ライフサイエンスコーパス: zeta

1 S by preventing recruitment of mutagenic POL zeta.

2 3 gene encoding the catalytic subunit of Pol zeta.

3 that interacts with the REV7 subunit of POL zeta.

4 etwork rigidity, through the binary variable zeta.

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

6 m injection or expression of phospholipase C zeta.

7 the ICL-G by Pol eta, Pol zeta, and Rev1-Pol zeta.

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

9 tro-kinetic potential was: zeta ~ -25 mV and zeta ~ -17 mV, respectively.

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

11 0.01 and the electro-kinetic potential was: zeta ~ -25 mV and zeta ~ -17 mV, respectively.

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

13 lic changes through stabilization of IkappaB-zeta, a critical pro-inflammatory mediator in chondrocyt

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

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

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

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

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

19 kene of the starting material, whereas the e-zeta alkene of the product is preserved.

20 pass synthesis, by 2-3 fold, compared to Pol zeta alone or Pol eta.

21 Rev1-Pol zeta, and particularly Pol zeta alone showed a tendency to stall before the ICL, wh

22 Pol zeta also includes REV7 subunits (encoded by Rev7 in yea

23 Pol zeta also participates in repair by microhomology mediat

24 at loss of diacylglycerol (DAG) kinase (Dgk) zeta, an enzyme which converts DAG into phosphatidic aci

25 al signatures associated with DNA polymerase zeta, an error-prone translesion polymerase, and the APO

26 Ag-independent tonic signaling termed CAR-28/zeta and 2) a nonstimulating control CAR construct lacki

27 that simultaneously expressed both 4-1BB/CD3-zeta and CD28/CD3-zeta endodomains.

28 We have used yeast DNA polymerases eta, zeta and Rev1 to study translesion synthesis (TLS) past

29 present the cryo-EM structure of polymerase zeta and show how it catalyzes the extension step of tra

30 are critical for the interaction with 14-3-3 zeta and sigma and for the efficient nuclear importation

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

32 synthesis was downstream of protein kinase C-zeta and was required for c-Myc-induced proliferation.

33 DNA polymerase zeta (Pol zeta) and Rev1 are essential for the repair of DNA inter

34 Rev1-Pol zeta, and particularly Pol zeta alone showed a tendency

35 deamination, replication error by polymerase zeta, and polymerase slippage at repeat junctions - on t

36 ly inserted across the ICL-G by Pol eta, Pol zeta, and Rev1-Pol zeta.

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

38 nality in spite of the smallest value of the zeta-angle yet observed for a helix of this type.

39 so a result of the narrow range of potential zeta-angles in our monomer.

40 c databases identified protein kinase C (PKC)zeta as a TRIM32-associated protein that contributes to

41 suggesting that the proposed function of Pol zeta as an extender DNA polymerase is also required for

42 nvolvement of mutagenic DNA synthesis by Pol zeta as well as diminished proofreading by Pol delta dur

43 mmunoprecipitation, we identified the kinase zeta-associated protein kinase of 70 kDa (Zap70) as a bi

44 and correct the T-cell immunodeficiency in a zeta-associated protein of 70 kDa (ZAP-70)-deficient mur

45 its associated CD3epsilon, delta, gamma, and zeta, but the contributions of different CD3 chains rema

46 xternal Bronsted base, electrophilic, remote zeta C-H activation takes place, for which the participa

47 The prediction quality factor zeta can be improved by ca. 20-50% by selecting an adequ

48 atio CD4:CD8 T-cell composition with a 4-1BB:zeta CAR targeting CD19 who also recieved early interven

49 roides containing the N = 7 carotenoid zeta (zeta)-carotene, not previously incorporated within a nat

50 ally utilized in light-harvesting complexes, zeta-carotene does not quench excited triplet states of

51 elative to the lifetime of the S(1) state of zeta-carotene in solvent, the lifetime decreases ~250-fo

52 lvent, the lifetime decreases ~250-fold when zeta-carotene is incorporated within LH2, due to transfe

53 ealed how an epistatic interaction between a zeta-carotene isomerase mutant (ziso-155) and ccr2 block

54 se the S(1) -> S(0) fluorescence emission of zeta-carotene overlaps almost perfectly with the Q(x) ab

55 es of BChl a, likely due to elevation of the zeta-carotene triplet energy state above that of BChl a

56 Others were zeta-carotene, phytofluene, phytoene and lutein.

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

58 n synthesis, eukaryotic DNA polymerase zeta (zeta) carries out extension from a wide range of DNA les

59 gnificantly affect phosphorylation of Zap70 (zeta chain of T cell receptor-associated protein kinase

60 o-oncogene SRC family tyrosine kinase (LYN), zeta chain of T-cell receptor-associated protein kinase

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

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

63 ibition of Csk revealed that CD45 suppressed zeta-chain phosphorylation and was necessary for a regul

64 influence on Lck activation, TCR-associated zeta-chain phosphorylation, and more downstream signalin

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

66 local changes in the flexibility of the TCR zeta-chain, this naturally leads to rate enhancements an

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

68 f the TCR with rapid phosphorylation of both zeta-chain-associated protein 70 and linker for activati

69 signaling events, such as phosphorylation of zeta-chain-associated protein kinase 70 (Zap70), Src hom

70 The Rev1-Pol zeta complex was most efficient in complete bypass synth

71 s (TLS) by releasing it from REV3 in the Pol zeta complex.

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

73 B-family DNA polymerases alpha, delta, e and zeta cooperate to accurately replicate the eukaryotic nu

74 We show that zeta correlates strongly to the T(g), and that this simp

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

76 chromosomal instability associated with pol zeta deficiency must be considered.

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

78 we identified alpha-enolase, 14-3-3 protein zeta/delta, cofilin-1, and heat shock cognate 71 kDa pro

79 lementation of alpha-enolase, 14-3-3 protein zeta/delta, cofilin-1, and heat shock cognate 71 kDa pro

80 other Pol zeta-proteins, suggesting that Pol zeta-dependent and -independent roles of Rev7 are releva

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

82 t that targeting diacylglycerol (DAG) kinase zeta (DGKzeta), a negative regulator of DAG-mediated cel

83 No stalling by Rev1-Pol zeta directly past the ICL was observed, suggesting that

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

85 CAR T cells expressing the 4-1BB/CD3-zeta endodomain were insufficient to prevent viral rebou

86 y expressed both 4-1BB/CD3-zeta and CD28/CD3-zeta endodomains.

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

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

89 3-kinase (PI3-K), protein kinase C-zeta (PKC-zeta), extracellular signal-regulated kinase 1/2 (ERK1/2

90 licity of Jensen polynomials for the Riemann zeta function [Formula: see text] at its point of symmet

91 Targeting of pol zeta function may be a useful strategy in cancer therapy

92 In the case of the Riemann zeta function, this proves the Gaussian unitary ensemble

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

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

95 7 (but not for Pol32) subunits of polymerase zeta in the survival of cells undergoing telomere losses

96 -DNA recombination, uncovering a role of Pol zeta in transferring genetic information from transcript

97 iverse functions of DNA polymerase zeta (pol zeta) in eukaryotes.

98 Converging evidence suggest that zeta inhibitory peptide (ZIP) eliminates memories for ex

99 Zeta inhibitory peptide (ZIP), a PKMzeta inhibitor, is w

100 The myristoylated zeta inhibitory peptide (ZIP), which was originally deve

101 le and female rodents.SIGNIFICANCE STATEMENT Zeta-inhibitory peptide (ZIP) has been shown to disrupt

102 For instance, pol zeta is also employed when the replisome operates sub-op

103 IkappaB-zeta is regulated bi-modally at the stages of transcript

104 e positions along the BIR track and that Pol zeta is responsible for the majority of both spontaneous

105 y adjustable parameter in the calculation of zeta is the ratio of mobility between conjugated and non

106 Pol zeta is used in response to circumstances that stall DNA

107 An effective mobility value, zeta, is calculated using an assigned atomic mobility va

108 In contrast, expression of the CAR-28/zeta led to elimination of mature CAR(+) T and B cells,

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

110 ns of PG were determined via zeta-potential (zeta) measurements after lipid exchange and after scramb

111 gene enhancer in B cells inhibitor (IkappaB) zeta (NFKBIZ, the gene encoding IkappaBzeta) was reduced

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

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

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

115 carbon chains (gamma-, delta-, epsilon-, and zeta-) or cyclic structures (cyclobutane, cyclopentane,

116 (mu(EP)((1))), the particle zeta potential (zeta(P)), the E(EEC), and the electrophoretic mobility o

117 ely directed G->A mutations; Pol eta and Pol zeta participated in error-prone bypass of the straight-

118 inositide 3-kinase (PI3-K), protein kinase C-zeta (PKC-zeta), extracellular signal-regulated kinase 1

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

120 triggers the activation of protein kinase C zeta (PKCzeta).

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

122 iptase, translesion DNA polymerase zeta (Pol zeta) plays a major role in R-TDR, and it is essential f

123 DNA polymerase zeta (Pol zeta) and Rev1 are essential for the repair of

124 rvey the diverse functions of DNA polymerase zeta (pol zeta) in eukaryotes.

125 se transcriptase, translesion DNA polymerase zeta (Pol zeta) plays a major role in R-TDR, and it is e

126 DNA polymerase zeta (Polzeta) belongs to the same B-family as high-fide

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

128 Extended sonication time (8 min) lowered the zeta potential (-47.5 to -40.8), and particle size (74.2

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

130 horetic mobility (mu(EP)((1))), the particle zeta potential (zeta(P)), the E(EEC), and the electropho

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

132 ter (Z-ave), polydispersity index (PDI), and zeta potential (ZP).

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

134 ulation efficiency in HSA particles (169 nm, zeta potential -31 mV).

135 about 75 nm, polydispersive index<0.2, and a zeta potential about 14), which were associated with a h

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

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

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

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

140 Changes in zeta potential and INP size, measured by dynamic light s

141 in molecular protonation are measured using zeta potential and modeled using DFT.

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

143 ning with HCl had a negligible impact on the zeta potential and performance of all membranes evaluate

144 tability was evaluated using liposomes size, zeta potential and polydispersity index.

145 On the other hand, the absolute values of zeta potential and surface hydrophobicity decreased as a

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

147 Zeta potential and turbidity measurements were employed

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

149 Studies of zeta potential at the bacterial cell membrane suggested

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

151 nd pass number increased (p < 0.05), whereas zeta potential did not change (p > 0.05).

152 The repulsive zeta potential for the rock and the oil in low-salinity

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

154 Zeta potential increase and formation of aggregates were

155 While the zeta potential is a convenient and commonly used measure

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

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

158 Adjusting size and zeta potential may allow investigators to further fine-t

159 ntly nanoparticles of 8 nm diameter and with zeta potential mean value of -33 mV.

160 Zeta potential measurements and X-ray photoelectron spec

161 oncentration and size determinations of EVs, zeta potential measurements for surface charge analysis,

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

163 urement, thermal gravimetric analysis (TGA), zeta potential measurements, and Fourier-transform infra

164 ion of pH using batch adsorption experiment, zeta potential measurements, in situ P K-edge X-ray abso

165 , X-ray photoelectron spectroscopy (XPS) and zeta potential measurements.

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

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

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

169 e charge of copper species, as determined by zeta potential measurements.

170 ed an average particle size of 76.6nm with a zeta potential of +16.5mV.

171 E) values of 67.4 and 63.1%, 26.6 and 22.7%, zeta potential of - 18.0 and - 18.6 mv, respectively.

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

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

174 75%, a hydrodynamic diameter of 292nm, and a zeta potential of -17.37mV.

175 ncy of 59.09, 48.30, and 55.00% and negative zeta potential of -18.05, -21.5 and -18.05 mv, respectiv

176 y modified HA, have a mean size of 130 nm, a zeta potential of -20 mV, and exhibit high docetaxel enc

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

178 The low sedimentation values, and the high zeta potential of mashua and melloco starches in cold di

179 NaOH affected the zeta potential of membranes with a greater concentration

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

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

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

183 n experimentally validated by modulating the zeta potential of the detection probe by conjugating neg

184 aried from 5 to 30 nucleotides, altering the zeta potential of the detection probe from -9.3 +/- 0.8

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

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

187 ia coli in a manner similar to NETs when the zeta potential of the microwebs is positive.

188 The zeta potential of the nanoliposomes was decreased during

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

190 Zeta potential studies provided information regarding th

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

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

193 tive with particle size of was 263 +/- 3 nm, zeta potential was 0.1 +/- 0.02 and entrapment efficienc

194 However, zeta potential was higher in mayonnaises with DEs contai

195 ng Characterization (MBC) (TGA, ATR-FTIR and zeta Potential), while at the "macroscopic" scale, micro

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

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

198 erized using dynamic light scattering (DLS), zeta potential, and quantitative UV-vis spectroscopy mea

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

200 for the particle size, polydispersity index, zeta potential, apparent viscosity, pH, color parameters

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

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

203 Zeta potential, disulfide-sulfhydryl groups, surface hyd

204 These functionalized GNPs were analyzed by Zeta potential, dynamic light scattering, electron micro

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

206 lly characterized in terms of their acidity, zeta potential, interfacial tension, microdispersion pro

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

208 Zeta potential, particle size, and polydispersity index

209 roperties such as morphology, particle size, zeta potential, pGFP encapsulation efficiency and biolog

210 py (TEM), dynamic light scattering (DLS) and zeta potential, respectively.

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

212 on using rheology, dynamic light scattering, zeta potential, surface tension, and FTIR spectroscopic

213 on that was enhanced by the 16% reduction in zeta potential.

214 ies regarding particle size distribution and zeta potential.

215 form infrared spectroscopy and measuring the zeta potential.

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

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

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

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

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

221 nd total fractions of PG were determined via zeta-potential (zeta) measurements after lipid exchange

222 ticles (2Rh = 450 nm, PDI = 0.118 +/- 0.014, zeta-potential = 21 mV and T(g) = 8 +/- 1 degrees C) are

223 noparticles of similar size, polydispersity, zeta-potential and antibody valency, and its lung accumu

224 rge densities of functional groups, produced zeta-potential and networking potential were dominating

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

226 ented droplet diameter lower than 200 nm and zeta-potential approaching -30 mV until the end of stora

227 aller, more uniform and homogenious size and zeta-potential as well as higher encapsulation efficienc

228 0.202 +/- 0.034 PDI and 81 +/- 4 mV zeta-potential at pH 6) using an emulsion-diffusion meth

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

230 The size and zeta-potential changes in the nanoemulsions were investi

231 owed that alkalization induced more negative zeta-potential compared to MPI control, reducing it from

232 e without the addition of gums; however, the zeta-potential decreases from 2.92 mV to -2.51 mV as pH

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

234 in the outer leaflet only was quantified by zeta-potential measurements for octaethylene glycol dode

235 ment of hair surface charge mainly relies on zeta-potential measurements which lack spatial resolutio

236 titration calorimetry (ITC), turbidity, and zeta-potential measurements.

237 able sizes (170-350 nm), good stability with zeta-potential of -25 mV, and high vitamin encapsulation

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

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

240 The zeta-potential of particles was opposite to the substrat

241 perties influenced the mean droplet size and zeta-potential of the fresh emulsions.

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

243 decreased after heat treatment, whereas the zeta-potential remained unchanged.

244 l of particles was opposite to the substrate zeta-potential that promoted their irreversible adsorpti

245 Neutralization had a relatively similar zeta-potential value as alkalized sample.

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

247 ectronegativity lower than 1.55 and positive zeta-potential were more likely to cause lysosomal damag

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

249 ace, as reflected in the decrease of surface zeta-potential with increasing pH.

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

251 characteristics (including counts, size and zeta-potential), and a limited number of differentially

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

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

254 rmined using dynamic light scattering (DLS), zeta-potential, and Scanning Electron Microscopy (SEM),

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

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

257 uring turbidity, particle size distribution, zeta-potential, as well as surface hydrophobicity of cas

258 LS), Transmission Electron Microscopy (TEM), zeta-potential, Inductively Coupled Plasma-Mass Spectrom

259 es, and exosome quantity, size-distribution, zeta-potential, marker-expression and RNA/protein qualit

260 ormation were investigated by state diagram, zeta-potential, rheological, and phase composition analy

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

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

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

264 consistent with the decrease in ferrihydrite zeta-potential.

265 larger oil droplet sizes, stronger negative zeta potentials (-69.9 mv), narrower size distributions

266 The particle sizes, zeta potentials and encapsulation efficiencies for the p

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

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

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

270 eractions even while having nearly identical zeta potentials.

271 ial values that are consistent with measured zeta potentials.

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

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

274 ously shown following targeting of other Pol zeta-proteins, suggesting that Pol zeta-dependent and -i

275 ich blocks the REV1-REV7 interaction and POL zeta recruitment.

276 Knockdown of either hPol iota or hPol zeta reduced the mutation frequency by nearly 50%.

277 ole of receptor protein tyrosine phosphatase zeta (RPTPzeta) in PNN structure.

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

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

280 Its zeta-subunit contains multiple cytosolic immunoreceptor

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

282 ol eta and hPol kappa with knockdown of hPol zeta, suggesting that these TLS polymerases play a criti

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

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

285 evidence that uncovers various roles of pol zeta that extend beyond translesion synthesis.

286 ilencing the Rev3l subunit of polymerase Pol zeta to impair DNA repair in combination with cisplatin;

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

288 Eligible patients from the ZETA trial were divided into 4 disease severity subgroup

289 phospholipase A2 receptor, protein kinase C zeta type, tubulin beta-4B class IVb, vimentin), only an

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

291 In contrast, the larger range of potential zeta-values observed for the corresponding trans-system

292 zeta-Values were in good agreement with exclusive outsid

293 s (TLS) DNA polymerases-hpol iota, kappa, or zeta-were individually deleted.

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

295 TLS) by DNA polymerases (Pol) delta, eta and zeta, which creates C>T transitions at pyrimidine dimers

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 slesion synthesis, eukaryotic DNA polymerase zeta (zeta) carries out extension from a wide range of D

299 sphaeroides containing the N = 7 carotenoid zeta (zeta)-carotene, not previously incorporated within

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