ライフサイエンスコーパス: halves

1 pod eye (midband and the upper and lower eye halves).

2 icodons, resulting in the generation of tRNA halves.

3 on and corresponding disomy 3 and monosomy 3 halves.

4 The protein is organized into two halves.

5 s normal to the membrane and between the two halves.

6 lack of sequence similarity between the two halves.

7 bacteriocins are located in their C-terminal halves.

8 s normal to the membrane and between the two halves.

9 t subdivide the CNS into bilateral symmetric halves.

10 ns to FeMoco by using one or both of its 4Fe halves.

11 mary structure of the Rossmann fold into two halves.

12 op cleavage of mature tRNAs to generate tRNA halves.

13 the internucleotide bond that joins the two halves.

14 We also show that MeCP2 has two functional halves.

15 ntially migrate into the anterior sclerotome halves.

16 te relaxase and its two, separate functional halves.

17 ormation and pinches the cell into two equal halves.

18 the mutual information between each pair of halves.

19 her smaller tRFs are generated from the tRNA halves.

20 ential for producing the stress-induced tRNA halves.

21 t they are generated independently from tRNA halves.

22 r anticodon stem loop (ASL) to generate tRNA halves.

23 er multiple random splits of the cohort into halves.

24 ing there are other RNases that produce tRNA halves.

25 ace manifested via a swiveling motion of two halves.

26 ons that have a split dendritic tree in both halves.

27 vering the free ends of the two rps12 intron halves.

28 BTS)-H2O2 reaction catalyzed by G-quadruplex halves.

29 d and anticorrelated motions between the two halves.

30 r the junction of the Rav1 N- and C-terminal halves.

31 , specifically 30-35 nucleotide-long 5' tRNA-halves (5' tRHs), were abundant in non-malignant liver a

32 (BC half) forms a propenone bearing the two halves (a hydrobilin analogue).

33 lease angiogenin to generate 5'- and 3'-tRNA halves: a novel class of small non-coding RNAs of 30-40

34 ArsA is composed of two homologous halves A1 and A2, each containing a nucleotide binding d

35 densation, and the choice of different upper halves allows for the facile tuning of their rotational

36 The abundant accumulation of 5'-tRNA halves also occur in HMDM-secreted extracellular vehicle

37 On the contrary, 5' tRNA halves and 5' RNA Y4-derived fragments of 31-33 were gre

38 ssentially form the right and left forebrain halves and are relatively weakly interconnected.

39 re common sequences with their corresponding halves and bsAb, it is not suitable to use peptides as s

40 ral studies in recent years showed that tRNA halves and distinct Y RNA fragments are abundant in the

41 f eukaryotic tRNases that also generate tRNA halves and inhibit translation in response to stress.

42 l RNAs (tsRNAs), mainly from 5' transfer RNA halves and ranging in size from 30 to 34 nucleotides, ex

43 viously uncharacterized link between 5'-tRNA halves and td-piRNAs.

44 and is not the only RNase that creates tRNA halves and that the shorter tRFs are not generated from

45 romosome arms (replichores) on opposite cell halves and the replication origin (oriC) close to midcel

46 s), tRNA(Asp), and tRNA(SeC) to produce tRNA halves and tRF-5s that are 26-30 bases long.

47 be achieved by splitting the cohort into two halves and using the average of the enrichment scores ev

48 as a strong candidate for generation of tRNA halves and Y RNA fragments in biofluids.

49 ll mutation of RNase 1 on the levels of tRNA halves and Y RNA fragments in the extracellular environm

50 ditions that induce the accumulation of tRNA halves, and the demonstration of a predominantly ribonuc

51 es in cell extract suggest that ciliate tRNA halves are degradation intermediates in an autophagy pat

52 biogenesis and biological functions of tRNA halves are emerging areas of research.

53 the nucleotide binding domains in these two halves are functionally nonequivalent.

54 consistent with our proposal that these two halves are functionally nonequivalent.

55 the aqueous environment while the N-terminal halves are not.

56 Its two Ge9-halves are the first examples of germanium deltahedra wi

57 At the interface of these two halves are two nucleotide-binding domains and a metalloi

58 g subprocesses: disengagement of the spindle halves, arrest of spindle elongation, and initiation of

59 ed to identify angiogenin-generating 5'-tRNA halves as a proof of principle, the method should be app

60 wo tRNAs as major substrates for the 5'-tRNA halves as well, suggesting a previously uncharacterized

61 al gentamicin of 260 mg) between the sternal halves at surgical closure (n = 753) vs no intervention

62 sion of the stomach into proximal and distal halves averaged 0.809 (SD, 0.083) for normal FA and 0.44

63 We found that the BET N-terminal halves bearing the bromodomains convey marked difference

64 tRNA splicing endonuclease to yield tRNA 3'-halves beginning with a 5'-hydroxyl, and 5'-halves endin

65 inkers of various lengths that separated the halves between 6 and 30 A (alpha-carbons).

66 some arms do not separate into distinct cell halves, but extend from pole to pole with the oriC regio

67 Wild-type and engineered interface halves can be mixed to create two distinct Cre mutants,

68 eptum which divide the cell in two identical halves can be used in daughter cells, irrespective of it

69 rdinated activities of its N- and C-terminal halves catalyze sequential steps in recycling cofilin an

70 indicates that the NTD consists of two rigid halves connected by a flexible hinge.

71 The halves contain a transmembrane domain (TMD) with six tra

72 between the groups were larger in the upper halves (Delta = 0.04 mL/mL, P </= .001-.002).

73 duction) in ICT lures and first minus second halves (DeltaL(1-2)) were used to determine learning of

74 introduces support for nanopore sequencing, halves depth-of-coverage requirements, and improves asse

75 This roughly halves differences in coverage and power between the pla

76 ntersomitic furrows and posterior sclerotome halves, disrupting metameric NCC streaming and DRG segme

77 ts from the lateral movement of the germband halves during spider embryogenesis.

78 coprotein (P-gp), consists of two homologous halves each comprising one nucleotide-binding domain and

79 ating the 2D plane to two gated intersecting halves, each with different fillings, counter-propagatin

80 be divided into two structurally homologous halves; each half assembles as an alpha-helical barrel t

81 ork is robust and flexible, as loss of end-3 halves ELT-2 levels in the early embryo but levels fully

82 -halves beginning with a 5'-hydroxyl, and 5'-halves ending in a 2',3'-cyclic phosphate.

83 led that the majority of stress-induced tRNA halves, except for the 5' half from tRNA(HisGTG) and the

84 nchor for directed assembly of the AD and BC halves, forming both the chlorin macrocycle and the isoc

85 unreplicated arms resolve into opposite cell halves, generating a left-ori-right pattern.

86 ce of tRNA-derived small RNAs called 5' tRNA halves hampers the detection of other small RNAs, like m

87 tRNA fragments (tRFs) and tRNA halves have been implicated in various cellular processe

88 ingle channel gating while those in the same halves have lesser impact.

89 of the molecule and another in which the two halves have moved sideways, thereby closing the central

90 inantly ribonucleoprotein-free state of tRNA halves in cell extract suggest that ciliate tRNA halves

91 d region that connects the N- and C-terminal halves in many eukaryotic ABC transporters, allowing all

92 approaches for targeted depletion of 5' tRNA halves in murine serum samples.

93 developmental boundary between the two tail halves in the chicken, then followed major developmental

94 An increase in levels of the 5'-tRNA halves, induced by BmNSun2 knockdown, enhanced the td-pi

95 heir target sites brought the split mCitrine halves into close proximity, allowing BiFC to occur and

96 rall, the spin density ratio between the two halves is in agreement with experimental determinations,

97 support of these results, formation of tRNA halves is recapitulated by recombinant human RNase 1 in

98 training the ideal to take two steps roughly halves its identification efficiency.

99 introduced into the mosquito Aedes aegypti, halves its life span.

100 for Ca2+/gelsolin C-terminal and N-terminal halves+/-monomeric G-actin.

101 nge in mature tRNAs, indicating that 5'-tRNA halves, not mature tRNAs, are the direct precursors for

102 possible by embryonic microsurgeries wherein halves of 2 differently colored embryos were joined, ind

103 at the representations of the left and right halves of a face are dissociable.

104 These perspectives represent two halves of a feedback loop: individual behaviour scales u

105 We show that Ribeye can exchange between halves of a ribbon within 1 minute in a manner that is c

106 ng fiber, which consists of two intertwining halves of a single circular nucleoprotein.

107 ania major TyrRS show that, instead, the two halves of a single molecule form a pseudo-dimer resembli

108 sister loci that have segregated to opposite halves of an E. coli cell.

109 In the hypocotyl assays, the basal halves of APY-suppressed hypocotyls contained considerab

110 The similarity of the N- and C-halves of archaeal TBPs is especially pronounced in the

111 iratory substrates, however, depends on both halves of Atp25p, indicating that the N-terminal half ha

112 disrupts correlated motions between the two halves of Bacillus thuringiensis PI-PLC, and Pro(245) va

113 of either Fos or Jun fused to complementary halves of beta-lactamase.

114 flexibility in the juxtaposition of the two halves of bipartite NRSE.

115 ired for cbox binding, the N- and C-terminal halves of C-RING1B can be separated and are able to inte

116 gesting that the flexibility between the two halves of CaM also contributes to the fine tuning of the

117 ein domains through the use of nonfunctional halves of CAX transporters.

118 transport, whereas co-expressing C-terminal halves of CAX variants with CAX1 conferred salt toleranc

119 Co-expressing variants of N- and C-terminal halves of CAX1 and CAX3 in yeast suggested that the N-te

120 Inactive halves of DAM (DNA adenine methyltransferase) were fused

121 an unexpected binding pocket between the two halves of E2.

122 mmunohistopathologic differences between the halves of each nevus were demonstrable even when in vivo

123 resegmentation, with anterior and posterior halves of each vertebra deriving from adjacent somites.

124 ke PIF3, PIF1 does not interact with the two halves of either phyA or phyB separately.

125 These functions, exerted by the two halves of EL5, are independent, because the loop can be

126 s high sequence similarity to the C-terminal halves of fibrinogen beta and gamma chains.

127 Trab group, and during the first and second halves of follow-up in the Comp group, were calculated.

128 sk (RR) and 95% CI, for the first and second halves of follow-up, adjusting for confounding variables

129 ged with the complementary C- and N-terminal halves of green fluorescent protein and in the presence

130 The right halves of halichondrins A-C (1a-c) were synthesized in 2

131 diated couplings were converted to the right halves of halichondrins A-C in excellent overall yields.

132 The right halves of halichondrins A-C were synthesized by coupling

133 A stereocontrolled synthesis of the left halves of halichondrins was reported.

134 With this approach, the left halves of halichondrins, homohalichondrins, and norhalic

135 that mutations in both the N- and C-terminal halves of ICP22 result in similar defects in viral late

136 and hinge loop joining the N- and C-terminal halves of IDE for catalysis.

137 site close to the interface between the two halves of inward facing LmrP.

138 istinct regions within the N- and C-terminal halves of IpaC.

139 acting as a molecular hinge between the two halves of lactose permease.

140 idence that UbcM2 can bind to the N-terminal halves of multiple cullins, implying that this E2 is a g

141 ormed by association of helices from the two halves of NarK.

142 Containing 10 transmembrane helices, the two halves of NCX_Mj share a similar structure with opposite

143 haeological sites in the western and eastern halves of North America by employing statistical tools u

144 nd EM projection images suggest that the two halves of P-gp are separated by a central cavity that cl

145 The homologous halves of P-gp each contain a transmembrane (TM) domain

146 Each of the homologous halves of P-gp is composed of a transmembrane domain (TM

147 by a 75-residue linker that connects the two halves of P-gp.

148 th the opening and closing motion of the two halves of P-gp.

149 ests that correlated motions between the two halves of PI-PLC may be more important for enzymatic act

150 ntly with both the N-terminal and C-terminal halves of Pol2 (Pol2N and Pol2C).

151 (P=0.007), and between the first and second halves of PROTECT AF and CAP, with 10.0%, 5.5%, and 3.7%

152 The C-terminal halves of PspA and PspC have some structural similarity

153 Analytical measurements of both halves of redox couples for dissolved iron, mercury, and

154 ion into a gap between the N- and C-terminal halves of Sec61.

155 movements of the amino- and carboxy-terminal halves of SecY.

156 ptides, fused to either the N- or C-terminal halves of split mCitrine, were engineered to recognize t

157 upling conformational changes across the two halves of the AAA ring.

158 assistant in their respective first and last halves of the academic year, but operative times within

159 hese molecules to interact with the distinct halves of the active site.

160 complex comprised of the target and the two halves of the aptamer.

161 nuously, in the amino- and carboxyl-terminal halves of the bundle and the linker domain.

162 ith the distinct hydrophobic and hydrophilic halves of the CA II active site were prepared.

163 irectly with the hydrophobic and hydrophilic halves of the CA II active site.

164 Thus, the two regulators act on different halves of the catalytic cycle in an unusual regulatory r

165 he fold of the unique domain between the two halves of the catalytic region.

166 the active site by a loop separating the two halves of the catalytic TIM barrel.

167 The resulting two halves of the cleaved mRNA accumulate to much higher lev

168 alpha-mu2 double mutants disrupt both halves of the complex and are lethal.

169 However, they model the halves of the complex as outputs of modules selected for

170 ontact area at the interface between the two halves of the composite photoanode.

171 can generate opposite velocities on the two halves of the condensate.

172 Most strikingly, the two halves of the crystallographic dimer pack together in a

173 cysteine scanning shows that the C-terminal halves of the cysteine-containing transmembrane segments

174 ded evidence of interactions between the two halves of the dimers.

175 , although the relative positions of the two halves of the dyad are reversed.

176 f germ band flexure, when the left and right halves of the embryo separate and the embryo folds deepl

177 xons originating from anterior and posterior halves of the embryonic day 14.5 dorsal thalamus respond

178 recorded at 3 sites: the proximal and distal halves of the enthesis and the adjacent calcaneal superi

179 the electrostatic attraction between the two halves of the enzyme, shifting the partitioning between

180 und that the flexible linker joining the two halves of the FH2 dimer has a strong influence on dissoc

181 ketone synthesis was used to couple the two halves of the final product at a late stage in the synth

182 nts were designed from approximately the two halves of the full-length peptide whereas the five short

183 ntified between rabbits in the top or bottom halves of the group as measured by the behavioral assay.

184 ay matter regions forming the right and left halves of the interbrain.

185 Both the CI and the CII halves of the KaiC hexamer harbor ATPases, but only the

186 In contrast, the top and bottom halves of the lipid tails surrounding MAO-B are more and

187 ectrons are localized at the two icosahedral halves of the metal core.

188 pindle is the only structure linking the two halves of the mitotic spindle, it is under mechanical te

189 central cavity between the N- and C-terminal halves of the molecule and another in which the two halv

190 umber of different labeling schemes, the two halves of the molecule can be distinguished, so that the

191 ts show that distinct domains of SecA on two halves of the molecule interact with two corresponding S

192 interacting regions on the N- and C-terminal halves of the MukB coiled coil through photoaffinity cro

193 relative alignment of the N- and C-terminal halves of the MukB coiled coil, obtained by a combinatio

194 mechanism for communication between the two halves of the nitrogenase complex is suggested by normal

195 esenting, respectively, the leading/trailing halves of the peak.

196 luating the segmental tilt angles of the two halves of the peptide, we substituted selected leucines

197 rn of basic and acidic residues in the first halves of the periodic repeats (periods) in tropomyosin.

198 wo equivalent structures located in opposite halves of the predivisional cell.

199 n NBDs and MSD cytoplasmic loops in opposite halves of the protein rapidly and reversibly arrest sing

200 t Lys16 and Lys335, located in the A1 and A2 halves of the protein, have different roles in ArsA cata

201 Asp142 and Asp447, located on the A1 and A2 halves of the protein, have different roles in ArsA cata

202 (NBD) and cytoplasmic loops (CL) in opposite halves of the protein, indicating that any structural re

203 acting as a molecular hinge between the two halves of the protein, must also exit from the membrane

204 place in the occlusion between the N- and C-halves of the protein.

205 on there is some flexibility between the two halves of the protein.

206 on and activation of ATPase activity in both halves of the protein.

207 e-spanning pore formed by the two homologous halves of the protein.

208 omain is located at the interface of the two halves of the protein.

209 ves a rocker-switch type movement of the two halves of the protein.

210 Unexpectedly, the two halves of the ring are structurally related to karyopher

211 result of this transition, the intracellular halves of the S6 helices bend and rotate by about 100 de

212 HRAS and NOTCH1 mutations identified in two halves of the same cSCC, suggesting polyclonal origin.

213 4 hydroxybutyrate (P4HB) sutures in opposite halves of the same wound.

214 sition point, data from the first and second halves of the sessions were compared.

215 to balance the locomotor output between both halves of the spinal cord, thereby ensuring a symmetrica

216 y distributing excitatory drive between both halves of the spinal cord.

217 The two halves of the spiroketalization precursor were joined vi

218 s by rigid-body relative rotation of the two halves of the synapse, mediated by a flat protein-protei

219 to proceed by rigid-body rotation of the two halves of the synaptic complex, following the cleavages

220 f electron delivery demonstrate that the two halves of the ternary complex between the MoFe protein a

221 ffects between myosin head arrays in the two halves of the thick filaments, have been claimed to prov

222 Between the early and latter halves of the time period, the major TC exceedance proba

223 Additionally, the N- and C-terminal halves of the TM helix form trimeric cores of opposite n

224 and transport substrate that showed the two halves of the transporter separated by a central cavity.

225 son of the structures of the two symmetrical halves of the transporter suggests conformational change

226 trate lead to a close association of the two halves of the transporter, thereby closing the central c

227 affinity and conformational changes in both halves of the transporter.

228 rand cleavage is coordinated between the two halves of the transpososome.

229 interface formed between the amino-terminal halves of the two protomers.

230 ed structural order of the N- and C-terminal halves of the uncomplexed SNARE motif suggests the forma

231 ein results in a covalent bonding of the two halves of the Venus molecule, the head-to-tail interacti

232 th reciprocal exchanges involving (i) the 3' halves of the viruses, including the Vif, OrfA, and Env

233 ch hemisphere receives information from both halves of the visual field.

234 ay crystallography shows that the N-terminal halves of their SNARE motifs bind the CALM(ANTH) domain

235 M4 are water-exposed, whereas the N-terminal halves of these TMs are not.

236 Thus, the N- and C-terminal halves of this bipartite channel may interact with other

237 Alternate transcription of the two opposing halves of this cluster appears to be the result of promo

238 Cys-285 are disulfide-bonded, the C-terminal halves of TM1 and TM4 are water-exposed, whereas the N-t

239 hinge-bending movements of the extracellular halves of transmembrane domains 1, 2 and 6, together wit

240 We find very clear signs that the two halves of tRNAs had an evident evolutionary relationship

241 ogy or complementarity between the 5' and 3' halves of tRNAs, even if there is strong evidence in fav

242 ength UNC-112 and that the N- and C-terminal halves of UNC-112 bind to each other.

243 The left and right halves of visual space had independent capacities and th

244 nce complementation of the N- and C-terminal halves of YFP attached to 5-HT(2C) receptors was observe

245 ma with distinct non-pigmented and pigmented halves on gross dissection and corresponding disomy 3 an

246 two chromosome arms reside in separate cell halves, on either side of a centrally located origin.

247 d 60-A-wide trimer divided into two globular halves: one containing N-terminal CRDs (N-CRDs) and the

248 We find that although manure storage halves oocyst loads, manure treatment, especially of cat

249 shorter tRFs are not generated from the tRNA halves or from independent tRNA cleavage by ANG.

250 hose centers connect two seemingly different halves or include a nitrogen atom.

251 arity and complementarity of their 5' and 3' halves or segments of them in intra-and inter-molecular

252 he intermolecular binding forces between two halves (or partners) of naturally split protein splicing

253 that angiogenin-induced accumulation of tRNA halves (or tiRNAs) is accompanied by increased survival

254 ndbrain, with activity in the left and right halves oscillating in antiphase, on a timescale of 20 s,

255 itute LTCC alpha1C-subunit from two distinct halves, overcoming the difficulty of expressing full-len

256 usion, blocks 40% of cardiac capillaries and halves perfused blood volume within the affected region.

257 abolish interaction of the N- and C-terminal halves, permit D382V UNC-112 to localize to adhesion str

258 only after extended contact with the vegetal halves prior to that time.

259 nts are biochemically distinct from the tRNA halves produced transiently in response to stress.

260 ArPIKfyve(WT), but not the N- or C-terminal halves, prolongs the Sac3(WT) half-life consistent with

261 uplex environment restricts local motion and halves QSSQ.

262 the optic tecta of the left and right brain halves reciprocally inhibit each other in birds.

263 In tetrapods, adjacent somite halves recombine to form a single vertebra through the p

264 Because of the linkage of their molecular halves (regiochemistry) and the configuration of the bia

265 n anticodon-binding domain; however, the two halves retain only 17% sequence identity to each other.

266 eplisomes separate and move to opposite cell halves shortly after initiation, migrating outwards as r

267 G) cleaves tRNA anticodons and produces tRNA halves similar to those produced in response to stress.

268 t NMD and promote translation of two protein halves, termed Split-ORFs, from the bicistronic SRSF7-PC

269 We engineered split-DddA halves that are non-toxic and inactive until brought tog

270 f the heterotrimeric complex consists of two halves that form an hourglass-shaped pore with a constri

271 subunit, SecY or Sec61alpha, consists of two halves that form an hourglass-shaped pore with a constri

272 The orthogonality constraint halves the effective size of the factor model and outper

273 On public benchmarks, Opal halves the error on precision/recall (F1-score) as compa

274 Meiosis is the cell division that halves the genetic component of diploid cells to form ga

275 nts with suspected appendicitis, and roughly halves the need of diagnostic imaging.

276 omosomes and the reductional division, which halves the number of chromosomes in daughter cells.

277 It also halves the overpotential during discharge, increases the

278 that resection of cavity shave margins (CSM) halves the rate of positive margins and re-excision in b

279 blishes that a low-frequency allele in CCND2 halves the risk of type 2 diabetes primarily through enh

280 ) binds both X chromosomes in XX animals and halves the transcription from each.

281 serves by a factor of 1.8, which effectively halves the uncertainty in the recruitment contribution o

282 With the use of a slight excess of the left halves, the desired ketones were isolated in yields of 8

283 n the lamina serving the upper and lower eye halves, the general morphology of the midband lamina ref

284 ob/ob mice, whereas Osteocalcin inactivation halves their hyperinsulinemia.

285 sition, resulted from assembly of two hollow halves through a joint also acting as a partition.

286 that the enzyme is able to join spliced tRNA halves to mature-sized tRNAs where the joining phosphodi

287 Fusions of the split-DddA halves, transcription activator-like effector array prot

288 Sequence identification of the 5'-tRNA halves using cP-RNA-seq revealed abundant and selective

289 by stitching together two similarly complex halves via a key Ru-catalyzed alkene-alkyne coupling and

290 (even in non-mammary cell lines), where tRNA halves were detected as part of approximately 45 kDa rib

291 QV ratios of upper to lower lung halves were lower in patients with CF than in control su

292 as it did not occur when N- and C-terminal "halves" were coexpressed.

293 bacteriocins, especially at their C-terminal halves where all contain a conserved KXXXGXXPWE motif, s

294 t the second pyrrole ring in one of three BC halves, whereas the other two were prepared by known rou

295 s are not subdivided into rostral and caudal halves, which is necessary for neural segmentation.

296 cap subdivides into nucleotide and acceptor halves whose motions, while coupled, exhibit an independ

297 We find that the per nucleus import rate halves with each cycle and construct a mathematical mode

298 lits insulin into inactive N- and C-terminal halves without breaking the disulfide bonds.

299 n cells of the anterior and posterior somite halves, without clear resegmentation.

300 red CHO cell lines expressing nonfluorescent halves (YN and YC) of yellow fluorescent protein attache