ライフサイエンスコーパス: delta

1 CD8(+) T cells from patients with hepatitis delta.

2 (S) comparable to measurements of YBa 2Cu3O7-delta.

3 naptic protein tyrosine phosphatase receptor delta.

4 one SHIP2 allele selectively in ECs (ECSHIP2(Delta/+)).

5 atterns among the canonical frequency bands (delta 0-3 Hz, theta 3-7 Hz, alpha 7-13 Hz, beta 13-30 Hz

6 were associated with specific sleep cycles: delta (0-3 Hz) activity during non-rapid eye movement (N

7 overall spike-field coherence (SFC) with V1 delta (0.5-4 Hz) and spindle (7-15 Hz) oscillations incr

8 elative strength of common input in both the delta (0.5-5 Hz) and alpha (5-13 Hz) bands was significa

9 The B (delta(11)B = 22.9 +/- 3.5 per thousand) and Sr ((87)Sr/(

10 Here, Cd isotopic compositions (delta(114/110)Cd) of archived fertilizer and soil sample

11 15-deoxy-Delta(12,14)-prostaglandin J2 (15d-PGJ2) is naturally pr

12 howed significant positive relationships for delta (13)C and a domed relationship for delta (15)N wit

13 delta (13)C and delta (15)N thus showed the inverse rela

14 ant relationship with trawling intensity for delta (13)C, but not for delta (15)N.

15 cids (delta (15)NAA) and bulk-tissue carbon (delta (13)Cbulk) and nitrogen (delta (15)Nbulk) isotopes

16 ogenesis but deep peat warming increased the delta(13) C of CH4 suggesting an increasing contribution

17 e region, the response, both delta(18) O and delta(13) C, is primarily to variations in relative humi

18 In delta(13) C, the response is via changes in stomatal con

19 volcanic emitters outgas carbon with higher delta(13)C and are located in mature continental arcs th

20 However, delta(13)C and Delta(14)C results on foraminifera from a

21 lation (p<0.0001) (n=54) was noticed between delta(13)C and delta(15)N in milk with that of hair whic

22 The delta(13)C and delta(15)N of pulp and the delta(18)O of

23 In contrast, delta(13)C and delta(15)N were not correlated with THg a

24 in nickel abundance correlate with negative delta(13)C and delta(18)O anomalies, suggesting that exp

25 andards of CO2 in air of known but differing delta(13)C and delta(18)O isotopic composition allows st

26 and and 0.48 per thousand to be achieved for delta(13)C and delta(18)O measurements, respectively.

27 Both delta(13)C and delta(18)O of the aragonite are enriched

28 ay lead to reassessment of the role that the delta(13)C record plays in reconstructing the oxygenatio

29 ere stronger in a global data base of foliar Delta(13)C samples than observed in P. balsamifera.

30 Correlation of delta(15)N versus delta(13)C values of NDMA resulted in trend lines that w

31 the effect of precipitation and elevation on Delta(13)C were stronger in a global data base of foliar

32 d changes in stable isotopes (delta(15)N and delta(13)C) in unexposed mayflies.

33 (delta(15)N) and C isotopic discrimination (Delta(13)C) measured in 755 specimens of a single widely

34 -calcium ratios (Ba/Ca) and carbon isotopes (delta(13)C) measured in long-lived coralline algae demon

35 had an average stable carbon isotope value (delta(13)C) of -66.2 +/- 6.4 per mil, consistent with a

36 these limits, the carbonate carbon isotope (delta(13)C) record becomes insensitive to changes in org

37 insight into this cycle, we combined carbon (delta(13)C), nitrogen amino acid (delta(15)NPhe), and Hg

38 housand to +0.54 per thousand for delta(2)H, delta(13)C, and delta(37)Cl values, respectively.

39 Both delta(13)C-CH4 and deltaD-CH4 correspond to the isotopic

40 Progressive enrichment of both delta(13)C-CH4 and deltaD-CH4 is observed with increasin

41 lated using emission inventories and updated delta(13)C-CH4 signatures.

42 than 10 mg/L (n = 12) were all found to have delta(13)C-CH4 values larger than -30 per thousand, typi

43 N by approximately 0.8 per thousand, but not delta(13)C.

44 he C(13)/C(12) ratio in atmospheric methane (delta(13)CH4) from 1983 through 2015.

45 However, delta(13)C and Delta(14)C results on foraminifera from a sediment core

46 delta (13)C and delta (15)N thus showed the inverse relationships to tho

47 for delta (13)C and a domed relationship for delta (15)N with trawling.

48 wling intensity for delta (13)C, but not for delta (15)N.

49 nitrogen isotopes of individual amino acids (delta (15)NAA) and bulk-tissue carbon (delta (13)Cbulk)

50 issue carbon (delta (13)Cbulk) and nitrogen (delta (15)Nbulk) isotopes for nine bat species from diff

51 We used the difference in delta(15) N between 20 ant conspecifics in 10 genera bet

52 onal isotope characterization', analysed the delta(15) N values from annual bone growth layer rings f

53 naturally occurring stable nitrogen isotope (delta(15) N) patterns that differentiate distinct ocean

54 vironments respectively, failed to vary with delta(15) N.

55 ne (TEA) solution as nitrite and nitrate for delta(15)N analysis using the denitrifier method.

56 analytical procedure is 0.6 per thousand for delta(15)N and 0.5 per thousand for delta(18)O.

57 We also measured changes in stable isotopes (delta(15)N and delta(13)C) in unexposed mayflies.

58 Metamorphosis also increased delta(15)N by approximately 0.8 per thousand, but not de

59 1) (n=54) was noticed between delta(13)C and delta(15)N in milk with that of hair which indicated tha

60 The delta(13)C and delta(15)N of pulp and the delta(18)O of juice can be co

61 n zinc concentrations coupled with increased delta(15)N signatures.

62 AD 1940-1975 is contemporaneous with higher delta(15)N values (wetter conditions).

63 Drier conditions indicated by delta(15)N values at AD 1848-1852 and AD 1880-1930 corre

64 Comparison of delta(15)N values between C. virginica shells shows rela

65 Using the relationship between NAO index and delta(15)N values in guano for the instrumental period,

66 The delta(15)N values were highest for Central Karoo, Semi-e

67 Correlation of delta(15)N versus delta(13)C values of NDMA resulted in

68 lta(18)O and fertilisation practices on pulp delta(15)N was demonstrated and must be considered with

69 In contrast, delta(13)C and delta(15)N were not correlated with THg among wetlands a

70 environmental gradients in foliar N isotope (delta(15)N) and C isotopic discrimination (Delta(13)C) m

71 s by analyzing the stable nitrogen isotopic (delta(15)N) values of the scleractinian coral Pocillopor

72 Fractionation of delta(15)NNO3 and delta(18)ONO3 during diffusion of nitr

73 high-spatial-resolution passive-samplers of delta(15)NNO3 and delta(18)ONO3 to investigate nitrogen

74 delta(15)NNO3 values from the DET gels ranged between 2.

75 ed carbon (delta(13)C), nitrogen amino acid (delta(15)NPhe), and Hg isotope (Delta(199)Hg, Delta(201)

76 precise measurements of the isotopic ratios delta(17)O and delta(18)O in CO2.

77 Here, we analyze Delta(17)O data from four places (Taipei, Taiwan; South

78 ate high-altitude region, the response, both delta(18) O and delta(13) C, is primarily to variations

79 mmediate delta(18) OV effect was highest for delta(18) O of leaf lamina water, but 40% lower on delta

80 18) O of leaf lamina water, but 40% lower on delta(18) O of main vein water.

81 plants and for our understanding of how the delta(18) O signal is incorporated into biomarkers.

82 The immediate delta(18) OV effect was highest for delta(18) O of leaf

83 A significant effect of crop cover on juice delta(18)O and fertilisation practices on pulp delta(15)

84 dance correlate with negative delta(13)C and delta(18)O anomalies, suggesting that explosive reaction

85 ory of Toba quartz traces an influx of a low-delta(18)O component into the magma reservoir just prior

86 assing two consecutive positive peaks of the delta(18)O curve (substages 13.3 and 13.1).

87 ements of the isotopic ratios delta(17)O and delta(18)O in CO2.

88 ying three BTs, electrical conductivity, and delta(18)O in high-frequency streamwater samples taken d

89 in air of known but differing delta(13)C and delta(18)O isotopic composition allows standard uncertai

90 r thousand to be achieved for delta(13)C and delta(18)O measurements, respectively.

91 rly constrained by marine records, including delta(18)O of benthic foraminiferal calcite (delta(18)Oc

92 negatively correlated with the delta(2)H and delta(18)O of feed and the delta(2)Hfat.

93 he delta(13)C and delta(15)N of pulp and the delta(18)O of juice can be considered effective tools fo

94 Both delta(13)C and delta(18)O of the aragonite are enriched above the expec

95 Here, we present another stalagmite delta(18)O record with multi-decadal time resolution fro

96 Based on our new stalagmite delta(18)O record, millennial-scale events since the mid

97 truction based on high-resolution speleothem delta(18)O records from the core region of the South Ame

98 new high-resolution deep-sea oxygen isotope (delta(18)O) record from the South Atlantic Ocean spannin

99 asonally-resolved stalagmite oxygen isotope (delta(18)O) records from Shihua Cave, North China to rec

100 nt from how it affects passive tracers, like delta(18)O, and call for caution when inferring water ma

101 sand for delta(15)N and 0.5 per thousand for delta(18)O.

102 sly, the observed phasing difference of deep delta(18)Oc likely reflects early warming of the deep no

103 ution when inferring water mass changes from delta(18)Oc records while assuming uniform changes in de

104 delta(18)O of benthic foraminiferal calcite (delta(18)Oc).

105 Fractionation of delta(15)NNO3 and delta(18)ONO3 during diffusion of nitrate through the DE

106 lution passive-samplers of delta(15)NNO3 and delta(18)ONO3 to investigate nitrogen cycling.

107 ution value of 2.7 +/- 0.4 per thousand, and delta(18)ONO3 values ranged between 18.3 +/- 1.0 and 21.

108 the circadian locomotor output cycles Kaput delta 19 N-ethyl-N-nitrosoure (ENU) mutation (ClockDelta

109 Delta(199)Hg was related to Hg levels of fish but we als

110 amino acid (delta(15)NPhe), and Hg isotope (Delta(199)Hg, Delta(201)Hg, delta(202)Hg) data for six s

111 effect: F1,68 = 5.4, P = .02, d = 0.50, and Delta = 2.4 [95% CI, 0.4-4.5]).

112 nal movements, we measured hydrogen isotope (delta(2) H) values of metabolically inert feathers and m

113 termediates in the photodenitrogenation of a Delta(2)-1,2,3-triazoline bearing a benzophenone group t

114 matrices and negatively correlated with the delta(2)H and delta(18)O of feed and the delta(2)Hfat.

115 -6.69 per thousand to +0.54 per thousand for delta(2)H, delta(13)C, and delta(37)Cl values, respectiv

116 the delta(2)H and delta(18)O of feed and the delta(2)Hfat.

117 elta(15)NPhe), and Hg isotope (Delta(199)Hg, Delta(201)Hg, delta(202)Hg) data for six species of Hawa

118 and Hg isotope (Delta(199)Hg, Delta(201)Hg, delta(202)Hg) data for six species of Hawaiian marine bo

119 s, we first constructed oncolytic adenovirus Delta-24-RGDOX expressing the immune costimulator OX40 l

120 ental information can be derived from pyrite delta(34)S records.

121 riations in the sulfur isotopic composition (delta(34)S) of sedimentary sulfate and sulfide phases ov

122 We found that delta(34)S, an indicator of sulfate reduction and habita

123 sulfur isotopic record preserved in pyrite (delta(34)Spyr) necessarily corresponds to local environm

124 per thousand for delta(2)H, delta(13)C, and delta(37)Cl values, respectively.

125 l as marked variations in Ca isotope ratios (delta(44/42)Ca).

126 on factors, is consistent with our resulting delta(56)FeNaAc.

127 In contrast, Delta(9)-tetrahydrocannabinol (Delta(9)-THC), the major

128 The main psychoactive compound in marijuana, Delta(9)-tetrahydrocannabinol (THC), and its metabolites

129 Reinforcing effects of Delta(9)-tetrahydrocannabinol (THC), the primary active

130 Bath applied Delta(9)-tetrahydrocannabinol depressed GABA cell activi

131 sible mechanism for the addictive effects of Delta(9)-tetrahydrocannabinol in juvenile-adolescents, b

132 ical for the brain's reward circuit, and how Delta(9)-tetrahydrocannabinol occludes this plasticity.

133 the synaptic remodeling that can occur after Delta(9)-tetrahydrocannabinol use.

134 rect cannabinoid receptor 1 stimulation with Delta(9)-tetrahydrocannabinol.

135 In contrast, Delta(9)-tetrahydrocannabinol (Delta(9)-THC), the major psychoactive component of canna

136 echnology, to detect and quantify CBD, CBDV, Delta(9)-THCV, and CBG in biological matrices.

137 PET), we investigated whether the effects of delta-9-tetrahydrocannabinol (delta-9-THC), the main psy

138 oncentrations of its main active ingredient, delta-9-tetrahydrocannabinol (THC), to be more harmful (

139 d by the modulation of amygdalar function by delta-9-THC and the extent of these effects are related

140 Relative to the placebo condition, delta-9-THC induced anxiety and modulated right amygdala

141 the effects of delta-9-tetrahydrocannabinol (delta-9-THC), the main psychoactive ingredient of cannab

142 stantaneous, overtone-dependent QCM data on (delta/a, -Deltaf/n) coordinates where delta is the visco

143 area (VTA) dopamine depletion had attenuated delta activity (1-4 Hz) in the medial frontal cortex (MF

144 ed periodic discharges, lateralized rhythmic delta activity, or bilateral independent periodic discha

145 reaction corresponds to the formation of the delta-adduct (the thermodynamic product).

146 Multiple imputation with delta adjustment provides a flexible and transparent mea

147 eed1Delta/Delta also excretes 10X more farnesol and while able to

148 the proofreading activity of DNA polymerase-delta, although the repair proteins Msh2, Mlh1 and Exo1

149 promotes heme biosynthesis by activation of delta-aminolevulinate synthase (ALAS), which catalyzes t

150 eta and alpha/gamma BSBHps, but not of alpha/delta analogues.

151 ite between cancers with mutated polymerases delta and epsilon, consistent with the role of these pol

152 Here we study epitaxial thin films of SrNbO3+delta and find that their bandgaps are approximately 4.1

153 g cell nuclear antigen) binds tightly to Pol delta and recruits it to the lagging strand.

154 ion is related to the scale-free dynamics of delta and theta bands, whereas this property in high-gam

155 We identified PKC delta and varepsilon as required and sufficient to activ

156 with a Zeb2 loss-of-function mutation (Zeb2(Delta)) and mice carrying a spontaneous recessive mutati

157 e replicative DNA polymerases Pol alpha, Pol delta, and Pol epsilon; and canonical maturation of Okaz

158 nscriptomes identified distinct alpha, beta, delta, and PP/gamma cell-type signatures.

159 RasGRP3 activation occurs via PKC delta- and varepsilon-dependent phosphorylation and PKC-

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

161 HDV immunoglobulin G wherein recombinant HDV delta antigen is printed by microarray on slides coated

162 sphatidylinositol-3-kinases (PI3K) gamma and delta are key regulators of T cell signaling.

163 polarization, and PKCdelta (protein kinase C delta) as a downstream target.

164 nucleotide binding (Kd , DeltaG, DeltaH, and DeltaS at 37 degrees C) and kinetic parameters for enzym

165 onal bursts, the most common of which is the delta brush.

166 terns were left and right posterior-temporal delta brushes which were associated in the left hemisphe

167 es as directing groups is evidenced by other delta-C(sp(2))-H functionalizations such as alkenylation

168 demonstrate that the [4Fe4S] cluster in Pol delta can act as a redox switch for activity, and we pro

169 (10,000 km(2)) CH4 flux map of the Mackenzie Delta, Canada, based on airborne CH4 flux data from July

170 centers in NO2-CLA located on the beta- and delta-carbons with respect to the nitro group.

171 y factors secreted by neighbouring beta- and delta-cells (paracrine regulation) have been proposed to

172 tivation of the beta-cells propagates to the delta-cells via gap junctions, and the consequential sti

173 ity via gap junction-dependent activation of delta-cells.

174 Both delta(13)C-CH4 and deltaD-CH4 correspond to the isotopic composition of the

175 essive enrichment of both delta(13)C-CH4 and deltaD-CH4 is observed with increasing distance and decr

176 CMG, and in the absence of a stabilizing Pol delta-CMG interaction, the collision release process is

177 r basal photosynthetic capacity, Ea , Hd and DeltaS co-acclimate across broad temperature ranges to d

178 t that can reliably diagnose CIRCI, although delta cortisol (change in baseline cortisol at 60 min of

179 erexpression of SAP2 or SAP5 in an efg1Delta/Delta cph1Delta/Delta mutant could restore the capacity

180 sion approach, N() -(4-azidobenzoxycarbonyl)-delta,-dehydrolysine, an allysine precursor is genetical

181 t lack EZH2 specifically in Treg cells (EZH2(Delta/Delta)FOXP3(+)).

182 respectively, Delta systolic BP P=3x10(-4), Delta diastolic BP P=5x10(-5)).

183 iazide versus noncarriers (Delta systolic BP/Delta diastolic BP: -12.3/-8.2 versus -6.8/-3.5 mm Hg, r

184 pring season and along the Mississippi River Delta during the fall season.

185 Zeb2(Delta/+) EPCs had increased neuronal differentiation com

186 or were heterozygous for the mutation (Zeb2(Delta/+) EPCs) were exposed to EDN3; we analyzed the eff

187 ice based on the model system Gd0.1 Ce0.9 O2-delta /Er2 O3 to set and tune the property of "memristan

188 Comparisons between the Jagged and Delta family show a huge diversity in the structures of

189 Tan delta findings reveal a more elastic-like behavior of th

190 t effects Microcystis blooms may have on the Delta food web were investigated.

191 By contrast, on subsecond (delta frequency) timescales, cortical oscillations can e

192 inked to K pathway spiking activity, whereas delta-frequency cortical oscillations entrain spiking ac

193 itor of phosphatidylinositol 3-kinase (PI3K)-delta/gamma isoforms currently in clinical development.

194 We found sites in river deltas had larger OC stocks (175-504 Mg/ha) than those i

195 eakest link by annotating timemin, powermin, Delta-Impmin, CFmin, FTImin, AImin, ILDmax, and ALCImin.

196 he function of the nuclear receptor PPARbeta/delta in cancer is dictated by ligand-mediated activatio

197 A comparison of the mean changes (delta) in the markers between groups showed that TGF-bet

198 ect was preserved in vivo after ex vivo PI3K-delta inhibition in CD8(+) T cells destined for adoptive

199 the discovery of a highly selective PI3Kbeta/delta inhibitor displaying excellent pharmacokinetic pro

200 sitol-3-kinase (PI3K) alpha/delta (PI3Kalpha/delta) inhibitor AZD8835 showed marked potency in ABC DL

201 ed in the presence of PI3K-alpha, -beta, or -delta inhibitors.

202 gh-threshold, as a result of a predominant A-delta input to high-threshold neurons, but not wide dyna

203 Collectively, our results show that PI3K delta is essential for survival during sepsis.

204 -doping of strontium and iron into PrBaCo2O5+delta is found to be very effective in enhancing intrins

205 ta on (delta/a, -Deltaf/n) coordinates where delta is the viscous penetration depth, a is the particl

206 Consequently, this study establishes that DeltaS is proportional to S0 and that the %Cvn is conser

207 p38 mitogen-activated protein kinase (MAPK) delta isoform (p38delta) is a poorly studied member of t

208 combines STRUCTURE analysis with the Evanno Delta K analysis and visualization of results using STRU

209 Pol delta, like bacterial replicases, undergoes collision re

210 hanced Notch1 binding to and activation from Delta-like 1, while modifications at EGF6 and EGF36 (add

211 Although Notch signaling mediated by Delta-like 1/4 (DLL1/4) Notch ligands has emerged as a m

212 esponsible for induction of the Notch ligand delta-like 4 (DLL4) in endothelial cells, we find that a

213 tracellular domain (ICD) of the Notch ligand Delta-like 4 (DLL4).

214 Recent studies have shown that Delta-like ligand 4 (Dll4) was upregulated on APC after

215 the balance between Notch ligands by driving Delta-like ligand 4 (Dll4) while repressing Jagged1 (Jag

216 ass antibody-drug conjugate directed against delta-like protein 3 (DLL3), a novel target identified i

217 Like the Pabpn1+/A17 mice, Pabpn1+/Delta mice have mild histologic defects, shorter poly(A)

218 in both wild-type Hsp90alpha and Hsp90alpha-Delta mice.

219 mediated vasodilation was blunted in ECSHIP2(Delta/+) mice, as was aortic nitric oxide bioavailabilit

220 ation rate was reached at 25% RH and 45% for delta-MnO2 and gamma-MnO2, respectively, possibly due to

221 reactivity towards SO2 uptake was highest on delta-MnO2 but lowest on beta-MnO2, with a geometric upt

222 3D porous nanostructures built from 2D delta-MnO2 nanosheets are an environmentally friendly an

223 nganates of varying initial vacancy content (delta-MnO2, hexagonal birnessite, and triclinic birnessi

224 transformation of a synthetic, Mn(III)-rich delta-MnO2.

225 SAP2 or SAP5 in an efg1Delta/Delta cph1Delta/Delta mutant could restore the capacity to cause immunop

226 f C. albicans bcr1Delta mutant and bcr1Delta/Delta mutant, which is known to be severely defective in

227 ayers was discovered within [(Pbx Sn1-x Se)1+delta ]n (TiSe2 )1 heterostructures using electron micro

228 the critical roles of volume of activation (Delta( not equal) V) and reaction volume (DeltaV) in und

229 We profile two such genes, Delta/Notch-like EGF repeat containing (Dner) and nuclea

230 s anti-Ri; 0.016%) and PCA-Tr (also known as delta/notch-like epidermal growth factor-related recepto

231 rns of erosion and accretion along the large deltas of the main rivers in the Arctic.

232 n release process is triggered, ejecting Pol delta on the leading strand.

233 Activation of the delta-opioid receptor (DOR) produces similar analgesia w

234 gnancy hormones (estrogen and progesterone), delta-opioid receptors, and T cells of the adaptive immu

235 l and genetic data suggest the importance of delta-opioid receptors.

236 re movement ceases, coherent thalamocortical delta oscillations (1-5 Hz) develop, distinct from concu

237 le mixed anaerobic enrichments from a Mekong Delta paddy soil.

238 n completing replication, and we propose Pol delta-PCNA collides with the slower CMG, and in the abse

239 uator based on the model material PrxCe1-xO2-delta (PCO).

240 wn, but sequence analysis has suggested that delta peptide could be a viroporin, belonging to a diver

241 information suggests a critical role for the delta peptide in Ebola virus disease pathology and as a

242 The function of the delta peptide is unknown, but sequence analysis has sugg

243 We show here that the Ebola virus delta peptide, a conserved nonstructural protein produce

244 esidue nonstructural polypeptide, called the delta peptide, that is produced in abundance during Ebol

245 e phosphatidylinositol-3-kinase (PI3K) alpha/delta (PI3Kalpha/delta) inhibitor AZD8835 showed marked

246 Inhibition of phosphatidylinositol 3-kinase delta (PI3Kdelta), a linchpin in the pre-B-cell receptor

247 endent for co-dependency on protein kinase C delta (PKCdelta).

248 a sucrose injection experiment in the Bengal Delta Plain to guide our model development and to constr

249 TDW maintenance in baseline wake and blunted delta power in SWS, reproducing, respectively, narcoleps

250 REM sleep frontal high delta power was a negative correlate of intelligence.

251 sitions between responsive states, while the delta power/connectivity changes were consistent with th

252 e peroxisome proliferator-activated receptor-delta (PPAR-delta), which is implicated in bile acid hom

253 Peroxisome proliferator-activated receptor delta (PPARdelta) regulates many genes involved in lipid

254 g Okazaki fragment length by restricting Pol delta progression.

255 e inhibition of the extracellular Hsp90alpha-Delta protein function by a monoclonal antibody targetin

256 s 889 to 1289 encompassing the 3' end of the delta protein-coding gene.

257 actors, pretreatment radiomics features, and delta-radiomics features.

258 nsitivity that fluctuate rhythmically in the delta range (at approximately 3 Hz), commencing approxim

259 When interpreted in terms of delta resilience, high nER configurations reflect an inc

260 We recorded from OFF delta retinal ganglion cells in the guinea pig retina an

261 Classical learning algorithms, such as the delta rule with constant learning rate, are not optimal.

262 nine protein kinase 2 (SRPK2) phosphorylates delta-secretase and enhances its enzymatic activity.

263 Our findings support that delta-secretase phosphorylation by SRPK2 plays a critica

264 delta-secretase, also known as asparagine endopeptidase

265 ntrast, inhibition of CIN firing with the mu/delta selective opioid [Met(5)]enkephalin (1 mum) decrea

266 te, however, a unified theory explaining how deltas self-organize to distribute water and sediment up

267 etermination by lateral inhibition via Notch/Delta signalling has been extensively studied.

268 We identified a 2- to 4-Hz delta signature that modulated posterior alpha activity

269 olera has emerged and spread from the Ganges Delta six times and from Indonesia once to cause global

270 infilling of GRK after 6 ka when the Indus delta started to grow.

271 s to intrasubunit sites within the alpha and delta subunits, photolabeling alphaVal-218 (alphaM1), de

272 Third, delta suppresses alpha6 synaptic localization by prevent

273 Activated PI3K Delta Syndrome (APDS) is a primary immunodeficiency dise

274 3/-8.2 versus -6.8/-3.5 mm Hg, respectively, Delta systolic BP P=3x10(-4), Delta diastolic BP P=5x10(

275 e to hydrochlorothiazide versus noncarriers (Delta systolic BP/Delta diastolic BP: -12.3/-8.2 versus

276 erent material phases: the perovskite SrCoO3-delta, the brownmillerite SrCoO2.5, and a hitherto-unexp

277 in Saccharomyces cerevisiae polymerase (Pol) delta, the lagging strand DNA polymerase.

278 delta, theta, and low-gamma oscillations followed the no

279 h the insertion of silence gaps, LRTC in the delta, theta, and low-gamma oscillations resumed the low

280 ave sleep, and for EEG spectral power in the delta, theta, and sigma ranges.

281 the individual subject scaling exponents of delta/theta oscillations, the greater the comprehension

282 ding to synchronized oscillations spanning d delta to beta frequencies; (2) the network can reach a b

283 artly attributed to miR-1 directly targeting Delta to decrease Notch signaling.

284 tagonistic effects were observed for (lutein-delta-tocopherol) and (alpha-tocopherol-delta-tocopherol

285 tein-delta-tocopherol) and (alpha-tocopherol-delta-tocopherol).

286 decrease in the concentration of gamma- and delta-tocopherol, as well as in the IP.

287 ha-tocopherol, beta-tocopherol, -tocopherol, delta-tocopherol, beta-tocotrienol, -tocotrienol, and de

288 opherol, beta-tocotrienol, -tocotrienol, and delta-tocotrienol.

289 ence factor PSMalpha, but not alpha-toxin or delta-toxin, contributed to the skin inflammation, which

290 Here, we report that centrioles in delta-tubulin and epsilon-tubulin null mutant human cell

291 ents in unicellular eukaryotes indicate that delta-tubulin and epsilon-tubulin, two less-studied tubu

292 ingly pervasive in the San Francisco Estuary Delta (USA) since the early 2000s and their rise has coi

293 several common monomers, including lactide, delta-valerolactone, epsilon-caprolactone, a cyclic carb

294 latory response (Delta VE control 74 +/- 6%, Delta VE AOPCP 64 +/- 5%, P < 0.05).

295 decreased the hypoxic ventilatory response (Delta VE control 74 +/- 6%, Delta VE AOPCP 64 +/- 5%, P

296 d changes in hepatitis B virus and hepatitis delta virus (HDV) viral loads (VL) during tenofovir-cont

297 osion potential is an important indicator of delta vulnerability.

298 fferent morphologies (alpha, beta, gamma and delta) was investigated using flow tube reactor and in s

299 proliferator-activated receptor-delta (PPAR-delta), which is implicated in bile acid homoeostasis.

300 using Rad51, Rad54, RPA, RFC, DNA Polymerase delta with different forms of PCNA.

301 We first compared super-delta with four commonly used normalization global, medi