ライフサイエンスコーパス: Z

1 Z-curve for trial sequential analyses of mortality assoc

2 Z-DNA-binding protein 1 (ZBP1) is an innate immune senso

3 Z-DNA-binding protein 1 (ZBP1; also known as DAI or DLM-

4 Z. tritici infection is symptomless for around 10 days,

5 Z = 0.023; P = 0.509) nor AFP model (-0.014, Z = -0.021; P = 0.492) provided significant net reclassi

6 Neither Metroticket 2.0 criteria (0.014, Z = 0.023; P = 0.509) nor AFP model (-0.014, Z = -0.021;

7 nctioning aortic valve was estimated at 0.05 Z score unit per year.

8 nged and expressed as two clusters: soxXY(1) Z(1) AB and soxCDY(2) Z(2) H, and sulfate was the sole m

9 Despite the absence of the soxXY(1) Z(1) AB cluster, strain CVO oxidized S(0) to thiosulfate

10 he soxCDY(2) Z(2) H cluster and not soxXY(1) Z(1) AB.

11 compounds: (E)-1-cyano-1,3-butadiene (E-1), (Z)-1-cyano-1,3-butadiene (Z-1), 4-cyano-1,2-butadiene (2

12 Higher concentrations of 13-Z- and 9-Z-zeaxanthin were identified in puffed grains (

13 yield, >98:2 alpha:gamma selectivity, >98:2 Z:E selectivity, and >99:1 enantiomeric ratio.

14 of model system PBDB-TF:Y6 (Y6 = 2,2'-((2Z,2'Z)-((12,13-bis(2-ethylhexyl)-3,9-diundecyl-12,13-dihydro

15 oil field strain CVO has only the soxCDY(2) Z(2) H cluster and not soxXY(1) Z(1) AB.

16 te and sulfate, demonstrating that soxCDY(2) Z(2) H genes alone are sufficient for S(0) oxidation in

17 two clusters: soxXY(1) Z(1) AB and soxCDY(2) Z(2) H, and sulfate was the sole metabolic end product.

18 ic acid (2) and 3alpha-hydroxytirucalla-7,24 Z-dien-27-oic acid (3).

19 nge in regioselectivity from 2:1 (E) to 1:5 (Z) for the monoacetylated products at room temperature.

20 dihydrodipyrrin afforded the enone (E, 70%; Z, 3%); subsequent double-ring cyclization of the E-enon

21 Higher concentrations of 13-Z- and 9-Z-zeaxanthin were identified in puffed grains (2x and 37

22 Aortic Z scores were determined, and a Z-score calculator was created for this population.

23 s further demonstrate that MnBi(4)Te(7) is a Z(2) antiferromagnetic TI with two types of surface stat

24 H-ketimines in situ, which then react with a Z-allyl boronate.

25 nient route has been demonstrated to access (Z)-1,2-diazido alkenes from the corresponding 1,2-diboro

26 Additionally, Z-nucleotide derivatives (AICAr, AICA) are detected at h

27 in analyses of HC data only, Weight for Age Z-score [WAZ]) regression to account for interaction bet

28 D was positively associated with BMI-for-age Z >1 and maternal education.

29 r underweight subgroups using weight-for-age Z-score (WAZ) thresholds of -2 and -3.

30 issue of Infection and Immunity, Hoy et al. (Z.

31 two Zalpha domains that bind Z-DNA(4,5) and Z-RNA(6-8).

32 lack the canonical FtsZ-membrane anchors and Z-ring regulators described for E. coli.

33 Benzodiazepines and Z-drugs are two of the most prescribed agents worldwide.

34 The biological function of Z-DNA and Z-RNA, nucleic acid structures with a left-handed double

35 o the small energy differences between E and Z isomers of trisubstituted alkenes (compared with 1,2-d

36 rination of alkynes to access both the E and Z isomers of vinyl fluorides.

37 different adduct distribution for the E and Z isomers, indicating that the covalent bis-functionaliz

38 E- and Z-dienes react in a stereoconvergent fashion, providing

39 vinyl cation intermediates, with the E- and Z-hydrofluorination products forming under kinetic and t

40 leading to failure in borosilicate glass and Z-cut quartz.

41 ing loss-of-function mutation intolerant and Z-scores of observed/expected synonymous and non-synonym

42 viation, intact 3D spheroidal morphology and Z' values above 0.5, and hence confirming their amenabil

43 antitrypsin (AAT), Null Hong Kong (NHK), and Z (ATZ), in Man1b1 knockout HEK293T cells were monitored

44 tween Z-crotyl-B(pin) (pin = pinacolato) and Z-dichloroethene, both of which are commercially availab

45 ses of western Baltic Sea F. vesiculosus and Z. marina populations to simulated near-natural marine h

46 clei collectively), external cuneate, X, and Z nuclei, and the median accessory nucleus.

47 l)-3,4-diphenylhex-3-ene-1,6-dione (D1) and (Z)-2,2'-(1,2-diphenylethene-1,2-bis(benzofuran-3(2H))-on

48 es of the E2' reactions leading to (E)- and (Z)-1-cyano-1,3-butadiene (1) were analyzed by density fu

49 Methyl, ethyl and (Z)-3-hexenyl benzoate with 50% of the volatile compositi

50 catalytic reactions: DPA hydrogenation and (Z)-stilbene isomerization.

51 ticular compounds (Z)-10-tritriacontene and (Z)-6-pentadecene, previously associated with unhealthy h

52 Similarly, antioxidant (Z)-N-tert-butyl-1-(2-chloro-6-methoxyquinolin-3-yl)metha

53 The mean ascending aorta Z score progression rate for BAV patient with a normally

54 Aortic Z scores were determined, and a Z-score calculator was c

55 post-translational modification of aquaporin Z (AqpZ), and surpasses previous reports of sequence cov

56 ermeability, which is about 50% of aquaporin Z's capacity, makes channel 1 the fastest among the exis

57 Proximal aorta diameters (expressed as Z scores) were modeled in relation to age and potential

58 icacy for dealing with problem behaviours at Z = 2.44 (I(2) = 0, SMD = 0.36, 95%CI = 0.05 to 0.67, p

59 um to large effect on reducing depression at Z = 1.99 (SMD = -0.74, 95%CI = -1.47 to -0.01, p = .05),

60 lum (SR) junctional cisternae, and apo-GP at Z disk.

61 ather than from genetic incompatibilities at Z-linked loci.

62 gical functions and establish a link between Z-RNA sensing via the Zalpha2 domain and promotion of in

63 ugh stereoretentive cross-metathesis between Z-crotyl-B(pin) (pin = pinacolato) and Z-dichloroethene,

64 r that contains two Zalpha domains that bind Z-DNA(4,5) and Z-RNA(6-8).

65 ted with HIV with low lumbar spine (LS) BMD (Z score < -1.5) were randomized to receive once-weekly a

66 , with a median immediate improvement in BMI Z-score of 0.2 per month following the institution of ga

67 essed this isomerization in the case of both Z- and E-PB and PI.

68 cell division site, involving FtsZ bundling, Z-ring tethering and membrane reshaping activities that

69 -butadiene (E-1), (Z)-1-cyano-1,3-butadiene (Z-1), 4-cyano-1,2-butadiene (2), and 2-cyano-1,3-butadie

70 gh OAVs were determined for ethyl butanoate, Z-3-hexenal, linalool and methyl benzoate responsible fo

71 Expression of ECG variables by Z-scores lends an objective and reproducible evaluation

72 itical to the success of this system, called Z-lock, is that the linkers connecting the dimer compone

73 rifurcated fiber optic assembly, a capillary Z-type flow cell, and photodiodes.

74 l transitions to CDN "Y" and back or to CDN "Z" and back.

75 ion of CDN "X" to CDN "Y" or CDN "X" to CDN "Z".

76 y was defined as having a head circumference Z score <-2 according to the 2000 US Centers for Disease

77 plexus in 24.5% +/- 2.4% of flattened colon Z-stack area.

78 ion proportion; (2) Relative to the combined Z values of depressive symptoms and processing speed, sl

79 the hypothesis that the cuticular compounds (Z)-10-tritriacontene and (Z)-6-pentadecene, previously a

80 We provided 280 adult human colon confocal Z-stacks from persons without known bowel motility disor

81 than its unique tetranuclear active site Cu(Z), the binuclear electron entry point Cu(A) is also uti

82 yr, and Trp showed that although both the Cu(Z) and Cu(A) sites were present in all the variants, onl

83 to the effect of the Z-value reduction (Z(D)/Z(F) from 3 to 20).

84 cross-coupling can then furnish the desired Z-homoallylic alcohol in high enantiomeric purity.

85 ose left ventricular end-diastolic dimension Z score before intervention is >2, irrespective of basel

86 y revealed that ZnTPP-P-Ipa partly displaced Z-(Aib)(6)-Ipa, forming a coadsorbed monolayer on the ox

87 dominant haplotypes more evenly distributed; Z. cucurbitae has a single dominant haplotype with close

88 es include epigenetic modifiers of the ESC/E(Z) complex, an effector of response to ovarian steroids.

89 ective conversion of the cryptand to the E,E,Z isomer inside CB[8].

90 n is stereospecific in the regard that the E-Z-geometry of the olefin governs the stereochemistry of

91 nerate (E)-1-cyano-1,3-butadiene (1) (10:1 E/Z) via tandem S(N)2 and E2' reactions.

92 lkyl bromides (>130 examples, mostly >95:5 E/Z, >20:1 rr).

93 dienes that are commercially available as E/Z mixtures to be used as substrates for the cycloadditio

94 At (E/Z)-ratios of 75 and 23%, rhodoxanthin (E/Z)-isomer mixtu

95 rovided several epoxypolyenes as expected (E/Z, ca. 2-3:1).

96 observation of cyclic structures (MALDI), E/Z isomerism from maleic to fumaric acid, and the statist

97 hin across an unprecedented wide range of (E/Z)-ratios by thermal (E/Z)-isomerization, lyotropic aggr

98 (E/Z)-ratios of 75 and 23%, rhodoxanthin (E/Z)-isomer mixtures in acetone revealed color hues (CIE-h

99 Lyotropic aggregation of rhodoxanthin (E/Z)-isomer mixtures in acetone/water yielded red (CIE-h d

100 ted wide range of (E/Z)-ratios by thermal (E/Z)-isomerization, lyotropic aggregation, and two differe

101 ective bromoboration of acetylene yielding E/Z mixtures of dibromo(bromovinyl)borane with the Z-isome

102 ions solubilization in tomato seed oil and E:Z ratios of 75:25, 59:39 and 25:75, full and partial equ

103 copene (lyc) amount and (all-E)-lyc:Z-lyc (E:Z) ratio as driving parameters of the tomato pomace (TP)

104 pe 3-vectored Ebola Zaire vaccine (ChAd3-EBO-Z) and boosted with modified vaccinia Ankara Ebola Zaire

105 accinia Ankara Ebola Zaire-vectored (MVA-EBO-Z) vaccine.

106 The efficient Z-selective cross-metathesis between acrylamides and com

107 tion, and a modified Horner-Wadsworth-Emmons Z-selective olefination.

108 vide evidence that the sensing of endogenous Z-form nucleic acids by ZBP1 triggers RIPK3-dependent ne

109 Excellent Z/E-stereoselectivity has been achieved with cheap and v

110 onstrate HTS compatibility with an excellent Z'-factor of 0.67 +/- 0.03.

111 s in high to excellent yields with exclusive Z diastereoselectivity.

112 al expression, providing evidence for a fast-Z effect.

113 live mouse imaging of RIT labeled with FNIR-Z-759.

114 ta shows that the reduction of gene flow for Z-linked loci primarily reflects female-biased gene flow

115 r modeling program for designing linkers for Z-lock.

116 repair complex, Msh2-Msh3, are required for Z-DNA-induced genetic instability in yeast and human cel

117 ptic Ca(2+) are necessary and sufficient for Z-LTD induction.

118 FtsZ and SepF for formation of a functional Z-ring in C. glutamicum.

119 he unprecedented and densely functionalized (Z)-alpha-phosphino-beta-boryl acrylate products.

120 [Y = U or C]), glutamic acid (coded by GAZ [Z = A or G]), glycine (coded by GGX), Ser (coded by AGY)

121 ver 20-fold enhancement in binding upon E -> Z isomerization, which can be triggered with red light.

122 ansition dipole moment between reversible E->Z photoisomerization to the microscopic torque can quali

123 H2A.Z initially localizes downstream of the transcription st

124 H2A.Z.1 and H2A.Z.2 can replace each other at Transcription

125 s already present downstream, additional H2A.Z accumulates upstream.

126 ate that the balance between H2A.Z.1 and H2A.Z.2 at promoters is critically important to regulate spe

127 H2A.Z.1 and H2A.Z.2 can replace each other at Transcription Start Sites,

128 rometry analysis showed that H2A.Z.1 and H2A.Z.2 have specific interactors, which can mediate their f

129 r data indicate that the balance between H2A.Z.1 and H2A.Z.2 at promoters is critically important to

130 of H2A with the evolutionarily conserved H2A.Z via the SWR1 histone chaperone complex has been extens

131 This hierarchical H2A.Z accumulation coincides with improved nucleosome positi

132 stone acetyltransferase NuA4 and histone H2A.Z exchanger SWR1.

133 ic regulators of memory, whereby histone H2A.Z suppresses fear memory.

134 cleosomes with the non-canonical histone H2A.Z, thereby focusing the pathway on select sites such as

135 of the transcription start site, and if H2A.Z is already present downstream, additional H2A.Z accumu

136 Using conditional-inducible H2A.Z knockout (cKO) mice, we showed that H2A.Z binding is h

137 These findings link H2A.Z eviction to transcription initiation, promoter escape

138 1 nucleosomes genome-wide would obligate H2A.Z turnover, we propose that global transcription at yeas

139 The localization of H2A.Z almost exclusively at the +1 nucleosome suggests that

140 omoters, suggesting that the presence of H2A.Z is not related to transcriptional control.

141 little is known about how a reduction of H2A.Z levels can be achieved.

142 However, the determinants of H2A.Z occupancy at specific nucleosomes and its relationship

143 cessibility through subtle refinement of H2A.Z patterns, providing a means to reprogram chromatin sta

144 activity, are essential determinants of H2A.Z positioning in vicinity of the promoters, suggesting t

145 incorporates H2A.V (the fly ortholog of H2A.Z) genome-wide in an ATP-dependent manner, like the yeas

146 ow that NRP proteins cause a decrease of H2A.Z-containing nucleosomes in Arabidopsis under standard g

147 eby preventing excessive accumulation of H2A.Z.

148 promoters is responsible for eviction of H2A.Z.

149 2A.Z knockout (cKO) mice, we showed that H2A.Z binding is higher in females and that H2A.Z cKO enhanc

150 .Z binding is higher in females and that H2A.Z cKO enhanced fear memory only in males.

151 ngle-molecule resolution, and found that H2A.Z eviction is dependent on RNA Polymerase II (Pol II) an

152 These data suggest that H2A.Z may be a sex-specific epigenetic risk factor for PTSD

153 Mass spectrometry analysis showed that H2A.Z.1 and H2A.Z.2 have specific interactors, which can med

154 karyotic transcription to erasure of the H2A.Z epigenetic signal.

155 The H2A.Z histone variant, a genome-wide hallmark of permissive

156 multiple chromatin marks, including the H2A.Z histone variant, H3K4me3 modification, and nucleosome

157 We tracked H2A.Z in living yeast at single-molecule resolution, and fou

158 s implicated in removing histone variant H2A.Z from the -1 and +1 nucleosomes flanking NDRs; however,

159 osomes incorporating the histone variant H2A.Z.

160 ased toward females, we examined whether H2A.Z cKO also has sex-specific effects on fear sensitizatio

161 formation (heptanal, (E,E)-2,4-heptadienal, (Z)-2-heptenal, octanal, pentanal, (E)-2-hexenal, (E)-2-o

162 High Z(va) and low tricuspid annulus plane systolic excursion

163 Irrespective of treatment arm, high Z(va) and low tricuspid annulus plane systolic excursion

164 yclic alkene is generally obtained with high Z selectivity.

165 ere identified using Z-scores of LGI (hyper: Z >= 2.58, hypo: Z <= - 2.58).

166 ing Z-scores of LGI (hyper: Z >= 2.58, hypo: Z <= - 2.58).

167 Valvulo-arterial impedance (Z(va)), which reflects total left ventricular hemodynami

168 These results implicate Z-RNA as a new pathogen-associated molecular pattern and

169 cal shift perturbations for methyl groups in Z AAT (E342K).

170 In contrast, no corresponding skew in Z genotype was detected in their (hemizygous) sisters.

171 Incremental Z-score values between -2.5 and 2.5 were calculated to e

172 y cotreatment with the pan-caspase inhibitor Z-VAD-FMK.

173 ygdala, occipitotemporal cortex, and insula (Z > 2.3; p < 0.05; whole-brain corrected).

174 Our method, PIZSA (Protein Interaction Z-Score Assessment), is a binary classification scheme f

175 s (approximately 10%-20%) with heavier ions (Z >= 3) contributing the remainder.

176 e isomerization of the (E)-azobenzene to its Z isomer enhances diol binding, and the magnitude of thi

177 sformation of natural product ligustrazine, (Z)-N-tert-butyl-1-(3,5,6-trimethylpyrazin-2-yl)methanimi

178 also adopt alternative DNA structures, like Z DNA, triplexes, G quadruplexes, and I motifs.

179 idered lycopene (lyc) amount and (all-E)-lyc:Z-lyc (E:Z) ratio as driving parameters of the tomato po

180 3-(anthracen-9-yl)allylidene)malononitrile ((Z)-DVAM) can be continuously actuated when exposed to a

181 to store thermal energy in their metastable Z isomer liquid phase and release the energy by opticall

182 association studies using Z-scores, modified Z'-scores, p-values and Jaccard indices.

183 What is more, Z-trisubstituted allyl boronates may be used.

184 Moreover, Z tests revealed that the correlations between the resti

185 lly attaching the sarcolemma to myofibrillar Z-lines.

186 two crucial classification parameters named Z(1kHz) and IPS (impedance phase slope in the frequency

187 ylpropionate, and two new compounds, namely (Z)-1,6-bis(2-hydroxyphenyl)-3,4-diphenylhex-3-ene-1,6-di

188 the Dirac and flat bands, endowing a nonzero Z(2) invariant to the flat band.

189 ich suggests that ZBP1 may recognize nuclear Z-form nucleic acids.

190 omal structures, including recently observed Z-loops.

191 s appears to be responsible for the observed Z-selectivity.

192 y correlated with their temporal occurrence (Z = 3.43, p = 2.7e-04).

193 The biological function of Z-DNA and Z-RNA, nucleic acid structures with a left-han

194 Homozygosity of Z chromosome blocks was produced by daughter-father back

195 We found that upon U. maydis infection of Z. mays, KWL1-b is expressed at significantly lower leve

196 A in eukaryotes, representing a mechanism of Z-DNA-induced genomic instability.

197 red boramidine, which exists as a mixture of Z and E isomers.

198 Furthermore, a monolayer of Z-(Aib)(6)-Ipa on TiO(2)(110) was exposed for different

199 ommon to all tissues, a higher proportion of Z-linked genes than autosomal genes showed differential

200 and omission tests, showed the relevance of Z-3-hexenal, linalool and methyl benzoate as odour activ

201 emonstrating remarkable thermal stability of Z isomers at high temperatures and liquid-phase stabilit

202 Herein, a metal-free domino synthesis of Z-selective alpha,beta-diphenylthio enones is developed

203 hat can be used to prepare a wide variety of Z-homoallylic alcohols with significantly higher efficie

204 hese results confirm biological activity of (Z)-6-pentadecene and reveal (Z)-10-tritriacontene as a n

205 olecular crystalline microwires composed of (Z)-2-(3-(anthracen-9-yl)allylidene)malononitrile ((Z)-DV

206 Changes of -omega*Z(imag), an impedance factor that gives information of t

207 sis of conjugated polyenes with at least one Z-configured C=C bond.

208 of responses measured in both species, only Z. marina growth was impaired by the accumulative heat s

209 ts with the lowest use of benzodiazepines or Z-drugs (odds ratio=1.08, 95% CI=1.01, 1.15) compared wi

210 sociations between use of benzodiazepines or Z-drugs and subsequent dementia, even when exposures wer

211 and the cumulated dose of benzodiazepines or Z-drugs at baseline were not associated with dementia.

212 f patients had any use of benzodiazepines or Z-drugs, and during the median follow-up of 6.1 years (i

213 r is the viral protein Zta (BZLF1, ZEBRA, or Z).

214 al conserved uORF, herein referred to as ORF-Z, was also found in exon 2 of POLG.

215 nts cause amino acid changes in ORF-Y or ORF-Z.

216 ystem that mimics the natural photosynthetic Z-scheme.

217 PI Z-containing compound heterozygotes (ZS/ZV(R); n = 7) ha

218 sease cohort, we confirmed the effects of PI Z heterozygote and compound heterozygote genotypes.

219 INA1.Measurements and Main Results: White PI Z heterozygotes confirmed by sequencing (MZ; n = 74) had

220 ared with 1,411 white individuals without PI Z, S, or additional rare variants denoted as V(R).

221 Homozygosity for the Pi*Z variant of the gene that encodes the alpha-1 antitryps

222 otype, but higher than adults without the Pi*Z variant.

223 biochemical features associated with the Pi*Z variant.

224 Notably, the products possess Z-stereochemistry with regard to the exocyclic C=C doubl

225 which these complexes recognize and process Z-DNA in eukaryotes, representing a mechanism of Z-DNA-i

226 on in the structured limbs-exercise program (Z= 9.294, p<0.01); (3) Processing speed was affected by

227 haping activities that are needed for proper Z-ring assembly and function.

228 activated protein C, protein S, and protein Z.

229 The polar organizing protein Z (PopZ) is necessary for the formation of three-dimensi

230 ase plane distances observed in prototypical Z-DNA CpG steps remains unclear.

231 composition of their E-isomer provided pure (Z)-(2-bromovinyl)boronates in 57-60% overall yield.

232 able to the effect of the Z-value reduction (Z(D)/Z(F) from 3 to 20).

233 induced down-regulation of immune regulator Z-DNA binding protein 1.

234 al activity of (Z)-6-pentadecene and reveal (Z)-10-tritriacontene as a novel hygiene trigger.

235 of the model chromophore leads to reversible Z -> E photoisomerization followed by reversible photocy

236 Nineteen white heterozygotes for five non-S/Z coding variants associated with lower alpha-1 antitryp

237 SI-Z in patients with previous ablation (SI-Z: coefficient, 0.004; P<0.001 and LGE: coefficient, 0.0

238 trogram fractionation was associated with SI-Z (coefficient, 0.012; P=0.03) and LGE (coefficient, 0.0

239 gram activation delay was associated with SI-Z in patients with previous ablation (SI-Z: coefficient,

240 tion induced LTP of synaptic zinc signaling (Z-LTP), evidenced by enhanced zinc-mediated inhibition o

241 f size, with small (DeltaAla), medium-sized (Z-DeltaAbu), and bulky (DeltaVal) DeltaAAs exerting simi

242 More specifically, Z-chloro-substituted allylic pinacolatoboronate is first

243 al, or combined) for generating liquid-state Z isomers capable of storing thermal energy.

244 le cells of the pigmented E. gracilis strain Z and two bleached mutants that lack detectable plastid

245 the lipid composition of E. gracilis strain Z mitochondria and plastids, and of plastid subfractions

246 FtsZ is the polymeric, ring-like structure (Z-ring) assembled at the future division site during cel

247 an alkyl-, a chloro-, or a bromo-substituted Z-alkene, can either be purchased or prepared by catalyt

248 Here, we discover that Z-DNA is mutagenic in yeast as well as human cells, and

249 ion, and drift, and our results suggest that Z-linkage of SCN4A may make significant contributions to

250 sensor probing zinc release, supported that Z-LTD is expressed, at least in part, via reductions in

251 The Z allele of SERPINA1 encodes a mutant AAT, named ATZ, th

252 tary lipid content that strongly affects the Z-value of the diet, the capability of an animal to dige

253 ion was carried out between polymers and the Z-1,4-diacetoxy-2-butene as a chain transfer agent in di

254 o influences the BMF(lim) by controlling the Z-values of their feces and the volume reduction of the

255 between two gapped states changes either the Z(2) invariant or the locally stable valley Chern number

256 seased livers of children homozygous for the Z allele.

257 human livers of patients homozygous for the Z allele.

258 cell surface for the proper location for the Z-ring.

259 served and with complete selectivity for the Z-stereoisomer.

260 cle where it spans half a sarcomere from the Z-disc to the M-band and is essential for muscle organis

261 domains, which bind to nucleic acids in the Z-conformation.

262 which is evidenced also to take part in the Z/E isomerization of the product.

263 t formation and subsequent assembly into the Z-ring are still not understood.

264 two-step excitation processes mimicking the Z-scheme of natural photosynthesis are currently develop

265 s in understanding the dynamic nature of the Z-ring and its role in coordinating septal cell wall syn

266 ZBP1 sensing of the Z-RNA produced during influenza virus infection induces

267 4 to 15) was comparable to the effect of the Z-value reduction (Z(D)/Z(F) from 3 to 20).

268 antitative PCR, we show that SCN4A is on the Z chromosome in Thamnophis and other advanced snakes.

269 on autosomes and mitochondria but not on the Z chromosome.

270 ed reactions are proposed to rationalize the Z-selective allyl additions.

271 otofilaments form a ring-like structure, the Z-ring, in most bacterial species.

272 We tested the hypothesis that the Z chromosome in the butterfly Bicyclus anynana carries a

273 While it is clear that the Z-ring plays an essential role in orchestrating cytokine

274 Photoisomerization to the Z isomer transforms the intercalator into a chain capper

275 Photoisomerization of the E- to the Z-azobenzene catalyst (monitored via NMR) with an LED (l

276 ocalization away from the A-band towards the Z-disk of the sarcomere.

277 xtures of dibromo(bromovinyl)borane with the Z-isomer as a major product (up to 85%).

278 ds of analysis that we applied here with the Z. mobilis transposon mutant dataset, could easily be ut

279 cation intermediate required to produce the (Z)-C8,C9 alkene bond in sobralene has identified new con

280 While the (Z) geometry is predominant in nature, only a handful of

281 Moreover, these Z nucleotides are shown to also activate the nonrelated

282 Both ERCC1-XPF and MSH2-MSH3 bind to Z-DNA-forming sequences, though ERCC1-XPF recruitment to

283 rease in length when switching from the E to Z isomer of m-BTA in the copolymer with inert a-BTA.

284 Both technologies induced E-to Z-isomerization of all-E-lutein and puffing also of all-

285 g sequences, though ERCC1-XPF recruitment to Z-DNA is dependent on MSH2-MSH3.

286 between colony-level hygienic responses to (Z)-10-tritriacontene and the traditional freeze-killed b

287 What is more, trisubstituted Z-alkenyl chloride moiety can be accessed with similar e

288 le: The role of PI (protease inhibitor) type Z heterozygotes and additional rare variant genotypes in

289 981 radiomic features were extracted using Z-Rad software implementation.

290 n in 68 cortical areas were identified using Z-scores of LGI (hyper: Z >= 2.58, hypo: Z <= - 2.58).

291 and comparison of association studies using Z-scores, modified Z'-scores, p-values and Jaccard indic

292 rmative ECG standards in the young utilizing Z-scores.

293 -BMF(lim)) by determining the ratio of the V.Z-products of undigested and digested food.

294 When Z-RNA is sensed, ZBP1 recruits RIPK3 and caspase-8 to ac

295 ures in female heterozygous animals, whereas Z-band streaming could be observed in the jump muscle of

296 onjugate addition at room temperature, while Z-DeltaAbu- and DeltaVal-containing peptides were inert

297 y of proteins under optogenetic control with Z-lock.

298 library size and positively correlated with Z' value for the assay.

299 stabilizing the isomers of the cryptand with Z-configurations.

300 damascenone and massoia lactone, likely with Z-1,5-octadien-3-one for fruit-in-syrup and alcoholic no

301 Ye Z, Rochwerg B, Wang Y, et al.