コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 , leading to inhibition of mTORC1 and cancer cell growth arrest.
2 that significantly exceed those required for cell growth arrest.
3 p21 and p27, the tumor suppressor, p53, and cell growth arrest.
4 to isolate minigenes whose expression causes cell growth arrest.
5 gized with IFN-gamma in the promotion of NB4 cell growth arrest.
6 ins is necessary to induce apoptosis but not cell growth arrest.
7 /Cdk4 protein complexes were associated with cell growth arrest.
8 a Schwann cell-specific protein that induces cell growth arrest.
9 imed HalA complex and induce protective host cell growth arrest.
10 Cellular senescence is a stable cell growth arrest.
11 alectin-9-induced colon cancer apoptosis and cell growth arrest.
12 ulate cellular senescence, a state of stable cell growth arrest.
13 interact with CypD, triggering necrosis and cell growth arrest.
14 erentially induce FGFR1c phosphorylation and cell growth arrest.
15 ppression of cyclin D1 promoter activity and cell growth arrest.
16 d MCM7 DNA replication licensing and induced cell growth arrest.
17 hed 5 S and 45 S ribosomal RNA synthesis and cell growth arrest.
18 cyclin-dependent kinase inhibitor 1A-induced cell growth arrest.
19 to be necessary and sufficient for normal T-cell growth arrest.
20 A sensitizes LNCaP-RF cells to apoptosis and cell growth arrest.
21 her binding to tubulin by ITCs could lead to cell growth arrest.
22 nces to inhibit protein synthesis leading to cell growth arrest.
23 results in p53- and p21-dependent mesodermal cell growth arrest.
24 activity, leading to vascular smooth muscle cell growth arrest.
25 CA nucleotide sequences, results in complete cell growth arrest.
26 for ceramide-induced vascular smooth muscle cell growth arrest.
27 sm of UV-dependent checkpoint activation and cell growth arrest.
28 ort interference RNA treatment results in MM cell growth arrest.
29 gnified in a manner consistent with enhanced cell growth arrest.
30 factor alpha (TNF-alpha) that induced tumor cell growth arrest.
31 an important role in lytic cycle-associated cell growth arrest.
32 ssociated with decreased viability and tumor cell growth arrest.
33 ow levels of p202 are upregulated during the cell growth arrest.
34 ribute to senescence-associated irreversible cell growth arrest.
36 esveratrol (10 microM, 48 hr) induces both a cell growth arrest and a metabolic reprogramming in colo
37 ive oxygen species (ROS) are able to mediate cell growth arrest and activate proteins that inhibit th
43 ere, we show that Tip60 is required for both cell growth arrest and apoptosis mediated by p53 and als
45 ion of Akt by API-1 resulted in induction of cell growth arrest and apoptosis selectively in human ca
46 creased expression of cell cycle inhibitors, cell growth arrest and apoptosis, but not tumour formati
56 but the inter-relationships among autophagy, cell growth arrest and cell death induced by these ligan
58 and trigger signaling pathways essential to cell growth arrest and death by inducing an HSP90-active
60 n reduced susceptibility of TGF-beta-induced cell growth arrest and decreased phosphorylation of Smad
62 toxin module wherein MazF(Sa) leads to rapid cell growth arrest and loss in viable CFU upon overexpre
66 messengers with opposing roles in mammalian cell growth arrest and survival; their relative cellular
67 tant component of p53-mediated apoptosis and cell growth arrest and that inactivation of the apoptoti
69 RG1 and pRB is not required for induction of cell growth arrest and transcriptional repression of E2F
70 ylase (HDAC) inhibitors (HDACi) cause cancer cell growth arrest and/or apoptosis in vivo and in vitro
71 on of this protein, which is associated with cell growth arrest and/or apoptosis under various stress
72 down-regulating survivin expression induced cell-growth arrest and subsequent cell death regardless
73 e treatment of tumor cells with induces both cells growth arrest and alter the spectral lines in a do
74 ne M1 myeloblastic leukemia cells, where the cells growth arrest and ultimately undergo programmed ce
75 y peptidic inhibitors, GrB induced in Jurkat cells growth arrest and, over a delayed time period, cel
76 mRNA-specific endoribonuclease causing host cell growth arrest, and culture condensation) to facilit
77 f MCM8 in PC3, DU145 and LNCaP cells induced cell growth arrest, and decreased tumour volumes and mor
79 nses including induction of target genes and cell growth arrest, and this inhibition is dependent on
81 inase inhibitor p21(Waf1/Cip1/Sdi1) triggers cell growth arrest associated with senescence and damage
82 or p21Waf1/ Cip1/Sdi1 is an integral part of cell growth arrest associated with senescence and damage
85 le progression, as evidenced by induction of cell growth arrest at the G0/G1 phase, inhibition of DNA
86 ed activation of CCN5 in TNBC cells promotes cell growth arrest at the G0/G1 phase, reduces cell prol
88 nhibited VEGF-induced EC proliferation, with cell growth arrested at the G(0)/G(1) phase and a concom
90 n of supplementation) are maintained through cell growth arrest by serum depletion and when prolifera
93 lialization) underlies a state of reversible cell growth arrest called tumor dormancy, which enables
94 adation and that wts mutants have defects in cell growth arrest, caspase activity, and autophagy.
95 The PTEN-induced localization defect and the cell growth arrest could be rescued by the expression of
96 -UCA and SSR were associated with apoptosis, cell growth arrest, cytokines, and oxidative stress.
97 ts play in histone deacetylase inducement of cell growth arrest, differentiation, or apoptotic cell d
98 vival, but that its overexpression may cause cell growth arrest due to an accumulation of sphingosine
99 B or NIR causes p53-dependent apoptosis and cell growth arrest, due to the up-regulation of p21 and
101 rotestosterone (DHT) treatment by undergoing cell growth arrest in association with cytoskeletal reor
102 de that telomerase inhibition by PPA induces cell growth arrest in BEAC cells and demonstrate the pot
107 These studies show that LY290181 induces cell growth arrest in prometaphase/metaphase, and tubuli
111 nd cross-filament contacts are essential for cell growth arrest in vivo and reveal a stepwise mechani
112 tion of p33(QIK)-specific kinase activity of cells growth-arrested in the quiescent phase and deactiv
113 ation of the gene, A20 induced apoptosis and cell growth arrest, indicating a tumour suppressor role.
114 t MetAP-2 is responsible for the endothelial cell growth arrest induced by Fg and its derivatives.
115 Stra13 expression is closely associated with cell growth arrest induced by several triggers such as r
121 ial role for Zta's basic domain in eliciting cell growth arrest, its amino terminus is required for e
122 s associated with a dose- and time-dependent cell growth arrest, mitochondrial damage, and apoptosis
123 DNA nanoparticles can transfect nondividing cells, growth-arrested neuroblastoma and hepatoma cells
124 uently, MDM2 suppressed p21waf1/cip1-induced cell growth arrest of human p53(-/-) and p53(-/-)/Rb(-/-
126 een MDM2 and p53, activates p53 resulting in cell growth arrest or apoptosis in various cancer cells.
131 kinase inhibitor p21WAF1/CIP1 and subsequent cell growth arrest or senescence is one mechanism by whi
133 (neo) gene whose expression leads to potent cell growth arrest, restricting the viral infection.
135 tion of YjhX (85 amino acid residues) causes cell-growth arrest resulting in cell death, while YjhQ (
136 are often induced into pathways that lead to cell growth arrest, senescence, and/or apoptosis in resp
139 Cellular senescence defines an irreversible cell growth arrest state linked to loss of tissue functi
141 duced M-MITF expression, leading to melanoma cell growth arrest that was rescued by ectopic expressio
142 mote osteoblastic differentiation and induce cell growth arrest, the highly related ZEB-2/SIP1 protei
143 ghtforward mechanism for C/EBPalpha-mediated cell growth arrest through repression of E2F-DP-mediated
144 This constitutes the first demonstration of cell growth arrest through telomerase inhibition, upon t
146 These D1/CDK4 inhibitors inhibited tumor cell growth, arrested tumor cells at the G1 phase, and i
147 stress response characterized by persistent cell growth arrest under various stress conditions, incl
148 K-mediated Bax activation and that increased cell growth arrest was associated with elevated expressi
149 ha down-regulation using shRNA, which caused cell growth arrest, was accompanied by increased H3K27me
150 elevant aspects of HIF-1 function in primary cell growth arrest, we examined two different primary di
154 ggest that overexpression of HO-1 results in cell growth arrest, which may facilitate cellular protec
155 atment of cultured human PA-SMCs resulted in cell growth arrest with the induction of senescence but