ライフサイエンスコーパス: Z

1 Z score models involved indexed parameters (X/BSA(alpha)

2 Z tests were used to compare cancers on DM versus DBT ex

3 Z-DNA-binding protein 1 (ZBP1), initially reported as an

4 Z-rings were diffuse in cells lacking zapA or zauP and,

5 Z-scan measurements revealed a high third-order nonlinea

6 Z: Little is known about the influence of multiple conse

7 Z[Cu(II)OH] complexes, although shown to be inactive, ar

8 substrate scope is demonstrated (up to 99:1 Z:E) together with evidence of mechanistic dichotomy via

9 products in 47-88% yield and 90:10 to >98:2 Z:E selectivity.

10 cyclic alkenes in 40-70% yield and 96:4-98:2 Z:E selectivity; here too, reactions were more efficient

11 mall-molecule electron acceptor, 2,2'-((2Z,2'Z)-((6,6'-(5,5,10,10-tetrakis(2-ethylhexyl)-5,10-dihydro

12 e produced 16 SCO-active [Fe(II)(bpp(X,Y))2](Z)2 complexes (Z = BF4 or in one case PF6) in (CD3)2CO s

13 edian = 12.5pg/ml; IQR = 10.7, 15.0; n = 23; Z = 2.6; p < 0.01).

14 alysed photoisomerisation showed that the (5'Z)-isomer gazaniaxanthin is the main (Z)-isomer of rubix

15 irradiation with 470 to 530 nm light and 99% Z isomer with 590 up to 680 nm light.

16 accessible valine-derived aminophenol and a Z- or an E-gamma-substituted boronic acid pinacol ester.

17 ccessible diene starting materials bearing a Z-olefin moiety.

18 tive cyclizations of substrates containing a Z-allylic phosphate tethered to an alkyne are described.

19 In chicken, which has a Z/W sex chromosome system, expression output of genes on

20 Previous results suggested that ZipA is a Z-ring stabilizer, since in vitro experiments it is show

21 s catalyzed by trace copper salts and that a Z- to E-hydrazone isomerization occurs through an enehyd

22 nduces a sequential reaction path in which a Z-E photoisomerization of C2-C3 is followed by a rotatio

23 termediates show an innate preference for a (Z)-configuration, although this can be suppressed by ste

24 se of alpha-methyl-beta-anisylvinyl acetate (Z/E = 58:42).

25 suggest a model where multiple alpha-actinin/Z-repeat interactions cooperate to ensure long-term stab

26 ular version of this approach also afforded (Z)-alpha,beta-unsaturated amino esters in moderate to go

27 benthamiana as a system to study NHR against Z. tritici.

28 -1.36, 95% CI -1.44 to -1.27, weight-for-age Z score -1.20, -1.28 to -1.11, and head circumference Z

29 ritional status at 24 months (length-for-age Z score -1.36, 95% CI -1.44 to -1.27, weight-for-age Z s

30 rimary outcome was children's length-for-age Z score at 18 months of age.

31 s), and seven had implausible length-for-age Z scores (<-5 SD; one in intervention cluster; six in co

32 with low-to-moderate vagility (T. aedon and Z. capensis).

33 allows precise quantification of each E and Z isomer of the enantiomer.

34 istic interconversion zone between the E and Z isomers.

35 d with substantially improved efficiency and Z selectivity.

36 here too, reactions were more efficient and Z-selective than when the other catalyst classes are emp

37 s enantioseparation of E(R), Z(R), E(S), and Z(S) isomers, with a characteristic interconversion zone

38 matic, especially for highly substituted and Z-enamides.

39 tly related to the reference temperature and Z-value commonly used for kinetic analysis in food micro

40 adapter-inducing interferon-beta (TRIF) and Z-DNA-binding protein 1 (ZBP1)/DNA-dependent activator o

41 ly imperils the persistence of L. tumana and Z. glacier throughout their ranges, highlighting the rol

42 Welch's t-test assuming unequal variance and Z test of comparison of proportions.

43 tive index difference between the axis X and Z gradually decreased with decreasing temperature, which

44 360 degrees along all three axes (X, Y, and Z), by employing the geometric property of a 3D structur

45 A series of new (E) and (Z)-benzoyl-homoquinones have been prepared in good yield

46 A borocyclopropanation of (E)- and (Z)-allylic ethers and styrene derivatives via the Simmon

47 eaves [(Z)-3-hexenal, (Z)-3-hexen-1-ol, and (Z)-3-hexenyl acetate] were drastically reduced by blanch

48 Another Z-linked miRNA, the male-biased miR-2954-3p, shows conse

49 ary artery luminal dimensions, normalized as Z scores, and is calibrated to both past and current inv

50 Other homologues, such as Z-d-Phe, are less effective but may act through the same

51 baceous and green aromas were identified as (Z)-1,5-octadien-3-one and 3-isobutyl-2-methoxypyrazine.

52 ng, the desmin cytoskeleton and the attached Z-band-bound thin filaments are degraded after ubiquitin

53 By incorporation of commercially available Z-butene together with robust and readily accessible Ru-

54 retention of oscillatory behavior for the B-Z reaction with the formation of giant vesicles bring a

55 d movement of FtsZ clusters around bacterial Z-rings that is powered by GTP hydrolysis and guides cor

56 g the treatment period than at the baseline, Z >/= -1.97, p </= .04.

57 d arylations of allylamines were found to be Z-selective.

58 ic product and was mediated by a beneficial (Z)-1 --> (E)-1 interconversion.

59 re used to establish the interaction between Z. tritici and N. benthamiana.

60 including adhesion plaques and dense bodies (Z-disks) of striated muscles and attachment plaques of s

61 CUX1 drives EMT, which can be antagonized by Z-FY-CHO.

62 C) were achieved for tetra-CBDs followed by (Z)-1,1,2,3,4-penta-CBD and hexa-CBD.

63 ty in the hydrogenation of E/Z mixtures (ca. Z/E = 75:25) of alpha,beta-dialkylvinyl substrates, whil

64 docrine-refractory metastatic breast cancer, Z-endoxifen provides substantial drug exposure unaffecte

65 The inhibitors carbobenzoxy (Z)-d-Phe-l-Phe-Gly (fusion inhibitor peptide [FIP]) and

66 1.20, -1.28 to -1.11, and head circumference Z score -0.51, -0.59 to -0.43).

67 associated with a smaller head circumference Z score.

68 CO-active [Fe(II)(bpp(X,Y))2](Z)2 complexes (Z = BF4 or in one case PF6) in (CD3)2CO solution: again

69 ge from baseline to 36 months on a composite Z score combining four cognitive tests (free and total r

70 Initial hit compound (Z)-5-((1-(4-bromophenyl)-2,5-dimethyl-1H-pyrrol-3-yl)met

71 owth, centronuclear myopathy, central cores, Z-disc streaming, and SR dilation.

72 axanes in up to 85% yield; the corresponding Z-hydrazone thread affords no rotaxane under similar con

73 This process requires cytokinetic Z-rings formed by the bacterial tubulin homolog FtsZ, an

74 GTP-dependent manner to form the cytokinetic Z ring.

75 assemble at midcell to form the cytokinetic Z-ring, which coordinates peptidoglycan (PG) remodeling

76 The MRCI/aug-cc-pV(T+d)Z results on the evolution of the low-lying singlet elec

77 The CASSCF/aug-cc-pV(T+d)Z results suggest that the ground state of SiH2OO is sev

78 This multicenter study sought to determine Z scores for common measurements adjusted for body surfa

79 the type I IFN locus on the sex-determining Z chromosome.

80 um from the inactive, predominantly dimeric (Z)-1.

81 ggering the reverse isomerization direction (Z --> E) by the same wavelength of light, which normally

82 aline-like bodies adjacent to a disorganized Z-line on electron microscopy, recapitulating the diseas

83 o the access to different 1,4-disubstituted (Z)-enynyl esters in excellent yields.

84 DURA-Z coating effectively solves several key challenges prev

85 The fabricated DURA-Z coating retains antifouling property after 90 d of imm

86 trongly immobilize the superhydrophilic DURA-Z coating through interpenetration.

87 The DURA-Z coating achieves a rarely reported long-term biofilm r

88 d ultrarobust antifouling zwitterionic (DURA-Z) coating is created that can be easily and universally

89 aled, among others, over-expression of ESC/E(Z) complex genes (an ovarian steroid-regulated gene sile

90 Finally, mRNA expression of several ESC/E(Z) complex genes were increased by progesterone in contr

91 RNA and protein expression of the 13 ESC/E(Z) complex genes were individually quantitated.

92 In contrast, protein expression of ESC/E(Z) genes was decreased in untreated PMDD LCLs with MTF2,

93 These natural products have in common an E,Z-configured conjugated diene linked to a di- or triyne

94 lection of components of a diastereomeric (E,Z) and enantiomeric (R,S) oxime into a third reactor col

95 plant volatile compound pear ester ethyl-(E,Z)-2,4-decadienoate, while CpomOR6a responds to the stro

96 method to stereoselectively establish the E,Z-diene part, an ester-tethered ring-closing metathesis/

97 approach based on abs conversion type (i.e. Z = |X 1 - X 2|) and t-test, to detect interactions in s

98 ti/syn) and E-linear products (up to >20:1 E/Z) in high selectivity with aromatic, alpha,beta-unsatur

99 cts at a yield of up to 73 per cent and an E/Z ratio greater than 98/2.

100 t the enantioselective, regioselective and E/Z-selective allylic oxidation of unactivated internal al

101 This is followed by E/Z separation in a fourth analytical column.

102 Finally, a predictive model for E/Z selectivity was developed using DFT calculations.

103 ess to generate enals from ynals with good E/Z selectivity, our early studies found that an asymmetri

104 enantioselectivity in the hydrogenation of E/Z mixtures (ca. Z/E = 75:25) of alpha,beta-dialkylvinyl

105 However, thermodynamic ratios E/Z were reached as the reaction proceeded to equilibrium.

106 The reversible E/Z isomerization of the alkenylnickel species is essentia

107 The E/Z isomerization process of a uracil-azobenzene derivativ

108 , provides orthogonal means to control the E/Z state of the system.

109 t formation of photoisomers from CBDs with E/Z configuration must be taken into account because of th

110 y responses in participants in the ChAd3-EBO-Z group (63.5%) and in those in the rVSVG-ZEBOV-GP group

111 s (in 28.5% of the patients in the ChAd3-EBO-Z group and 30.9% of those in the rVSVG-ZEBOV-GP group,

112 n in 40 participants (8.0%) in the ChAd3-EBO-Z group, in 47 (9.4%) in the rVSVG-ZEBOV-GP group, and i

113 e chimpanzee adenovirus 3 vaccine (ChAd3-EBO-Z) and the recombinant vesicular stomatitis virus vaccin

114 Echocardiographic Z scores based on BSA were derived from a large, diverse

115 A highly efficient, Z-selective ring-closing metathesis system for the forma

116 20) in aqueous extracts and heavy elements (Z > 20) in acid extracts, coming from materials and degr

117 on was developed to quantify light elements (Z </= 20) in aqueous extracts and heavy elements (Z > 20

118 have formed in low-metallicity environments (Z=0.001) from progenitor binaries with typical total mas

119 rate to high yields (67-79 %) with excellent Z-selectivity (95-99 %).

120 btained with yields of 60-99% and excellent (Z)-selectivity.

121 ower law function of P with scaling exponent Z [group conflict mortality (GCM)].

122 d hydrogels directly from conventional AFM F-Z experiments, thereby creating a common platform for th

123 -ZapB provide additional positional cues for Z-ring formation and may help coordinate its assembly wi

124 decrease in kH has been instead measured for Z = OAc, NPhth, CO2Me, Cl, Br, and CN, indicative of alp

125 bacteria, indicating a common mechanism for Z-ring assembly.

126 H2 activation toward CumO(*) is observed for Z = Ph, OH, NH2, and NHAc, as evidenced by an increase i

127 ted with the average SS firing rate only for Z+ cells.

128 es resulted in hydroboration, 84-86% ee for (Z)-alkenes, but (E)-alkenes or 1,1-disubstituted alkenes

129 Z, and the stabilization of the newly formed Z-rings is crucial for completion of septum synthesis.

130 desuccinylase (DapE) facilitates functional Z ring formation by strengthening the Ter signal via Zap

131 eoretentive catalysts that not only generate Z-olefins selectively, but also kinetically produce E-ol

132 led cross-metathesis reactions that generate Z- or E-trisubstituted alkenes are disclosed.

133 Macrocyclization reactions generated Z-products from easily accessible diene starting materia

134 a-aminoxylation reaction, and Still-Gennari (Z)-selective olefination reactions.

135 rmal ring openings of the cyclobutenes give (Z,Z)-1,3-diene products, again for thermodynamic reasons

136 gy to include a bioinspired, catalytic E --> Z isomerization of alpha,beta-unsaturated nitriles, ther

137 Combined with light-controlled E --> Z isomerization, this enables controllable fractional tu

138 ngth of light, which normally triggers E --> Z isomerization.

139 H2A.Z impairs transcription elongation, suggesting that spli

140 H2A.Z is a histone H2A variant that contributes to transcrip

141 H2A.Z nucleosomes are enriched at temperature-responsive gen

142 H2A.Z occupancy, but not distribution, changes in parallel w

143 loss upon transcriptional activation and H2A.Z gain upon repression.

144 nder providing a surprising link between H2A.Z, chromosome segregation, and organ development.

145 is impaired in H2A.Z deposition, and by H2A.Z profiling in stress conditions, we investigated the im

146 In Saccharomyces cerevisiae, H2A.Z is deposited by the SWR-C complex, which relies on sev

147 In Saccharomyces cerevisiae, H2A.Z is deposited into chromatin by the SWR-C complex, is f

148 rones including Nap1 and Chz1 to deliver H2A.Z-H2B dimers to SWR-C.

149 re-mRNA splicing and indicate a role for H2A.Z in coordinating the kinetics of transcription elongati

150 that this suppressed the requirement for H2A.Z in splicing of that intron.

151 tably, affected introns are enriched for H2A.Z occupancy and more likely to contain nonconsensus spli

152 g of SWR to both H2A nucleosome and free H2A.Z induces SWR ATPase activity and engages the histone ex

153 ed protein6 mutant, which is impaired in H2A.Z deposition, and by H2A.Z profiling in stress condition

154 a redundant role for these chaperones in H2A.Z deposition.

155 While PWWP2A does not influence H2A.Z occupancy, the C-terminal tail of H2A.Z is one importa

156 intron-containing genes in cells lacking H2A.Z is impaired, particularly under suboptimal splicing co

157 Two internal protein regions mediate H2A.Z-specificity and nucleosome interaction, whereas the PW

158 of H2A.Z and identify PWWP2A as a novel H2A.Z-nucleosome binder.

159 Thus, PWWP2A is a novel H2A.Z-specific multivalent chromatin binder providing a surp

160 In particular, we observed H2A.Z loss upon transcriptional activation and H2A.Z gain up

161 propose that the antagonistic effects of H2A.Z and HSF1 provide a mechanism to activate gene expressi

162 termine the comprehensive interactome of H2A.Z and identify PWWP2A as a novel H2A.Z-nucleosome binder

163 t in drought-responsive genes, levels of H2A.Z in the gene body correlate with transcript levels.

164 H2A.Z occupancy, the C-terminal tail of H2A.Z is one important mediator to recruit PWWP2A to chromat

165 ch cause a rapid and dynamic eviction of H2A.Z nucleosomes at target genes.

166 ects, indicating that, in the absence of H2A.Z, stalled spliceosomes are disassembled, and unspliced

167 ucleosomes and the selective exchange of H2A.Z-H2B dimers out of nucleosomes and replacement by H2A-H

168 ed by well-positioned nucleosomes and/or H2A.Z-containing nucleosomes.

169 n of disassembly factor Prp43 suppresses H2A.Z-mediated splice defects, indicating that, in the absen

170 These data suggest that H2A.Z has a repressive role in transcription and counteracts

171 Together, these data demonstrate that H2A.Z is required for efficient pre-mRNA splicing and indica

172 t spliceosome rearrangements are tied to H2A.Z's role in elongation.

173 Together, our findings reveal unique H2A.Z surface dependences for Nap1 and Chz1 and a redundant

174 Our data support a model where H2A.Z in gene bodies has a strong repressive effect on trans

175 ments for Nap1 and Chz1 interaction with H2A.Z.

176 column for E right harpoon over left harpoon Z isomerization under controlled oven temperature and fl

177 acid-binding domains for left-handed helix (Z-form) and receptor-interacting protein homotypic inter

178 n volatiles in fresh leaves [(Z)-3-hexenal, (Z)-3-hexen-1-ol, and (Z)-3-hexenyl acetate] were drastic

179 The high Z chalcohalides Hg3Q2I2 (Q = S, Se, and Te) can be regar

180 The high-Z bcc metals with large spin-orbit-induced bandgaps are

181 Facile, highly Z-selective isomerizations are observed for allyl ethers

182 However, Z. rouxii promoted alcohols formation and produced a mor

183 r the unique than for the intermediate hues (Z = -2.9, p = 0.004).

184 his class of reactions four pathways (Type I Z, Type I E, Type II Z, Type II E) are possible, leading

185 We have recently identified Z-DNA-binding protein 1 (ZBP1) as an innate sensor of in

186 For the first time, we identify (Z)-2-(3,4-dichlorophenyl)-3-(1H-pyrrol-2-yl)acrylonitril

187 s four pathways (Type I Z, Type I E, Type II Z, Type II E) are possible, leading to different enantio

188 assessed based on recording total impedance |Z| in different individual frequencies.

189 tionally defined growth faltering as fall in Z score between 3 months and 21 months of age.

190 e strong support for a CO2 response of gm in Z. mays, and indicate that gm in maize is probably drive

191 to maintaining K(+) and Na(+) homeostasis in Z. xanthoxylum was investigated.

192 peculiarity of cultivation nor inbreeding in Z. mays.

193 that mutation of key amino acids involved in Z-DNA/RNA binding in ZBP1's ZBDs prevented necroptosis u

194 the amplitudes of the phases were larger in Z+ cells.

195 losing of Z-hexatriene, the [1,5]-H shift in Z-pentadiene, and the Cope rearrangement.

196 uses the premature disassembly of individual Z-rings, leading to the frequent abortion of septum synt

197 f mesenchymal cells with the Cat L inhibitor Z-FY-CHO led to nuclear-to-cytoplasmic relocalization of

198 Interestingly, Z-ring formation occurs coincidently with initiation of

199 e distal esophagus, also called an irregular Z line, are encountered.

200 ltivariate analysis, patients with irregular Z line and patients with BE of >/= 1 cm did not differ s

201 None of the patients with irregular Z line developed HGD or EAC during a median follow-up pe

202 study, we found that patients with irregular Z line do not develop HGD or esophageal cancer within 5

203 ce of HGD and EAC in patients with irregular Z line with intestinal metaplasia.

204 epening of the ocean's 26 degrees C isotherm Z 26 .

205 yzed (119 in the lutein plus zeaxanthin [L + Z] group and 120 in the placebo group).

206 The main volatiles in fresh leaves [(Z)-3-hexenal, (Z)-3-hexen-1-ol, and (Z)-3-hexenyl acetat

207 properties (quantitative switching and long Z isomer half-life).

208 ubixanthin and the (13Z)-isomer is the main (Z)-isomer of lycopene.

209 the (5'Z)-isomer gazaniaxanthin is the main (Z)-isomer of rubixanthin and the (13Z)-isomer is the mai

210 Seasonal patterns of mean Z scores were obtained by Fourier regression.

211 a high optical resolution (X-Y, 0.17 microm; Z < 3 nm).

212 cient cytokinesis by stabilizing the midcell Z-ring through a bundling-independent mechanism.

213 iny (NMR-invisible) population of monomeric (Z)-1 that was formed in a mobile equilibrium from the in

214 propyl ketone added rapidly to the monomers (Z)-1&3THF and (E)-1&3THF with a rate ratio of at least 1

215 for both zebrin positive (Z+) and negative (Z-) cells, though the amplitudes of the phases were larg

216 f cyclobutene, electrocyclic ring-closing of Z-hexatriene, the [1,5]-H shift in Z-pentadiene, and the

217 were resistant to the inhibitory effects of Z-d-Phe-l-Phe-Gly.

218 role in controlling the activation energy of Z-E isomerization as well as the shape of the DSC exothe

219 uided purification of the aqueous extract of Z. jujuba Mill.

220 he typhoon intensity change as a function of Z 26 and other environmental variables.

221 iferated (3 log increase) in the presence of Z. rouxii, while Z. rouxii growth was suppressed by 4 lo

222 thodologies have resulted in a wide range of Z scores for a single measurement.

223 n in Escherichia coli occurs at the stage of Z ring formation.

224 -, regio-, and stereoselective synthesis of (Z) and (E) styryl pyrazoles and benzpyrazoles by the add

225 The subsequent treatment of (Z)-1 with a minimum amount of THF afforded exclusively (

226 I) cation [Au(PPh3)](+), a large variety of (Z)-beta-iodoenol esters (39 examples) could be synthesiz

227 inery and that they mediate their effects on Z-ring stability during developmentally controlled cell

228 stereoselective synthesis of either the E or Z alkene from a single isomer of a vinyl coupling partne

229 ne shift affords stereospecifically the E or Z isomer of the 5-alkenyl-4-iminohydantoin products from

230 ti relationship from the corresponding E- or Z-crotylboronate used in the reaction.

231 depending on the imine configuration (E- or Z-imine) and on the nucleophilic attack site (top or bot

232 oducts from the corresponding starting E- or Z-N'-alkenyl urea, each of which may be formed from the

233 partner provides access to either the E- or Z-olefin with excellent yield and stereochemical fidelit

234 iated with the male determining region, Y or Z).

235 Methods We performed a phase I study of oral Z-endoxifen to determine its toxicities, maximum tolerat

236 viglumis, Z. mays mexicana, and particularly Z. mays huehuetenangensis.

237 and its wild relatives Z. mays parviglumis, Z. mays mexicana, and particularly Z. mays huehuetenange

238 e decades ago, the small hydrophobic peptide Z-d-Phe-l-Phe-Gly (FIP) was shown to block MeV infection

239 ion of SS activity for both zebrin positive (Z+) and negative (Z-) cells, though the amplitudes of th

240 (1)Denant) yields enantioseparation of E(R), Z(R), E(S), and Z(S) isomers, with a characteristic inte

241 ing C-C bond formation step leading to the R-Z and S-Z product respectively with TMSQ and MeQd cataly

242 centromeres in maize and its wild relatives Z. mays parviglumis, Z. mays mexicana, and particularly

243 Sonogashira coupling of representative (Z)-beta-iodoenol esters with terminal alkynes, alkynols,

244 As demonstrated, a rearrangement of (S,Z)-allyl carbamates provides (S)-teriary allylamines, wh

245 bond formation step leading to the R-Z and S-Z product respectively with TMSQ and MeQd catalysts is p

246 IF-1, independent of PKM2-JMJD5.-Schoepflin, Z.

247 s that have a twisted (rather than T-shaped) Z isomer conformation.

248 L was classified into Band-shaped, Y-shaped, Z-shaped, Trident-shaped, and Complex-shaped configurati

249 one added less rapidly to the less shielded (Z)-1 [but never to (E)-1]; this singly diastereoconverge

250 mice with a nonsense mutation in Mypn showed Z-streaming and nemaline-like bodies adjacent to a disor

251 ion half-lives adopt a T-shaped ground state Z isomer conformation and proceed through a T-shaped iso

252 lective synthesis of fluoroalkyl-substituted Z-homoallylic tertiary alcohols has been developed.

253 ows; 5-sulfo-(E)-caftaric acid (a), 2-sulfo-(Z)-caftaric acid (b), 2-sulfo-(E)-caftaric acid (c), (E)

254 on protein, E3, which contains an N-terminal Z-nucleic acid binding (Zalpha) domain that is critical

255 In addition, the Z-isomers have long thermal half-lives in the dark of up

256 the E-isomers (4-6) or predominantly as the Z-isomer (3) which in solution is converted to the E-iso

257 egions of more recent divergence between the Z and W chromosomes.

258 MYPN encodes the Z-line protein myopalladin implicated in sarcomere integ

259 med in livers of patients homozygous for the Z allele, with severe liver disease requiring hepatic tr

260 % MS SI restoration for the Z-Gly-Gly-Val and bradykinin peptides were 75-83% while

261 e main candidates for anchoring titin in the Z-disk is the actin cross-linker alpha-actinin.

262 ic protofilaments, whose organization in the Z-ring is an unresolved problem.

263 thelial cells by enhancing expression of the Z and R proteins.

264 divisome that promotes the integrity of the Z ring by acting through ZapB and raises the possibility

265 ciated with the Z-disc, with over 74% of the Z-disc proteins experiencing robust changes in phosphory

266 me system, expression output of genes on the Z Chromosome is expected to be male-biased, since there

267 preference for dosage-sensitive genes on the Z Chromosome, based on computational and experimental da

268 ace, and ethnicity have small effects on the Z scores that are statistically significant but not clin

269 division proteins are thought to require the Z-ring for recruitment to the future division site.

270 lectronic effect that largely suppresses the Z --> E photoisomerization (the tau torsion) reaction, w

271 c disorders and the liver disease due to the Z mutant of AAT (ATZ) is a prototype of conformational d

272 bond are converted by UV irradiation to the Z-isomers having bifurcated O-H...O...H-X hydrogen bond.

273 in-like domain of alpha-actinin binds to the Z-repeats of titin.

274 structures form without a connection to the Z-ring.

275 und on proteins that are associated with the Z-disc, with over 74% of the Z-disc proteins experiencin

276 period than at baseline and end of therapy, Z >/= -2.27, p </= .023.

277 Therefore, Z-FY-CHO may be an important therapeutic tool to antagon

278 onal barrier and thus in accelerated thermal Z --> E isomerization.

279 isomerization kinetics show that the thermal Z --> E interconversion is 4-fold accelerated upon forma

280 l disubstituted alkynes that were reduced to Z-olefins followed by borepin formation either through a

281 ides a more efficient and selective route to Z-macrocycles relative to previously reported systems.

282 reaction mechanism involving a crucial E-to-Z vinyl-Pd isomerization and a carbon-halogen bond-formi

283 e explore the effects of one such transcript-Z+Agrin-known to be a critical organizer of the NMJ.

284 vealed that the phosphorylation state of two Z-disc kinases (striated muscle-specific serine/threonin

285 of K(+) and Na(+) , as compared to wild-type Z. xanthoxylum grown under 50 mm NaCl.

286 hibited stunted growth compared to wild-type Z. xanthoxylum.

287 of FtsZ assemblies in solution that underlie Z-ring assembly, employing time-resolved x-ray scatterin

288 helical conformations, including the unusual Z-conformation.

289 their investigative work.-Liu, C.-H., Wang, Z., Sun, Y., Chen, J.

290 s in stereoselective olefin metathesis where Z-alkene substrates are required.

291 ncrease) in the presence of Z. rouxii, while Z. rouxii growth was suppressed by 4 log in concurrence

292 low-affinity protein binding (affibody with Z protein), elusive enzyme-substrate interaction (ubiqui

293 tochondrial redox status did not change with Z-3-hexenol, another abundant GLV.

294 We identify compounds with Z isomer half-lives ranging from seconds to hours, to da

295 xternal ED-XRF calibration for elements with Z > 20 in acid extracts was optimized as a faster and cl

296 RF calibration methodology for elements with Z </= 20 was proposed as an alternative to ion chromatog

297 and non-stereoselective transformations with Z-1,2-dichloroethene and 1,2-dibromoethene can be effect

298 d on the transformation status of cells.-Yu, Z., Ruter, D.

299 uch inhibitors as rapamycin.-Xiong, M., Zhu, Z., Tian, S., Zhu, R., Bai, S., Fu, K., Davis, J.

300 , and (iv) a chitosan derivative called ZWC (Z) to trigger pH-sensitive drug release.