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 itutively activated in FA-C cells in a STAT1-independent fashion).
2 1 in the PI3K signaling cascades in a ligand-independent fashion.
3 winds ~2 turns of the double helix in an ATP-independent fashion.
4 ated by the Rad54 paralog Rdh54 in an ATPase-independent fashion.
5 isms within the injured heart, in a GH/IGF-1 independent fashion.
6 othelial NO production in a cyclooxygenase-1-independent fashion.
7 proteasomal degradation in an ubiquitination-independent fashion.
8 , interacts with incoming dNTP in a sequence-independent fashion.
9 signaling across all cell types in a ligand-independent fashion.
10 ted autophagy in neurons in an Akt- and mTOR-independent fashion.
11 d the BRCA1/BARD1 heterodimer in a ubiquitin-independent fashion.
12 etic identity in situ in a completely gender-independent fashion.
13 ay, 2% strain) inactivated GSK3beta in a Wnt-independent fashion.
14 assessed the two data sets in a blinded and independent fashion.
15 matrices allowing for EC migration in an MMP-independent fashion.
16 d divalent cations and requires Bak in a Bax-independent fashion.
17 n an acetylation-dependent and transcription-independent fashion.
18 a heterologous protein, LacZ, in a position-independent fashion.
19 eg-dependent allograft acceptance in an IL-6-independent fashion.
20 ases allergic airway inflammation in a STAT6-independent fashion.
21 ytosolic monothiol glutaredoxins, in an iron-independent fashion.
22 and Fra2 interact in the cytosol in an iron-independent fashion.
23 PF0610 does bind DNA, at least in a sequence-independent fashion.
24 nthesize aminoacylated polyketides in an ATP-independent fashion.
25 late sigma(E)-dependent promoters in an RseA-independent fashion.
26 virus particles in an entry- and replication-independent fashion.
27 the tubulin-rich centrioles in a microtubule-independent fashion.
28 (DDITS) and induced apoptosis in a protease-independent fashion.
29 rotein accumulation in a dose-dependent, p53-independent fashion.
30 ced in a cell density-dependent and reporter-independent fashion.
31 in mouse dendritic cells occurred in a MyD88-independent fashion.
32 ass switch DNA recombination (CSR) in a CD40-independent fashion.
33 by BRCA1 deficiency can also occur in a p53-independent fashion.
34 to decarboxylate the substrate in an oxidant-independent fashion.
35 lated by PACAP38 in a cAMP-dependent but PKA-independent fashion.
36 expectedly, also respond to salt in a ppk301-independent fashion.
37 o inducers of oxidative stress in a receptor-independent fashion.
38 osted with peptide (plus adjuvant) in a CD40-independent fashion.
39 neurons discharged in a place- and direction-independent fashion.
40 k phosphorylation in a Raf-dependent but Rac-independent fashion.
41 ntain SIV nef can replicate in a cyclophilin-independent fashion.
42 on of AMP-activated protein kinase in an Akt-independent fashion.
43 both an IFN-gamma-dependent and an IFN-gamma-independent fashion.
44 pressing Rat1a cells to grow in an anchorage-independent fashion.
45 era toxin, or forskolin induced GEP in a PKA-independent fashion.
46 de-chain in driving TCR binding in a peptide-independent fashion.
47 ction through both a VEGF-dependent and VEGF-independent fashion.
48 suggests that EGFR is activated in a ligand-independent fashion.
49 n's N terminus in a CIA1-, CIA2B-, and MMS19-independent fashion.
50 mplexes is regulated in an inhibitor kappa B-independent fashion.
51 res the PmrD protein and by Fe(3+) in a PmrD-independent fashion.
52 brane-associated microtubules in a rhodopsin-independent fashion.
53 e (MAPK)/p90(rsk) signaling cascade in a p53-independent fashion.
54 egulate osteoblast differentiation in a CTGF-independent fashion.
55 t allow cell cycle progression in a cyclin D-independent fashion.
56 -like viral protein that signals in a ligand-independent fashion.
57 and cell cycle progression occurred in a Btk-independent fashion.
58 nt cytoskeletal events, possibly in a kinase-independent fashion.
59 2 and Smad3 moving to the nucleus in a Smad4-independent fashion.
60 . pneumoniae in a pneumolysin-dependent and -independent fashion.
61 RNA induction by cytokines and LPS in a PI3K-independent fashion.
62 s-link to a portion of this region in an ATP-independent fashion.
63 and of duplex DNA, moving 5'-to-3' in an ATP-independent fashion.
64 ducing p21waf1/cip1 stability in a ubiquitin-independent fashion.
65 ing lies near the phagocytic cup in a myosin-independent fashion.
66 ed to the periplasm in a SecA-dependent, SRP-independent fashion.
67 eceptor-transcriptional activity in a ligand-independent fashion.
68 directly within the pituitary in a dopamine-independent fashion.
69 ely 60 and 100 %, respectively, in a voltage-independent fashion.
70 n remodeling and locus opening in a cytokine-independent fashion.
71 a subset of BL-CFCs that develop in a Runx1-independent fashion.
72 -induced growth arrest and did this in a p53-independent fashion.
73 adrenoreceptor in vitro in a phosphorylation-independent fashion.
74 n of IL-18Ralpha/IL-12Rbeta2 in an IFN-gamma-independent fashion.
75 er editing by E. coli ProRS occurs in a tRNA-independent fashion.
76 ion is required for rDNA silencing in a Sir2-independent fashion.
77 main, and hormone binding domain in a ligand-independent fashion.
78 e GBV-B NS3 protease in an HCV NS4A cofactor-independent fashion.
79 er, these cells proliferated in an anchorage-independent fashion.
80 e, silencing occurs in a histone deacetylase-independent fashion.
81 or beta receptor tyrosine kinase in a ligand-independent fashion.
82 n of PlexinA1 associate with NP1 in a Sema3A-independent fashion.
83 repress other C. albicans genes in a CaTup1-independent fashion.
84 aused release of both APP and Abeta in a COX-independent fashion.
85 d several rounds of proliferation in an IL-2-independent fashion.
86 oth in vitro and in vivo in a Janus kinase 3-independent fashion.
87 e with the nonvisual arrestins in an agonist-independent fashion.
88 yet are secreted in a constitutive, calcium-independent fashion.
89 ating the NF-kappa B pathway in a MAP kinase-independent fashion.
90 ) caused similar cytotoxicity, but in a CRBN-independent fashion.
91 arly 2 orders of magnitude in an orientation independent fashion.
92 between fragments of genes in a DNA homology-independent fashion.
93 lls produce IL-2 but proliferate in an IL-2--independent fashion.
94 murine macrophage cell lines in an invasion-independent fashion.
95 ive, has been shown to activate sGC in an NO-independent fashion.
96 egulation is exerted on both promoters in an independent fashion.
97 c G-protein signaling pathways in a receptor-independent fashion.
98 l in response to IR exposure in a cell cycle-independent fashion.
99 e development of BM-derived CNS APC in an Ag-independent fashion.
100 hown to assist allograft rejection in a CD28-independent fashion.
101 e able to generate these signals in a ligand-independent fashion.
102 it class II histone deacetylases in a mSin3A-independent fashion.
103 ndly suppressed IL-12 production in an IL-10-independent fashion.
104 T cells in a copy number-dependent, position-independent fashion.
105 expression of Siamois in a protein synthesis independent fashion.
106 t not immature T cells in a largely position-independent fashion.
107 rrent was weakly blocked by TEA in a voltage-independent fashion.
108 ription in a position-dependent but sequence-independent fashion.
109 As suggest that MSY2 binds RNA in a sequence-independent fashion.
110 in its N-terminal region in an RNA sequence-independent fashion.
111 mes that are arrested after step 1 in an ATP-independent fashion.
112 rophages in an opsonin-dependent and opsonin-independent fashion.
113 ha release from isolated monocytes in a CD14-independent fashion.
114 Epo-induced event in a dose-dependent, STAT5-independent fashion.
115 ion of interleukin-2 gene synthesis in a TCR-independent fashion.
116 lls, hot spots were dispersed in a stimulus- independent fashion.
117 in mature mammalian cells, in an interferon-independent fashion.
118 embrane-anchored protein, albeit in a ligand-independent fashion.
119 c42 controls anchorage independence in a Rac-independent fashion.
120 viral and host cell plasma membranes in a pH-independent fashion.
121 proteins in either a Rev-dependent or a Rev-independent fashion.
122 ently derived transgenic plants in a variety-independent fashion.
123 also significantly activated in a buttonhead-independent fashion.
124 directly targeted to the promoter in an E2F-independent fashion.
125 his cellular maturation can occur in an IL-2-independent fashion.
126 rigenicity 2 receptor (ST2) (IL-33 receptor)-independent fashion.
127 asma membrane and the virus envelope in a pH-independent fashion.
128 kinase, GCN2, in an apparent deacylated tRNA-independent fashion.
129 rated degradation of GABABin a catalytically independent fashion.
130 n by the DNA-binding protein Rbp-J in a Tead-independent fashion.
131 idges SHP to THEMIS in a Tyr-phosphorylation-independent fashion.
132 lated genes (ISGs) in an IRF3-dependent, IFN-independent fashion.
133 n mast cells for degranulation in an antigen-independent fashion.
134 eneic murine pancreatic cancers in an immune-independent fashion.
135 CAT-induced cyclin D1 expression in a kinase-independent fashion.
136 ator factor-4 in a programmed death-1 and B7-independent fashion.
137 ective, IL-4-producing T cells in an antigen-independent fashion.
138 creases after starvation in cells in an mTOR-independent fashion.
139 vel role of DSS1 to regulate BRCA2 in an RPA-independent fashion.
140 variability of vmPFC threat assessment in an independent fashion.
141 increased Cif packaging into OMVs in a CifR-independent fashion.
142 of the LMP2 proteasome subunit in a caspase-independent fashion.
143 MET(N375S) to interact with HER2 in a ligand-independent fashion.
144 etion exacerbated apoptotic death in a KCNB1-independent fashion.
145 l of cisplatin ICLs, acting in a replication-independent fashion.
146 V, a target gene repressed by H-NS in an Hha-independent fashion.
147 inhibitor inhibits factor XIa in a protein Z-independent fashion.
148 st general relativity in a nuclear structure-independent fashion.
149 d-restricted, MyD88-independent and dectin-1-independent fashion.
150 protein B-containing lipoproteins in an LDLR-independent fashion.
151 nagen re-entry but does so in a calcium flux-independent fashion.
152 s represses IL-17 expression in a type I IFN-independent fashion.
153 ase/AKT pathway in a predominantly HIF1alpha-independent fashion.
154 itor of metalloproteinase-3 (TIMP3) in a P53-independent fashion.
155 inder of the peptides/proteins in a sequence-independent fashion.
156 in-dependent but flotillin-1- and caveolin-1-independent fashion.
157 Asp310Lys change bound to PCSK9 in a Ca(2+)-independent fashion.
158 We compared results in a blinded, independent fashion.
159 proliferation in an IL-35-dependent, contact-independent fashion.
160 and early progenitor cells, likely in a p53-independent fashion.
161 lial cells leads to Rap1 activation in a PKA-independent fashion.
162 l migration and actin organization in a ROCK-independent fashion.
163 ll growth and glioma formation in a TSC/Rheb-independent fashion.
164 -trisubstituted piperidines in a substituent-independent fashion.
165 is required for development of AHR in an MC-independent fashion.
166 B cells diversify their repertoire in an Ag-independent fashion.
167 tion of human T cells by HIV-R3A in a fusion-independent fashion.
168 tory effects in both B7-1/B7-2 dependent and independent fashions.
169 toxins work in receptor-mediated or receptor-independent fashions.
170 both PCNA monoubiquitination-dependent and -independent fashions.
171 lation in both ovarian hormone-dependent and independent fashions.
172 phosphorylation in a PKC-dependent, but GRK6-independent, fashion.
173 associates with the nuclear matrix in a DNA-independent fashion, 3) zebrafish Sp2 is inherited as a
175 tivate the complement system in an Ab and C1-independent fashion after binding of the lectin to appro
176 lasmic domain of Fc gamma RIIa in activation-independent fashion, although SHIP binding increases upo
177 rrest of the five cell lines in a cell cycle-independent fashion, although some cell lines accumulate
178 sing trapped-ion qubits in a continuous time-independent fashion (analogous to optical pumping of ato
179 84 cell line, cAMP activates ERK1/2 in a PKA independent fashion and a physiological consequence of t
180 with FAs but are established in an integrin independent fashion and are responsible for anchoring ba
181 y elevates mutagenesis at epsilonC in an SOS-independent fashion and at AP sites in an SOS-dependent
182 ecrosis factor-alpha (TNF-alpha) in a kinase-independent fashion and at higher levels relative to the
183 precursor protein (APP) in a phosphotyrosine-independent fashion and can markedly inhibit the process
184 ns of the two processes have developed in an independent fashion and different explanations offered a
185 , translocates into the nucleus in a caspase-independent fashion and directly phosphorylates H2B at S
187 tein (IGFBP)-3 regulates apoptosis in an IGF-independent fashion and has been shown to localize to nu
188 ith Dicer partners TRBP and PACT in an siRNA-independent fashion and in the absence of effects on int
190 hypoxia occurs in a hypoxia-inducible factor-independent fashion and is catalyzed by the DHC desatura
191 perlipidemia and atherosclerosis in a CX3CR1-independent fashion and plays a potential role in endoth
193 ed DNA synthesis in an IGF-IGF receptor axis-independent fashion and resulted in the subsequent induc
194 p53 by suppressing MDM2 expression in a p53-independent fashion and subsequently, massive cell death
195 of interacting with HIV-1 Env in a receptor-independent fashion and that a chimeric 5-Helix/Pseudomo
196 (hairpins) in heteroduplex DNA in a DNA end-independent fashion and that automodification of PARP in
197 auxin gradients control leaf shape in a KNOX-independent fashion and that inappropriate KNOX activity
198 t perifosine induces p21(waf1/cip1) in a p53-independent fashion and that induction of p21(waf1/cip1)
199 hat DNA damage occurs in a bacterial contact-independent fashion and that Streptococcus pyruvate oxid
200 nite induces GADD45alpha expression in a p53-independent fashion and that this GADD45alpha induction
201 yr281Ala-Gln-Val occurs in a phosphotyrosine-independent fashion and to the motif Thr-Val-Tyr327Ala-S
202 ivate glutamate in presence of ATP in a tRNA-independent fashion and to transfer glutamate onto tRNA(
203 ansduced DC induced CTL in vivo in a Th cell-independent fashion and vaccinated against OVA-expressin
204 igh levels of Pol-specific antigens in a Rev-independent fashion and were able to induce potent Pol-s
205 ucing RV-specific intestinal IgA in a T-cell-independent fashion and, therefore, be responsible for a
206 ly blocks distal enhancers in an orientation-independent fashion, and can function when located far f
207 -33 is functionally active in vivo in an ST2-independent fashion, and its effects are partially diffe
208 ediate the AI growth of LNCaP cells in an AR-independent fashion, and that both Akt and Bcl-2 are not
209 nfected cells both in a U(S)3-dependent and -independent fashion, and that depletion of PDCD4 by siRN
211 s show that AF inhibits HIF-1alpha in an AhR-independent fashion, and they unveil additional activiti
212 LR3 or TLR4 agonists, this occurs in a dsRNA-independent fashion, and VP35 does not inhibit TLR-media
213 vitro; 3) is cell cycle-regulated in a SWI6-independent fashion; and 4) maximally stimulates retinob
214 tivated transcription of rpoS in an enhancer-independent fashion; and finally, (iv) rpoN is required
215 ation of GLI1 appears to occur in a Hedgehog-independent fashion as blockade of Hedgehog signaling ha
216 A mRNA accumulated to high levels in a light-independent fashion as long as a segment encoding a stem
217 n promotes tumor cell proliferation in a p53-independent fashion, as observed both in cultured cells
218 ns were released constitutively in a calcium-independent fashion, as shown using both intact and stre
219 able to polymerize nucleotides in a template-independent fashion before using these primers to initia
220 urvival analysis, that neurons die in a time-independent fashion but one that is dependent on mutant
221 at the level of transcription in a promoter-independent fashion but was not caused by stabilization
222 Th1 and Th17 differentiation in an aromatase-independent fashion, but also exacerbated cell death in
223 ab4A associates with inclusions in a species-independent fashion by 2 h postinfection by mechanisms t
224 ce that venetoclax kills CLL cells in a TP53-independent fashion by inhibition of BCL2 in patients an
225 s I-binding peptides were generated in a TAP-independent fashion by the action of various exopeptidas
227 n inhibition can also be activated in a MinD-independent fashion by the DicB protein of cryptic proph
228 Each lesion was classified in a blinded and independent fashion by using the VNC or unenhanced image
229 activity is activated in a Smoothened (Smo)-independent fashion, consistent with it acting downstrea
230 ptor peripheral terminals in a transcription-independent fashion, contributes to the maintenance of i
231 s, in a cell cycle-, and developmental stage-independent fashion, creating a platform for systematic
232 es cultured with M-CSF and IL-4, in a GM-CSF-independent fashion, differentiated into IL-10(high)IL-1
233 esponse to HIV-1 that persists in an antigen-independent fashion during antiretroviral therapy but se
234 e third event can occur to a degree in a Rho-independent fashion, gathering preassembled filaments to
235 BCs, abnormal Lyn kinase activation in a Syk-independent fashion has been reported recently, resultin
236 r cells to promote growth in an angiogenesis-independent fashion; however, this autocrine VEGF pathwa
239 ) decrease luciferase activity in a promoter-independent fashion in both viral and eukaryotic promote
240 tate cancer cells, and functions in a ligand-independent fashion in many prostate cancers when they b
241 NP34) that is presented by H-2Db in a Tap-1-independent fashion in mice expressing the influenza NP6
242 signals in either an SH2-dependent or an SH2-independent fashion in photoreceptor (R cell) growth con
243 e-switched (sw) Ig(+) memory B cells in a GC-independent fashion in response to strong CD40 stimulati
244 processing in fast, selective, yet attention-independent fashion in sensory and motor systems, for di
245 dulates inflammatory responses in a protease-independent fashion in tandem with its trafficking to th
246 vary gland (SG) NK cells develop in an Nfil3-independent fashion in the steady-state in the absence o
247 proliferation and megakaryopoiesis in a TPO-independent fashion, inducing LPS-like responses, such a
248 r short-lived protein(s) which acts in a MEK-independent fashion is required in order for egg cytopla
249 ome c release from mitochondria in a caspase-independent fashion leading to activation of caspase-9 a
250 olled in a pRB-dependent, but p107- and p130-independent fashion, likely through the pRB-dependent E2
251 nsensitive multiple myeloma cells in an IL-6 independent fashion may offer exciting new therapeutic o
252 nds that activate GPR109A in a beta-arrestin-independent fashion may represent an improved therapeuti
254 rred TGF-beta1 responsiveness, in a position-independent fashion, on a heterologous minimal promoter.
255 m the Nkx2.1 lineage either occur in a FoxO1-independent fashion or are compensated for through devel
256 affects stress processing, however in a sex-independent fashion: participants with lower self-esteem
257 tes HDC transcription in a Rafdependent, Ras-independent fashion predominantly through activation of
259 Increases in signaling occur in a ligand-independent fashion, require gamma-secretase activity, a
261 ilin-2 to interact with RhoA in a nucleotide-independent fashion, Rho-induced serum response element
262 s when Mn2+, which activates sGC in a ligand-independent fashion, served as the substrate cation cofa
263 nriched to UV-damaged DNA in an NER-incision-independent fashion, suggesting that recruitment of the
264 is triggered by steroids in a transcription-independent fashion that involves an unusual positive fe
265 by formation of reactivated enzyme in an ATP-independent fashion that is not regulated by redox, calc
266 ell cycle and cancer cell apoptosis in a RAR-independent fashion, thereby avoiding atRA's toxicity ca
267 A and FtsA join this structure in a mutually independent fashion through direct interactions with the
268 cyclin E facilitates MCM loading in a kinase-independent fashion, through physical interaction with C
269 ut rather activates the receptor in a ligand-independent fashion, thus providing a unique system to e
270 naling homologues cooperate in a similar but independent fashion to help set the threshold for TCR-in
272 Thus, the beta-phosphate may bind in a state-independent fashion to K185 to destabilize channel openi
273 2) Va-HC bound reversibly and in a Ca2+-independent fashion to membranes composed of neutral pho
274 fashion and then cross-links them in an ATP-independent fashion to oppose their subsequent sliding b
275 sity by also responding in a foreign antigen-independent fashion to some infectious agents, similar t
276 l domain of polycystin-1, acting in a ligand-independent fashion, triggers unique signaling pathways
277 strandedness of the telomere in a cell-cycle-independent fashion, unlike wild-type cells which form 3
278 iated by DeltaN89beta-catenin in a cyclin D1-independent fashion, up-regulation of cyclin D1 occurs i
279 murine CD4+ T cells to proliferate in an Ag-independent fashion using anti-CD3, as well as an Ag-dep
280 c cellular signaling pathways in a chemokine-independent fashion, vGPCR binds a broad spectrum of CC
281 regulates angiogenesis in a VEGF- and VEGFR2-independent fashion via ABL1 suggests that ABL1 inhibiti
282 d, in which PKGIalpha is activated in a cGMP-independent fashion via oxidation of Cys(43), resulting
283 ivated p38alpha MAPK in a Toll-like receptor-independent fashion via the lasI/lasR quorum-sensing sys
284 ar macrophages and can infect cells in a CD4-independent fashion, was highly sensitive to neutralizat
285 that transduces BMP-2/4 signals in a ligand-independent fashion, we demonstrate that signals provide
286 nhibitor 1 (PAI-1) transcription in a ligand-independent fashion when its nuclear localization is for
287 uggest that Dkk1 is acting in a beta catenin independent fashion when modulating gastrulation movemen
288 emained associated with membrane in a Ca(2+)-independent fashion whereas C2 domain rapidly dissociate
289 traviolet B-induced apoptosis in a caspase-3-independent fashion, whereas co-incubation with a caspas
290 a transforming growth factor beta (TGFbeta)-independent fashion, whereas it down-regulated matrix me
291 atalyze the condensation reaction in a metal-independent fashion, whereas the Class II enzymes (e.g.
292 level of MAP kinase kinase in a Ras- and Raf-independent fashion, whereas the JNK pathway stimulation
294 lR/GrlA activate LEE2 transcription in a Ler-independent fashion, whereas transcription of grlRA is a
295 NF)-induced apoptosis in an oxidative stress-independent fashion, which could not be explained by int
296 ermination of monochromatic light in a power-independent fashion with a single metal-insulator-metal
297 a chromosomal scale and in a marker density-independent fashion, with chromosomes 2, 15, and 18 bein
298 CD8+ T cells also secrete IFN-gamma in an Ag-independent fashion within 16 h of infection with L. mon
300 recruited, were highly activated in an MyD88-independent fashion, yet failed to clear the infection i