ライフサイエンスコーパス: dependent

1 MCs to T cells was partially FGF2b and FGFR1 dependent.

2 ts activity was both time- and concentration-dependent.

3 minant negative or their effects are context dependent.

4 er-evoked responses is highly internal-state dependent.

5 ation selectivity was carbohydrate structure dependent.

6 hoice of the appropriate tool is application-dependent.

7 duced reductions in Miro1 levels were Parkin dependent.

8 nd s.c. tumor growth, and this was IFN-gamma dependent.

9 ative stress, and this upregulation is CLOCK-dependent.

10 gests that the asymmetry of the three ATPase-dependent 120 degrees power strokes imposed by the relat

11 we further validate its detection with data-dependent acquisition and targeted analyses.

12 ion of MutLalpha endonuclease, PCNA- and DNA-dependent activation of MutLalpha ATPase, and MutLalpha

13 alpha interaction with PCNA, as well as PCNA-dependent activation of MutLalpha endonuclease, PCNA- an

14 Calcium/PKCalpha-dependent activation of NUAK1 supports engagement of the

15 ification increases receptor tyrosine kinase-dependent activation of RAS more potently in colorectal

16 sis of the decoy effect could be the context-dependent activation of the valuation area.

17 TRIF) and Z-DNA-binding protein 1 (ZBP1)/DNA-dependent activator of IFN-regulatory factors (DAI) that

18 We report a new distance- and orientation-dependent, all-atom statistical potential derived from s

19 Unexpectedly, we identified PABPN1-dependent ALYREF binding near the 3' end of the mRNA.

20 ory protein required for efficient, activity-dependent AMPAR endocytosis.

21 significantly inhibited both phosphoantigen-dependent and -independent activation of Vgamma9Vdelta2

22 We assessed neuronal-dependent and -independent contributions by activating o

23 that stimulus, and this effect was stimulus dependent and action independent.

24 Furthermore, DDX21 is both an ATP-dependent and ATP-independent helicase, and both ATPase

25 hus constitute a common endpoint of both EMT-dependent and EMT-independent cancer dissemination progr

26 ation of the AR/AR-V7 target genes in ligand dependent and independent manners respectively.

27 uses on recent progress on the roles of NFIC-dependent and NFIC-independent signaling pathways in too

28 Temporal, dose-dependent and specific disruption of the TJ-associated Z

29 in vivo (using rainbow trout fry) in a dose-dependent and time-dependent manner.

30 marker that is reliable, cheap, less device-dependent, and can be easily and repeatedly used on a la

31 h three competing cancer "species": androgen dependent, androgen producing, and androgen independent.

32 tion of ERalpha, which in turn increases TAM-dependent anti-estrogen chemosensitivity in vitro and in

33 resenting cells and we aimed at studying IgE-dependent antigen presentation in both cell types.

34 l subsets whose phenotype and migration were dependent ( approximately 30%) or independent ( approxim

35 Thus sortilin-dependent as well as sortilin-independent sorting mechan

36 Furthermore, there was a dose-dependent association between the prevalence of low VA a

37 event occurring in the airways of prednisone-dependent asthmatic patients with increased eosinophil a

38 d humoral immune responses that included IgE-dependent basophil activation and measurement of serum i

39 is a major factor, which determines sequence-dependent behavior of peptides in HILIC.

40 -nucleotide polymorphisms, considering depth-dependent behavior of similarity metrics for identical a

41 Thus, we demonstrated peptide-dependent binding of the activating NK cell receptor KIR

42 licit greatly exaggerated blood-oxygen-level-dependent (BOLD) responses in the anterior insular corte

43 ted within a context, and blood oxygen level dependent (BOLD) signals in the ventromedial prefrontal

44 In an in vitro and cell-based model of MMP-dependent breast cancer cellular invasiveness, this N-TI

45 trols lysosome positioning through Ragulator-dependent, but mTORC1-independent, modulation of BORC.

46 Most induced changes were TCF dependent, but TCF-independent TSSs exhibited the same h

47 s and caused only a minor inhibition of P2X1-dependent Ca(2+) entry.

48 tes in vivo, GsD is expressed and allows CNO-dependent cAMP signaling and glycogen breakdown.

49 wide association study data on 2080 cannabis-dependent cases and 6435 cannabis-exposed controls of Eu

50 In root cells, HS triggered an iron-dependent cell death pathway that was characterized by d

51 DAC) PAR2 protein is necessary for TGF-beta1-dependent cell motility.

52 lls and involved a switch from BCL2 to BCLXL-dependent cell survival.

53 at they contain a highly conserved sortase A-dependent cell wall-anchored C terminus, whereas the sur

54 suggest that 5-HT neurons exert a frequency-dependent, cell-type-specific control over BA circuitry

55 Our current studies show that K-Ras-dependent cells are refractive to PKCdelta-driven apopto

56 , but remains poorly understood in substrate-dependent cells.

57 re is growing interest in utilizing antibody-dependent cellular cytotoxicity (ADCC) to eliminate infe

58 e previously showed that the differentiation-dependent cellular transcription factors KLF4 and BLIMP1

59 orthogonal to the rips, inducing an angular-dependent change in the reversal mechanism.

60 ucture of many mineral soils could undergo N-dependent changes as atmospheric CO2 concentrations rise

61 esults could be accounted for by temperature-dependent changes in both Km and kcat (three substitutio

62 Here, oxygen-dependent changes in C. jejuni physiology were studied a

63 ocaine CPP extinction and lack of extinction-dependent changes in hippocampal PSD CaMKII expression a

64 quantitative proteomics to characterize Hat1-dependent changes in the composition of nascent chromati

65 Here, we identify several novel CO2-dependent changes in the NF-kappaB pathway.

66 we observed that 1B6 displayed a rapid dose-dependent clearance (t(1/2) 10-60 h) in contrast to 1F11

67 base of the lamellipodium, where a vinculin-dependent clutch couples actin to previously positioned

68 oactive component of cannabis, produced dose-dependent conditioned place aversion and a reduction in

69 nization of RNA synthesis and ligand binding-dependent conformational refolding.

70 rameter combinations, which represent myosin-dependent contractility, a characteristic viscosity-adhe

71 The wavelength-dependent conversion of two rapid photoinduced ligation

72 Time-dependent Cox regression models were used to calculate h

73 me 2 (CRY2) can simultaneously undergo light-dependent CRY2-CRY2 homo-oligomerization and CRY2-CIB1 h

74 cytotoxic T-lymphocyte-associated protein 4-dependent (CTLA4-dependent) manner.

75 onses through the initiation of a type I IFN-dependent DDR.

76 on of pre-change exposure, suggesting a time-dependent decision threshold.

77 e changes in follicle populations showed age-dependent decreases in total follicles and percentages o

78 able RAD51 filament formation prevents MRE11-dependent degradation of the newly synthesized DNA at st

79 in kinase (MAPK) cascade and triggers a dose-dependent differentiation response.

80 itis B in China, we propose an age- and time-dependent discrete model and use the method of non-linea

81 active targets for the treatment of estrogen-dependent diseases like endometriosis and breast cancer.

82 n of pressure to the complex causes its time-dependent dissociation and the loss of both DHO and ATC

83 nd parabolic barrier approximation) and spin-dependent drift-diffusion model.

84 ans for interrogating mechanisms of mutation-dependent drug response, which will have a significant i

85 iatric risk gene TCF4 enhances NMDA receptor-dependent early network oscillations.

86 Position-dependent effects on peptide retention for different res

87 s of auxin-induced SAUR expression and auxin-dependent elongation growth were closely correlated.

88 alyzing the temperature and excitation power dependent emission spectra, thermal quenching ratios, fl

89 e majority of sequences examined display p53-dependent enhancer activity during the DNA damage respon

90 rt a versatile S-adenosyl-l-methionine (SAM)-dependent enzyme, LepI, that can catalyse stereoselectiv

91 olite that can competitively inhibit alphaKG-dependent enzymes.

92 ol efflux do not necessarily represent inter-dependent events, but MafB is broadly involved in both t

93 superlattice period-, temperature- and field-dependent evolution of these structures, we observe seve

94 sed by hydrogen bonding to water, where a pH-dependent excitation energy appears to be an intrinsic p

95 Inhibition of PI3K-dependent exocytosis of TRPC6 is thought to be the under

96 od mononuclear cells elicited a cell contact-dependent expansion of MDSCs.

97 ls, we show that B cells primarily use force-dependent extraction and resort to enzymatic liberation

98 The local sequence-dependent features of DNA found in high-resolution struc

99 On the one hand, models of scale-dependent feedbacks, whereby plants facilitate neighbour

100 reversal characteristics captured by angular-dependent first order reversal curve measurements indica

101 ess the spatiotemporal changes of actomyosin-dependent force and stiffness along the antero-posterior

102 This mechanism is distinct from the BRCA2-dependent fork protection pathway, in which stable RAD51

103 ion and inhibition of a broad range of actin-dependent functions, including phagocytosis, granule exo

104 to adjacent uninfected cells through contact dependent gap junctions.

105 subtilis causes strand- and sequence-context-dependent GC --> AT transitions.

106 ing an infrared laser, for reproducible heat-dependent gene expression in small sublineages (one to f

107 e that Rap1 contains an AD required for Rap1-dependent gene transcription.

108 induce GRalpha nuclear translocation and GRE-dependent GILZ expression.

109 Thus, GCK-dependent glycolysis regulates Treg cell migration.

110 epresents a new class of zinc-binding flavin-dependent halogenases and provides new insights into a p

111 Flavin-dependent halogenases are useful enzymes for providing h

112 ndependent helicase, and both ATPase and ATP-dependent helicase activities are inhibited by Rev in a

113 We found that PEGylation prevented dose-dependent hemolysis in the concentrations studied (0-10

114 The accumulation of AGO4-dependent het-siRNAs also requires several factors known

115 ene) electrochemical devices exhibit voltage-dependent heterogeneous swelling consistent with device

116 er-range interactions connecting replication-dependent histone genes on chromosome 6, potentially rep

117 ed one substitution severely impaired OGFOD1-dependent hydroxylation of a neighboring proline residue

118 ed that autophagy in NP cells was not TonEBP-dependent; hyperosmolarity did not upregulate autophagy

119 verexpression results in a significant, dose-dependent increase in EGFR tyrosine phosphorylation, par

120 Taurocholate induced a time-dependent increase in LPC proliferation and expression o

121 Plants use context-dependent information to calibrate growth responses to t

122 ors, which is a prevailing mechanism for use-dependent inhibition in the nucleus accumbens core and d

123 Notably, 12 was able to cause concentration-dependent inhibition of cell proliferation, yielding an

124 gesting a possible mechanism underlying KCC2-dependent insulin release.

125 induce pyroptosis, as measured by caspase-1-dependent interleukin-1beta release, though this phenoty

126 inally, we describe a novel form of activity-dependent intrinsic plasticity that persistently elimina

127 In this study, we generated Zwitch, a Cre-dependent invertible gene-trap cassette, enabling the es

128 ranscriptome gene expression analyses on WNT-dependent KDR(+)CD235a(-) definitive hematopoietic mesod

129 totic activation of Gwl requires both cyclin-dependent kinase 1 (CDK1)-dependent phosphorylation and

130 lar, to THZ1, a covalent inhibitor of cyclin-dependent kinase 7 (CDK7).

131 ontaining 4 (BRD4) with NF-kappaB and cyclin-dependent kinase 9 (CDK9).

132 is strictly controlled by a number of cyclin-dependent kinases (CDKs) and CDK inhibitors (CKIs), the

133 ibitors of mTOR and inhibitors of the cyclin-dependent kinases CDK4 and CDK6 substantially improve pr

134 Time-dependent leukocyte density and diversity and the magnit

135 a crucial role for this pathway in activity-dependent long-term depression (LTD) at hippocampal Scha

136 Model-predicted deficits in PEEP-dependent lung recruitment correlate with altered lung l

137 decompensation, mortality, and HCC in a dose-dependent manner (P for trend <0.0001, <0.0001, and 0.00

138 these cellular phenotypes in a dose- and age-dependent manner in cortex and striatum of mice.

139 a rich extracellular environment in a stage-dependent manner producing complex microstructural patte

140 27 suppressed osteoclastogenesis in an Egr-2-dependent manner that up-regulates Id2, the repressor of

141 Suc affects the circadian oscillator in a GI-dependent manner was unknown.

142 se activities are inhibited by Rev in a dose-dependent manner, although ATP-independent helicase acti

143 ti-proliferation gene transcripts in a Cnot3-dependent manner, and promoted their degradation.

144 on inflammation in a CC-chemokine receptor 2-dependent manner, and the nonclassical blood resident mo

145 est migration in Xenopus embryos in a Snail1-dependent manner, indicating that the mechanism of actio

146 Stat3-phosphorylation/activation in an LKB1-dependent manner, preventing its recruitment to canonica

147 amphetamine-induced hyperactivity in a dose-dependent manner, similar to the atypical antipsychotic,

148 y initiation of liver regeneration in a dose-dependent manner, without modifying the peak regenerativ

149 telomeres after damage in an ATM activation-dependent manner.

150 ed skin cancer development in mice in a TSLP-dependent manner.

151 -helical domains in a position- and organism-dependent manner.

152 tly activated to bind GPIbalpha in a tension-dependent manner.

153 nbow trout fry) in a dose-dependent and time-dependent manner.

154 topoisomerase II activity in a concentration-dependent manner.

155 vated smooth muscle gene promoters in an SRF-dependent manner.

156 e-induced apoptosis occurring in a Bax, Drp1-dependent manner.

157 ied that these proteins induce TREM-1 in p65-dependent manner.

158 of endotoxin-induced inflammation in an MPO-dependent manner.

159 k controlling phosphate accumulation in zinc-dependent manner.

160 obular proteins, such as mCherry, in a light-dependent manner.

161 inactivates dopamine D2 receptors in a PRDX6-dependent manner.

162 antibodies reduced tau uptake in an epitope-dependent manner: N-terminal (Tau13) and middomain (6C5

163 hocyte-associated protein 4-dependent (CTLA4-dependent) manner.

164 can be ascribed to an interplay between time-dependent many-particle scattering and phase-space filli

165 ase C- and Gbetagamma-metalloproteinase/EGFR-dependent MAPK/ERK signaling cascades.

166 properties while the latter results in size-dependent mechanical properties at the nanometer scales.

167 ing as an on-off switch controlling an RbohD-dependent mechanism in response to different stresses, s

168 o a cholesterol-rich diet and uncover a PDL1-dependent mechanism through which MZB cells use their in

169 inflammatory cytokines via a Wnt5a signaling-dependent mechanism.

170 nction protein expression through an IL-10RA-dependent mechanism.

171 formed synapses via dendritic calcium spike-dependent mechanisms.

172 ivo evidence for contributions of complement-dependent membrane perturbations to prothrombotic TF act

173 cking PRMT8 also exhibit reduced hippocampus-dependent memory.

174 Cell-dependent minimal to no toxicity of Inh2-B1, and its abi

175 through a synergistic induction of NF-kappaB-dependent MMP1 expression in cancer cells.

176 nt connections act as transistor-like, angle dependent momentum filters, whereas triangular networks

177 EFL mutations eliminated off-target antibody-dependent monocyte phagocytosis of cynomolgus monkey pla

178 1-CXCR2 signaling axis identified HIF-2alpha-dependent neutrophil recruitment as an essential mechani

179 ne rapidly with age, culminating in activity-dependent, non-apoptotic cell death.

180 ceruleus is associated with decreased 5-HT2A-dependent noradrenergic transmission.

181 ctivity, supporting the conclusion that RIMA-dependent nuclear IYO accumulation triggers cell differe

182 Progress in science is dependent on a strong foundation of reliable results.

183 s the immune response progressed, and it was dependent on antigen formulation and delivery.

184 n of multiple viruses, and this activity was dependent on both its RING E3 ligase and ADP-ribosylatio

185 ry necrosis and GSDMD-induced pyroptosis are dependent on caspase activation, we propose that they ar

186 ulosis (Mtb) inside its host cell is heavily dependent on cholesterol and fatty acids.

187 independent of filament lifetime and sharply dependent on crosslink dynamics.

188 to the transcriptional stat site of MYC was dependent on EBNAs.

189 The IRES was dependent on eIF4G, but not eIF4E, for activity.

190 g constitutive caspase-8-mediated cell death dependent on FADD but independent of Ser(533) phosphoryl

191 We find that silencing is dependent on germline nuclear RNAi factors and post-tran

192 the uterine wall and perceived by the fetus, dependent on how light interfaces with maternal tissue.

193 hrough beta-catenin, whereas hypertrophy was dependent on mammalian target of rapamycin complex 1.

194 lating, MinC exhibits a midcell localization dependent on MinD and the DivIVA-like protein Cdv3, indi

195 cle growth by 1.5-fold (P < 0.05), which was dependent on MMP-1 activation.

196 cale UF assessments which have hitherto been dependent on proxy data for UF.

197 ranscription of nearly all mRNAs is strongly dependent on TFIID function.

198 The analysed responses were dependent on the applied drying parameters and the pre-t

199 We show that recorded spectra are highly dependent on the cluster morphology and size of particle

200 The sensitivity values are dependent on the excitation power, and reach two maximum

201 trated that the effect of vasopressin is not dependent on the level of maturation (depolarizing vs. h

202 Potent methylation is dependent on the multimerization of Dnmt3a/Dnmt3L comple

203 In mammalian cells, this process is dependent on the recognition of the hexanucleotide AAUAA

204 correction to optic flow, a response that is dependent on the spatial structure of the visual environ

205 sful therapeutic intervention will be highly dependent on the specific therapeutic target and the sta

206 gly, activation of NF-kappaB by netrin-1 was dependent on UNC5A receptor, because suppression of UNC5

207 that particle morphology and evaporation is dependent on whether SOA from limonene is formed before

208 t lung cancer cell lines classified as K-Ras-dependent or -independent for co-dependency on protein k

209 Together, our data reveal an HSPG-dependent pathway that specifically allows dendrites of

210 n, acting to drive immune escape via a C3/C5-dependent pathway.Significance: This provocative study s

211 ne potential, facilitates downstream Ca(2+) -dependent pathways and becomes concentrated in specific

212 s as well as alcohol expectancies in alcohol-dependent patients and healthy controls and assessed tre

213 cell division pattern indicating a position-dependent patterning mechanism may be in place.

214 we were able to identify several major time-dependent phenotypic changes in blood immune cell subset

215 Scaffolding the calcium/calmodulin-dependent phosphatase 2B (PP2B, calcineurin) focuses and

216 al tubule by the action of the apical sodium-dependent phosphate transporters, NaPi-IIa/NaPi-IIc/Pit2

217 quires both cyclin-dependent kinase 1 (CDK1)-dependent phosphorylation and its autophosphorylation at

218 Alterations in the Cdk/Cdc14-dependent phosphorylation status of Spc110, or its inact

219 Interestingly, in the absence of sodium-dependent Pi transport activity, the PiT1-PiT2 heterodim

220 ides enriched in lipid rafts to inhibit raft-dependent PI3K signaling.

221 By inducing activity-dependent plasticity in the visual cortex of adult rats

222 an early developmental time when experience-dependent plasticity shapes such circuits.

223 implicated in mediating several forms of use-dependent plasticity, but the mechanisms by which it con

224 ce of glibenclamide, an inhibitor of the ATP-dependent potassium (KATP)-channels, thus suggesting a p

225 reduced functional expression of the voltage-dependent potassium channel subunit Kv1.1 substantially

226 red 35 proteins mainly related to nucleotide-dependent processes and lipid metabolism.

227 he mother centriole mediates most centrosome-dependent processes, the role of the daughter remains po

228 a subset of odor combinations, this history-dependent processing was useful in helping to identify t

229 f these cytokines, inhibiting interleukin-23-dependent production of interleukin-17.

230 m Toxoplasma gondii is hydroxylated by an O2-dependent prolyl-4-hydroxylase (PhyA), and the resulting

231 We have recently reported that HPV E7-dependent promoter hypermethylation leads to downregulat

232 high-avidity epitope provided strong, T cell-dependent protection against viruses or tumors.

233 tuin 1 (SIRT1), a conserved mammalian NAD(+)-dependent protein deacetylase, senses environmental stre

234 ors (BKIs) of Cryptosporidium parvum calcium-dependent protein kinase 1 (CpCDPK1) are leading candida

235 ) H]ryanodine binding and Ca(2+) /calmodulin-dependent protein kinase II (CaMKII) phosphorylation of

236 A group of "plant-like" Ca(2+)-dependent protein kinases (CDPKs) transduces cytosolic C

237 erse biological processes by phosphorylation-dependent protein-protein interactions.

238 aintaining proper neddylation levels for CRL-dependent proteostasis.

239 Activity-dependent pruning also occurs at embryonic Drosophila ne

240 rophysiological recordings show that Sema-1a-dependent R axon lamination is required for preventing t

241 roposed to be formed using CysS, a cobalamin-dependent radical S-adenosylmethionine (SAM) methyltrans

242 roventricular injection of 10 nM oxytocin in dependent rats.

243 strands, respectively, in an NTP-hydrolysis dependent reaction.

244 Ch25h deficiency results in cholesterol-dependent reduced mitochondrial respiratory capacity and

245 However, the mGluR-dependent reduction in ICa was not mimicked by Gbetagamm

246 stimulation also elicited a Ca(2+)- and PKC-dependent reduction in synaptojanin1 recruitment to clat

247 Patients who received inclisiran had dose-dependent reductions in PCSK9 and LDL cholesterol levels

248 rate how sensory information regulates state-dependent reflexes in the lower urinary tract and contri

249 aint that is mediated by muscarinic receptor-dependent regulation of mitochondrial function via AMPK.

250 Thus, species-dependent regulation of PlexA1 expression may have been

251 ontal sensorimotor control and rapid, reward-dependent reorganization of control dynamics.

252 s as a molecular linker between the synapsin-dependent reserve pool and the presynaptic endocytosis m

253 perturbing S phase and by blocking the Chk1-dependent response to replication fork damage.

254 95% confidence intervals (CI), for the time-dependent risk related to ENE positivity.

255 t RNAs suggests that localization of the APC-dependent RNA subgroup is functionally important for cel

256 sed approach to specifically mislocalize APC-dependent RNAs suggests that localization of the APC-dep

257 nal theory calculations, show distinct layer-dependent semiconductor-to-semimetal evolution of 2D lay

258 The study of temperature-dependent sex determination (TSD) in vertebrates has att

259 e epilepsy, alpha-related blood oxygen level-dependent signal changes demonstrated lower decreases re

260 se that phosphorylates MyD88, promoted MyD88-dependent signaling and mediates dermatosis in Ptpn6(spi

261 iously that Rab8a recruits PI3Kgamma for Akt-dependent signaling during TLR4 activation to limit the

262 implementing GBAi in vivo, we show that GBA-dependent signaling modulates phenotypes during Xenopus

263 cted in MKs and platelets, the impact of CK2-dependent signaling on MK/platelet (patho-)physiology ha

264 Sse1sbd was fully competent to support Hsp90-dependent signaling through heterologously expressed glu

265 a distinct meaning for the encoding of time-dependent signals.

266 Nicotine-dependent smokers and nonsmokers completed a probabilist

267 el RT neurons are predisposed to an activity-dependent switch from GABA-mediated inhibition to excita

268 me proliferator-activated receptor signaling-dependent switch from glycolysis to fatty acid oxidation

269 arized light, so-called all-optical helicity dependent switching, has renewed interest in the physics

270 By modifying rules that govern activity-dependent synaptic plasticity, addictive drugs can derai

271 in network parameters arising from learning-dependent synaptic plasticity.

272 -independent mechanism that involves caspase-dependent T cell apoptosis and upregulation of inhibitor

273 n A small but statistically significant dose-dependent T1-weighted signal enhancement was observed in

274 Using a novel activity-dependent technology called CANE developed in our labora

275 alcified PFP, purified DNA triggered contact-dependent thrombin generation (TG) and amplified TG init

276 Condors' routines reflect a sexual-size dependent trade-off that may underpin ecological and soc

277 romoting AMP-activated protein kinase (AMPK)-dependent trafficking of KATP and Kv2.1 channels to the

278 A selective peptide inhibitor of AMPH-dependent trafficking of the neuronal excitatory amino a

279 e ability of HMGA1 to stimulate beta-catenin-dependent transcription, suggesting that interactions be

280 s are examined through time- and temperature-dependent transport measurements.

281 Dose- and time-dependent tumor uptake was studied in nude BALB/c mice b

282 In summary, ARID1A has context-dependent tumor-suppressive and oncogenic roles in cance

283 gical means as a potential treatment for MYC-dependent tumors.

284 ACD11) in planta and promotes the proteasome-dependent turnover of ACD11 in cell-free degradation ass

285 alters species stoichiometry and proteasome-dependent turnover of nuclear MAF1.

286 NQO1 is a FAD-dependent, two-domain multifunctional stress protein act

287 we demonstrate that key RQC activities-Ltn1p-dependent ubiquitination and Rqc2p-mediated Carboxy-term

288 ression of proteins associated with the BMI1 dependent ubiquitination pathway.

289 e findings suggest a new paradigm where IL-4-dependent up-regulation of Cox-1 expression may play a k

290 us, and this coincides with TCP20 and NLP6&7-dependent up-regulation of nitrate assimilation and sign

291 Further, this reconsolidation-dependent updating process appears to reorganize the neu

292 ver nanoparticle (Ag NP) exposure, which was dependent upon key physicochemical properties.

293 Biological functions of RNA molecules are dependent upon sustained specific three-dimensional (3D)

294 aphy of a cuticular drusen distribution; age-dependent variations in cuticular drusen phenotypes, inc

295 stress, associated impairment of endothelium-dependent vasorelaxation, and preserves endothelial Sirt

296 distinct signalling mechanisms direct stress-dependent versus homeostatic regeneration, and highlight

297 ne inhibition was splice variant and isoform dependent, with a 5- to 11-fold lower sensitivity to Cav

298 acellular protein that enhances beta-catenin-dependent Wnt signaling and has previously been shown to

299 tion of the ALOX5 is responsible for the Hcy-dependent worsening of the AD phenotype in a relevant mo

300 The phosphorylation of STAT5B on the JAK2-dependent Y699 site is significantly reduced in the live