gulation of AKT/mTOR or in those involved in epithelial to mesenchymal transition.
3 ponents and their regulators associated with epithelial to mesenchymal transition.
4 a result SNAI1 is stabilized, triggering an epithelial to mesenchymal transition.
5 e and altered the expressions of markers for epithelial to mesenchymal transition.
6 factors best known for their role in driving epithelial to mesenchymal transition.
7 eat shock protein 27 (HSP27); and markers of epithelial-to-mesenchymal transition.
8 induces markers of the primitive streak and epithelial-to-mesenchymal transition.
9 enhancing expression of the genes related to epithelial-to-mesenchymal transition.
10 sed extracellular matrix, cell adhesion, and epithelial-to-mesenchymal transition.
11 ression of twist1b-a well-known regulator of epithelial-to-mesenchymal transition.
12 onize distant sites, including the so-called epithelial-to-mesenchymal transition.
13 , including cell cycle arrest, apoptosis and epithelial-to-mesenchymal transition.
14 poorly differentiated state with features of epithelial-to-mesenchymal transition.
15 (MUC1-CT) represent initiating steps in the epithelial-to-mesenchymal transition.
16 static potential through the upregulation of epithelial-to-mesenchymal transition.
17 arcinomas marked by poor differentiation and epithelial-to-mesenchymal transition.
18 as computationally designed and that impairs epithelial-to-mesenchymal transition.
19 n of a set of transcription factors to drive epithelial-to-mesenchymal transition.
20 proliferation, cancer stem cell biology, and epithelial-to-mesenchymal transition.
21 experimental metastases in fact undergo the epithelial-to-mesenchymal transition.
22 rd chemokine loop that further drives an IBC epithelial-to-mesenchymal transition.
23 re correct epithelial cell shape and prevent epithelial-to-mesenchymal transitions.
25 and gene expression analysis of oncogenesis, epithelial to mesenchymal transition and apoptosis pathw
26 ysis, angiogenesis, cell-matrix interaction, epithelial to mesenchymal transition and metastatic abil
27 catenin signaling acts as a switch to induce epithelial to mesenchymal transition and promote colorec
28 Given that DDR2 has a crucial role in the epithelial-to-mesenchymal transition and cancer progress
29 in tumor progression and resistance, such as epithelial-to-mesenchymal transition and cell adhesion p
30 itabine recovers FBXL7 expression and limits epithelial-to-mesenchymal transition and cell invasion i
31 ERK1/2 hyperactivation drives ZEB1-dependent epithelial-to-mesenchymal transition and chemoresistance
33 es we show MBC-specific increases related to epithelial-to-mesenchymal transition and extracellular m
34 PEB2B isoform inhibited pathways driving the epithelial-to-mesenchymal transition and hypoxic respons
35 aling cascade culminating in Slug induction, epithelial-to-mesenchymal transition and increased invas
37 the posterior side of the embryo undergo an epithelial-to-mesenchymal transition and ingress through
39 invasive abilities and higher expression of epithelial-to-mesenchymal transition and mammary stem ce
40 mals, various in vitro and in vivo models of epithelial-to-mesenchymal transition and metastasis, an
41 on protein products of genes instrumental to epithelial-to-mesenchymal transition and metastasis.
43 knockdown enhanced the invasiveness, induced epithelial-to-mesenchymal transition and promoted metast
44 dergo an order-to-disorder transition via an epithelial-to-mesenchymal transition and sort symmetrica
45 te-induced airway remodeling by facilitating epithelial-to-mesenchymal transition and STAT3/NF-kappaB
46 henotypes were also affected at the level of epithelial-to-mesenchymal transition and the ERK1/2 sign
47 -8), real-time polymerase chain reaction for epithelial-to-mesenchymal transition and tight junction
48 ve enhanced glycocalyx height in response to epithelial-to-mesenchymal transition and to oncogenic KR
49 structure and gene expression suggestive of epithelial-to-mesenchymal transition and transdifferenti
50 ures and exhibited features of self-renewal, epithelial-to-mesenchymal transition and tumor initiatio
51 e report the novel functions of PHF8 in EMT (epithelial to mesenchymal transition) and breast cancer
52 ic cells were used to evaluate the CSC, EMT (epithelial-to-mesenchymal transition), and metabolic pro
53 issue remodeling, cytoskeletal organization, epithelial-to-mesenchymal transition, and cellular migra
54 including profibrotic genes, genes promoting epithelial-to-mesenchymal transition, and genes associat
55 point were associated with moderate hypoxia, epithelial-to-mesenchymal transition, and inflammatory r
56 XCL11 significantly induced tumor migration, epithelial-to-mesenchymal transition, and matrix remodel
57 minal layer, led epithelial cells to undergo epithelial-to-mesenchymal transition, and resulted in la
58 al and resistance to environmental stresses, epithelial-to-mesenchymal transition, and the emergence
59 regulation, extracellular matrix remodeling, epithelial-to-mesenchymal transition, and the enrichment
60 umor angiogenesis, cell adhesion, migration, epithelial-to-mesenchymal transition, and transendotheli
61 cal processes, including tissue homeostasis, epithelial-to-mesenchymal transition, and wound repair.
62 uire mobility and invasiveness by undergoing epithelial-to-mesenchymal transition, and yet most metas
63 s in altered expression of genes involved in epithelial-to-mesenchymal transition, angiogenesis, and
65 t and -independent AR signaling mediated HCC epithelial-to-mesenchymal transition by regulating the t
66 nd metastasis, including analysis of partial epithelial-to-mesenchymal transition, cell isolation and
67 tes several key oncogenic processes, such as epithelial-to-mesenchymal transition, cellular migration
68 population of progenitor cells that undergo epithelial-to-mesenchymal transition displaying characte
69 6-E7 proteins augmented invasion and induced epithelial to mesenchymal transition (EMT) accompanied b
70 ODH promotes NSCLC tumorigenesis by inducing epithelial to mesenchymal transition (EMT) and IKKalpha-
71 l glycine t-butylester) abrogates GH-induced epithelial to mesenchymal transition (EMT) and is associ
72 (UTR) nucleic acid regulatory motif, driving epithelial to mesenchymal transition (EMT) and metastasi
74 gests that cell-fate transitions such as the epithelial to mesenchymal transition (EMT) are associate
75 (miRNA-200) family have a regulatory role in epithelial to mesenchymal transition (EMT) by suppressin
76 tion with canonical Wnt signaling during the epithelial to mesenchymal transition (EMT) from NMP to m
80 icroenvironment and acts as a key inducer of epithelial to mesenchymal transition (EMT) in lung cance
81 ow that the initiation of limb formation, an epithelial to mesenchymal transition (EMT) in the latera
84 detachment, misplaced retinal cells undergo epithelial to mesenchymal transition (EMT) to form contr
85 dherens junctions, dedifferentiation, and an epithelial to mesenchymal transition (EMT) transcription
87 is study, we investigated ST6Gal-I's role in epithelial to mesenchymal transition (EMT) using the Sui
88 the chorioamniotic membranes consistent with epithelial to mesenchymal transition (EMT) with loss of
89 ) a hormone related subtype, associated with Epithelial to Mesenchymal Transition (EMT), and gain of
90 harbor its receptor, leads to occurrence of epithelial to mesenchymal transition (EMT), in time and
93 ar event during embryonic development called epithelial to mesenchymal transition (EMT), we hypothesi
101 nit, caused HME cells to undergo spontaneous epithelial-to-mesenchymal transition (EMT) and aberrant
102 a (GBM) is, in part, attributed to increased epithelial-to-mesenchymal transition (EMT) and enhanced
103 riptional factor is essential for triggering epithelial-to-mesenchymal transition (EMT) and inducing
104 lso play essential roles in the induction of epithelial-to-mesenchymal transition (EMT) and induction
107 ognosis is potentially due to cancer-related epithelial-to-mesenchymal transition (EMT) and poor chem
108 ingle-cell population shifts toward invasive epithelial-to-mesenchymal transition (EMT) and prolifera
109 ant induction of apoptosis and inhibition of epithelial-to-mesenchymal transition (EMT) and stemness
110 ional reprogramming of the cells, leading to epithelial-to-mesenchymal transition (EMT) and stimulati
111 taRIII-SS in lung cancer cell models induces epithelial-to-mesenchymal transition (EMT) and that thes
113 senchymal-to-epithelial transition (MET) and epithelial-to-mesenchymal transition (EMT) are important
114 uring implantation, cytotrophoblasts undergo epithelial-to-mesenchymal transition (EMT) as they diffe
116 n-regulation of TRPS1 in TNBC cells promoted epithelial-to-mesenchymal transition (EMT) by deregulati
117 -3 supports the TIC/CSC state and induces an epithelial-to-mesenchymal transition (EMT) by driving ex
118 a master regulator of cellular identity and epithelial-to-mesenchymal transition (EMT) directly repr
119 can transcriptionally regulate SNAI1, a key epithelial-to-mesenchymal transition (EMT) driver, which
121 man mammary epithelial cells that undergo an epithelial-to-mesenchymal transition (EMT) following tra
122 Transcriptome sequencing identified a strong epithelial-to-mesenchymal transition (EMT) gene signatur
126 urvival, and migration; however, its role in epithelial-to-mesenchymal transition (EMT) has been scar
127 d gene expression changes consistent with an epithelial-to-mesenchymal transition (EMT) have been ass
129 translational regulatory programs underlying epithelial-to-mesenchymal transition (EMT) in breast epi
132 Snail and Zeb transcription factors induce epithelial-to-mesenchymal transition (EMT) in embryonic
133 ession on the Wnt/beta-catenin signaling and epithelial-to-mesenchymal transition (EMT) in human CRC
136 atic cancer, especially in the regulation of epithelial-to-mesenchymal transition (EMT) in Pancreatic
137 cent study has revealed that MT1-MMP induces epithelial-to-mesenchymal transition (EMT) in prostate a
138 prostate adenocarcinoma through induction of epithelial-to-mesenchymal transition (EMT) in Pten-null
141 ce temporary or transient cell fate, such as epithelial-to-mesenchymal transition (EMT) in tumor meta
142 olarized epithelial phenotype, and ESRP1, an epithelial-to-mesenchymal transition (EMT) inhibitor.
157 red to maintain expression of metastasis and Epithelial-to-mesenchymal transition (EMT) markers and t
158 activities of lung cancer cells and reduced epithelial-to-mesenchymal transition (EMT) markers as N-
159 ssays together with qRT-PCR determination of epithelial-to-mesenchymal transition (EMT) markers were
160 n of the EOC cells and reduced expression of epithelial-to-mesenchymal transition (EMT) markers ZEB1,
162 monstrate that LRIG1 is downregulated during epithelial-to-mesenchymal transition (EMT) of human mamm
164 h STAT4 mediated EOC metastasis via inducing epithelial-to-mesenchymal transition (EMT) of ovarian ca
165 itary tumor transcriptome data revealed the "epithelial-to-mesenchymal transition (EMT) pathway" as o
166 stases requires cell dissemination utilizing epithelial-to-mesenchymal transition (EMT) program.
167 Metastatic lung cancer cells can undergo an epithelial-to-mesenchymal transition (EMT) regulated by
168 ells to undergo VM and that knockdown of the epithelial-to-mesenchymal transition (EMT) regulator, Zi
169 esicular trafficking that is associated with epithelial-to-mesenchymal transition (EMT) remains uncle
170 ased migration phenotype along with enhanced epithelial-to-mesenchymal transition (EMT) signature aft
171 confers distinct proliferative and invasive epithelial-to-mesenchymal transition (EMT) states in sub
173 e of the neural tube, these cells undergo an epithelial-to-mesenchymal transition (EMT) to delaminate
175 were characterized by a higher expression of epithelial-to-mesenchymal transition (EMT) traits and by
176 cellular matrix organization, TGFbeta genes, epithelial-to-mesenchymal transition (EMT) transcription
178 omoter methylation of three genes regulating epithelial-to-mesenchymal transition (EMT), a key mechan
180 adherin to N-cadherin is associated with the epithelial-to-mesenchymal transition (EMT), a process re
181 cells is a bona fide physiological model of epithelial-to-mesenchymal transition (EMT), a process th
182 twork of transcription factors that controls epithelial-to-mesenchymal transition (EMT), a reversible
183 s lncRNA was proven a pivotal element of the epithelial-to-mesenchymal transition (EMT), a transdiffe
184 within primary breast cancers can undergo an epithelial-to-mesenchymal transition (EMT), although the
185 eir clusters and become motile by undergoing epithelial-to-mesenchymal transition (EMT), an essential
186 cells lose PDX1 expression while undergoing epithelial-to-mesenchymal transition (EMT), and PDX1 los
187 ast cancer, increased ECM stiffness promotes epithelial-to-mesenchymal transition (EMT), cell invasio
189 ion of a beta-catenin/TCF4-dependent partial epithelial-to-mesenchymal transition (EMT), followed by
190 RNAi-mediated silencing of RASSF1A induced epithelial-to-mesenchymal transition (EMT), fomenting a
191 applied to a proposed 22-gene network of the Epithelial-to-Mesenchymal Transition (EMT), from which w
192 asticity, including transdifferentiation and epithelial-to-mesenchymal transition (EMT), in the devel
193 oor prognosis owing to its role in promoting epithelial-to-mesenchymal transition (EMT), invasiveness
194 mnion membranes during labor were subject to epithelial-to-mesenchymal transition (EMT), mediated, in
195 altered level or activity of p53, markers of epithelial-to-mesenchymal transition (EMT), or MIR34A or
196 n hepatocytes is associated with HCV-induced epithelial-to-mesenchymal transition (EMT), providing an
198 h suggested PrP and ZIP6 are critical during epithelial-to-mesenchymal transition (EMT), we investiga
199 h factor-beta (TGF-beta) is major inducer of epithelial-to-mesenchymal transition (EMT), which associ
200 derstood about the contribution of lncRNA to epithelial-to-mesenchymal transition (EMT), which correl
201 pithelial ovarian cancer (EOC) cells undergo epithelial-to-mesenchymal transition (EMT), which influe
202 ny tissue types, metastasis is fueled by the epithelial-to-mesenchymal transition (EMT)-a dynamic pro
204 ithelial cell transformation by promoting an epithelial-to-mesenchymal transition (EMT)-like phenotyp
205 difficult to treat, especially the squamous/epithelial-to-mesenchymal transition (EMT)-like subtype.
241 fumarate in mouse and human cells elicits an epithelial-to-mesenchymal-transition (EMT), a phenotypic
246 shared features, including cells undergoing epithelial-to-mesenchymal transitions (EMTs), collective
249 cific long non-coding RNA that modulates the epithelial-to-mesenchymal transition, facilitates cell m
250 ed CD133-mediated cancer stemness and hybrid epithelial-to-mesenchymal transition features in advance
251 types and correlates with the expression of epithelial-to-mesenchymal transition gene signature, a f
252 ded by ALDH5A1), and with the presence of an epithelial-to-mesenchymal transition gene signature, imp
253 r, time to formation, proliferation, volume, epithelial to mesenchymal transition, gene expression, o
254 s developmental gene programs that stimulate epithelial-to-mesenchymal transition; however, it is not
255 rP(C)), a neuronal protein known to modulate epithelial-to-mesenchymal transition in a variety of cel
257 nsion of primary cancer cells, and induce an epithelial-to-mesenchymal transition in cancer cells.
259 how plastic CSCs are, and the importance of epithelial-to-mesenchymal transition in conferring CSC p
260 of IL-8 after 24 hours, but possibly induces epithelial-to-mesenchymal transition in epithelial cells
262 GFB in platelets led to enhanced hypoxia and epithelial-to-mesenchymal transition in the primary tumo
263 cally, we found that ABHD5 knockdown induces epithelial to mesenchymal transition, increasing aerobic
268 , increased proliferation, and activation of epithelial-to-mesenchymal transition leading to increase
269 ial for stimulating stem cells to undergo an epithelial to mesenchymal transition-like process necess
270 d with cancer associated fibroblasts (CAFs), epithelial to mesenchymal transition, mesenchymal stem c
271 Concurrently, the proteins associated with epithelial-to-mesenchymal transition, N-cadherin and Vim
272 n of MRC-5 fibroblasts and TGF-beta-mediated epithelial-to-mesenchymal transition of A549 cells by in
273 n the proliferation, survival, migration and epithelial-to-mesenchymal transition of cancer cells.
274 is frequently citrullinated in cells during epithelial-to-mesenchymal transition of metastasizing ep
276 and transforming growth factor beta-induced epithelial-to-mesenchymal transition of SKOV-3 cells.
277 endothelial cells and platelets and induced epithelial-to-mesenchymal transition of tumor cells, pro
278 Snai1 activities that promote an incomplete epithelial to mesenchymal transition on a subset of epib
279 ound to promote and/or maintain the state of epithelial to mesenchymal transition on CTCs through pla
280 to tumorigenesis including TGF-beta induced epithelial-to-mesenchymal transition on NMuMG cells and
282 o a drug-tolerant state, for example through epithelial-to-mesenchymal transition or transition to a
285 7a increased expression of genes involved in epithelial-to-mesenchymal transition pathways, consisten
286 In the absence of USP9X, cells exhibited an epithelial-to-mesenchymal transition phenotype, acquired
287 d enhances cell migration especially in post-epithelial-to-mesenchymal transition (post-EMT) cancer c
288 eta-catenin and TGF-beta signalling, and pro-epithelial-to-mesenchymal transition/pro-metastatic prot
289 p53 inactivation activates a cell-autonomous epithelial-to-mesenchymal transition program leading to
290 proteins and with an increased expression of epithelial-to-mesenchymal transition-related genes.
291 n breast cancer cells increased MEK-EMT (MEK-epithelial-to-mesenchymal transition) signaling, transwe
292 tory: initiated in basal cells exhibiting an epithelial-to-mesenchymal transition signature, tumorige
293 late-stage cancer cells could facilitate the epithelial-to-mesenchymal transition, stemness, and mobi
294 C-like cells, with these cells undergoing an epithelial-to-mesenchymal transition to form clonogenic,
295 s the ability of cancer cells to undergo the epithelial-to-mesenchymal transition to invade and disse
297 uence hormone signaling, cell-cell adhesion, epithelial-to-mesenchymal transition, transforming growt
298 and differentiation, resistance to anoikis, epithelial-to-mesenchymal transition, tumor cell dormanc
300 vitro-derived epicardial cells underwent an epithelial-to-mesenchymal transition when treated with P