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1 n of RGS6, which in turn blocked Ras-induced cellular transformation.
2  the DNA-damage-induced G2/M checkpoint, and cellular transformation.
3 down was sufficient to inhibit Ras-dependent cellular transformation.
4 lic effects differ depending on the stage of cellular transformation.
5 sor pathway is a key barrier to Ras-mediated cellular transformation.
6 I3K membrane recruitment, and PI3K-dependent cellular transformation.
7 t1 in non-transformed cells did not initiate cellular transformation.
8 ed in the absence of BRCA1 may contribute to cellular transformation.
9 IP1 ubiquitination, NF-kappaB activation and cellular transformation.
10 ction-deficient hERG1 mutants also prevented cellular transformation.
11 ignaling with relevance to wound healing and cellular transformation.
12 e show that several of these mutations drive cellular transformation.
13 ssion of the carcinoma variant E295K induces cellular transformation.
14 apeutic drug-induced DNA damage and enhances cellular transformation.
15 B (BRAF) recurrent V600E mutation to promote cellular transformation.
16 hanced motility is another characteristic of cellular transformation.
17 naling is implicated in bone development and cellular transformation.
18 te viral latency and contribute to malignant cellular transformation.
19 APH-2 is dispensable for viral infection and cellular transformation.
20 ncreased chromosomal aberrations and induced cellular transformation.
21 r, leading to changes in gene expression and cellular transformation.
22 ression and is required for BCR-ABL-mediated cellular transformation.
23 er cells and may be a contributing factor to cellular transformation.
24 ch for the latter protein, is sufficient for cellular transformation.
25 lation, NF-kappaB nuclear translocation, and cellular transformation.
26 metabolism are common hallmarks of malignant cellular transformation.
27 ment, cell cycle progression, apoptosis, and cellular transformation.
28 ggered by active Galphao proteins to promote cellular transformation.
29 atory networks that if disrupted can lead to cellular transformation.
30 nase activity, leading to Src-Y527F-mediated cellular transformation.
31 vity of hVPS34 is essential for Src-mediated cellular transformation.
32  host immune evasion, cellular survival, and cellular transformation.
33 ectal cancers and are an initiating event in cellular transformation.
34 572(STOP) mutant for downstream signaling or cellular transformation.
35 modifiers is modulated at specific stages of cellular transformation.
36 , let-7, and miR-155, that are implicated in cellular transformation.
37 sufficient to cause hepatocyte dysplasia and cellular transformation.
38 pathway to repair damaged DNA and to prevent cellular transformation.
39 undamental biological events associated with cellular transformation.
40 ments contributing to normal cell growth and cellular transformation.
41 of histone-modifying complexes in regulating cellular transformation.
42 ate that elevated tRNA synthesis can promote cellular transformation.
43  regulation of the polarity machinery during cellular transformation.
44 ir influence on protein expression vis-a-vis cellular transformation.
45 ut how a gene or pathway works in regulating cellular transformation.
46 transcription were not sufficient to promote cellular transformation.
47 ivity and regulates DNA topology to suppress cellular transformation.
48 ich requires normal gene function to prevent cellular transformation.
49 th and glandular hypertrophy associated with cellular transformation.
50 mutations, leading to genome instability and cellular transformation.
51  defined epigenetic reprogramming leading to cellular transformation.
52 ymes, alterations to DNA occur that initiate cellular transformation.
53 ooperated with the HTLV-I Tax oncoprotein in cellular transformation.
54  to play an important role in virus-mediated cellular transformation.
55  play an important role in embryogenesis and cellular transformation.
56 tes and it cooperates with Ha-ras to promote cellular transformation.
57  PTEN, overexpression of NEDD4-1 potentiated cellular transformation.
58 ins c-Ski and related SnoN in the control of cellular transformation.
59 lasts and epithelial model cells resulted in cellular transformation.
60 RK-c-Jun pathway to induce antiapoptosis and cellular transformation.
61 echanisms by which EBV infection can lead to cellular transformation.
62  have an important impact on HTLV-1-mediated cellular transformation.
63 Expression of the E295K variant also induces cellular transformation.
64  organization of chromatin during EBV-driven cellular transformation.
65 otoxic stress, resulting in a higher rate of cellular transformation.
66  BRD4 downstream oncogenes and abrogation of cellular transformation.
67 ts interaction with A-Raf, and thus promotes cellular transformation.
68 , while MWFs inhibit fibrogenesis and induce cellular transformation.
69  depletion led to a decrease in LMP1-induced cellular transformation.
70  a cell-type specific function for Dnmt3a in cellular transformation.
71 -dependent inhibition of enzyme activity and cellular transformation.
72 c screen identifies genes that contribute to cellular transformation.
73                          Senescence prevents cellular transformation.
74 acted as a key regulator of Bcr-Abl-mediated cellular transformation.
75 E2F1-mediated FOS induction in As2O3-induced cellular transformation.
76 e expression as well as the implications for cellular transformation.
77 antisense protein of HTLV-3 (APH-3) promoted cellular transformation.
78 ic rearrangements, some of which can lead to cellular transformation.
79 bal protein synthesis, significantly impeded cellular transformation.
80 n 3T3 cells and are also known inhibitors of cellular transformation.
81 enes that contribute to inflammation-induced cellular transformation.
82 PP2A, E7 provides these functions related to cellular transformation.
83 ate substrates, chromosomal aberrations, and cellular transformation.
84 Because overexpression of eIF4E is linked to cellular transformation, 4E-BP is a tumor suppressor, an
85 air pathways and ROS detoxification systems, cellular transformation after apoptosis by the blebbishi
86 MECs by altering multiple pathways linked to cellular transformation and breast cancer.
87 ceptor tyrosine kinases (RTK) contributes to cellular transformation and cancer progression by disrup
88 uracil and dihydrothymine is associated with cellular transformation and cancer progression.
89 proliferation, epigenetic reprogramming, and cellular transformation and cancer.
90 loss of regulation can lead to, for example, cellular transformation and cancer.
91 f this pathway is frequently associated with cellular transformation and cancer.
92 idy-inducing gene deficiencies contribute to cellular transformation and carcinogenesis involving the
93 f the degree of dysregulation by AML1-ETO in cellular transformation and demonstrate that AML1-ETO-W6
94    We also explore the role of aneuploidy in cellular transformation and discuss the possibility of d
95 utation or oncogenic viruses is required for cellular transformation and eventually carcinogenesis.
96  Chronic inflammation in the stomach induces cellular transformation and gastric cancer primarily in
97 rms found in breast cancer may contribute to cellular transformation and genomic instability by impai
98  highlight a role for MV in the induction of cellular transformation and identify tTG and FN as essen
99  from the KSHV genome abolished KSHV-induced cellular transformation and impaired angiogenesis.
100  and phenformin in an Src-inducible model of cellular transformation and in mammosphere-derived breas
101 e the first evidence that MUC4 alone induces cellular transformation and indicates a novel role of MU
102 c expression of the ACTG1-MITF fusion led to cellular transformation and induced the expression of do
103 pathway has been shown to play a key role in cellular transformation and invasion.
104 tein whose expression is up-regulated during cellular transformation and is associated with disease p
105 ce by oncogenic signals acts as a barrier to cellular transformation and is attained, in part, by the
106 hus, Myc may be a key cellular node coupling cellular transformation and KSHV latency.
107 which Nup98 translocations may contribute to cellular transformation and leukemogenesis.
108  inversions that have the potential to cause cellular transformation and lymphoid tumors.
109                      These responses inhibit cellular transformation and mediate the response to many
110        This stress consequentially inhibited cellular transformation and melanoma growth via senescen
111 cts cancer progression by directly promoting cellular transformation and metastasis.
112  RhoA activity has previously been linked to cellular transformation and metastatic potential of epit
113  tumor viruses is a vital step in initiating cellular transformation and represents a major shortcomi
114 in retrospective clinical analyses, inhibits cellular transformation and selectively kills breast can
115 st-line drug for treating diabetes, inhibits cellular transformation and selectively kills cancer ste
116 rmin, a standard drug for diabetes, inhibits cellular transformation and selectively kills cancer ste
117 o-inflammatory pathways are not required for cellular transformation and suggests a need for further
118 r, we show that SIRT5 is up-regulated during cellular transformation and supports proliferation and t
119 and tumor suppressor pathways that regulates cellular transformation and survival.
120                                              Cellular transformation and the accumulation of genomic
121 P48/TIP49 as well as MYC in MTBP function in cellular transformation and the growth of human breast c
122 rotein that has been shown to be involved in cellular transformation and to activate the phosphatidyl
123 overexpression of Ran in fibroblasts induces cellular transformation and tumor formation in mice.
124 dy, we found that the FoxM1B molecule causes cellular transformation and tumor formation in normal hu
125 h STAT3, block gene expression, and suppress cellular transformation and tumor growth in vivo.
126  in vitro and in vivo assays that screen for cellular transformation and tumor growth.
127 s overcome the inhibitory effect of Dok-1 on cellular transformation and tumor progression.
128 ic members of the Ras superfamily to promote cellular transformation and tumor progression.
129 139 site, to be important for suppression of cellular transformation and tumorigenesis.
130 tated, caspase-2 lost its ability to inhibit cellular transformation and tumorigenesis.
131 ly understood escape mechanism that promotes cellular transformation and tumorigenesis.
132            They have also been implicated in cellular transformation and tumorigenesis.
133 d RNA pol III transcription is essential for cellular transformation and tumorigenesis.
134  and intestinal commensals can contribute to cellular transformation and tumorigenesis.
135 ed growth suppression, ultimately leading to cellular transformation and tumorigenesis.
136 obal repression of miRNA maturation promotes cellular transformation and tumorigenesis.
137            Altered MYC protein level lead to cellular transformation and tumorigenesis.
138 s shed light on the roles of viral miRNAs in cellular transformation and viral latency.
139 rrant enzyme function in vitro and to induce cellular transformation and/or genomic instability in vi
140 ffects on growth in soft agar, a hallmark of cellular transformation, and also assessed in vivo intra
141 inhibition in human HCC cell lines decreases cellular transformation, and anti-miR-494 treatment of p
142 ption, DNA damage response, snoRNP assembly, cellular transformation, and cancer metastasis.
143  are pivotal to understanding the process of cellular transformation, and illustrate key targets for
144 ciency, a strong mutator phenotype, enhanced cellular transformation, and increased cancer susceptibi
145                         We further show that cellular transformation, and thus initiation of liver tu
146 that, in turn, promotes genomic instability, cellular transformation, and tumorigenesis.
147 ne-regulated pathways underlying this unique cellular transformation are not fully understood.
148        Mechanisms whereby the virus promotes cellular transformation are poorly understood.
149            Effects of GRIM-19 on src-induced cellular transformation are reversible in the presence o
150 effects on a constitutively active STAT3 and cellular transformation are unknown.
151                                              Cellular transformations are driven by environmentally t
152 d-type NTH1 leads to genomic instability and cellular transformation as assessed by anchorage-indepen
153 ification for transcriptional activation and cellular transformation as well as functional difference
154 cogenes is important for distinct aspects of cellular transformation, as well as tumor growth and col
155 ulting in endogenous genomic instability and cellular transformation, as well as tumor growth in a mo
156 tion has been observed in carcinogenesis and cellular transformation associated with arsenic exposure
157 activity in LMP1-induced gene expression and cellular transformation associated with LMP1.
158 ally modified mouse models that recapitulate cellular transformation at specific developmental stages
159                        During the process of cellular transformation, biguanide treatment prevents th
160                 Wild-type GRIM-19 suppressed cellular transformation by a constitutively active form
161 hat hERG1 expression is sufficient to induce cellular transformation by a mechanism distinct from hEA
162          Mutational activation of src causes cellular transformation by altering transcription and cy
163 tem cells can evade cell death by undergoing cellular transformation by constructing "blebbishields"
164                            miR-193a inhibits cellular transformation by directly targeting the 3' unt
165                      This JM mutant promotes cellular transformation by EGFR in vitro and is tumorige
166 S) family member RGS6 suppresses Ras-induced cellular transformation by facilitating Tip60-mediated d
167 denovirus E4-ORF1 protein mediates oncogenic cellular transformation by human adenovirus type 9, augm
168 cal to our understanding of the mechanism of cellular transformation by oncogenic transcription facto
169 1 confers a specific resistance to oncogenic cellular transformation by phosphoinositide 3-kinase (PI
170 d in certain human tumours may contribute to cellular transformation by promoting genomic instability
171 sferase 1 (Dnmt1) is essential for oncogenic cellular transformation by Ras, and Dnmt1 is overexpress
172             Overexpression of eIF4E promotes cellular transformation by selectively increasing the tr
173 nd provide a rationale for the efficiency of cellular transformation by the adenoviral E1A oncoprotei
174 gh TC21 activates some pathways that mediate cellular transformation by the classical Ras proteins, t
175 l hypoacetylation of H3K18Ac associated with cellular transformation by the viral oncoprotein E1A.
176                                   Yet, human cellular transformation can be accomplished by a few gen
177        Glycosylation changes associated with cellular transformation can facilitate the growth and pr
178 sion levels in cancer and are able to affect cellular transformation, carcinogenesis and metastasis,
179  insights into morphological and biochemical cellular transformations caused by diseases.
180  adopt a Xi-like conformation in response to cellular transformation, characterized by CpG hypomethyl
181 pressed in an antisense orientation, induced cellular transformation, consistent with a tumor suppres
182 , these results reveal that Bcr-Abl-mediated cellular transformation critically requires silence of t
183 on of LMP1-activated genes and LMP1-mediated cellular transformation, demonstrating an essential role
184  in multistep process of tumorigenesis, from cellular transformation, disease progression to metastat
185 t into the molecular mechanisms that control cellular transformation driven by activation of protein
186     Mammalian spermiogenesis is a remarkable cellular transformation, during which round spermatids e
187 ility-associated genes at distinct phases of cellular transformation, exhibited chromosomal instabili
188 ugh genetic and epigenetic alterations drive cellular transformation, genomic plasticity, and evoluti
189 an T-cell leukemia virus 1 (HTLV-1)-mediated cellular transformation has not been described.
190 isease process; however, its precise role in cellular transformation has not been explored.
191 ever, the mechanism of effect of Aurora-B on cellular transformation has not been fully explored.
192  viral persistence, host immune evasion, and cellular transformation--have been ascribed to viral ncR
193 pression has been observed to correlate with cellular transformation; however, the importance to tumo
194                    Metformin strongly delays cellular transformation in a manner similar to that occu
195          Elevated Mdmx levels also increased cellular transformation in a p53-independent manner.
196 d gene transcription activities and promotes cellular transformation in a TOP1-dependent manner.
197 tor (HBZ) is dispensable for HTLV-1-mediated cellular transformation in cell culture, but is required
198 10gamma or p110delta is sufficient to induce cellular transformation in chicken embryo fibroblasts.
199 ic epithelial tissue types and contribute to cellular transformation in cooperation with other biolog
200  drives the stem cell-like proliferation and cellular transformation in NMC cells.
201 increased presence of DCLK1+ve cells promote cellular transformation in response to a second hit.
202                   RGS6 functions to suppress cellular transformation in response to oncogenic Ras by
203  key mediators of regional cell behavior and cellular transformation in the adult body.
204 e stress and DNA damage in the initiation of cellular transformation in the prostate gland.
205 RIM-19 suppresses constitutive STAT3-induced cellular transformation in vitro and in vivo by down-reg
206  we show that GRIM-19 suppresses src-induced cellular transformation in vitro and in vivo by down-reg
207 EGFR CTD deletion mutants are able to induce cellular transformation in vitro and in vivo in the abse
208 ion accelerates cell proliferation, triggers cellular transformation in vitro and in vivo, and stimul
209   Ectopic expression of mutated RIT1 induces cellular transformation in vitro and in vivo, which can
210  mir-200 expression compromised KRAS-induced cellular transformation in vitro and tumor formation in
211 if (PBM) required for E4-ORF1 to induce both cellular transformation in vitro and tumorigenesis in vi
212                  LIN28 and LIN28b facilitate cellular transformation in vitro, and overexpression is
213  in soft agar is the gold-standard assay for cellular transformation in vitro, but it is unsuited for
214   Both pathways also cooperated in promoting cellular transformation in vitro, demonstrating their ce
215 s type 16 (HPV16) oncoproteins contribute to cellular transformation in vitro.
216 ht combine to uniquely affect the process of cellular transformation (in vitro) and environmental car
217 IP) has been shown to have a crucial role in cellular transformation, in which it is vital for the su
218 d the dynamic m(6)A mRNA modification during cellular transformation induced by chemical carcinogens
219 rtantly demonstrate that PI3K activation and cellular transformation induced by E4-ORF1 require two s
220                                              Cellular transformation induced by oncogenic tyrosine ki
221     GRIM-19 had no significant effect on the cellular transformation induced by other oncogenes such
222 enatal transgenic founders exhibited a gross cellular transformation into a secretory epithelium.
223 ression, resulting in hyperproliferation and cellular transformation into cancer cells in vivo.
224 r converting our increasing understanding of cellular transformation into intelligently designed anti
225 ted T cells) upregulation has been linked to cellular transformation intrinsically, but it is unclear
226     MicroRNA profiling in isogenic models of cellular transformation involving either breast epitheli
227                          Hence, KSHV-induced cellular transformation is a suitable model for investig
228                                 Importantly, cellular transformation is accompanied by elevated stead
229                                              Cellular transformation is associated with altered gluta
230                                              Cellular transformation is associated with dramatic chan
231                                              Cellular transformation is associated with the reprogram
232 he requirement of Cat-1 for this hallmark of cellular transformation is coupled to its ability to bin
233 lucidating the pathways by which they induce cellular transformation is critical.
234 ever, whether Cat-1 might also contribute to cellular transformation is currently unknown.
235       In contrast to hEAG1, the mechanism of cellular transformation is dependent on ion conduction.
236  the major metabolic changes associated with cellular transformation is enhanced nutrient utilization
237                                              Cellular transformation is mediated directly by the expr
238 however, whether this is sufficient to drive cellular transformation is not clear.
239  critical cellular response that counteracts cellular transformation is oncogene-induced senescence (
240 ing knowledge of the role of large ncRNAs in cellular transformation is pointing towards their potent
241 However, the molecular mechanism of IRF-4 in cellular transformation is unknown.
242           The mechanism by which Ras induces cellular transformation is, however, not fully elucidate
243 V-1 E7 by itself is not sufficient to induce cellular transformation, it enhances the abilities of th
244                   In a model of KSHV-induced cellular transformation, KSHV upregulated expression of
245 human mammary cell line, MCF10A, resulted in cellular transformation marked by epidermal growth facto
246 e that the contribution of E7 to BPV-induced cellular transformation may involve its ability to inhib
247                  In a Src-inducible model of cellular transformation, metformin inhibits the earliest
248 ostate cancer variants, respectively, induce cellular transformation most likely due to sequence-spec
249 tumor-derived HSP70 was neither required for cellular transformation nor for in vivo tumor growth.
250                                              Cellular transformation occurred at as early as day 4 af
251 ges with overactive IGF signaling to promote cellular transformation of DS fetal progenitors, reveali
252               This efficient system for KSHV cellular transformation of primary cells might facilitat
253  lack of an adequate experimental system for cellular transformation of primary cells.
254      Here, we report efficient infection and cellular transformation of primary rat embryonic metanep
255 rect effects of oncogenic RAS(G12V)-mediated cellular transformation on the mitochondrial dynamics ma
256 desired outcomes such as DNA translocations, cellular transformation or acute cell death.
257 as does not trigger increased proliferation, cellular transformation or EMT, and prevents MUC1 upregu
258 it has been hypothesized that it may promote cellular transformation or exacerbate tumor growth.
259 n attributed to MCPyV tumor antigen-mediated cellular transformation or replication, to date, no stud
260 initial infection or subsequently during the cellular transformation process.
261 otal role for SIRT7 in chromatin regulation, cellular transformation programs and tumour formation in
262                     F-circRNAs contribute to cellular transformation, promote cell viability and resi
263 ioning as a tumour promoter that facilitates cellular transformation, promotes tumour growth and scul
264 chanisms and structural domains required for cellular transformation remain largely unknown.
265 ar functions, additional targets involved in cellular transformation remain to be explored.
266 their role in cell homeostasis as well as in cellular transformation remains poorly explored.
267 mensional cell culture and that HER2-induced cellular transformation requires p62, as well as NRF2, w
268                     During genotoxic stress, cellular transformation requires that promitotic activit
269                       Here, we find that the cellular transformation resulting from combined expressi
270 uppressor surveillance, preventing potential cellular transformation resulting from the growth-induci
271  of mutation have exhibited the capacity for cellular transformation, several aspects of this transfo
272 ke Factor 5 (KLF5) has been shown to mediate cellular transformation signaling events downstream of o
273 och and Crabtree now show that the resulting cellular transformation stems from disruption of the nor
274                        They induce oncogenic cellular transformation, stimulate cellular proliferatio
275 loop in the regulation of c-Myc activity and cellular transformation, supporting/suggesting a role of
276 transcription-3 (STAT3) has been linked with cellular transformation, survival, proliferation, chemor
277 ic H3K9 acetylation is a better predictor of cellular transformation than are global histone acetylat
278               Here, we describe an assay for cellular transformation that involves growth in low atta
279  Cu(I) deficiency induced by oncogene-driven cellular transformation that promotes fluctuations in gl
280  epigenetic control mechanisms contribute to cellular transformation, these results, together with th
281 g the STING pathway in cancer cells promotes cellular transformation through accumulation of chromoso
282  limits aberrant cell division and potential cellular transformation through autophagic death inducti
283 ransformed cells and are proposed to promote cellular transformation through mechanisms such as inhib
284 ctor alpha (TGFalpha) is a potent inducer of cellular transformation, through its binding and activat
285 nly known inhibitors of STING that allow for cellular transformation, thus, our findings are the firs
286 iple stages of oncogenesis, from the initial cellular transformation to the hierarchical organization
287 with a wide variety of molecules that induce cellular transformation to various extents.
288 n relation to disease progression and drives cellular transformation, tumorigenesis, and metastatic p
289 hese somatic alterations, is associated with cellular transformation, tumorigenesis, cancer progressi
290                                              Cellular transformation was examined using NIH3T3 cells
291 g an inducible, inflammatory model of breast cellular transformation, we describe the transcriptional
292  abolish E4-ORF1-induced PI3K activation and cellular transformation, we reasoned that E4-ORF1 must p
293 , a massive lymphoproliferative disorder and cellular transformation were observed in Ag-experienced
294 reported in some patients, leads to enhanced cellular transformation when compared with either mutati
295 e degree to which these substitutions induce cellular transformation when introduced into full-length
296 s were dependent on Jak1 kinase activity for cellular transformation, whereas the JAK3 kinase domain
297 GFbetaRII in CD8(+) T cell proliferation and cellular transformation, which is caused by a mechanism
298 m that underlies the ability of SKI to cause cellular transformation while unraveling a novel connect
299 rexpression of SEMA4C promotes properties of cellular transformation, while RNAi knockdown of SEMA4C
300 al life cycle and might not be necessary for cellular transformation, yet HPV integration is frequent

 
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