1 e provide evidence that the hedgehog pathway
is activated in 20% of T-ALL samples.
2 The same PF3D7_1255200 var gene
was activated in 4 different experimental infections.
3 The mobile-phone positioning system
was activated in 667 out-of-hospital cardiac arrests: 46
4 In particular, these components
are activated in a sequential manner in order to success
5 Here, we show that although caspases
are activated in a well-studied neoplastic tumor model i
6 This system can
be activated in a convertase-independent manner from int
7 vocal evidence that naive CD4(+) T cells can
be activated in a nonlymphoid organ.
8 The purified protein was shown to
be activated in a pH-dependent manner.
9 and involves approximately 10% of the genome
being activated in a highly dynamic pattern.
10 e, could be used to change the way a prodrug
is activated in a "programmable" manner.
11 vation has been proposed, in which PKGIalpha
is activated in a cGMP-independent fashion via oxidation
12 polarity-responsive enhancer in upd3, which
is activated in a coincident manner by both JNK-dependen
13 galactose, the galactose regulatory pathway
is activated in a fraction of the cell population hours
14 The innate immune system
is activated in a number of degenerative and inflammator
15 RIM pathway, and, accordingly, pH signaling
is activated in a phosphodeficient Rim8 mutant and impai
16 Moreover, Notch1
is activated in a small subset of SCC cells at the invas
17 roblasts, in which constitutive Gli activity
is activated in a Smoothened (Smo)-independent fashion,
18 chemically-induced injury, Ascl3 expression
is activated in a subset of horizontal basal cells (HBCs
19 ke the other phospholipase C family members,
is activated in a sustained manner.
20 ysical studies have shown that alpha-catenin
is activated in a tension-dependent manner that in turn
21 em2)(-/-) Tg-AD reveals that the DAM program
is activated in a two-step process.
22 The complement system
is activated in a wide spectrum of CNS diseases and is s
23 lones expressing an array of Vbeta receptors
were activated in a dose-, time-, and processing-depende
24 Jag1 are expressed in, and Notch2 signaling
is activated in,
a subset of human HCC samples.
25 oves glucose tolerance and insulin signaling
is activated in AAV mice.
26 eroceptive insular cortex (a region known to
be activated in acute MWD) also prevented the establishm
27 Toll-like receptor 2 was shown to
be activated in AD lesional skin (immediately proximal t
28 both vascular pathology and inflammation and
is activated in AD patients and AD mice.
29 A third IL17 subfamily
is activated in adult immune cells indicating that expre
30 The JAK-STAT pathway appears to
be activated in all myeloproliferative neoplasms, regard
31 The mTOR pathway
was activated in all 6 TCL cell lines tested and everoli
32 After this visit, both leads
were activated in all patients for an additional 3 month
33 ts signals from cytokines IL-4 and IL-13 and
is activated in allergic airway disease.
34 The complement pathway
is activated in Alzheimer's disease.
35 alleles have not been identified and T cells
are activated in an allele unrestricted manner.
36 er spinal cord injury (SCI), meningeal ILC2s
are activated in an IL-33-dependent manner, producing ty
37 MAIT cells
are activated in an MR1-restricted manner by diverse str
38 RhoA, cdc42, Rac1, and FAK
were activated in an EPAC1/2-dependent manner, and there
39 ents where it was unknown whether the target
was activated in any individual patient.
40 The WNT signaling pathway
is activated in APAs.
41 they have restricted mobility but reside and
are activated in apposition to CX3CR1(+) macrophages.
42 rget for the transcription factor ERG, which
is activated in approximately 50% of human prostate canc
43 The PI3K pathway
is activated in approximately 70% of breast cancers.
44 post infection, indicating that ET signaling
was activated in Arabidopsis early by SCN infection.
45 trast, no new cohesion is detected when Rec8
is activated in arrested oocytes by tamoxifen despite co
46 over PI3K/AKT2 as a direct PDGFA target that
is activated in ASCs during WAT hyperplasia and is funct
47 NK cells
are activated in asthma; however, their role in allergic
48 report in this study that TGF-beta signaling
is activated in astrocytes during toxoplasmic encephalit
49 The PERK-elF2 pathway
was activated in astrocytes of the spinal dorsal horn in
50 We conclude that HIF1alpha
is activated in ATII cells after lung injury and promote
51 , a cytosolic sensor of double-stranded DNA,
is activated in autoinflammatory disorders and by DNA da
52 Stat3
is activated in basal cells and their daughters early in
53 We establish that beta-catenin signaling
is activated in basal cells during early pregnancy, and
54 howed that nuclear factor kappaB (NF-kappaB)
is activated in BCR-ABL1-expressing cells, but the mecha
55 gene encoding the nuclear receptor PPARgamma
is activated in bladder cancer, either directly by gene
56 In the infarcted heart, Smad3 signaling
is activated in both cardiomyocytes and interstitial cel
57 ike endoplasmic reticulum (ER) kinase (PERK)
was activated in both intact and Gcn2(-/-) mice.
58 The autophagy and proteasome pathways
were activated in both muscles at varying intensities ov
59 Several inflammatory pathways
were activated in both subtypes.
60 cancer samples, indicating that this pathway
is activated in breast cancers that are clinically resis
61 Its expression
is activated in breast cancers, where high tumor levels
62 We report here a mechanism by which they
are activated in cancer cells, involving release of the
63 EMT may
be activated in cancer cells by reactive oxygen species
64 These results show that PP2A can
be activated in cancer cells to inhibit proliferation.
65 Furthermore, this pathway
is activated in cancer cells, and correlates with pro-in
66 We show that the MRTF-SRF pathway
is activated in cancer-associated fibroblasts (CAFs).
67 NF2
was activated in cardiomyocytes subjected to H2O2 and in
68 expression demonstrated that the Hh pathway
is activated in CD34(+) CP-CML stem/progenitor cells.
69 The mechanistic target of rapamycin (mTOR)
is activated in CD4(-)CD8(-) double-negative (DN) T cell
70 edia, whereas transcription of MDH1 and MDH2
is activated in cells cultured in YNB + Glu but not in Y
71 Although nuclear factor-kappaB
is activated in cells from patients with inflammatory di
72 Many enzymes
are activated in chemotransduction to hydrolyze ATP.
73 Here we show that both pathways
are activated in chondrocytes after treatment with TGF-b
74 RET can
be activated in cis or trans by its co-receptors and lig
75 , we evaluate whether the kynurenine pathway
is activated in clinical HAT and associated with CNS inf
76 o1-CIN tissues upregulated pathways known to
be activated in colon cancer, including lipid metabolism
77 rget of rapamycin complex 1 (mTORC1) pathway
was activated in Cpt2M(-/-) hearts; however, daily rapam
78 by several 2'-O-methyl-modified nucleotides
was activated in culture supernatants of S. aureus but n
79 Subsequently, Wnt/beta-catenin signaling
is activated in cushion mesenchymal cells where it suppo
80 Villin-CreER(T2)
was activated in developed tumors by administration of t
81 e time, the BMP signal transducers SMAD1/5/8
were activated in developing coronary arteries.
82 ings provide the first evidence that the UPR
is activated in DTC in the bone marrow from cancer patie
83 y of colonic muscles; different conductances
are activated in each cell type of the SMC-ICC-PDGFRalph
84 Differential genetic programs
are activated in each cell type to construct functionall
85 DDK, despite
being activated in early S phase, does not phosphorylate
86 Once the program
is activated in early embryos, Fli1 then takes over to s
87 The finding that MAPK
was activated in early differentiating and mature D2J os
88 levels are increased in ECs, stress pathways
are activated in ECs, and ISCs overproliferate.
89 sponsive reporter, we demonstrate that Notch
is activated in endothelial progenitors during vasculoge
90 Under normal conditions, S1P1
was activated in endothelial cells of lymphoid tissues a
91 showed that the steroid biosynthesis pathway
is activated in enzalutamide-resistant prostate cancer c
92 Both Pdgfrb and Igf1r
were activated in ex vivo T-ALL cells, and coculture wit
93 numerous genes that control inflammation and
is activated in glomerular cells in glomerulonephritis (
94 the present study, we showed that ER stress
was activated in granulosa cells of PCOS patients as wel
95 The renin-angiotensin system (RAS)
is activated in heart failure (HF) and inhibition of RAS
96 Hypoxia-inducible factor-1alpha (HIF-1alpha)
is activated in hepatic stellate cells (HSCs) by hypoxia
97 pegIFN-alpha in serum, the Jak/STAT pathway
was activated in hepatocytes only on the first day after
98 endent HIF1alpha/VEGF-A/FOXO1/TWIST1 pathway
was activated in high-grade PCa specimens, and knockdown
99 silent in the genome, this group of viruses
is activated in HIV-1-infected and cancer cells.
100 After carbon tetrachloride, HIF-1alpha
was activated in HSCs.
101 Importantly, BCAT1 expression not only
is activated in human blast crisis CML and de novo acute
102 n patients with AAV indicated that NF-kappaB
is activated in human NCGN also.
103 es have shown that homologous cortical areas
are activated in humans during tongue movement tasks, th
104 scle cells of the human intestinal tract and
is activated in inflamed and fibrotic tissue.
105 epithelial A1-adenosine receptors (A1-AdoR)
are activated in influenza A virus-infected mice.
106 We found that Ikkepsilon
was activated in intestinal tumors forming upon loss of
107 bited by the Hippo tumor suppressor pathway,
are activated in KSHV-infected cells in vitro, KS-like m
108 In this study, we found that caspase-3
is activated in L88 bone marrow stroma cell-derived exos
109 nal-regulated kinase (ERK) signaling pathway
is activated in Langerhans cell histiocytosis (LCH) hist
110 Hence, type I cytokine receptors may
be activated in leukemia through 2 types of transmembran
111 nuclease inositol-requiring enzyme 1 (IRE1),
is activated in lipid-laden macrophages that infiltrate
112 A bidirectional response
is activated in &
lt;5 min of training, in which phosphoryla
113 hown to be an eat-me signal on cancer cells,
is activated in macrophages for secretion and cell-surfa
114 Here we report that caspase-1
is activated in macrophages under hypertonic conditions.
115 SCF E3 ligases
are activated in many cancers and inhibitors could have
116 The Hedgehog (Hh) signaling pathway
is activated in many cancers and is a promising target f
117 sis of epithelial barrier tissues; how MASPs
are activated in mature epithelia is unknown.
118 Here, we show that, when ERK1/2
are activated in mature quiescent oligodendrocytes durin
119 Abl kinases (Abl/Arg)
are activated in melanomas and drive progression; howeve
120 cal adhesion formation and FAK/SRC signaling
is activated in mesenchymal tumor cells by crosslinked c
121 We previously showed that beta1 integrins
are activated in metastatic prostate cancer (PCa) cells,
122 We show that CGRP(PBN) neurons
are activated in mice implanted with Lewis lung carcinom
123 e propose that the noncanonical inflammasome
is activated in mice during acute intestinal inflammatio
124 egulation of critical cellular processes and
is activated in more than 30% of human cancers.
125 Oncogenic NOTCH signaling, which
is activated in more than 65% of T-ALL patients by activ
126 In these studies, we show that RA signaling
is activated in mouse and zebrafish models of AKI, and t
127 We found that Jak/Stat-signaling
is activated in Muller glia in response to NMDA-induced
128 1 knockouts, indicating that the endocardium
is activated in multiple cases where sinus venosus angio
129 data demonstrate that the NOD2-RIP2 pathway
is activated in murine and human VL and plays a role in
130 TS whereby p53 is deleted and oncogenic Kras
is activated in muscle satellite cells via a Pax7(CreER)
131 on; (2) beta1 Integrin/FAK signaling pathway
was activated in myeloma cells under hypoxic condition.
132 activated kinase (AMPK), a metabolic sensor,
was activated in myotubes exposed to high CO2, and loss-
133 quires intact TLR9, but how the TLR9 pathway
is activated in NASH is not clear.
134 d and are tightly linked, since beta-catenin
is activated in nearly all of the CAR-dependent tumours
135 Lin28B
is activated in neuroblastoma (NB), a childhood tumor in
136 SPOT can
be activated in neuron cell bodies or uncaged in dendrit
137 We found that these channels can
be activated in neurons of the medial nucleus of the tra
138 We found that Cdc25A
is activated in neurons undergoing ischemic stress media
139 oot cap regulators SOMBRERO and BEARSKIN1/2,
are activated in nlp7-1 seedlings.
140 m of the large, membrane fission GTPase, can
be activated in nonneuronal cells downstream of cancer-r
141 AEP
is activated in normal mice in an age-dependent manner,
142 For example, the murine protein p204 can
be activated in numerous tissues by distinct transcripti
143 lays a vital role in cell cycle progression,
is activated in numerous human malignancies, and is link
144 The AKT pathway
was activated in one subtype while MAP kinase pathway wa
145 , and the ErbB3-binding protein-1 (Ebp1) can
be activated in oral tumorigenesis and can serve as a tr
146 Hedgehog signaling
is activated in osteoarthritis, where it promotes chondr
147 enhancers are evolutionary conserved and can
be activated in other tissues, in contrast to enhancers
148 In addition, proapoptotic pathways
are activated in P1 knock-in premegakaryocyte/erythroid
149 SPHK1/Akt/NF-kappaB signaling pathway, which
is activated in pancreatic cancer.
150 We also reveal that ATM
is activated in pancreatic precancerous lesions in the c
151 cyclin-dependent kinase 4/6 (CDK4/6) pathway
is activated in parallel with renal cell-cycle entry but
152 ormal adult lymphatic endothelial cells, but
is activated in pathological situations such as inflamma
153 However, how beta1 integrins
are activated in PCa cells is unknown.
154 We found here that although MSKs
are activated in peritoneal B cells in response to TLR4
155 found that the WNT/beta-catenin pathway can
be activated in PHHs, as assessed by universal beta-cate
156 In nature, this strategy may
be activated in phytochrome-disabling, vegetation-dense
157 gen-specific B lymphocytes and T lymphocytes
are activated in piperacillin-hypersensitive patients.
158 Multi-layered defense responses
are activated in plants upon recognition of invading pat
159 We found that necroptosis
was activated in postmortem human AD brains, positively
160 NR1D1
was activated in primary mouse and human macrophages by
161 When beta-catenin
was activated in Prom1+ DP cells there was an increase i
162 roblastoma RAS viral oncogene homolog (NRAS)
is activated in PSC cholangiocytes.
163 OR), which governs most protein translation,
was activated in rat spinal dorsal horn neurons after re
164 The JAK/STAT3 pathway
was activated in reactive astrocytes in two transgenic m
165 istence of enhancer regulatory elements that
are activated in regenerating tissue.
166 murine leukemia virus envelope protein (Env)
are activated in relation to each other, sequentially or
167 The NLRP3 inflammasome can indeed
be activated in resident macrophage/monocyte-like cells
168 rentiating epiblast shows that CDX2 and ELF5
are activated in response to BMP4.
169 eptor potential vanilloid 4 (TRPV4) channels
are activated in response to changes in plasma membrane
170 The inflammatory caspases 1 and 11
are activated in response to different agonists and act
171 g IFN-gamma-producing NKG2D(+) NK cells that
are activated in response to DS-induced stress signals.
172 We report here that mTORC1 and mTORC2
are activated in response to exogenously supplied fatty
173 MAPKs
are activated in response to G protein-coupled receptor
174 Innate type 2 immune cells
are activated in response to helminths, allergens, and c
175 em cell population in adult skeletal muscle,
are activated in response to hypertrophic stimuli and gi
176 8(MAPK) molecules and 36.5% of MK2 molecules
are activated in response to IL-1beta.
177 In the CNS, microglia
are activated in response to injury or infection and in
178 ndicating that the label-retaining (LR) GBCs
are activated in response to injury.
179 lammatory caspases (caspases 1, 4, 5 and 11)
are activated in response to microbial infection and dan
180 These promoters
are activated in response to unique signals.
181 ptionally repressed in ES cells but ready to
be activated in response to differentiation signals.
182 HSCs) are dormant in the bone marrow and can
be activated in response to diverse stresses to replenis
183 alateral prefrontal cortex are also shown to
be activated in response to INMS.
184 While RTKs are generally known to
be activated in response to ligand binding, many of thes
185 A aminoarabinose transferase ArnT, known to
be activated in response to limiting magnesium.
186 omponent of the innate immune system and can
be activated in response to microbial and endogenous dan
187 a homotetrameric transcription factor which
is activated in response to a variety of cellular stress
188 diated proteasome degradation mechanism that
is activated in response to abnormal Ca(2+) homeostasis.
189 cocorticoid production in the adrenal cortex
is activated in response to an increase in cyclic AMP (c
190 Chaperone-mediated autophagy (CMA)
is activated in response to cellular stressors to preven
191 However, the mechanism by which p53
is activated in response to centrosome loss remains unkn
192 The allelochemical DIMBOA gene cluster
is activated in response to co-cultivation with rice, wh
193 The non-receptor tyrosine kinase c-Abl
is activated in response to DNA damage and induces p73-d
194 The DNA damage checkpoint pathway
is activated in response to DNA lesions and replication
195 ine the molecular mechanism by which PKCzeta
is activated in response to hyperglycemia and suggest th
196 In particular, IRF3
is activated in response to infection by a range of viru
197 Cyclooxygenase-2 (COX-2)
is activated in response to ischemia and significantly c
198 ess their own unfolded protein response that
is activated in response to mitochondrial protein foldin
199 sive Polycomb complexes in growing cells but
is activated in response to oncogenic stress.
200 Autophagy
is activated in response to stress, but its regulation i
201 Alkaloid accumulation in plants
is activated in response to stress, is limited in distri
202 p38 MAPK signaling
is activated in response to stretch, and inhibition of p
203 (UPR) is a cellular adaptive mechanism that
is activated in response to the accumulation of unfolded
204 The complement system
is activated in response to tissue injury.
205 cell line and animal models showed that Pak1
is activated in response to UV-B radiation, and this act
206 did not attain the levels observed when p53
was activated in response to etoposide treatment and rem
207 n-activated protein kinase kinase-1 (MEKK-1)
were activated in response to TNF-alpha.
208 Calcium oscillations
were activated in rice atrichoblasts by CO4, but not the
209 Yap and Taz
are activated in Schwann cells by mechanical stimuli and
210 onstrates that oncogenic ErbB2 signaling can
be activated in SCs but not impede transdifferentiation
211 The Rho family GTPases Rac1 and Cdc42
were activated in senescent cells, and simvastatin reduc
212 Here we show that complement
is activated in skeletal muscle injury and plays a key r
213 nfiguration and proximal or distal geometry,
were activated in solution by ultrasound-generated elong
214 logical pathway caused by epigenetic changes
is activated in some forms of congenital neuromuscular d
215 at NRF2 and protumorigenic NRF2 target genes
were activated in some actinic keratoses, the major prec
216 Consistently, NF-kappaB
was activated in sorafenib-resistant HCC cells, and this
217 ompeting functional roles, only one of which
was activated in speech production.
218 s, and we present evidence that this pathway
is activated in sporadic CCM patients.
219 Both ER and mitochondrial stress responses
are activated in sqrd-1 mutant animals exposed to H2S, b
220 ulation of the right and left phrenic nerves
were activated in synchrony with mechanically ventilated
221 The mechanism by which mast cells (MCs)
are activated in T cell-mediated inflammatory processes
222 NF-kappaB
was activated in T cells by inducing the expression of a
223 pathways linked to epigenetic reprogramming
were activated in TBDM above levels observed with DM alo
224 fied a group of CTNNB1/TCF target genes that
are activated in the absence of TCF7L1, including EPHB3,
225 ests that serine-aspartyl proteases-caspases
are activated in the AD brain.
226 tes are pivotal in this process because they
are activated in the attempt to digest Abeta which start
227 DNA damage nor the intra-S phase checkpoints
are activated in the first cell cycle, demonstrating tha
228 Indeed, 4 of 11 enzymes of this cycle
are activated in the light through dithiol/disulfide int
229 farnesoid X receptor (FXR, encoded by NR1H4)
are activated in the liver in the fasted and fed state,
230 ase- and oxidative stress-dependent pathways
are activated in the lung tissue of C57/BL6J-betaENaC-Tg
231 al nervous system tumors and found that MNKs
are activated in the majority of tumors tested.
232 a, determination of which cells and pathways
are activated in the network of APCs remains elusive.
233 mmune encephalitis (EAE), autoimmune T cells
are activated in the periphery before they home to the C
234 We examined whether macrophages
are activated in the skin of imiquimod (IMQ)-treated mic
235 monstrating that the PGLYRP1/TREM-1 axis can
be activated in the absence of bacterial products.
236 signaling pathways (e.g., ERK signaling) can
be activated in the absence of nuclear strain transfer,
237 Because Notch signaling is known to
be activated in the bleomycin model of pulmonary fibrosi
238 first time that this prominent catalyst can
be activated in the dark even when electrically insulate
239 low and it is unclear how Ca(2+) release can
be activated in the interior of atrial cells.
240 rently expressed genes and were predicted to
be activated in the intestine of insulin-resistant subje
241 investigated whether the NLRP3 inflammasome
is activated in the adipose tissue of burned patients, a
242 dings suggest that the CgA-angiogenic switch
is activated in the BM of multiple myeloma patients and
243 Our studies demonstrate that p53
is activated in the brain following reovirus infection a
244 onstrate that DR-induced apoptotic signaling
is activated in the brain following WNV infection and su
245 c-Abl
is activated in the brain of Parkinson's disease (PD) pa
246 Here we show that IIS
is activated in the cells surrounding an epidermal wound
247 orkhead boxO family of transcription factors
is activated in the diaphragm during mechanical ventilat
248 s, and that the ubiquitin-proteasome pathway
is activated in the diaphragm.
249 model, the Yap protein of the Hippo pathway
is activated in the eyes, and blood vessels near the les
250 Here, we demonstrate that Gi
is activated in the Golgi by GIV/Girdin, a non-receptor
251 r AMP-dependent enzyme, AMP deaminase (AMPD)
is activated in the liver of diabetic mice, which parall
252 The MAPK pathway
is activated in the majority of melanomas and is the tar
253 analyses reveal that miR-200a-3p expression
is activated in the pre-ameloblast cells to enhance epit
254 In yeast, PKA
is activated in the presence of high glucose concentrati
255 On the contrary, Snf1/AMPK
is activated in the presence of low glucose or alternati
256 system, the human sex-determining gene hSRY
is activated in the single-cell embryos of the mouse.
257 Tryptophanase
is activated in the stationary phase by the stationary-p
258 EGFR
is activated in the ventral midline and neurogenic ectod
259 The same region
was activated in the aphasic patients as they listened t
260 A mirror right-lateralized FTP network
was activated in the Count and Decision trials, but not
261 ly translocate between both compartments and
was activated in the cytoplasm.
262 GUS fusion assays we established that miR827
was activated in the initial feeding cells and this acti
263 LBOW
was activated in the intestinal epithelium, and a year-l
264 ated in one subtype while MAP kinase pathway
was activated in the other.
265 Here, we found that the mTOR pathway
was activated in the parathyroid of rats with secondary
266 Neurostimulation
was activated in the sham group at 3 months and outcomes
267 Multiple cell death-related pathways
were activated in the degenerating D stump, whereas acti
268 tein signaling, such as bmp2, nog, and dlx5,
were activated in the extraction wounds of the ALN-treat
269 sical complement pathway associated proteins
were activated in the glaucoma samples suggesting an inn
270 ozoon cuniculi infection, CD11b(-) CD8(+) DC
were activated in the lamina propria (LP) and acquired t
271 entially expressed and 94 signaling pathways
were activated in the topical MSCs transplanted onto the
272 in the hearing condition at those sites that
were activated in the two conditions.
273 components of insulin/insulin-like signaling
are activated in their discs.
274 egulated in daughters of overweight fathers,
was activated in their mammary tissues and tumors.
275 llular signal-regulated kinase (ERK) kinases
are activated in these knockout animals.
276 gation in megakaryocytes, an endomitotic SAC
is activated in these cells upon Plk1 inhibition.
277 However, the immune receptors that
are activated in this context remain elusive.
278 at the level of activation, but how TGF-beta
is activated in this disease is unknown.
279 It is not clear how ARL-8
is activated in this process.
280 How the inflammasome
is activated in this untreatable disease is largely unkn
281 Here we report that XOD
is activated in THP-1 human myeloid cells in response to
282 anaerobe nanovesicle mimic that can not only
be activated in THRs but also induce hypoxia in tumors b
283 Here we report that XBP1
is activated in TNBC and has a pivotal role in the tumor
284 lls and demonstrate that specific mechanisms
are activated in tolerant T helper cells to directly rep
285 nd other Treg cell signature genes, began to
be activated in Treg precursor cells.
286 use and contains multiple MYC enhancers that
are activated in tumor cells.
287 RhoA
is activated in tumors from neuroblastoma patients, and
288 cytidine deaminase-induced mutagenesis might
be activated in tumourigenesis and limited therapeutical
289 Cdc42
is activated in two temporal steps in the G1 phase: the
290 iety of DNA repair mechanisms, many of which
are activated in vascular disease.
291 MKK4
is activated in vitro by reduced Trx but not oxidized Tr
292 Thus, we found that when donor cells
were activated in vitro and injected intraperitoneally,
293 Primary pancreatic stellate cells
were activated in vitro by C5a.
294 Human CD19(+) B cells
were activated in vitro in the presence or absence of 9c
295 In the current study, human neutrophils
were activated in vitro with immobilized extracellular m
296 Finally, we demonstrate that ERK1/2
are activated in vivo in the colon of Stx2-intoxicated i
297 rial diseases, we show that the ATF4 pathway
is activated in vivo upon mitochondrial stress.
298 and that in human lung cancers this pathway
is activated in vivo.
299 in vitro and injected intraperitoneally, or
were activated in vivo, they migrated simultaneously to
300 Previously we demonstrated that FOXO1
was activated in wound healing but to higher levels in d