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