ライフサイエンスコーパス: dependent

1 as refractory to ruxolitinib vs ruxolitinib dependent.

2 ilm-promoting brp exopolysaccharide was IamA-dependent.

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

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

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

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

7 nescent circadian reporter mice that are Cre dependent, allowing the circadian properties of genetica

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

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

10 multi-organ immune dysregulation via kinase dependent and independent mechanisms.

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

12 erring tamoxifen resistance via both ERalpha dependent and independent pathways.

13 L2 production by GPBAR1 agonism was promoter dependent and involved FOXO1.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

29 Different temperature dependent band splitting behaviors are observed at the [

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

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

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

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

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

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

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

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

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

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

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

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

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

43 ATP-dependent chromatin-remodeling enzymes control accessibi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

67 alphaKG-dependent dioxygenases consume the metabolite alphaKG (a

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

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

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

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

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

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

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

75 ADi as a resource for studying YAP1/TAZ-TEAD dependent effects.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

93 Activity-dependent global scaling therefore operates on both the

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

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

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

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

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

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

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

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

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

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

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

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

106 680I/M680I) FMF knock-in mice exhibited IL-1-dependent increased survival relative to wild-type knock

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

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

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

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

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

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

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

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

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

116 We have previously demonstrated that copper dependent inhibitors (CDIs), a class of antibiotics that

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

170 This structure-dependent mechanism therefore enables cells to selective

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

187 reversible competitive inhibition of CLK1 is dependent on a Michael acceptor forming an irreversible

188 et electrification, however, was found to be dependent on a rapid transition to a cleaner grid.

189 G(i/o) -mediated TRPC4 activation is dually dependent on and bimodally regulated by phosphatidylinos

190 Honey bees are highly dependent on circadian clocks to regulate critical behav

191 SDE15 suppression of plant immunity is dependent on CsACD2, and overexpression of CsACD2 in cit

192 l cord, detailing synaptic diversity that is dependent on developmental stage, anatomical region and

193 ir effector function, was, at least in part, dependent on formation of the microbiome, and consequent

194 Wnt signaling is dependent on four Wnts (Wg, Wnt5, 6,10) that are express

195 Optimal NK cell responses were dependent on IL-18 and IL-12, whereas IFN-gamma secretio

196 was sufficient to induce itching in a manner dependent on IL-31 expression.

197 omoted capsule retention through a mechanism dependent on its C-terminal lysine residue; its deletion

198 We show that oxygen delivery through PMCs is dependent on its permeability through the polymeric shel

199 The inhibition of Lp-PLA(2) by darapladib is dependent on many factors such as concentrations of dete

200 The pre- and post-division migrations are dependent on microtubules and actin, respectively, and t

201 ent culture that exhibits exponential growth dependent on Mn(II) oxidation to a co-culture of two mic

202 or these species, reproduction appears to be dependent on pollinator identity such that reduced repro

203 the neuronal response rate to ultrasound is dependent on pulse repetition frequency (PRF); and (3) u

204 nt therapy is not effective generally become dependent on red-cell transfusions.

205 Management of fisheries that are highly dependent on reefs may need to adapt to declining produc

206 -crystal TiO(2)(110)) was found to be highly dependent on the anchor group, with Ipa establishing a m

207 ensity for post-mating effects on females is dependent on the component of baseline immunity.

208 ffold, and consequently axon pathfinding, is dependent on the expression of an atypical RHO-GTPase, R

209 rted that metastatic pancreatic cancers were dependent on the glucose-metabolizing enzyme phosphogluc

210 ithin cultivars and was found to be strongly dependent on the growing environment.

211 n increased growth rate, virulence was still dependent on the mevalonate pathway in 10403S strains ex

212 BAIAP2L2 localization to stereocilia tips is dependent on the motor protein MYO15A and its cargo EPS8

213 ovir-diphosphate incorporation by PrimPol is dependent on the n-1 nucleotide.

214 rtitions POLE tumors into distinct subgroups dependent on the nature of the POLE allele, its expressi

215 al populations at higher latitudes is highly dependent on the persistence of up-current tropical syst

216 nal TA pair and essentiality of darG(Mtb) is dependent on the presence of darT(Mtb) , but simultaneou

217 Cancer cells then become very dependent on the proper function of those pathways, and

218 ot microbiota under iron deprivation that is dependent on the secretion of plant-derived coumarins.

219 These findings were not dependent on the trajectory of the implanted electrode n

220 expansion and differentiation are critically dependent on the transcription factor c-Myc (Myc).

221 acy of many nucleoside analogues is strongly dependent on their intracellular activation by host cell

222 neurofibromin, whose function is completely dependent on this interaction.

223 ort that YtgR repression at P(trpBA) is also dependent on tryptophan by regulating YtgR levels throug

224 inear slopes), PQ intervals were found to be dependent on underlying cycle length in a highly curvili

225 orrelates of frequency were highly electrode dependent: On some electrodes, changes in frequency were

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

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

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

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

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

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

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

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

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

235 ing of circuit changes underlying experience-dependent plasticity.

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

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

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

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

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

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

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

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

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

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

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

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

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

249 Calcium dependent protein kinase 1 (CDPK1) is an essential Ser/T

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

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

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

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

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

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

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

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

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

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

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

261 2 (SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily D, member 2)

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

263 ve nanoparticles (CGPU) displayed a GSH-dose dependent release of cisplatin.

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

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

266 erstanding of poorly characterized ER stress-dependent RIP.

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

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

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

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

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

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

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

274 In this study, we used morphine dependent SIVmac251 infected rhesus macaque (RM) model t

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

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

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

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

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

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

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

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

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

284 Although less rate dependent than the QT intervals (36 +/- 19% of linear sl

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

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

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

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

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

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

291 cule manipulation studies of the temperature dependent unfolding and refolding of a titin immunoglobu

292 However, their detection is still heavily dependent upon conventional biochemical assays that reta

293 heir cognate amino acids in a manner that is dependent upon intact lysosomal function.

294 e radionuclide analogs (RAs) was shown to be dependent upon their chemical speciation in solution, th

295 ELF was evaluated as a time dependent variable by generating time-dependent Cox mode

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

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

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

299 Rates of categorization were class dependent with best performance for alcohols and acetate

300 on of ER proteins by the KDEL receptor is pH dependent, with binding occurring under acidic condition