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 vering the free ends of the two rps12 intron halves.

3 t subdivide the CNS into bilateral symmetric halves.

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

5 mary structure of the Rossmann fold into two halves.

6 op cleavage of mature tRNAs to generate tRNA halves.

7 the internucleotide bond that joins the two halves.

8 We also show that MeCP2 has two functional halves.

9 ntially migrate into the anterior sclerotome halves.

10 te relaxase and its two, separate functional halves.

11 ormation and pinches the cell into two equal halves.

12 ail to completely separate into two distinct halves.

13 ell migratory streams through rostral somite halves.

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

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

16 d and anticorrelated motions between the two halves.

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

18 icodons, resulting in the generation of tRNA halves.

19 on and corresponding disomy 3 and monosomy 3 halves.

20 The protein is organized into two halves.

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

22 lack of sequence similarity between the two halves.

23 bacteriocins are located in their C-terminal halves.

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

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

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

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

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

29 unit, ArsA, is an ATPase with two homologous halves, A1 and A2, connected by a short linker.

30 ytic subunit of the pump, has two homologous halves, A1 and A2.

31 sA, the catalytic subunit has two homologous halves, A1 and A2.

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

33 and 4 are proteolytically processed into two halves and are differentially regulated by nuclear recep

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

35 categorise the sample into richer and poorer halves and examine caesarean rates within rural areas.

36 ecies assembled from separate 5' and 3' tRNA halves and four species derived from tRNA precursors con

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

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

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

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

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

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

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

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

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

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

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

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

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

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

51 visual evidence that vaults disassemble into halves as the solution pH is lowered from 6.5 to 3.4.

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

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

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

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

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

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

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

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

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

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

62 194 nM, respectively), indicating that both halves contribute to the interaction in a synergistic ma

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

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

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

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

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

68 formation by the opening of two linked SecY halves during polypeptide translocation.

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

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

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

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

73 ombinant gamma-module (gamma148-411) and its halves, gamma148-286 and gamma287-411 fragments containi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

88 n, in Chinese character recognition, the two halves of a centrally fixated character may be initially

89 We propose that the forward and reverse halves of a flash-induced protein-protein electron trans

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

91 intrachromosomal association that holds the halves of a single broken sister chromatid together in m

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

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

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

95 he average level of matching between the two halves of an individual tRNA and the average level of ma

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

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

98 poration of labeled nucleotides into the two halves of ArsA.

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

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

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

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

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

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

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

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

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

108 ar interactions between the basic and acidic halves of CHMP3 and CHMP4B, these results suggest that t

109 ndency toward higher densities in the distal halves of chromosome arms.

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

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

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

113 e level of sequence identity between the two halves of each of a large sample of tRNAs and compare th

114 el of the thin filament, with the N-terminal halves of each period (i.e., the so-called "alpha zones"

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

131 Previously, it has been shown that the two halves of MinC have two distinct functions.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

146 his paper we report syntheses of the eastern halves of ritterazines B, F, G, and H and address the en

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

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

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

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

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

152 for mediating the interaction between dimer halves of the active tetramer.

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

154 hese results suggest that the two homologous halves of the ArsA may be functionally nonequivalent.

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

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

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

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

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

160 he average level of matching between the two halves of the chimeric tRNAs in any of the sets we const

161 ed on the distal halves than on the proximal halves of the chromosome arms.

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

163 es six iron atoms in two MFe(3)S(3) cuboidal halves of the cluster.

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

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

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

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

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

169 t flexible, with flexibility between the two halves of the dimer conferred by the linker segments.

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

171 ded and ejects bidirectionally into opposite halves of the dividing cell.

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

173 ents with little cooperativity among the two halves of the E-box.

174 re step--in which the anterior and posterior halves of the embryo are developing at different tempera

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

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

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

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

179 either one of two sites located in distinct halves of the enzyme.

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 of its GTPase-defective mutants causes both halves of the first meiotic spindle to extend symmetrica

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

184 , whose premature activation would close the halves of the grasper and induce it to pull inedible mat

185 tiparallel arrangement across the partnering halves of the IS supports reciprocal Notch signal propag

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

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

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

189 higher eukaryotes, microtubules (MT) in both halves of the mitotic spindle translocate continuously a

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

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

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

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

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

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

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

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

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

199 ne-rich motifs in both the N- and C-terminal halves of the polypeptide, cluster at a common site betw

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

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

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

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

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

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

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

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

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

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

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

211 en each from the carboxy- and amino-terminus halves of the protein.

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

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

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

215 4 hydroxybutyrate (P4HB) sutures in opposite halves of the same wound.

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

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

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

219 The two halves of the spiroketalization precursor were joined vi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

235 ly with the interaction between the carboxyl halves of the VP16 AD, VP16C, and TATA-binding protein-a

236 ymmetry has opposite orientations in the two halves of the vulva.

237 nstroke has led to the assumption that these halves of the wingbeat cycle contribute equally to weigh

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

239 The N-terminal halves of these helices superimpose well on each other,

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

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

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

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

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

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

246 recombination of the anterior and posterior halves of two adjacent sclerotomes on both sides of the

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

265 uplex environment restricts local motion and halves QSSQ.

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

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

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

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

270 e significantly more matches between the two halves than do random sequences that can form the tRNA s

271 nd duplicated loci were mapped on the distal halves than on the proximal halves of the chromosome arm

272 sed of highly similar anterior and posterior halves that are arranged in a mirror symmetric pattern.

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

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

275 hes for widely separated genes encoding tRNA halves that, on the basis of structural prediction, coul

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

277 , negates the effects of central insulin and halves the effects of systemic insulin on hepatic glucos

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

279 Meiosis is a specialized cell division that halves the genome complement, producing haploid gametes/

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

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

282 It also halves the overpotential during discharge, increases the

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

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

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

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

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

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

289 moval of tRNA introns and processing of tRNA halves to be joined in trans.

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

291 s genome reveals nine genes that encode tRNA halves; together they account for the missing tRNA genes

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

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

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

295 f the isolated gamma148-286 and gamma287-411 halves were much lower (K(d)'s = 521 and 194 nM, respect

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

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

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

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

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

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