ライフサイエンスコーパス: in vitro,

1 ot upon direct exposure of glia to morphine (in vitro).

2 In vitro, (11)C-Me-NB1 binding was independent of the si

3 In vitro, 2-deoxyglucose and radiation synergistically u

4 elial electrical resistance in an all-human, in vitro, 3-dimensional, blood-brain barrier model exemp

5 uch timing as demonstrated by animal studies in vitro [3, 4] and in vivo [5, 6], suggesting a causal

6 In vitro, about 20 days after infection with EBV lacking

7 In vitro, acute high glucose treatment reduces ER-mitoch

8 In vitro, adiponectin reduced apoptotic, anti-proliferat

9 In vitro, AGO10-bound miR165/6 is more susceptible to SD

10 In vitro, AGR2 expression was stimulated by tunicamycin-

11 We isolated four G4 conformations in vitro, all of which bear unusual structural features:

12 sed the level of IL-10 production by B cells in vitro, although the frequencies of CD1d(hi) CD5(+) an

13 fect the process of cellular transformation (in vitro) and environmental carcinogenesis (in vivo), in

14 R mutation confers enhanced FcRn interaction in vitro, and Abs harboring either the Q311R or TLQ muta

15 drial biogenesis and function dosed to cells in vitro, and also dosed in vivo to mice and humans.

16 All ILC subsets are functionally competent in vitro, and are sufficient to provide enhanced protect

17 ues can bind interchangeably with each other in vitro, and at least in the fission yeast, heterologou

18 MSCs can be grown in large numbers in vitro, and autologous MSCs transfused into tuberculos

19 C motif) ligand 2 in neonatal cholangiocytes in vitro, and blockade of the corresponding chemokine (C

20 ed neurons treated with recombinant TNFalpha in vitro, and by repeated intrathecal injection of recom

21 cultured in G-CSF failed to respond to G-CSF in vitro, and Csf3r gene expression could not be detecte

22 mphopoiesis in a non-cell-autonomous fashion in vitro, and depletion of the Hh effector Smoothened (S

23 rreversible growth inhibition and senescence in vitro, and diminishes growth of cell line and patient

24 s (RBCs) demonstrate procoagulant properties in vitro, and elevated hematocrit is associated with red

25 the presence of G4 in human P1-HNF4A-5' UTR in vitro, and establishes a novel working model of stron

26 orescently labelled particles are detectable in vitro, and explore the utility of the method in vivo

27 characterization of cell/tissue development in vitro, and for long-term in vivo monitoring the miner

28 een essential for generating human organoids in vitro, and how organoids are now being used as a prim

29 mutations showed similar behaviors in yeast, in vitro, and in Drosophila, a few showed anomalous beha

30 Systematic profiling of ex vivo (in yeast), in vitro, and in vivo activities of type-2 diacylglycero

31 In sum, our complementary in silico, in vitro, and in vivo analysis argues that interface add

32 (NMU), the ligand of NMUR1, activated ILC2s in vitro, and in vivo co-administration of NMU with IL-2

33 Here, we combine a theoretical model, in vitro, and in vivo experiments revealing how protein

34 biology approach integrating computational, in vitro, and in vivo experiments to identify TRIM25 (tr

35 eceptor trafficking, enhanced cell migration in vitro, and increased the metastatic efficiency of NSC

36 oalveolar lavage macrophages were stimulated in vitro, and iNOS expression and NO production were inv

37 istics for specific peptide binding to cells in vitro, and investigated peak peptide uptake in tumors

38 GFBR3-PLAG1 promotes a tumorigenic phenotype in vitro, and is absent in 723 other salivary gland tumo

39 1 bound fatty acids with micromolar affinity in vitro, and its function was essential for fatty acid

40 cells exhibited sustained clonogenic growth in vitro, and lineage-tracing of Prox1(+) cells revealed

41 hat in vivo SARs differ from those collected in vitro, and most importantly, we identify four UBPs wh

42 ated uptake in HCT116-C19 cells was observed in vitro, and PET/CT imaging of normal mice showed uptak

43 ricted expansion of antigen-pulsed Tfh cells in vitro, and possessed a unique gene expression pattern

44 ated enhanced responses to autologous blasts in vitro, and primed CD56bright cells controlled leukemi

45 o, interacting directly with the RRE and Rev in vitro, and promoting Rev oligomerization in vitro.

46 t-transcriptional assembly of yeast U6 snRNP in vitro, and propose a model for U6 snRNP assembly.

47 lls harboring ALK amplification or mutations in vitro, and resulted in complete and durable responses

48 c80 complex's ability to bind two Dam1 rings in vitro, and results in kinetochore biorientation and m

49 block the growth of the breast cancer cells in vitro, and stimulate apoptosis.

50 abilizes microtubules using cell biological, in vitro, and structural approaches.

51 their proliferation and clonogenic capacity in vitro, and suppressed tumor xenograft growth in sever

52 otes osteoblast migration and mineralization in vitro, and systemic administration of PTHrP1-17 augme

53 ymes are capable of polyubiquitylating NEIL1 in vitro, and that both catalyse ubiquitylation of NEIL1

54 protein is similar in vivo to that observed in vitro, and that, at least for a predominant part of t

55 RAS-binding domain of the adenylate cyclase in vitro, and the cAMP analogue 8-bromo-cyclic AMP parti

56 iciently cleaved DSP into distinct fragments in vitro, and the deletion of Mmp9 caused improper proce

57 ophila, the mutation accelerates aggregation in vitro, and the mutant prion-like domain can substitut

58 al of several glioblastoma neurosphere lines in vitro, and this activity was further augmented by hyp

59 BIM, led to apoptosis and growth inhibition in vitro, and tumor regression in vivo.

60 he nonessential proteins affect viral growth in vitro, and two affect virulence in vivo; and (iv) a m

61 ad no apparent defect in platelet activation in vitro, and vessel wall platelet deposition and initia

62 anges in the HA stalk domain replicated well in vitro, and viruses incorporating two of the stalk mut

63 Data from in-vitro, animal, and human lung injury models suggest t

64 We found that, in vitro, approximately 10% of genes in T. brucei are ex

65 mmune-modulating properties both in vivo and in vitro, as characterized by secretion of both proinfla

66 Furthermore, under Th1 culture conditions in vitro, as well as in an IFN-gamma-rich inflammatory e

67 al role in retinoblastoma cell proliferation in vitro, as well as in orthotopic xenografts.

68 sive and less anchorage-dependent for growth in vitro, as well as more metastatic in vivo.

69 eath, migration and invasion of cancer cells in vitro, as well as tumor progression in vivo.

70 5-E-VP -modified siRNA to human Argonaute-2 in-vitro, as well as the enhanced silencing in the conte

71 In vitro, Astragaloside IV regulated energy metabolism b

72 In vitro, autophosphorylation of Ser-500 is found to req

73 In vitro, baicalein down-regulated the TLR4/MyD88 signal

74 We found that, in vitro, bone marrow stromal cells exposed to IR enter

75 ties of MCs across the MOB and AOB, using an in vitro, brain slice approach in postnatal 15-30 day mi

76 atory principal neurons and Purkinje neurons in vitro (brain slices) and in vivo.

77 aspase-mediated processing of the prohormone in vitro, but also the ability of prosystemin to trigger

78 sing approach to directing HSC specification in vitro, but current protocols are not capable of gener

79 en derived from human pluripotent stem cells in vitro, but generating a human ovarian follicle remain

80 ct of succinate was observed on cancer cells in vitro, but interestingly, we found that succinate cau

81 ave well documented immunomodulatory effects in vitro, but not following oral administration in human

82 al strains of the H1 and/or H3 virus subtype in vitro, but only KLK5 promoted the infectivity of A/Pu

83 sers at monoamine transporters as determined in vitro, but only methylone and MDC (1, 3 mg/kg, iv) pr

84 d agave Rca form functional hetero-oligomers in vitro, but only the rice isoforms denature at nonperm

85 inib effectively inhibited tumor cell growth in vitro, but the combination of trametinib and BKM120 o

86 se CHDs can mediate nucleosome translocation in vitro, but their in vivo mechanism is unknown.

87 siRNAs increases their potency and efficacy in vitro, but when delivered systemically to mice, the 5

88 pecifically degraded single-strand (ss) RNAs in vitro; but neither miRNAs nor miRNA*s in vivo.

89 To bind large amounts of calcium in vitro, calsequestrin must polymerize and then depolym

90 ano-enzymatic pathway of TTR fibrillogenesis in vitro, catalysed by selective proteolytic cleavage, w

91 h destabilized the N-terminal Fe4 S4 cluster in vitro, caused mild growth defects and a significant d

92 In vitro, CD14(pos)- and CD15(pos)-cell depletion increa

93 In vitro, CD44TA-SMP accumulated in macrophages infected

94 In vitro, CFI-402257-mediated inhibition of Mps-1 result

95 We stimulated human NK cells through CD16a in vitro, characterized CD16a-inducible transcripts, and

96 Cs were isolated from mouse hearts, expanded in vitro, characterized, and evaluated for therapeutic e

97 In vitro, Cmr (a member of the CRP/FNR super-family of t

98 y effective inhibitor of human alpha-amylase in vitro, comparable to the drug acarbose.

99 UC-MSCs in vitro, compared with bone marrow-derived mesenchymal

100 The Ctk1 kinase complex binds RNA in vitro, consistent with direct EF-RNA interaction.

101 refer neutral over anionic membrane surfaces in vitro, consistent with their localization to the earl

102 he C-terminal region of TPX2 regulates Kif15 in vitro, contributes to motor localization in cells, an

103 In vitro, crocin inhibited the assembly of pure tubulin

104 Following TCR-driven stimulation in vitro, CXCR5+ but not CXCR5- CD8 T cells generated bo

105 Electrophysiological data over 95 days in vitro (DIV) showed an age-dependent increase of axona

106 In vitro, effects of ConA-conditioned HSC medium on hepa

107 The use of in vitro, engineered surrogates in the field of cancer r

108 We show that decidualization (even in vitro) enhances the ability to communicate with the f

109 single-walled carbon nanotubes (SWCNT) under in vitro, ex vivo and in vivo settings.

110 A systematic approach involving in silico, in vitro, ex vivo and in vivo studies is employed to ide

111 nhancer and SE repertoires in cultured VSMCs in vitro, ex vivo, and in AngII-infused mice aortas in v

112 In vitro, ex vivo, and in vivo analyses show that TLR-in

113 Using in vitro, ex vivo, and in vivo approaches, we demonstrat

114 om patients with sPE, which dedifferentiated in vitro, failed to redecidualize in culture.

115 fferentially expressed in vivo compared with in vitro (false discovery rate, </=0.001; 2-fold change)

116 In vitro, fibroblast extracellular cathepsin K activity

117 cytoskeletal proteins has been demonstrated in vitro, fluorescence recovery after photobleaching ana

118 human neurons may be useful for studying VZV in vitro, for growing preparations of virus with high ti

119 In vitro, FTDP-17 mutant versions of tau can reduce micr

120 In vitro, FXa stably associated with TF-FVIIa activates

121 We show that in vitro, GHRH(1-44)NH2 attenuates phenylephrine-induced

122 osphate) promote alpha-synuclein aggregation in vitro, glucosylsphingosine triggers the formation of

123 nduce autophagy at micromolar concentrations in vitro, have aggregate-clearing activity in a cellular

124 ng has no effect on radiation-induced EndoMT in vitro, Hey2 overexpression is sufficient to induce ph

125 Recapitulating this process in vitro, Hfq guides RNase E cleavage of a representativ

126 In vitro, hnRNP F overexpression stimulated Sirtuin-1 an

127 When activated in vitro, however, IFN-gamma production by naive wild ty

128 r ZauP influenced FtsZ dynamics or bundling, in vitro, however.

129 s virus (MHV)-A59 infection both in vivo and in vitro; however, its mechanism and association with lo

130 by islet cells and induced their destruction in vitro; however, passive transfer of the same DSAs did

131 In vitro, HpRppH converts RNA 5'-triphosphates and dipho

132 In vitro, hSef-b inhibited proliferation of TRAMP C2 cel

133 In vitro, human LS174T goblet-like cells were depleted o

134 Both in vitro (human BMEC) (HBMEC) and in vivo (mice) models

135 In vitro, IFNR degradation was conserved across multiple

136 hese proteins are essential for viral growth in vitro; (iii) seven of the nonessential proteins affec

137 In vitro, IL-10 expression was detected only when tendon

138 In vitro, IL-17A enhanced IL-13-induced gene expression

139 In vitro, IL-4 blockade inhibited while addition of exog

140 In vitro, IL4I1-deficient B cells proliferate more effic

141 In vitro, ILC2 were increased and potently expressed IL-

142 ntagonism modified PTH secretion in vivo and in vitro, implying roles for these specific miRNAs.

143 entiation of oligodendrocyte precursor cells in vitro, in animal models, and in human cells.

144 exhibits selectivity for hypoxic activation in vitro, in living cells, and in multiple disease model

145 sion of retinal degeneration in models of RP in vitro, in vivo analyses were not possible with PR1.

146 displays broad-spectrum anticancer activity in vitro, in vivo in preclinical animal models, and in a

147 for BD2, to modulate inflammatory processes in vitro, in vivo, and ex vivo.

148 f the interesting properties of graphene for in vitro, in vivo, and point-of-care electrochemical bio

149 in the presence of an antimicrobial peptide in vitro, inactivation of both phoP and Sant_4061 is nec

150 a transition between distinct MK populations in vitro, including one that is primed for platelet rele

151 s also enhanced P. mirabilis urease activity in vitro, including recent clinical isolates of Escheric

152 suppressed neutrophil activation ex vivo and in vitro, including reduced l-selectin shedding, oxidati

153 atrix of many different monospecies biofilms in vitro, including some of those produced by oral bacte

154 In vitro, increased HER2 uptake by DC increased cross-pr

155 In vitro, increased room temperature incubation of optis

156 Sucrose, a tuber-promoting factor in vitro, increases StPP2Ac2b expression.

157 In vitro, increasing the hematocrit increased thrombin g

158 -induced maturation of osteoclast-precursors in vitro, indicate the commensal microbiota induces sust

159 lations exhibited erosion-controlled release in vitro, indicated by similar polymer mass loss kinetic

160 interact with known paramyxoviral receptors in vitro, indicating an independence from well-character

161 uced smaller neurospheres than control cells in vitro, indicating reduction of self-renewal and expan

162 D4(+)LAP(+)Foxp3(-) T cells were suppressive in vitro, inhibiting proliferation of naive CD4(+) T cel

163 In vitro, insulin increased proliferation of intestinal

164 In vitro, ISG15 deficiency also leads to persistently hi

165 In vitro, islets cultured under 140 mm Hg oxygen showed

166 hat while the ISR protects OPCs from hypoxia in vitro, it does not appear to play a major role in eit

167 not essential for H3-H4 tetrasome deposition in vitro, it is required for efficient DNA synthesis-cou

168 the functions of dendritic cells in vivo and in vitro, IVM impaired T-cell activation, proliferation,

169 essed its pharmacological properties through in vitro (kinase assay), ex vivo (human liver microsomes

170 In vitro, knockdown of T-cadherin from human aortic smoo

171 In vitro, KPAF3 stimulates KPAP1 activity and inhibits m

172 s T cell activation and IFN-gamma production in vitro, leading to a significant reduction in tumour g

173 In vitro, leptospiral PerR could bind to the perR promot

174 In vitro, M2 macrophages inhibit CD4(+) and CD8(+) T cel

175 In vitro, M2-polarized macrophages protected hepatocytes

176 In vitro, macrophages from CalpTG mice produced less IL-

177 In vitro (macrophages, endothelial cells, skeletal muscl

178 so strongly inhibits metallo-beta-lactamases in vitro, major contributors to clinical carbapenem resi

179 A total of only 520 compounds were tested in vitro, making this method broadly applicable for tool

180 Mcm10 forms oligomers in vitro, mediated by the coiled-coil domain at the N-te

181 In vitro, Meg3 regulated the production of matrix metall

182 Although PCR is highly effective in vitro, methods that can function without prior sample

183 Here we report that, in vitro, Meto prevents catecholamine-induced down-regul

184 In vitro, miR-542-3p suppressed the expression of the mi

185 I3K pathway, we assessed Treg cell induction in vitro, mitochondrial depolarization, and recruitment

186 In vitro, MSCs from individuals with coronary artery dis

187 rt morphology, biochemistry and pharmacology in vitro, offering a promising alternative to animals an

188 In vitro, OIS melanocytes activate T-cell proliferation.

189 ctivity of guarana extracts, after digestion in vitro, on carbohydrates-metabolism enzymes and to ass

190 fibrils by prion-like seeded polymerization in vitro, only some are transmissible and pathogenic in

191 cological inhibition or lentiviral silencing in vitro, or by genetic inactivation in neurons in vivo,

192 s1-Cas2 alone integrates spacers efficiently in vitro; other Cas proteins (such as Cas9 and Csn2) hav

193 tly to aromatase inhibition both in vivo and in vitro, our findings suggest that E2 signaling in BLA

194 blood was exposed to the same radiation dose in vitro (P<0.0001).

195 silico (p < 0.001) and moderate associations in-vitro (p = 0.015 and p = 0.085).

196 In vitro, pan-histone deacetylase inhibition elevates he

197 In vitro, PDGF-BB attracted myoblasts and activated thei

198 In vitro, placental endothelial cells were deficient in

199 In vitro, Polo directly binds and is required for Nuf ph

200 y, rIFN-lambdas enhanced epithelial barriers in vitro, preventing transcellular bacteria disseminatio

201 In vitro, primary keratinocytes derived from IL1r(-/-) m

202 and gastruloids have recently been generated in vitro, providing a unique opportunity to explore comp

203 resulted in severe defects both in vivo and in vitro, providing additional support for this unpreced

204 In vitro, purified RPA directly enhances the association

205 In vitro, radiotracer incorporation and efflux was simil

206 h concentrated platelets from healthy donors in vitro, raising platelet counts by 0% (unsupplemented

207 mitant dominant-negative effect on other E3s in vitro, raising the possibility that short circuiting

208 In vitro, recombinant TSN initiated the decay of both pr

209 tromal cells for normal collagen remodelling in vitro, regulating fibroblast interaction and engageme

210 element that is critical to PD-1 expression in vitro, responds to NFATc1, FoxO1, and/or NF-kappaB si

211 nal culture derived from timed pregnant rats in vitro, resulting in a much higher C99 level and C99/C

212 LRRK2 directly phosphorylates synaptojanin1 in vitro, resulting in the disruption of endophilin-syna

213 In vitro, silencing of Nox5 in human mesangial cells was

214 In vitro, siRNA-mediated FABP4 knockdown in endothelial

215 In vitro, SNAREs are sufficient to mediate effective fus

216 In vitro, splenic Tregs from IL233-treated mice suppress

217 In vitro, succinyl-CoA was used to succinylate liver mit

218 orkhead box P3 (Foxp3)(-) regulatory T cells in vitro, such that beta subunit of IL-27 (Ebi)(-/-) (ie

219 Our results, while confirming ADE in vitro, suggest that pre-existing DENV immunity does n

220 strong immunoreactivity with patient T cells in vitro, suggesting long-lasting immunological memory.

221 establishment of several gammaherpesviruses in vitro, suggesting that ATM is proviral in the context

222 in the white flour fraction was bioavailable in vitro, suggesting that food products made from the bi

223 m, effectively inhibited phenazine reduction in vitro, suggesting that most phenazine reduction deriv

224 in vivo, STAT4 failed to induce EMT directly in vitro, suggesting that STAT4 might mediate EMT proces

225 ledge, that HsPrp40Ap interacts with centrin in vitro, supporting a coupled functional role for these

226 sCD83 inhibits T cell proliferation in vitro, supports allograft survival in vivo, prevents

227 o examined the activity of the three enzymes in vitro; surprisingly, all three are active toward oxam

228 In vitro, testosterone treatment not only decreased Th1

229 In vitro, TGR5 stimulation enhanced cAMP production, cel

230 Additionally we report, in vitro, that increased concentrations of active caspas

231 In vitro, the activation of RANK-dependent signals is en

232 In vitro, the afferent nerve calyx surrounding type I ha

233 n vivo and on primary human pulp fibroblasts in vitro, the authors reveal that C5L2 and C5aR are co-e

234 In vitro, the Caulobacter S-layer protein, RsaA, enters

235 In vitro, the compounds induce misfolding of chromatin f

236 ad to modulation of their chaperone activity in vitro, the in vivo functions of alphaB-crystallin in

237 scosity and diffusion on a single cell level in vitro, the in vivo viscosity monitoring has not yet b

238 e that, using the RHOA biosensor in vivo and in vitro, the initiation of NCC polarization is accompan

239 Given the absence of external causes in vitro, the interplay of structurally differently cons

240 In vitro, the lipidic mediator resolvin D1 (RvD1) down r

241 In vitro, the mutant proteins were abnormally processed

242 In vitro, the PMM2 promoter mutation associated with dec

243 In vitro, the responses to sotalol were highly variable

244 ast Rad51 has been extensively characterized in vitro, the stringency of its search and sensitivity t

245 alize or enhance Zika virus (ZIKV) infection in vitro, their contribution to ZIKV infection in vivo r

246 and decreased endothelial barrier integrity in vitro, therefore increasing permeability.

247 In vitro, these dendrimers reduced the secretion of proi

248 Following the abrogation of AdipoR1 in vitro, these protective effects of adiponectin were a

249 When mixed in vitro, these two sHSPs form a polydisperse oligomer a

250 ells generally display a growth disadvantage in vitro, they grow significantly better in low adherenc

251 In vitro, this change can be reversibly induced by overc

252 When recapitulated with purified protein in vitro, this modification completely ablated the activ

253 Sertoli cells in a mitotically active state in vitro, thus enabling transfection experiments that al

254 promotes the degradation of mutant myocilin in vitro, to date no Grp94-selective inhibitors have bee

255 a facultative intracellular bacterium known, in vitro, to invade a large diversity of cells through t

256 transmembrane protein which has been shown, in vitro, to participate in the cellular efflux of desmo

257 ttachment factors for AKAV and SBV, at least in vitro, to promote virus replication in susceptible ce

258 though hPL inhibits GSTP1 enzymatic activity in vitro, treatment of cells susceptible to PL with hPL

259 In vitro, treatment with NE attenuated TGF-beta-induced

260 peptides disrupted the targeted interaction in vitro; two act by binding to CMG2 while one binds PA.

261 ptible mice and inhibited by IL-4R-signaling in vitro, uncoupling parasite killing from expulsion mec

262 ts, and biochemical characterization of DH10 in vitro, using polyketide substrate mimics with varying

263 NV), infectivity was significantly inhibited in vitro (using the epithelioma papulosum cyprini [EPC]

264 To unwind duplex DNA in vitro, UvrD needs to be activated either by self-asse

265 In vitro, we assessed cholangiocyte proliferation, cAMP

266 s E. histolytica does not readily form cysts in vitro, we assessed membrane trafficking gene expressi

267 To study these host-microbe interactions in vitro, we developed a human three-dimensional (3-D) e

268 To model hydrostatic pressure-induced edema in vitro, we developed a method of applied pressure to t

269 reement with predictions from determinations in vitro, we discovered a decline of noradrenergic proje

270 cessfully reconstituting Search-Capture-Pull in vitro, we discovered that formin Cdc12 is a mechanose

271 in cholangiocytes and hepatic stellate cells in vitro, we evaluated angiogenesis and fibrosis gene ex

272 Given the effectiveness of RpoN* in vitro, we explored its effects in a Caenorhabditis el

273 le assays for measuring honey's cytotoxicity in vitro, we found honey is cytotoxic towards prostate c

274 In vitro, we found that insulin increased pAKT, prevente

275 In vitro, we found that the disruption of glpG had polar

276 In vitro, we found that the loss of Twist1 in IPF lung f

277 nement and screening for biological activity in vitro, we identified 21 hit compounds which inhibited

278 rt-butyl hydroperoxide and hypochlorous acid in vitro, we identified additional covalent oxidative mo

279 Corroborating the results in RB-KO organoids in vitro, we observed ectopically localized Tuj1(+) cell

280 By reconstituting purified Smoothened in vitro, we show that cholesterol within the bilayer is

281 In vitro, we showed RTN1A mediates albumin-induced ER st

282 In vitro, we studied Smad-dependent and Smad-independent

283 nation of analytical and biophysical methods in vitro, we tested whether EVs isolated from pancreatic

284 rimary hepatocytes facilitates HBV infection in vitro, where all replicative intermediates including

285 icient attL x attR recombination in vivo and in vitro, whereas attP x attB recombination efficiency i

286 ls with GATA2 mutation proliferated normally in vitro, whereas lineage-negative progenitors displayed

287 M, providing a substrate for monocytic cells in vitro, whereas lung fibroblasts from Vcan(-/-) mice d

288 s LD abundance and reduces TNBC 2D migration in vitro, which can be partially rescued by the ACSL inh

289 generate dendritic action potentials (DAPs) in vitro, which can profoundly influence neural computat

290 tion of tight junctions in endothelial cells in vitro, which is blocked by pharmacological inhibition

291 ncogene c-Myc and the neural ESC marker CDK2 in vitro, which was accompanied by altered expression of

292 s greatly reduced the synthesis of viral RNA in vitro, which was detected only for the 7- and 21-nucl

293 ipitate complex (IP) displayed MMEJ activity in vitro, which was significantly elevated after irradia

294 , these cells show increased differentiation in vitro, with rapid loss of HSC-enriched LSK cells.

295 dy levels triggered eosinophil degranulation in vitro, with release of extensive histone-rich extrace

296 ortical neurons from slow excitotoxic injury in vitro, without influencing NMDA-induced intracellular

297 In vitro, WNT5A promoted the expression of IL6 in human

298 In vitro, Y141C-Prph2 showed signs of retention in the e

299 phagy gene ATG5 is dispensable in A549 cells in vitro, yet promotes tumorigenesis in mice.

300 thelial cells can be propagated indefinitely in vitro, yet retain the capacity to become fully differ