ライフサイエンスコーパス: -dependent

1 d macrophages induce an interleukin-1 (IL-1)-dependent inflammatory cytokine response by recruited mo

2 ults from cancerous cervical cells, K(Ca)3.1-dependent H33258 uptake was rarely observed in epithelia

3 EBE and TIE is essential for mediating AF-1-dependent transactivation.

4 680I/M680I) FMF knock-in mice exhibited IL-1-dependent increased survival relative to wild-type knock

5 hening and intravascular crawling in a Mac-1-dependent manner.

6 ot VEGF-A, was PPARbeta/delta- and sirtuin-1-dependent.

7 e discovery of the cadherin family of Ca(2+)-dependent cell-cell adhesion proteins, which play essent

8 negatively charged phospholipids in a Ca(2+)-dependent manner.

9 Our study demonstrates that AP-2-dependent internalization of PM proteins via the recogni

10 rocessed into RNA-dependent RNA polymerase 6-dependent small RNAs, resulting in their continued turno

11 of receptor tyrosine kinase AXL in an m(6)A-dependent way.

12 constitutively active form of acetylcholine-dependent K(+) current (I(KACh)), called I(KH); this is

13 2 (SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily D, member 2)

14 cy of APTi with two gene families, the actin-dependent motor, myosin XI (a,b), and the putative chiti

15 Activity-dependent global scaling therefore operates on both the

16 w that Zn(2+) inhibits AMPARs in an activity-dependent manner, opening up this pathway as a means to

17 In this study, we used an activity-dependent tagging system in mice to determine the epigen

18 Within mammalian brain circuits, activity-dependent synaptic adaptations, such as synaptic scaling

19 Conclusion: (225)Ac-L1 demonstrated activity-dependent efficacy with minimal treatment-related organ

20 HVDAS is caused by mutations in activity-dependent neuroprotective protein (ADNP).

21 Despite the growing interest in activity-dependent plasticity, it is still unclear whether synapt

22 namic functions for various MAPs in activity-dependent synaptic plasticity.

23 y thought to reflect the outcome of activity-dependent forms of synaptic plasticity, yet activity-ind

24 bilise target cell activity through activity-dependent global scaling have been observed only within

25 the question remains as to whether adjuvant-dependent modulation of T(fh) cells enhances HIV-1 vacci

26 irus (SINV) is an alphavirus that causes age-dependent encephalomyelitis in mice.

27 We found age-dependent changes in five song traits (duration, maximum

28 nown, and may play a fundamental role in age-dependent changes in reproductive success.

29 urrent respiratory infections, revealing age-dependent variation and suggesting a role for IgG glycos

30 detected lipids, 95% showed significant age-dependent concentration differences clustering into four

31 Specific, age-dependent expansion of ovalbumin-specific regulatory T c

32 Here, we show that the age-dependent downregulation of lamin B1, one of the nuclear

33 ) is a particularly vulnerable tissue to age-dependent degeneration.

34 dogenic processing of APP, combined with age-dependent iron elevation in the tissue, increases pro-ox

35 progenitors and that it may do so in an AhR-dependent fashion.

36 These responses are nucleated via the AKAP5-dependent clustering of P2Y(11)/ P2Y(11)-like receptors,

37 Likewise, BMP9/10 treatment induced an ALK1-dependent phenotypic switch from synthetic to contractil

38 alphaKG-dependent dioxygenases consume the metabolite alphaKG (a

39 ppression, which subsequently triggered AMPK-dependent autophagic cell death.

40 er (NK) cells resulting in crippled antibody-dependent cellular cytotoxicity (ADCC).

41 d natural cytotoxicity but enhanced antibody-dependent cellular cytotoxicity (ADCC).

42 Our findings demonstrate that ATG5-dependent autophagy uncouples T-cell proliferation from

43 ATP-dependent chromatin-remodeling enzymes control accessibi

44 table complex with Pol II and acts as an ATP-dependent processivity factor that helps Pol II across a

45 ynamic nucleosome unwrapping governed by ATP-dependent chromatin remodelers.

46 ate that both condensin I and II exhibit ATP-dependent motor activity and promote extensive and rever

47 droxylation signals for dioxgen availability-dependent HIF-alpha degradation via the ubiquitin protea

48 carrier and multicarrier mechanisms for axis-dependent conduction polarity and their identifying band

49 h in turn activates a nuclear factor kappa B-dependent metabolic pathway, leading to aerobic glycolys

50 in a TGF-beta receptor/PI3K/protein kinase B-dependent manner, to regulate hepatic acetyl-CoA and cho

51 -4Ralpha regulation of MMC9s is in part BATF-dependent and occurs via modulation of metabolic transcr

52 ional B cells, through B cell receptor (BCR)-dependent positive selection of fetally derived precurso

53 tors at the plasma membrane to modulate BDNF-dependent gene expression and neuronal dendritic growth

54 e inhibitors will be useful in treating BRAF-dependent tumors.

55 d in microglial activation and complement C3-dependent synapse elimination in vivo.

56 on autophagy flux and apoptosis in a calcium-dependent manner.

57 Here, we report that the Arabidopsis calcium-dependent protein kinase CPK3 is a key regulator of both

58 acellular Ca(2+) through a Ca(2+)/calmodulin-dependent protein kinase II (CaMKII)-mediated mechanism,

59 The calcium-calmodulin-dependent protein kinase kinase-2 (CaMKK2) is a key regu

60 of the cyclic adenosine monophosphate (cAMP)-dependent protein kinase (PKA), leading to activation of

61 Baloxavir is a cap-dependent inhibitor of the polymerase acid (PA) protein

62 ted B cells)-dependent inflammation, caspase-dependent apoptosis, or necroptosis in response to extra

63 -dependent component of the Wnt/beta-catenin-dependent transcriptional complex.

64 on in the C-repeat/DREB binding factor (CBF)-dependent and CBF-independent cold signaling pathways to

65 reporter mice; it also exploited both CCL17-dependent and unique CCL17-driven inflammatory pain and

66 educed FcepsilonRI binding and enhanced CD23-dependent serum clearance.

67 th specific binding sites promote rapid Cdk8-dependent Notch turnover, and thereby reduce Notch-depen

68 g IMs in the development of acute T(H)2-cell-dependent allergic airway inflammation.

69 urine model, Alp1 elicits helper T (Th) cell-dependent lung eosinophilia that is initiated by the rap

70 a-light-chain-enhancer of activated B cells)-dependent inflammation, caspase-dependent apoptosis, or

71 Type 1 cGMP-dependent protein kinases (PKGs) play important roles in

72 capacities, implicating dysregulation of CoA-dependent intermediary metabolism rather than respirator

73 dy [cPRA] class I and/or II >99%, complement-dependent cytotoxicity panel reactive antibody [CDC PRA+

74 e inflammation via elaboration of complement-dependent anaphylatoxins.

75 s in infected macrophages in a concentration-dependent manner and demonstrated activity against Trypa

76 d reduction was revealed to be concentration-dependent interfacial chemistry that only occurs among c

77 to membranes in a cholesterol concentration-dependent manner and that the binding is facilitated by

78 ental niche is associated with the condition-dependent expression of immune function and stress respo

79 products, thereby defining a form of contact-dependent, aquatic chemosensation.

80 broad terms developmental stage and context-dependent functions of lineage-defining transcription fa

81 Our work implicates TBX3 as context-dependent component of the Wnt/beta-catenin-dependent tr

82 sferred thyroid hormones (THs) exert context-dependent effects on offspring survival and physiology b

83 ing CRISPR-Cas9 technology or in a Postn-Cre-dependent manner (Eprs(flox/+); Postn(MCM/+)) strongly r

84 s degraded by the proteasome 26S in a Cullin-dependent manner.

85 Cell cycle-dependent redox changes can mediate transient covalent m

86 To determine whether cell-cycle-dependent gene regulation occurs in mycobacteria, we cha

87 ell-cycle entry program by activating cyclin-dependent protein kinase 4/6 (CDK4/6).

88 Cip1) /p27(Kip1) ) inhibit cyclin and cyclin-dependent kinase (CDK) complex that promotes fibrosis an

89 , cyclin-specific docking motifs help cyclin-dependent kinases (CDKs) phosphorylate different substra

90 Genetic depletion of cyclin-dependent kinase 12 (CDK12) or selective inhibition of a

91 he Arabidopsis (Arabidopsis thaliana) cyclin-dependent kinase G1 (CDKG1) is necessary for recombinati

92 CYP4Z1-dependent metabolism of arachidonic acid preferentially

93 luenced by DP, but also observed apparent DA-dependent priming activity, with the ADDD+DADD fraction

94 alues are a major issue in quantitative data-dependent mass spectrometry-based proteomics.

95 e involves both telomere cohesion and a DAXX-dependent pathway.

96 demonstrating the importance of demographic-dependent selection in shaping functional phenotypic var

97 ps to coordinate their behavior in a density-dependent manner.

98 s related to top-down, bottom-up and density-dependent regulation of demographic rates in an imperill

99 experiments beyond range boundaries, density-dependent population models built from long-term demogra

100 positions, which strongly influence density-dependent growth and survival.

101 has never previously been linked to density-dependent proliferation.

102 Here, we review these DG-dependent mnemonic functions in light of the new finding

103 ings suggest that PIR-1 modulates both Dicer-dependent and Dicer-independent Argonaute pathways and p

104 These data argue that diet-dependent alterations in taste weaken satiation by impai

105 te, also showed a phthiocerol dimycocerosate-dependent growth compromise upon limitation of the corre

106 is catalyzed by MenD, a thiamine diphosphate-dependent enzyme comprising three domains.

107 f GOLPH3 and its colocalization with the DNA-dependent protein kinase catalytic subunit (DNA-PKcs).

108 tion of multilocus region 34 protein (Dom34)-dependent ribosome recycling system, which splits Lso2-c

109 and baseline reach kinematics in a dopamine-dependent manner.

110 regulates meiotic recombination in a dosage-dependent manner.

111 Dose-dependent repression of methionine adenosyltransferase 1

112 However, a dose-dependent deformability increase upon latrunculin B-indu

113 blocker of HCNs-for 24 h resulted in a dose-dependent higher HRV and lower heart rate at 5 days post

114 in the cochlea, rather cisplatin had a dose-dependent impact on cochlear clock rhythms only after tr

115 ve male NSCLC cell lines demonstrated a dose-dependent induction of linc-SPRY3-2/3/4 following irradi

116 er epithelial progenitor cell line in a dose-dependent manner, achieving far higher efficiency and co

117 levels in both dams and offspring in a dose-dependent manner, but did not change TSH levels, weight,

118 ion and restorative division rates in a dose-dependent manner, leading to tumorous overproliferation

119 pacia and P. aeruginosa in CF MDMs in a dose-dependent manner.

120 nhibited by LJM17, LJM11, and DSG1 in a dose-dependent manner.

121 highest lipase inhibition (~ 70%) in a dose-dependent way.

122 ministration of (212)Pb-L2 demonstrated dose-dependent inhibition of tumor growth in the PSMA(+) flan

123 rhbeta-gal uptake by the fibroblasts is dose-dependent and saturable and can be competitively inhibit

124 Below 10 ug/ml, there were no dose-dependent cellular ROS increases or effects in MEA burst

125 Similarly, there was no dose-dependent relationship between PPS exposure and diagnosi

126 Similar dose-dependent relationships were observed for subjective wak

127 e near absence of mTOR, CDK1 activates eIF4E-dependent translation in MPs through phosphorylation of

128 ere that a Transcriptional Repressor of EIN3-dependent Ethylene-response 1 (TREE1) interacts with EIN

129 tic hypothesis involves impaired endothelium-dependent vasodilation through reactive oxygen species (

130 response in a conductor involves the energy-dependent mean free path of the charge carriers and is a

131 invariant polynomials or sums of environment-dependent atomic contributions, which have recently emer

132 ing of circuit changes underlying experience-dependent plasticity.

133 Hypoxia activates hypoxia-inducible factor-dependent signaling, which in turn regulates metabolic r

134 Patients were classified into food-dependent exerciseinduced anaphylaxis (FDEIA) group and

135 tial FXR agonistic activity in vitro and FXR-dependent gene modulation in vivo.

136 hereas levels of the other incretin, glucose-dependent insulinotropic polypeptide, were not as profou

137 n cob(II)alamin intermediate via glutathione-dependent alkyltransferase or reductive elimination acti

138 e death of tumor cells in a granzyme B (GrB)-dependent manner.

139 derived from human tissue, stimulated HDAC3-dependent proliferation and countered butyrate inhibitio

140 ed contributions of GAS1, CDON and BOC to HH-dependent mammalian craniofacial development.

141 y inhibits beta-tryptase activity in a hinge-dependent manner.

142 Here we implement robust, scalable history-dependent programs by distributing the computational lab

143 -independent as well as the pubertal hormone-dependent branching of the mammary epithelium and for pr

144 ermined by the tissue niche in a sex-hormone-dependent manner to limit adipose tissue inflammation.

145 Our findings suggest that HSI2- and HSL1-dependent histone methylation plays critical roles in re

146 ilm-promoting brp exopolysaccharide was IamA-dependent.

147 a from alpha-gal allergic subjects in an IgE-dependent manner suggesting a role for glycolipid in the

148 sistance, explaining why short-term, insulin-dependent glucose utilization does not promote insulin r

149 n human aortic SMCs resulted in increased IP-dependent cAMP production and consecutive facilitation o

150 Ferroptosis is an iron-dependent form of nonapoptotic cell death associated wit

151 ted fatty acyl tails are oxidized in an iron-dependent manner.

152 ) mutant that, even when undamaged, shows JA-dependent leaf growth restriction.

153 YBX1 inactivation induces apoptosis in JAK2-dependent mouse and primary human cells, causing regress

154 ive autophagy and hepatosteatosis in a JMJD3-dependent manner.

155 However, the NF-kappaB-dependent production of pro-inflammatory mediators is no

156 zone under Pi deficiency increased with LAC2-dependent lignification, suggesting a direct relationshi

157 strogen receptor alpha (ERalpha) is a ligand-dependent transcription regulator, containing two transa

158 ramework for therapeutic targeting of ligand-dependent Hh signaling in human cancers with somatic mut

159 ts two alternate conformations in the ligand-dependent and the ligand-independent states.

160 tamalin plays a critical role in the ligand-dependent internalization of mGluR1 and mGluR5, members

161 ot fully understood how plants control light-dependent FAS regulation to meet the cellular demand for

162 In Drosophila, light-dependent degradation of the clock protein TIMELESS by t

163 ated auxin distribution in addition to light-dependent auxin biosynthesis.

164 sical visual cycle works together with light-dependent processes in both the RPE and neural retina to

165 study reveals a previously undiscovered Lyn-dependent exit route of flaviviruses in LC3+ secretory o

166 phosphorylation and is thus exclusively MAT1-dependent by positioning the CDK7 T-loop in its active c

167 ntext (RdRP mice) exhibit constitutive, MDA5-dependent, and quantitatively dramatic upregulation of m

168 id production in a Mediator Subunit 5 (MED5)-dependent manner.

169 lite concentrations and considers metabolite-dependent regulation while still retaining many computat

170 e show that Agd3 deacetylates GAG in a metal-dependent manner, and is the founding member of carbohyd

171 Eleven metal-dependent lysine deacetylases (KDACs) have been identifi

172 n of IL1beta in vivo was driven by microbial-dependent activation of toll-like receptor 4 (TLR4) sign

173 findings establish a key role for microbiome-dependent circadian GLP-1 secretion in the maintenance o

174 ine N-oxide (TMAO), an intestinal microbiome-dependent metabolite, worsens graft-versus-host disease

175 in an IL-4/IL-13- and intestinal microbiota-dependent manner.

176 t mice compromises suppression of microbiota-dependent activation of CD8(+) T cells, resulting in col

177 in FOS correlation networks in the morphine-dependent state.

178 However, the magnitude of antimicrobial MR1-dependent activation remained as potent and polyfunction

179 of SDE2 or TIM results in an excessive MRE11-dependent degradation of reversed forks.

180 replicated the existence of the two mutation-dependent episignatures.

181 acts intracellular NAD(+) content and NAD(+)-dependent DNA repair capacity.

182 sms that distinguish SIRT6 from other NAD(+)-dependent deacylases.

183 ite for the stable immobilisation of an NADH-dependent dehydrogenase (i.e. lactate dehydrogenase), vi

184 However, utilisation of NADH-dependent enzymes for (2)H-labelling is not straightforw

185 n, (5) S-nitrosothiols did not promote NADPH-dependent reduction of tetra-nitro-blue tetrazolium (TNB

186 former reaction being catalyzed by the NADPH-dependent dehydrogenase CofA.

187 of its targets, and show how numerous NEDD8-dependent interprotein interactions and conformational c

188 as astrocytes, which exhibit norepinephrine-dependent Ca(2+) elevations during vigilance, are not we

189 ent Notch turnover, and thereby reduce Notch-dependent transcription at other loci and sensitize tiss

190 debenone combination treatment promoted NQO1-dependent Complex I bypass activity in these cells.

191 generating potential underlying fibrin(ogen)-dependent bacterial clearance.

192 nzymes (PHDs) are Fe(II)- and 2-oxoglutarate-dependent oxygenases that act as hypoxia-sensing compone

193 s FBXL5 binding to IRP2 to effect its oxygen-dependent degradation, unveiling a novel and previously

194 CoxFluor enabled the detection of oxygen-dependent changes in COX-2 activity that are independent

195 ring fractionated radiotherapy, using oxygen-dependent quenching of phosphorescence, oxygen probe Oxy

196 would raise the hope for a cure to many P2X7-dependent pathologies, including inflammatory, neurologi

197 tric cancers that are sensitive to other p53-dependent cytotoxic drugs, also display increased sensit

198 ailable, the limited overlap of reported p63-dependent genes has made it difficult to decipher the p6

199 eveal the dynamics and specificity of Parkin-dependent ubiquitylation under endogenous expression con

200 This pathway-dependent targeting of kidney cancer arises from the fac

201 f atelectasis, and 2) ventilate in a patient-dependent manner that minimizes the number of lung units

202 Our results indicate that Pel-dependent biofilm formation requires a UDP-GlcNAc C4-epi

203 by anchoring to cancer cell surfaces in a pH-dependent manner.

204 Their results demonstrate a pH-dependent monomer-to-dimer transition, clear evidence of

205 We establish a pH-dependent oligomerization pathway forming tetrameric DEC

206 ent CpHMD(MSlambdaD) provides a realistic pH-dependent model for membrane proteins.

207 iviral targeting and understanding of the pH-dependent transitions involved in cell entry.

208 inhibits Wnt/beta-catenin signaling via PHB1-dependent activation of Axin1.

209 we show that this system exhibits physiology-dependent temperate dynamics at environmentally relevant

210 In addition to the HY5/PIF-dependent shoot module, a regulatory axis composed of au

211 The Pif1-dependent stimulation of DNA synthesis across strong pro

212 drenergic stimulation of BAT activates a PKA-dependent mitochondrial Ca(2+) extrusion via the mitocho

213 tion of EP2 receptors and the subsequent PKA-dependent phosphorylation of alpha3GlyRs within the intr

214 conclusion, our results reveal distinct PKC-dependent regulation of CF transdifferentiation and prol

215 s to arginine-vasopressin (an inhibitory PKC-dependent response).

216 ions between TRPC1 and PKCdelta and PKCdelta-dependent phosphorylation of TRPC1.

217 at PKA-mediated phosphorylation and PP1/PP2A-dependent dephosphorylation of the alpha2 subunit play a

218 reporting protein-protein interaction (PPI)-dependent, mutation-specific, and drug-driven changes of

219 that EWSR1 is essential for promoting PRDM9-dependent histone methylation and normal meiotic progres

220 xhibited a significant reduction of pristane-dependent induction of splenocyte number and weight.

221 agic targeting of L. monocytogenes by a RavZ-dependent mechanism.

222 ctly address this question for NMDA receptor-dependent long-term depression (LTD) in the hippocampus.

223 Replication-dependent histones (RDH) are required for packaging of n

224 The virus encodes an RNA-dependent RNA polymerase, which replicates and transcrib

225 Together our data show that DNA-PK has RNA-dependent, cNHEJ-independent functions during ribosome b

226 AD(+) capping are instead processed into RNA-dependent RNA polymerase 6-dependent small RNAs, resulti

227 ransgenic mice expressing a picornavirus RNA-dependent RNA polymerase (RdRP) outside the viral contex

228 The RNA-dependent-RNA polymerase (L) gene revealed phylogenetic

229 ions as a molecular switch that triggers RNA-dependent LLPS in response to a rise in intracellular fr

230 p53, p53, and p21(Waf1/cip1) levels in a ROS-dependent manner.

231 degradation via the endosomal/vacuolar RSL1-dependent pathway or 26S proteasome.

232 MG53 inhibits IFNbeta induction in an RyR-dependent manner.

233 c42EP5 affects these functions through SEPT9-dependent F-actin cross-linking, which enables the gener

234 This could be attributed to sex-dependent differential expression of genes (DEGs) involv

235 anism relative to well-characterized sigmaA4-dependent transcription activators.

236 lular detachment, which is followed by SIRT3-dependent increases in SOD2 mRNA during sustained anchor

237 spindle density but failed to enhance sleep-dependent procedural memory consolidation.

238 hanism that enables Drosophila to form sleep-dependent and sleep-independent memory.

239 of the gut microbiome that elicit a Smarcad1-dependent colitis response, including members of the poo

240 a membrane and promotes activation of an SRC-dependent signaling cascade that controls YAP nuclear sh

241 vented EphB1 binding to Cav-1 as well as Src-dependent Cav-1 phosphorylation, indicating the importan

242 ndicate that it is required for Pnr- and Srp-dependent gene expression, suggesting general GATA cofac

243 of GABA and insulin signaling in starvation-dependent modulation of olfactory sensory neuron (OSN) f

244 (AKT) inhibitor MK2206 blocks the starvation-dependent increase in lysosomal V-ATPase activity withou

245 MS3-6 expression strongly inhibits STAT3-dependent transcriptional activation and disrupts STAT3

246 er and activator of transciription-6 (STAT6)-dependent inhibition of Tgfb1 transcription.

247 memories of unique valence and provide state-dependent motivational control [1].

248 Robust literature has examined social status-dependent brain gene expression profiles across vertebra

249 nscription factors that regulate stimulation-dependent E-P interactions.

250 -type (WT), but not FX synapses, by stimulus-dependent ATP synthase beta subunit translation; this in

251 We report an unexpected stimulus-dependent diversity in Na(V) channel-mediated itch signa

252 release and thus activates the TMEM173/STING-dependent DNA sensor pathway, which results in macrophag

253 erstanding of poorly characterized ER stress-dependent RIP.

254 This structure-dependent mechanism therefore enables cells to selective

255 xible decision-making functions in substance-dependent individuals are a consequence of drug-induced

256 with experiments that probe proteins in a T-dependent fashion, e.g., for assessing the stability of

257 ile conjugation of long-chain Vi generates T-dependent antigens, the conjugates also retain T-indepen

258 e temperature range, paving the way toward T-dependent high-throughput screening applications by HDX-

259 synapse degeneration through an array of tau-dependent and independent mechanisms.

260 , S. carpocapsae IJs exhibited a temperature-dependent quiescent period.

261 ute a major role to post-melting temperature-dependent diffusion of hydrogen occurring above the melt

262 ese results identify a plausible temperature-dependent molecular mechanism, which contributes to the

263 ELISA)-based assay that uses the temperature-dependent loss of conformational epitopes to measure the

264 -dynamics simulations reveal the temperature-dependent morphological changes in poplar wood biomass d

265 We show a testosterone-dependent lower excitability in male versus female vHPC-

266 C-NAc neurons and corresponding testosterone-dependent male resilience to reduced sucrose preference

267 Chronic hypoxia (CH) produces a time-dependent increase of resting ventilation and the hypoxi

268 enotypic rankings of transpiration in a time-dependent manner.

269 at that same time (unexposed), using a time-dependent propensity score.

270 subtypes in the mPFC produced dose and time-dependent antidepressant effects in the forced swim and

271 count for confounding by indication and time-dependent confounding.

272 can bind to GO in a concentration- and time-dependent manner.

273 a time dependent variable by generating time-dependent Cox models; HRs at an ELF threshold of 10.51 w

274 In time-dependent covariate adjusted models, post-procedure MALE

275 Quantum mechanical time-dependent density functional theory (TDDFT) calculations

276 ings, an alternative method of modeling time-dependent inhibition that simplifies assay setup and all

277 t-operative survival was assessed using time-dependent Cox proportional hazard regression analysis an

278 h current criteria increased the 5-year time-dependent area under the curve from 0.68 to 0.81 (P=0.00

279 ermined the role of GSK3beta in spike timing-dependent long-term potentiation (tLTP) in the chronic u

280 hat EPEC induces pyroptosis in IECs in a Tir-dependent but actin polymerisation-independent manner, w

281 sists in muscle, and we asked if this tissue-dependent persistence was linked to MHC expression.

282 interactions, which explains the topography-dependent diversity in fibroblast phenotypes observed he

283 even in the solid state and exhibit topology-dependent pai transmission and exciton migration; these

284 Transfusion-dependent beta-thalassemia (TDT) and sickle cell disease

285 tors used in adult patients with transfusion-dependent haemoglobinopathies.

286 We confirmed the presence of Trem2-dependent DAM and identified a previously undiscovered S

287 that viperin appears to facilitate ubiquitin-dependent proteasomal degradation of some of the protein

288 e use of small molecules to induce ubiquitin-dependent degradation of proteins.

289 supernatant of DMOG-treated HSC induced VEGF-dependent proliferation of LSEC.

290 esters and siloxanes suggest that volatility-dependent partitioning processes modulate airborne SVOC

291 r in external Ba(2+) than in Ca(2+); voltage-dependent kinetics of activation, inactivation, and deac

292 ceptor currents in a dose-, pH-, and voltage-dependent manner.

293 terminants of S4 helix motion during voltage-dependent transition from the intermediate to the activa

294 Two candidate modules featuring voltage-dependent Ca2+-channels link these outputs to the downst

295 Concordantly, we demonstrate Vpr-dependent rescue of HIV-1 replication in human macrophag

296 show that WAPL-dependent cohesin removal is needed to restart DNA synth

297 he stiffness gradient corresponds to a Wnt5a-dependent domain of fibronectin expression, raising the

298 study demonstrates that proximal tubule YAP-dependent paracrine mechanisms play an important role in

299 loss of RIPK1 in keratinocytes induces ZBP1-dependent necroptosis and skin inflammation.

300 of the active site compared with other zinc-dependent nucleotide deaminases.