ライフサイエンスコーパス: trans

1 the IL-1-induced response of fibroblasts in trans.

2 -five of the replicated pQTLs are located in trans.

3 the lack of inhibition of the pro-domain in trans.

4 how editing is regulated both in cis and in trans.

5 tein complex that can nick DNA substrates in trans.

6 we now can differentiate the most prevalent trans-1,2-diols in pyranoses systematically and predicta

7 cloaddition of 3-hydroxyflavones with trans, trans-1,4-diphenyl-1,3-butadiene is described.

8 Hitherto unknown cis- and trans-1-amino-3-hydroxy-3-methylcyclobutanecarboxylic ac

9 or 1h, 13:0 and iso 16:0 were separated from trans-12:1 and 13-14:1, respectively, whereas iso 18:0 w

10 -(+)-MR200], cis-(-)-1a [cis-(-)-MR201], and trans-(+/-)-1a [trans-(+/-)-MR204], have been identified

11 An in vivo evaluation evidenced that trans-(+)-1d, in contrast to trans-(-)-1d, cis-(+)-1d, o

12 The most promising compound, trans-(+)-1d, showed remarkable selectivity over a panel

13 evidenced that trans-(+)-1d, in contrast to trans-(-)-1d, cis-(+)-1d, or cis-(-)-1d, which behave as

14 The 2,3-trans, 2,4-cis trisubstituted chroman moiety was formed

15 developed by our own group to construct the trans-2,6-disubstituted dihydropyran ring, asymmetric al

16 The ring-opening reaction of trans-2-aroyl-3-styrylcyclopropane-1,1-dicarboxylates wa

17 alyzed the oxidation of fatty acyl-CoAs into trans-2-enoyl-CoA and produced H2 O2 .

18 ion was loaded with the antifungal compound, trans-2-hexenal, and coated with the surfactant, sorbita

19 were obtained, cis-beta-ocimene (2.0-40.0%), trans-2-hexenol (2.4-19.4%), cis-3-hexenol (2.5.16.4%),

20 e higher alcohols (1-hexanol, cis-3-hexenol, trans-2-hexenol) and monoterpenes (beta-myrcene, cis-bet

21 Conformational analysis suggested that trans-3''-substituted trioxolanes would exhibit Fe(II) r

22 (ANABA), anatabine (ANATA), cotinine (COT), trans-3'-hydroxycotinine (COT-OH), N-nitrosoanabasine (N

23 oration of a representative internal alkene, trans-3-hexenyl 2,4,6-trichlorobenzoate, which undergoes

24 it 2, resulting in identification of racemic-trans-(3-((4-(aminomethyl)-6-(trifluoromethyl)pyridin-2-

25 ates through cis-1,2-diol, cis-3,4-diol, and trans-4,6-diol.

26 minor amounts of cis- and up to 35 mug/L of trans-4-MCHM into water, indicating 4-MCHM was present i

27 ectric field showed a significant release of trans-(4.01+/-0.48) and cis-(5.04+/-0.26mug/g) lycopene,

28 y established by X-ray analysis of precursor trans-(+)-5a as camphorsulfonyl derivative 9.

29 in the individual values of cis-6-propenyl-, trans-6-propenyl- and 3-vinylguaiacol.

30 Trans performed best in base coverage, while Trans-ABySS performed best in gene coverage and number o

31 The antioxidant properties of trans-aconitic acid (TAA) alone or in the presence of us

32 w how evolutionary changes in cis as well as trans acting signals have played a fundamental role in d

33 f libraries to provide a prediction of which trans -acting factors binding sites are disrupted/create

34 slation could be specifically enhanced using trans-acting agents that counter the function of negativ

35 We also identified cis- and trans-acting chromatin contacts to other genomic regions

36 their biogenesis is partially dependent on a trans-acting factor FPA.

37 abidopsis relies in large part on binding of trans-acting factors to cis-localized DNA sequence motif

38 t start codon selection is regulated by many trans-acting initiation factors as well as sequence/stru

39 y complex) to bind foreign DNA and recruit a trans-acting nuclease for target degradation.

40 miRNA target mimics and lncRNAs that produce trans-acting or phased small-interfering RNA (tasiRNA/ph

41 omolecular machinery consisting of dozens of trans-acting proteins.

42 3 by ARGONAUTE7 results in the production of trans-acting small interference RNAs, which target mRNAs

43 by promoting the biogenesis of TAS3-derived trans-acting small interfering RNA (ta-siRNA), which rep

44 putative colonization factor PrpB by the two trans-acting sRNAs RcoF1/2.

45 us demonstrate that our approach can uncover trans-acting transcriptional control circuits that affec

46 additive inheritance, while those linked to trans-acting variants are most often dominantly inherite

47 Furthermore, CCL5 was directly trans-activated by cancer-FOXP3 and promoted the recruit

48 onment via recruiting Treg cells by directly trans-activating CCL5.

49 The EGR1 promoter was engineered to enhance trans-activation capacity and optimized for simple scree

50 that the neurotoxic HIV-1 regulatory protein trans-activator of transcription (Tat) continues to be e

51 protein concentration in aggregation assays (trans-activity), irrespective of linker length between l

52 The inhibition by trans addition of alcohols implies that they alter the p

53 undergoes rapid autocatalytic processing in trans after its secretion from cells.

54 We also found trans ALA in mayonnaise samples.A high intake of ALA was

55 Seven-membered-ring trans-alkenes undergo rapid, uncatalyzed carboboration r

56 cis-Allostery persisted, but trans-allostery was lost in an oligomerization-deficient

57 rial fibrillation, we performed large-scale, trans-ancestry meta-analyses of common and rare variant

58 m the Global Lipids Genetics Consortium in a trans-ancestry meta-analysis.

59 In a nitrogen matrix, the cis-to-trans and trans-to-cis conversions of HOCO is also found

60 0.9) and the following parameters: AUGC90, K(trans), and maximum slope enhancement (intraclass correl

61 ), androgens (androstenedione, androsterone, trans-androsterone, and testosterone), progestins and me

62 The synthesis of the A-B-cis,B-C-trans-annulated cyclohepta[e]hydrindane core of a gaguni

63 broblast-specific loss of beta-catenin after trans-aortic constriction in vivo.

64 ligomers; (ii) mutational analysis reveals a trans-arginine finger, R158, indispensable for ATP hydro

65 nd it can be considered as an alternative to trans-arterial embolization when the pseudoaneurysm cann

66 rm a heterotetramer, in which MST2 undergoes trans-autophosphorylation.

67 A multicomponent trans-aziridination of aldehydes, amines, and diazo comp

68 The optimal protocol for the trans-aziridination of aliphatic aldehydes did not requi

69 on-rich aryl aldehydes were screened to give trans-aziridines in 73-90% yield with 82-99% ee and tran

70 he fused benzene rings to those with cis- or trans-bent connectivities.

71 The retention of all-trans-beta-carotene in breads containing 10, 20 and 30%

72 ing the Friedel Crafts addition of indole to trans-beta-nitrostyrene.

73 terpenes (beta-myrcene, cis-beta-ocimene and trans-beta-ocimene).

74 ction) matches the GHG impact of preconsumer trans-boundary food waste reduction.

75 hree BP-N (2)-dG adducts, namely the 10S (+)-trans-BP-N (2)-dG, 10R (+)-cis-BP-N (2)-dG, and 10S ( -

76 hotooxidation products that include fumaric (trans-butenedioic) and muconic (trans,trans-2,4-hexadien

77 late gene expression changes in both cis and trans by the ceRNA mechanism.

78 w that receiver dimers are phosphorylated in trans by the donor; this process requires the kinase act

79 nium and thorium bis(carbene) complexes with trans C=M=C cores where experimental and theoretical dat

80 ver (ASF) is endemic in Africa, parts of the Trans Caucasus, the Russian Federation, and several Euro

81 Compared to APP, APLP1 exhibits increased trans-cellular binding and elevated cell-surface levels

82 Though cadherins typically function via trans-cellular homophilic interactions, our results sugg

83 es encoding putative trans-chrysanthemol and trans-chrysanthemal dehydrogenases.

84 hile TcALDH1 encodes an enzyme that oxidizes trans-chrysanthemal into trans-chrysanthemic acid.

85 enzyme that oxidizes trans-chrysanthemol to trans-chrysanthemal, while TcALDH1 encodes an enzyme tha

86 nzyme that oxidizes trans-chrysanthemal into trans-chrysanthemic acid.

87 fy several candidate genes encoding putative trans-chrysanthemol and trans-chrysanthemal dehydrogenas

88 that TcADH2 encodes an enzyme that oxidizes trans-chrysanthemol to trans-chrysanthemal, while TcALDH

89 employed to install a pyridyl to the alkene trans-cinnamaldehyde while Ag(I) ions are used in a seco

90 tion of ammonia from l-phenylalanine to give trans-cinnamate.

91 Five monoacyl and three diacyl esters of trans-cinnamic acids and quinic acid were identified by

92 ounds were phenolics derived from quinic and trans-cinnamic acids.

93 ziridines in 73-90% yield with 82-99% ee and trans/cis selectivities of 19:1 to >99:1.

94 through the ionization yields and the ratio (trans/cis) of each stereoisomer pair as a function of in

95 ed the collapse in the central domain of the trans-cisternae accompanying polysaccharide synthesis wi

96 nol dasyscyphin E was achieved starting from trans-communic acid.

97 H3P38 is in the trans configuration, and the cis configuration is incomp

98 s that are differentiated based on a cis- or trans-configured Glu(18)-Pro(19) peptide bond.

99 into either the gauche-gauche or the gauche-trans conformation (respectively, axial or equatorial to

100 is found to be catalyzed; additionally, the trans conformation is selectively solvated within the bu

101 ltiscale approach, we found that the cis and trans conformers have different positions and orientatio

102 ur of the synthesized bipyrroles indicates a trans coplanar geometry of the pyrrole rings.

103 ) chelates of pentetic acid (Fe-DTPA) and of trans-cyclohexane diamine tetraacetic acid (Fe-tCDTA) we

104 nucleophilic amines to yield highly valuable trans-cyclopropylamines in good yields and high diastere

105 In multivariate analysis sniff trans-diaphragmatic and esophageal pressure, twitch tran

106 iaphragmatic and esophageal pressure, twitch trans-diaphragmatic pressure (Tw Pdi), age, and maximal

107 ne that was found to be the cis- and not the trans-diastereomer.

108 in hepatic fibrosis, and is characterized by trans-differentiation of quiescent HSCs to HSC myofibrob

109 ped to evaluate human mesenchymal stem cells trans-differentiation to endothelial lineage of over a p

110 A trans-dimensional Markov Chain Monte Carlo (MCMC) algori

111 The mechanism involves trans-dimerization between GTPase heads and a favorable

112 ry aliphatic amines lead to the formation of trans-disubstituted beta-lactams in excellent yields and

113 providing a means for discrimination of cis/trans double bonds in complex lipids.

114 o determine the relative contribution of the trans double-bond isomer in the mixed samples.

115 EIEIO spectra can be used to discern cis and trans double-bond isomers by virtue of the differences i

116 sed method for the identification of cis and trans double-bond isomers within intact complex lipid mi

117 Bonding and stability depend strongly on the trans effect and steric factors.

118 (e.g., thermosensors, riboswitches, cis- and trans-encoded RNAs) used for adaptation to the specific

119 Using micropatterning with a receptor trans-endocytosis assay, we show that signaling between

120 ediated homophilic adhesion is necessary for trans-endocytosis, and adhesive junctional PCP complexes

121 mics and cytokines on leukocyte adhesion and trans-endothelial migration (TEM) and subsequent accumul

122 Selective disruption of trans engagement of E-cadherin in an otherwise cohesive

123 er body fluid loss and higher mortality in a trans-epidermal body fluid loss test.

124 perm methylomes and point to a divergence in trans-epigenetic mechanisms that govern the organization

125 ctivation of endogenous target genes through trans-epigenetic remodeling.

126 posterior midgut and thereby facilitates the trans-epithelial migration of the primordial germ cells

127 human polyTE loci correspond to both cis and trans eQTL, and their regulatory effects are directly re

128 In addition, we identified 13 trans-eQTL hotspots, affecting from ten to hundreds of g

129 riance attributed to all identified cis- and trans-eQTL.

130 We identified 2,350 trans-eQTLs (at p < 10(-7)); more than 80% of them were

131 es simultaneously and found that hundreds of trans-eQTLs each affect hundreds of transcripts in lymph

132 Q-r; 1498 genes) was enriched for genes with trans-eQTLs in hotspots coinciding with GLS resistance Q

133 We hypothesized that some trans-eQTLs regulate expression of distant genes by alte

134 nd suggests biological mechanisms underlying trans-eQTLs, both of which are relevant for understandin

135 h detecting local, cis-eQTLs is now routine, trans-eQTLs, which are distant from the genes of origin,

136 Application of MR-MEGA to trans-ethnic GWAS of kidney function in 71,461 individua

137 Our findings show the utility of trans-ethnic GWASs for discovery and characterization of

138 th Tie2 in cis and across EC-EC junctions in trans Except for the binding of the C-terminal angiopoie

139 f the sodium, added sugar, saturated fat, or trans fat content.Nutrition label information (e.g., ser

140 ess sodium, added sugars, saturated fat, and trans fat has been recommended.

141 (e.g., serving size, sodium, saturated fat, trans fat) for 1032 infant and toddler foods was collect

142 The consumption of trans fatty acids (TFAs) is associated with an increased

143 Trans-fatty acids (TFAs) have deleterious cardiovascular

144 gents (cinnamon bark oil, zinc gluconate and trans-ferulic acid) in oil-in-water emulsions to control

145 The incorporation of zinc gluconate or trans-ferulic acid, independently of the concentration u

146 lic acids as gallic acid and antioxidants as trans-ferulic and p-coumaric acids were found and quanti

147 re much more difficult to stabilize than the trans forms.

148 eported that </=40% of ALA can be present as trans forms.We aimed to evaluate the associations betwee

149 Herein we report the total synthesis of the trans-fused 8,12-guaianolide (+)-mikanokryptin in 10 ste

150 tion/reduction cascades furnish the cis- and trans-fused azadecalin subunits present in Aspidosperma

151 riven reaction mechanism en route to the 5,7-trans-fused bicyclic pseudolaratriene scaffold.

152 rtner, the calcium-binding centrin Cdc31, in trans-Golgi network (TGN) to endosome traffic and TGN ho

153 irectly required both for transport from the trans-Golgi network (TGN) to the late endosome/prevacuol

154 tromer in the sequence-dependent endosome-to-trans-Golgi network (TGN) transport of the cation-indepe

155 re, we show that Rab29 recruits LRRK2 to the trans-Golgi network and greatly stimulates its kinase ac

156 gh the binding of regulatory proteins in the trans-Golgi network, followed by full activation by PI4P

157 nces of GPCR-mediated signaling at the Golgi/trans-Golgi network.

158 led to a disruption in the structure of the trans-Golgi network.

159 ked to cargo retrieval from endosomes to the trans-Golgi network.

160 To minimize energetic costs, trans-Gulf migrants should stop over when they encounter

161 the cis and trans head-tail isomers and the trans head-head isomer, where the CHF group is defined a

162 oxidative cycloaddition of TrFE: the cis and trans head-tail isomers and the trans head-head isomer,

163 Trans-hemispheric breeding attempts have occurred previo

164 le epigenetic changes of gene regulation and trans-homologue interactions.

165 A trans-human skull porcine model was designed for the pre

166 st of choice for stereochemically unorthodox trans-hydrometalations of internal alkynes.

167 on Gag assembly competency when provided in trans In contrast, artificially tethering full-length vi

168 We identified 11,204 cis and 3,791 trans independent expression quantitative trait loci (eQ

169 This work suggests that the inverse-trans-influence may occur beyond high oxidation state 5f

170 Thus, the inverse-trans-influence might be a more general f-block principl

171 ical data suggest the presence of an inverse-trans-influence.

172 to myoblasts and myotubes through homophilic trans-interactions.

173 No cis-trans interconversions and only one case of catalytic re

174 Trans-internalized Celsr1 carries with it additional cor

175 il weaning, potentially indicating prolonged trans-intestinal transfer of IgG.

176 To prove this concept, trans-/intramucosal and lymph-node delivery of PLGA-PEG

177 peptides encoded by the peptidyl-prolyl cis-trans isomerase A (PPIA) gene whose abundance was increa

178 ophilin A, also known as peptidylprolyl cis-/trans-isomerase A (PPIA), is a mediator of the neuroinfl

179 dingly, the rER-resident peptidyl prolyl cis/trans isomerases (PPIases) play an important role in the

180 the peptide bond undergoes a spontaneous cis-trans isomerism, and the cis isomers are much more diffi

181 ibits splitting of NMR resonances due to cis/trans isomerization of a single proline near the C-termi

182 idyl-prolyl isomerase that catalyzes the cis/trans isomerization of peptide bonds between proline and

183 large number of proline residues, so the cis/trans isomerization of proline peptide bonds is the rate

184 o trigger the enol-keto tautomerisim and cis-trans isomerization.

185 ation, namely ring-opening reactions and cis-trans isomerizations, respectively.

186 When DMS could not separate cis and trans isomers completely, as was the case with sphingomy

187 The content of cis/trans isomers in certain dietary supplements exceeded th

188 benzisoxazol-5(3H)-ylidene)ethanal (10), the trans isomers recombined forming the corresponding nitro

189 tary supplements exceeded the content of all trans K2MK-7 by up to 3.7 times.

190 The content of all trans K2MK-7 was in the range between 5.5 and 49microg i

191 repair pathway, while others participate in trans-lesion synthesis to allow replication past damaged

192 e converted by thiols and free radicals into trans lipids, which are therefore a valuable tell-tale f

193 All-trans-lutein was the unique carotenoid identified and qu

194 corresponding traits, as well as examples of trans-mediators (TAGAP for LDL cholesterol).

195 uded state with the substrate trapped in the trans-membrane translocation cavity.

196 TP hydrolysis, ABC transporters catalyze the trans-membrane transport of molecules.

197 Exploiting co-complexation and trans-metal-trapping strategies with lower polarity orga

198 of its components, suggest that for G:C W:W Trans , Mg(2+) binding can fine tune the basepair geomet

199 -(-)-1a [cis-(-)-MR201], and trans-(+/-)-1a [trans-(+/-)-MR204], have been identified as new potent s

200 munity faces growing challenges that require trans-national cooperation.

201 pillars of aging research" identified by the Trans-NIH Geroscience Initiative and loss of proteostasi

202 rus RdRPs are able to perform replication in trans of genomic or DI RNAs in the yeast Saccharomyces c

203 id formation and act as potent inhibitors in trans of simple polyQ peptide aggregation.

204 a common epitope of BTLA, whether engaged in trans or in cis, that is shared with a BTLA antibody ago

205 tailed investigation of Mg(2+)-bound G:C W:W Trans pairs occurring in high-resolution RNA crystal str

206 d(IPr)2(eta(2)-O2)] adds a second O2 to form trans-[Pd(IPr)2(eta(1)-O2)2].

207 with H2O in methanol/ether solution to form trans-[Pd(IPr)2(OH)(OOH)].

208 The crystal structure of trans-[Pd(IPr)2(OOH)(OH)] is reported.

209 SOAPdenovo-Trans performed best in base coverage, while Trans-ABySS

210 ation was the rate-limiting step during Jak3 trans-phosphorylation of beta-catenin, where Jak3 direct

211 f the transcription factor Foxp3 in T cells, trans-presentation of IL-6 by DC-bound IL-6Ralpha (calle

212 r alpha-chain (IL-6Ralpha), Sirpalpha(+) DCs trans-presented IL-6 to T cells during the process of co

213 trans-QTL are more frequent but tend to have smaller ind

214 end on GR SUMOylation, which leads to stable trans-recruitment of the GR-N-CoR/SMRT-HDAC3 corepressor

215 Additional work to uncover -cis and -trans regulators of EIF2B5 splicing identified several f

216 h requires concerted action of both cis- and trans-regulatory features.

217 yses, we reveal a logical organization where trans-regulatory modules (TRMs), which consist of subset

218 re able to measure the abundance of cis- and trans-regulatory variation between genotypes for both st

219 l all-carbon quaternary stereocenters having trans relative stereochemistry are constructed early in

220 Regulatory 3WJs generated in trans represent a newly identified regulatory category t

221 clear receptors, dexamethasone (Dex)-induced trans-repression of the estrogen E2 program appears to d

222 rves as an effective biological strategy for trans-repression, with clear implications for breast can

223 ng this repression by providing MHV68 RTA in trans rescued KLKI MHV68 replication in tissue culture a

224 ever, the content of stilbene represented by trans resveratrol-3-glucoside was only 18.5-70.5mg/100gd

225 Lavallee had also both the highest levels of trans-resveratrol and piceid, and Muscat de Hambourg the

226 The identification of all-trans retinoic acid (ATRA) as a potent Pin1 inhibitor pr

227 provides the first evidence showing that all-trans retinoic acid (ATRA) induces the interaction and c

228 cation of active vitamin D3 (VD3) and/or all-trans retinoic acid (RA) on wild-type mouse skin induces

229 In all-trans retinoic acid (RA)-induced differentiation of acut

230 Treatment with all-trans retinoic acid antagonizes stress-induced activatio

231 The combination of all-trans-retinoic acid (ATRA) plus arsenic trioxide (ATO) h

232 rmation and leukemogenesis, and inhibits all-trans-retinoic acid (ATRA)-induced AML cell differentiat

233 All-trans-retinoic acid (RA), a bioactive derivative of vita

234 Vitamin A (all-trans retinol) plays critical roles in mammalian develop

235 d approximately 2-fold higher vitamin A (all-trans-retinol (all-trans-ROL)) in the neural retina foll

236 ycle that catalyzes the isomerization of all-trans-retinyl esters to 11-cis-retinol, is also the isom

237 rolled generation of the highly strained 1,2-trans ring fusion of the final architecture.

238 in affects light-dependent regulation of all-trans-ROL uptake from photoreceptors into RPE cells thro

239 old higher vitamin A (all-trans-retinol (all-trans-ROL)) in the neural retina following a photobleach

240 odefluorination (HDF) of fluoroarenes by the trans-[Ru(IMe4 )4 H2 ] catalyst, 3, is reported.

241 -1) along with the T. cruzi Tc24 antigen and trans-sialidase antigen 1 (TSA1), induced significant nu

242 ings identify a novel mechanism linking IL-6 trans-signaling and angiogenesis in the peritoneal membr

243 130 fused to Fc transgenic mice lacking IL-6 trans-signaling are largely protected from tumor formati

244 Second, IL-6 trans-signaling directly induces endothelial cell prolif

245 rtant for innate and acquired immunity, IL-6 trans-signaling has been linked to accelerated liver reg

246 sing the membrane-anchored IL-6 receptor and trans-signaling using its soluble form.

247 combination with its soluble receptor (IL-6 trans-signaling).

248 tivity was reduced by interference with IL-6 trans-signaling.

249 croscopy, we find that GTPase activation and trans-SNARE complex zippering have opposing effects on f

250 When supplied in trans some truncated human ORF1 proteins suppress human

251 Wing vein phenotypes resulting from these trans-species enhancer replacements parallel features of

252 antibodies, "Bispecific Antibody by Protein Trans-splicing (BAPTS)".

253 olypeptides through a process termed protein trans-splicing (PTS).

254 and long non-coding RNAs (lncRNAs), undergo trans-splicing and polyadenylation.

255 Spliced leader (SL) trans-splicing is a critical element of gene expression

256 We demonstrate that the RNA trans-splicing technology combined with a SIN lentiviral

257 ammable DNA-binding protein by using protein trans-splicing to ligate synthetic elements to a nucleas

258 quence is added to the 5'end of each mRNA by trans-splicing.

259 This molecule also possesses a 1,3-trans stereochemical arrangement of substituents on one

260 that directly establishes the requisite 1,3-trans stereochemical arrangement on one ring while concu

261 The diastereoselective synthesis of cis and trans steroid-fulleropyrrolidines hybrids by reaction of

262 g benchmark materials such as solution-grown trans-stilbene crystals.

263 urthermore, under acidic conditions, two cis-trans styrylflavylium isomers were identified, which cou

264 rescued HIV-1 infection of CD4(+) T cells in trans, suggesting that HIV-1 exploits CD169 to attenuate

265 hesize that laminins are required for proper trans-synaptic alignment.

266 a2delta4 subunits link calcium channels to a trans-synaptic complex with glutamate receptors at the v

267 Late I-waves are thought to arise from trans-synaptic cortical inputs and have a crucial role i

268 anoreceptor neurons) resistant to direct and trans-synaptic infection from the spinal cord with rabie

269 Trans-synaptic interactions between neurexins (Nrxs) and

270 By combining trans-synaptic labeling, ultrastructural analysis, calci

271 egulated extracellular Wg ligand and nuclear trans-synaptic signal transduction, as well as downstrea

272 Thus, neurexins nucleate an overall trans-synaptic signaling network that controls synapse p

273 ting that Notum acts solely by inhibiting Wg trans-synaptic signaling.

274 in vivo opto/chemogenetic manipulations and trans-synaptic tracing of genetically identified dorsal

275 reactions create replicators trans-T(p) and trans-T(m).

276 e cycloaddition reactions create replicators trans-T(p) and trans-T(m).

277 These experiments establish trans-Tango as a flexible platform for transsynaptic cir

278 At the core of trans-Tango is a synthetic signaling pathway that is int

279 When compared to the gas phase, the trans to cis isomerization of glyoxal at the liquid wate

280 g nuclear receptors/transcription factors in trans to hot spot enhancers serves as an effective biolo

281 In a nitrogen matrix, the cis-to-trans and trans-to-cis conversions of HOCO is also found upon broa

282 NIR-activated UCNP effectively triggers the trans-to-cis photoisomerization of azobenzene, thus lead

283 he major deactivation pathway: excited-state trans-to-cis polyene rotation.

284 photocycloaddition of 3-hydroxyflavones with trans, trans-1,4-diphenyl-1,3-butadiene is described.

285 ude fumaric (trans-butenedioic) and muconic (trans,trans-2,4-hexadienedioic) acids was investigated.

286 n of PZA is entirely independent of RpsA and trans-translation in M. tuberculosis.

287 of ribosomal protein S1 (RpsA) and inhibits trans-translation leading to accumulation of stalled rib

288 These findings suggest that increased cis-to-trans UCA ratio in the epidermis is a distinct feature o

289 pathway distinct from DNA transposition and trans-V(D)J recombination that destabilizes the genome a

290 ies with reliably genuine examples of cis or trans vicinal disulfides and discuss their conformations

291 tereoselective fashion to exclusively afford trans-vinyldiboronates in good to excellent yields.

292 ases, the content of biologically active all trans vitamin K2MK-7 was below its declared content.

293 Five different isomers of cis/trans vitamin K2MK-7 were identified.

294 Confirmation that Sites 1 and 2 function in trans was demonstrated by examining the effect of E6APC8

295 ciated proteins tune microtubule dynamics in trans, we have yet to understand how tubulin genetic div

296 Combined in trans with a previously described endosome-disrupting ag

297 e HLA-DR1 allele is dominantly protective in trans with HLA-DR15 (ref.

298 switch in FnIII-1 regulates interactions in trans with the FnIII-2 domain, leading to open (monomeri

299 ypes in cis within skeletal myofibers and in trans within satellite cells and within motor neurons vi

300 e polyethylenes, where the chains are mostly trans within the crystals.