ライフサイエンスコーパス: zeta

1 ontaining only the CD3zeta endodomain (CD19R:zeta).

2 t interactions of AQP2 with 14-3-3theta and -zeta.

3 rated by another error-prone polymerase, Pol zeta.

4 nvolves a complex of Rev1 and DNA polymerase zeta.

5 ell culture model by siRNA knockdown of AP-5 zeta.

6 nthesis (TLS) as a subunit of DNA polymerase zeta.

7 ons that represent a unique signature of Pol zeta.

8 l kappa, and for O6-CMdG upon removal of Pol zeta.

9 m injection or expression of phospholipase C zeta.

10 protein, Fasiculation and Elongation Factor zeta 1 (FEZ1).

11 e Fez1 (fasciculation and elongation protein zeta 1), a gene previously reported to be regulated by H

12 logs of fasciculation and elongation protein zeta 2 (fez2) and leukocyte receptor cluster (lrc) membe

13 NPs conjugate from the AOx (pI 4.5) protein (zeta, -30mV) implied good stability of the in-situ synth

14 ity and exhibited a positive surface charge (zeta=36mV) at a neutral pH.

15 1)/2, (3)/2, (5)/2) and spin-orbit coupling (zeta = 464, 880, 3100 cm(-1)) on quantum decoherence.

16 r version, found naturally in eukaryotic Pol zeta (a family-B translesion synthesis polymerase).

17 s was dependent on atypical protein kinase C zeta, a mediator of stem cell polarity, with C5aR1 inhib

18 netic deletion of diacylglycerol kinase (DGK)zeta, a negative regulator of diacylglycerol-mediated si

19 ppaB member IkappaB (inhibitor of NF-kappaB) zeta, a selective coactivator of particular NF-kappaB ta

20 eptor atom close to 109 degrees , distance N(zeta)-acceptor atom ca. 2.7-3.0 A).

21 d by lysine NH3(+) group (angle C(epsilon)-N(zeta)-acceptor atom close to 109 degrees , distance N(ze

22 Accordingly, DNA polymerase zeta activity was essential for mutagenesis in cisplatin

23 Co-expression of 14-3-3 (zeta and ) and GluN1/GluN2C promotes the forward deliver

24 CD19 single-chain variable fragment plus TCR zeta and CD28 signalling domains.

25 the exact values of the anisotropy exponent zeta and the roughness exponents chix,y that characteriz

26 e latitudes observed on the Sun is absent on zeta And, which hosts global spot patterns that cannot b

27 DNA polymerase zeta (Pol zeta) and Rev1 are key players in translesion DNA synthe

28 tion, inhibited ROS production, degraded PKC-zeta, and activated caspases-3 and -8 to block transform

29 is necessarily connected with mammalian pol zeta, and there is accumulating evidence that REV7 and R

30 tiation via integrin-beta1, protein kinase C-zeta, and v-akt murine thymoma viral oncogene homolog.

31 l junctions in eukaryotic evolution and that zeta- and delta-tubulin are evolutionarily interchangeab

32 imaging of the old, magnetically active star zeta Andromedae using long-baseline infrared interferome

33 a, wt1b, and podxl, suggesting that prkciota/zeta are needed to maintain renal epithelial identity.

34 mitochondrial IF1 supported both the modeled zeta binding site at the alphaDP/betaDP/gamma interface

35 The N terminus of zeta blocks rotation of the gamma subunit of the F1-ATPa

36 lts showed that deficiency in Pol eta or Pol zeta, but not Pol kappa or Pol iota, led to pronounced d

37 -carotene desaturase activity encoded by the zeta-CAROTENE DESATURASE (ZDS)/CHLOROPLAST BIOGENESIS5 (

38 Biosynthesis of the signal depends on zeta-carotene desaturase activity encoded by the zeta-CA

39 Phytoene, phytofluene, zeta-carotene, neurosporene, tetra-cis-lycopene, all-tra

40 ne, phytoene, phytofluene, neurosporene, and zeta-carotene.

41 DNA polymerase zeta catalytic subunit REV3 is known to play an importan

42 way, Lck and ZAP-70, for the T cell receptor zeta chain and the scaffold proteins LAT and SLP-76.

43 further monitored LAT phosphorylation by TCR zeta chain-recruited ZAP-70, which suggests a weakly pro

44 ered TCR complex with reduced amounts of the zeta-chain (CD247).

45 The zeta-chain (TCR) associated protein kinase 70kDa (ZAP70)

46 sense mutations in the 70-kD T cell receptor zeta-chain associated protein (ZAP-70).

47 The TCR zeta-chain is a homodimer subunit that contains six ITAM

48 ction in molecular entropy of the disordered zeta-chain upon phosphorylation.

49 granzyme B-dependent degradation of the TCR-zeta-chain, resulting in significantly decreased prolife

50 exhibited reduced binding to phosphorylated zeta-chain, whereas mutation R360P in the N lobe of the

51 de of CXCR7 suppressed MIF-mediated ERK- and zeta-chain-associated protein kinase (ZAP)-70 activation

52 ysis revealed reduced phosphorylation of the zeta-chain-associated protein kinase of 70 kDa at the in

53 CLL cells that expressed zeta-chain-associated protein of 70 kDa (ZAP-70) or that

54 y study multisite phosphorylation of the TCR zeta-chain.

55 Physicochemical (zeta potential (zeta), conductivity, surface hydrophobicity (H0), protei

56 We conclude that pol kappa and pol zeta cooperatively carry out the majority of the error-p

57 cides: carbaryl, dimethoate, disulfoton, and zeta-cypermethrin; and fungicide pyraclostrobin) had sig

58 PEPITEM) proteolytically derived from 14.3.3 zeta delta (14.3.3.zetadelta) protein.

59 ding alpha-actinin-1, moesin, 14-3-3 protein zeta/delta, annexin A1/A3/A4/A5/A6, clathrin heavy chain

60 cient in the regulator diacylglycerol kinase zeta (DGKzeta) with or without PD-1/PD-L1 blockade.

61 amma1 are normalized in PLCgamma1/DAG kinase zeta double null cells.

62 of the mutagenic translesion DNA polymerase zeta during DNA replication.

63 We identified a common D-Q-Phi-X0,1-G-K-N-zeta-E motif in CsgC client proteins that is not found i

64 e a tandem CAR exodomain (TanCAR) and a CD28.zeta endodomain.

65 The final models show that zeta enters into F1-ATPase at the open catalytic alphaE/

66 We find that zeta-, epsilon-, and delta-tubulin form an evolutionaril

67 n fork to generate a first mutation, and Pol zeta extends the mismatch with a second mutation.

68 on carbides (alpha-Fe, gamma'-FeC, eta-Fe2C, zeta-Fe2C, chi-Fe5C2, h-Fe7C3, theta-Fe3C, o-Fe7C3, gamm

69 " blocking further gamma rotation, while the zeta globular domain anchors it to the closed alphaDP/be

70 Analysis of pol zeta has been hampered by difficulties in expression of

71 PhixGxzetax(P/A) (motif A; Phi, hydrophobic; zeta, hydrophilic), (Y/W)PhiGSxT (motif B), W (motif C),

72 rtial gamma rotations lock the N terminus of zeta in an "inhibition-general core region," blocking fu

73 bject to I/R expressed IL-34, c-FMS, and PTP-zeta in TECs during AKI that increased with advancing in

74 7 (but not for Pol32) subunits of polymerase zeta in the survival of cells undergoing telomere losses

75 es a damage-specific function of REV7 in pol zeta, in contrast to the distinct roles of REV3L and REV

76 negative regulator of diacylglycerol kinase zeta increased the suppressive ability of Tregs.

77 (PKMzeta), mainly because its inhibition by zeta inhibitory peptide (ZIP) interferes with previously

78 This evidence is heavily based on the use of zeta inhibitory peptide (ZIP), a supposed specific inhib

79 osubstrate fragment of the atypical PKCzeta, zeta inhibitory peptide (ZIP), has been extensively used

80 e molecular mechanisms that are sensitive to zeta-inhibitory peptide (ZIP) are the few manipulations

81 Significance statement: The zeta-inhibitory peptide (ZIP) is considered a candidate

82 The zeta-inhibitory peptide (ZIP) is considered a candidate

83 elied on the PKCzeta pseudosubstrate-derived zeta-inhibitory peptide (ZIP).

84 sms of maintenance (e.g., those sensitive to zeta-inhibitory peptide, ZIP) and those induced by memor

85 ding the catalytic subunit of DNA polymerase zeta involved in translesional synthesis, are significan

86 These data suggest that pol zeta is essential for processing AFB1-induced DNA adduct

87 DNA polymerase zeta (pol zeta) is exceptionally important for controlling mutagen

88 using knock-out mice, we determined that the zeta isoform of DGK (DGKzeta) is necessary for the mecha

89 t site in the atypical protein kinase C (PKC)zeta isoform, which removes N-terminal regulatory elemen

90 ha-helices 6, 7, and 8, respectively, within zeta-isoform as part of the GluN2C binding motif and ind

91 An enzyme called PKM zeta may have a role in long-term memory after all.

92 se of HMGB1 induced a rapid protein kinase C zeta-mediated internalization of surface tight junctions

93 The F1-ATPase and F1-zeta models of P. denitrificans were supported by cross-

94 Surprisingly, tubule cells in prkciota/zeta morphants displayed ectopic expression of the trans

95 e ectopic tubule gene expression in prkciota/zeta morphants.

96 a 3D structure configurationally isotypic to zeta-Nb2O5.

97 -N(zeta)-O close to 180 degrees , distance N(zeta)-O ca. 2.7-3.0 A).

98 axis of the NH3(+) group (angle C(epsilon)-N(zeta)-O close to 180 degrees , distance N(zeta)-O ca. 2.

99 The protein adopts the zeta or cis-prenyl transferase fold but remarkably, unli

100 up of atypical PKC (aPKC, isoforms iota and zeta), Par6, and Par3 determine asymmetry in several cel

101 THEMIS knock-down increased TCR-induced CD3-zeta phosphorylation, Erk activation and CD69 expression

102 We show that tonic CAR CD3-zeta phosphorylation, triggered by antigen-independent c

103 Atypical Protein Kinase C zeta (PKCzeta) forms Partitioning-defective (PAR) polari

104 resistance in vivo activate protein kinase C zeta (PKCzeta) in pancreatic islets and beta-cells.

105 raction between Galphaq and protein kinase C zeta (PKCzeta), leading to the stimulation of the ERK5 p

106 Protein kinase M zeta (PKMzeta), an atypical isoform of protein kinase C,

107 of "the memory molecule" is protein kinase M zeta (PKMzeta), mainly because its inhibition by zeta in

108 Sperm-specific phospholipase C-zeta (PLCzeta) is widely considered to be the physiologi

109 tion, a process initiated by phospholipase C zeta (PLCzeta), a sperm-specific protein.

110 DNA polymerase zeta (Pol zeta) and Rev1 are key players in translesion

111 DNA polymerase zeta (pol zeta) is exceptionally important for controlli

112 lyses demonstrated the ability of polymerase zeta (pol zeta) to incorporate an A opposite AFB1-Fapy-d

113 o additional accessory subunits of human Pol zeta, PolD2 and PolD3.

114 participation of error-prone DNA polymerase zeta (Polzeta) in replication of undamaged DNA.

115 Without H2Bub1, DNA polymerase zeta (Polzeta) is responsible for a highly mutagenic alt

116 7/Mad2l2 encodes a subunit of DNA polymerase zeta (Polzeta), 1 of 10 translesion DNA synthesis polyme

117 ghest emulsion stability index (179.5 h) and zeta potential (-67.4 mV) when compared to those of othe

118 The significant increase in zeta potential (zeta) value of -57mV for the synthesized

119 Physicochemical (zeta potential (zeta), conductivity, surface hydrophobic

120 Composite charge reversal (zeta potential -18 to 45 mV) increased the adsorption of

121 Zeta potential analysis indicated that charge neutraliza

122 Zeta potential analysis supports that antibacterial acti

123 ence and UV-visible absorption spectroscopy, zeta potential analysis, Fourier-transform infrared spec

124 on microscopy, dynamic light scattering, and zeta potential analysis.

125 incorporation as revealed by particle size, zeta potential and colour measurements.

126 raction, FTIR, thermal gravimetric analysis, Zeta potential and element analysis.

127 Size, zeta potential and encapsulation efficiency (EE) of the

128 pha-TOC) on mean size, polydispersity index, zeta potential and entrapment efficiency (EE) was evalua

129 his effect causes significant changes to the zeta potential and flow velocity.

130 ed the colloidal stability by increasing the zeta potential and hydrophilicity of CeO2 NPs.

131 ds (VOCs), particle size, size distribution, zeta potential and morphology of the liposomes.

132 The inflection point of the zeta potential and pH plot occurred at the first pKa of

133 PHs were evaluated for their particle sizes, zeta potential and surface hydrophobicity.

134 electrophoresis, which we attribute to their zeta potential and the suspension properties.

135 sing hydrophobicity and a decreasing surface zeta potential as the membranes fouled.

136 The polarity of the zeta potential at both interfaces must be determined whe

137 ing CSW is strongly correlated to changes in zeta potential at both the mineral-water and oil-water i

138 Studies of zeta potential at the bacterial cell membrane suggested

139 esults also show for the first time that the zeta potential at the oil-water interface may be positiv

140 rticles will lose the PEG layer and increase zeta potential by responding to tumor acidity, which sig

141 The high-resolution single particle size and zeta potential characterisation will provide a better un

142 Zeta potential data indicated that mixed hemi/ad-micelle

143 /- 2.21 nm to 88.64 +/- 1.25 nm and reversed zeta potential from -20.38 +/- 0.39 mV to 22.51 +/- 0.34

144 sh liposomes ranged from 75.7 to 81.0 nm and zeta potential from -64.6 to -88.2mV.

145 e, Ru(bpy)3Cl2, that changes the sign of the zeta potential in part of the channel from negative to p

146 Zeta potential increase and formation of aggregates were

147 The zeta potential is an electric potential in the Debye scr

148 Thus, characterizing the zeta potential is essential for many applications, but a

149 Brunauer, Emmett and Teller surface area and zeta potential measurement.

150 semblies, while dynamic light scattering and zeta potential measurements are employed for macroscopic

151 otential of particles in suspension, whereas zeta potential measurements of a solid wall in solution

152 Zeta potential measurements showed QS imparted higher dr

153 n of SDS molecules on the surface of MIONPs, zeta potential measurements were performed in different

154 addition, dynamic light scattering (DLS) and zeta potential measurements were used to study the effec

155 oflavin T and Congo Red fluorescence assays, zeta potential measurements) and quantitative assays on

156 tatic force microscopy (EFM) image analysis, zeta potential measurements, and charged nanoparticle bi

157 Zeta potential measurements, sedimentation experiments,

158 attern analysis with adsorption isotherm and zeta potential measurements, we show that the suppressio

159 tools such as FESEM, TEM, EDX, XRD, DLS and zeta potential measurements.

160 imised by dynamic light scattering (DLS) and zeta potential measurements.

161 (SEM), Raman spectroscopy, contact angle and zeta potential measurements.

162 e lowest negative charge as confirmed by the zeta potential measurements.

163 l shape, an average size of 205+/-4.24nm and zeta potential of -11.58+/-1.87mV.

164 was 47.5+/-7.3% and the nanoliposomes had a zeta potential of -16.2+/-5.5mV.

165 75%, a hydrodynamic diameter of 292nm, and a zeta potential of -17.37mV.

166 eedle-shaped particle ultrastructure, with a zeta potential of -35.5mV determined by electrophoretic

167 eal that Ca(2+) as well as Mg(2+) reduce the zeta potential of liposomes to nearly background levels

168 After PEI coating, zeta potential of MNPs shifted from -7.9 +/- 2.0 to +39.

169 Existing methodologies for measuring zeta potential of nanoparticles using resistive pulse se

170 robust method to simultaneously measure the zeta potential of particles in suspension and solid wall

171 scattering is typically used to measure the zeta potential of particles in suspension, whereas zeta

172 a after AgNP synthesis mainly depends on the zeta potential of the cell wall.

173 ted by X-ray photoelectron spectroscopy, the zeta potential of the food-grade TiO2 suspension in deio

174 No significant change in the PV and zeta potential of the liposome formulations with alpha-t

175 Additionally, lipolysis, particle size, and zeta potential of the micellar fractions were investigat

176 The zeta potential of the nanoliposomes was decreased during

177 espectively, which are both sensitive to the zeta potential of the particle and the wall.

178 The vesicle size and zeta potential of the phosphatiosomes were 154 nm and -3

179 HA increases the zeta potential of these nanosystems, but does not disrup

180 The conjugate was characterized by zeta potential UV-vis spectroscopy and field emission sc

181 ulations with minimum particle size and high zeta potential value were PW and BW+glycerol behenate sa

182 le size range of 200-300 nm and the absolute zeta potential varied between 8.4 and 10.6 mV.

183 of nanoliposomes was found to be 150 nm and zeta potential was -34 mV.

184 Absorbance at 600 nm, particle size, and zeta potential were analyzed at pH 4.0.

185 ntration of the electrolytes (and thus local zeta potential).

186 cal entity with ~90 +/- 6 nm having negative zeta potential, -37.7 +/- 2 mV, and has an ability to lo

187 erized by means of dynamic light scattering, zeta potential, and liquid chromatography-mass spectrome

188 owever, NOM inhibited Fe hydrolysis, reduced zeta potential, and suppressed the formation of filterab

189 Protein solubility, zeta potential, circular dichroism and gel strength of t

190 osing with FeCl3 increased Fe hydrolysis and zeta potential, decreased the fraction of colloidal Fe,

191 B-CDDSs were characterized by particle size, zeta potential, drug encapsulation efficacy, PB release

192 e particle size, polydispersity index (PDI), zeta potential, encapsulation efficiency (EE) and morpho

193 y droplet size, polydispersitiy index (PDI), zeta potential, entrapment efficiency (EE), in vitro per

194 solution ionic strength and characterized by zeta potential, FTIR, X-ray diffraction, and thermal gra

195 mpared for their size, polydispersity index, Zeta potential, loading rate, encapsulation efficiency a

196 haracterized for size, polydispersity index, zeta potential, morphology, loading rate (LR) and photo-

197 Particle size, zeta potential, span value, and pH of CSO-NP and oxidati

198 The protein zeta potential, the emulsifying capacity, the emulsion a

199 on transmission electron microscopy (HRTEM), zeta potential, UV-visible absorption, and photoluminesc

200 lity (p<0.001), lipolysis, particle size and zeta potential.

201 metric diameter (337-364 nm), and a negative zeta potential.

202 icating succinate as the main influence over zeta potential.

203 cle size (199-283nm), and slightly decreased zeta potential.

204 zed for their size, polydispersity index and zeta potential.

205 form infrared spectroscopy and measuring the zeta potential.

206 ies such as size, apparent surface area, and zeta potential.

207 asurements of interfacial tension, size, and zeta potential.

208 The zeta (zeta) potential values of all emulsions increased when r

209 cterized in terms of particle size and zeta (zeta) potential with average values of 148nm+/-39nm and

210 er transform-infra red spectroscopy (FT-IR), zeta-potential analysis, electrochemical impedance spect

211 te to a limited extent but retain a positive zeta-potential apparently due to nonuniform adsorption o

212 0.202 +/- 0.034 PDI and 81 +/- 4 mV zeta-potential at pH 6) using an emulsion-diffusion meth

213 dispersity index (PDI<0.5); furthermore, the zeta-potential changed from +3.9mV in uncoated liposomes

214 Zeta-potential data suggested the formation of LAE-lecit

215 The liposome zeta-potential depended on peptide molecular weight, sug

216 PNDDS having positive zeta-potential displayed strong adsorption onto silica s

217 repared and characterized regarding size and zeta-potential distribution, polidispersity index, entra

218 es to DNP hydrodynamic diameter and apparent zeta-potential in a concentration-dependent manner.

219 nes for the mixed hemi/ad-micelle formation, zeta-potential isotherms were investigated.

220 Turbidity and zeta-potential measurements indicated that pH 5 was the

221 e mixed hemi/ad-micelles of CTAB at Mag-NPs, zeta-potential measurements were performed.

222 a polydispersity index of 0.26+/-0.01, and a zeta-potential of -31.72+/-0.74mV.

223 opene NPs had a diameter of 152+/-32nm and a zeta-potential of 58.3+/-4.2mv as characterized with tra

224 As the zeta-potential of DDSNs increases with the doping level

225 ns gave a significant change in the size and zeta-potential of MFGs.

226 ion and density of HC together with size and zeta-potential of NP-HC complexes were tracked at each s

227 ming potential measurements confirm that the zeta-potential of the membrane surface is converted from

228 Tyrosinase did not have effect on zeta-potential or colloidal stability of either protein,

229 mic diameter by dynamic light scattering and zeta-potential under conditions where n-PCM is "invisibl

230 ive (16 kDa) formed stable polyplexes with a zeta-potential value of +34 mV and polyplex size of 61 n

231 equent enzymatic cross-linking increased the zeta-potential value.

232 Transglutaminase increased the absolute zeta-potential values and reduced the particle size of o

233 had similar surface properties, as shown by zeta-potential versus pH profiles and isoelectric point

234 tions differing in an average flake size and zeta-potential were prepared using centrifugation and co

235 posomes, as determined by electrical charge (zeta-potential) and FTIR analysis.

236 ized on the AgNPs, reducing surface charges (zeta-potential) and hence electrostatic repulsion betwee

237 entration, synthesis method, surface charge (zeta-potential), nor nominal size had any influence in t

238 tes (WPH), produced with Everlase (WPH-Ever; zeta-potential, -39mV) and papain (WPH-Pap; zeta-potenti

239 zeta-potential, -39mV) and papain (WPH-Pap; zeta-potential, -7mV), during simulated digestion.

240 mical properties such as size, distribution, zeta-potential, and siRNA condensation efficiency.

241 ease in particle size and a reduction of the zeta-potential, and the coating layer could be compresse

242 hemical and functional properties, including zeta-potential, surface morphology, emulsifying activity

243 er CaCO3 particles with a much more negative zeta-potential.

244 le and X-ray photoelectron spectroscopy, and Zeta-potential.

245 We further show that the measured zeta potentials and suspension properties are in excelle

246 By visualizing the particle dynamics, both zeta potentials can be determined independently.

247 allows measurement of both particle and wall zeta potentials, which suggests a cost-effective tool fo

248 terized regarding hydrodynamic diameters and zeta potentials.

249 the experimental conditions, using measured zeta potentials.

250 ial values that are consistent with measured zeta potentials.

251 The CCCs were correlated with material zeta-potentials (R(2) = 0.94-0.99), which were observed

252 constants (pKa) as the main contributors to zeta-potentials and thus material aqueous stability.

253 The zeta-potentials of these types of particles are not very

254 t microscope is used to demonstrate low-cost zeta potentiometry that allows measurement of both parti

255 we show that there is complete loss of AP-5 zeta protein and a reduction in the associated AP-5 micr

256 the CD247 gene that encodes the homodimeric zeta protein.

257 The zeta-protein is bound via its N-terminal alpha-helix in

258 ificans, inhibited by its natural regulatory zeta-protein, has been solved by X-ray crystallography a

259 IL-34 receptor, protein-tyrosine phosphatase zeta (PTP-zeta) were upregulated in the kidney after I/R

260 ressed protein tyrosine phosphatase receptor-zeta (PTPRZ), whereas PTN treatment did not induce RAS s

261 Rev1-pol zeta recruitment requires the Fanconi anemia core comple

262 eta function in one pathway and Pols eta and zeta, respectively, function in the other two pathways.

263 In addition, depletion of Pol zeta resulted in significant decreases in T-->C mutation

264 We show that Pol zeta/Rev1-dependent mutations occur at sites of replicat

265 B1, survival of mouse cells deficient in pol zeta (Rev3L(-/-)) was significantly reduced relative to

266 d that receptor protein-tyrosine phosphatase zeta (RPTPzeta)/phosphacan is hypoglycosylated in a mous

267 In vitro TLS using yeast pol zeta showed that it can extend G3*:A pair more efficient

268 ly modified to express HER2-CARs with a CD28.zeta-signaling endodomain (HER2-CAR VSTs).

269 esults reconcile conflicting findings of the zeta structure reported in previous studies and provide

270 In summary, the zeta subunit blocks the intrinsic rotation of the nanomo

271 The zeta subunit is a novel inhibitor of the F1FO-ATPase of

272 recipient rs2056626 (CD247: T-cell receptor zeta subunit) GG or GT genotypes were associated with hi

273 Its zeta-subunit contains multiple cytosolic immunoreceptor

274 lex formed by the gamma, delta, epsilon, and zeta subunits, which are invariable and ensure signal tr

275 ells deficient in Pol kappa, Pol iota or Pol zeta, suggesting the mutual involvement of multiple tran

276 ession of orthologues (except 14-3-3 protein zeta) suggests that parallel habitat adaptation or accli

277 e are seven known mammalian 14-3-3 isoforms (zeta,, tau, , eta, beta, and sigma), which generally fun

278 Thus ROS and the PKC-zeta to p47(phox) interaction are valid therapeutic targ

279 Here we demonstrate that a novel PKC-zeta to p47(phox) interaction is required for ROS produc

280 or BI-D1870 with TNF-alpha inhibited the PKC-zeta to p47(phox) interaction, inhibited ROS production,

281 nstrated the ability of polymerase zeta (pol zeta) to incorporate an A opposite AFB1-Fapy-dG and exte

282 itions, the Epsilon antidote neutralizes the Zeta toxin through the formation of a tight complex.

283 Humans lack zeta-tubulin but have delta-tubulin.

284 We conclude that zeta-tubulin facilitates interactions between the centri

285 In contrast with multiciliated cells, zeta-tubulin in cycling cells does not localize to centr

286 In Xenopus multiciliated cells, zeta-tubulin is a component of the basal foot, a centrio

287 Zeta-tubulin is the sixth and final member of the tubuli

288 Depletion of zeta-tubulin results in disorganization of centriole dis

289 The significant increase in zeta potential (zeta) value of -57mV for the synthesized AOx-AuNPs conju

290 oups showed significantly increased negative zeta values (from -37 to less than -10; P = .008).

291 With a tagged form of an active Pol zeta variant, we isolated two additional accessory subun

292 nd the error-prone translesion synthesis pol zeta were able to accurately bypass AFB1-N7-Gua.

293 When pol kappa and pol zeta were simultaneously knocked down, MF of the G1 and

294 ptor, protein-tyrosine phosphatase zeta (PTP-zeta) were upregulated in the kidney after I/R.

295 ein levels of AQP2 alongside 14-3-3beta and -zeta, whereas levels of 14-3-3eta and -theta were decrea

296 By utilizing cells lacking the DAG kinase zeta, which have increased DAG levels, we demonstrate th

297 enes was a single orthologue (14-3-3 protein zeta/YWHAZ) that was downregulated in temporary ponds in

298 The zeta (zeta) potential values of all emulsions increased

299 characterized in terms of particle size and zeta (zeta) potential with average values of 148nm+/-39n

300 Interactions of the cytosolic domain of zeta (zetacyt) with acidic lipids have been implicated i