ライフサイエンスコーパス: ring

1 bunits at defined positions in the hexameric ring.

2 in filaments for the cytokinetic contractile ring.

3 yze derivative linkages on the distal ribose ring.

4 s in the crystal structure of the PCNA-K20ac ring.

5 ics, all through tuning of the heteraromatic ring.

6 4 + 2)-cycloaddition for annulation of the B ring.

7 ut not by those tested containing a triazole ring.

8 of the podosome core but not of the adhesive ring.

9 eptins and in forming the subsequent midbody ring.

10 8.6 kcal/mol stabilization from the orotate ring.

11 ent attached to the nitrogen of the pyridone ring.

12 y the presence of substituents on the phenol ring.

13 ket of the AcCoA binding site by an aromatic ring.

14 hlorin macrocycle bearing an annulated fifth ring.

15 lation and a late-stage oxidation of a furan ring.

16 nitial enantiomerically enriched pyrrolidine ring.

17 P-dependent manner to form the cytokinetic Z ring.

18 re, leading to the formation of a cavitation ring.

19 ounds containing one, two, or three aromatic rings.

20 mbered rings, in preference to four membered rings.

21 oiety and assembly of the fused heterocyclic rings.

22 residing in infinity1Se chains versus in Se8 rings.

23 st mostly of five-fold and seven-fold carbon rings.

24 12-nm hexagonal lattice linked by CheA/CheW rings.

25 tes a trans coplanar geometry of the pyrrole rings.

26 importantly, to the conformation of its beta-rings.

27 als the mutual couplings between the antenna rings.

28 olecular competition with more electron-rich rings.

29 h alters the curvature of filamentous septin rings.

30 s after the initial appearance of gametocyte rings.

31 ositions 5,5' remain coplanar to the central rings.

32 ybrid" events, have HF onsets followed by LF ringing.

33 ion states involving six- and seven-membered rings (1,5 and 1,6 H-shifts, respectively) of alpha-OH h

34 e group between the thiazole and pyrrolidine ring (42) of compound 18 resulted in a dramatic increase

35 bstituted at the R-6 and R-7 position on the ring A, showed similar antioxidant activity to flavone w

36 ivity than the di-substituted flavone on the ring A.

37 ovalent interactions with associated benzene rings (a simple model of aromatic amino acid side chains

38 ent of substituents on one of its 5-membered rings, a pattern shared by a number of other terpenes.

39 ew pathway yielding oxidation of the benzene ring after the cleavage of the piperazine ring (e.g., CI

40 1 is capable of assembling normal actomyosin rings, although rings isolated from myo2-E1-Sup1 are def

41 We engineered a stable Rca hexamer ring and analyzed its functional interaction with Rubisc

42 preference for the centroid of the aromatic ring and distances near the sum of the van der Waals and

43 milled circumferentially around the division ring and drove the motions of the peptidoglycan-synthesi

44 ion was seen in 4 of 35 (11%) with a vaginal ring and in 4 of 34 (12%) with IVT.

45 n WT Arkadia is critical for the function of RING and that it depends on the nature of the residue at

46 engthen the interaction between this benzene ring and the agonist's quaternary ammonium (QA) and (2)

47 The proteolytic P-ring and the structurally similar R-ring form the core c

48 -en-3-one moieties, respectively, in their A-rings and differ in the position of their en-one structu

49 tively inhibited the sprouts of mouse aortic rings and neoangiogenesis in chick embryo chorioallantoi

50 primary phosphines to form cyclic phosphine rings and the first example of a non-metal-catalyzed hyd

51 to unequivocally demonstrate that 1) the Se8 rings and the infinity1Se chains are characterized by th

52 member of the PYBs, possesses three aromatic rings and these adopt a twisted "S"-shaped conformation

53 rise to fascinating everyday effects (coffee rings), and influence technologies ranging from printing

54 cleophilic attack, opening the cyanuric acid ring, and the mobile lysine guides products through the

55 d enables room-temperature lasing in protein rings, and circular and elliptical pillars with customiz

56 itions the QA to interact optimally with the rings, and weakly to Cho because a different H-bond teth

57 e construction of new classes of pyrrolidone-ring annulated thiophene/furan-based heterocyclic scaffo

58 In ex vivo rings, aortic and mesenteric vessels from SHR treated wi

59 hydroxyl or amino group in the newly formed ring are considerably more active than their axial diast

60 organic chemistry of an eta(2)-bound benzene ring are explored using the complex TpW(NO)(PMe3)(eta(2)

61 While bacterial FtsZ rings are composed of a single FtsZ, except in the basal

62 ctronic states can be ascribed to changes in ring aromaticity/antiaromaticity, with the switch from g

63 They are released from the contractile ring as it disassembles and then associate with type 1 n

64 The double-ring assembly of GroEL is required to function with GroE

65 acteria, indicating a common mechanism for Z-ring assembly.

66 uct the trans-2,6-disubstituted dihydropyran ring, asymmetric alpha-aminoxylation reaction, and Still

67 We also found that the RING B-box coiled-coil (RBCC) domain in KAP1 and the pro

68 thocyanidins depended on the substituents on ring B.

69 ce of two hydroxyl moieties in the flavone A-ring backbone are essential for potent inhibition of Las

70 olving spontaneous ring expansion of a fused-ring benzazirine into a seven-membered ring cyclic keten

71 ed vasoconstriction in an ex vivo rat aortic ring bioassay.

72 French Fries, chips, chicken nuggets, onions rings, breakfast cereals, biscuits, crackers, instant co

73 sembled starting from an easily accessible A ring building block by a (4 + 2)-cycloaddition for annul

74 d strongly by azoles containing an imidazole ring but not by those tested containing a triazole ring.

75 ricted to members of the inner and outer NPC rings, but it lacks numerous others including cytoplasmi

76 nerated bioprostheses or failed annuloplasty rings, but mitral ViR was associated with higher rates o

77 ivisome that promotes the integrity of the Z ring by acting through ZapB and raises the possibility o

78 harge within an aromatic cyclononatetraenide ring by the symmetric superposition of an alkyl ammonium

79 es report that FtsZ polymers move around the ring by treadmilling, which guides and regulates the inw

80 fused to graphene edges through two pyrrole rings by thermal annealing.

81 n the position of their en-one structures in ring C.

82 ouette mechanism for automerization of outer ring carbons in phenanthrene, a reaction demonstrated pr

83 Saturn's A- and B-rings cast a shadow on the planet that reduced ionizatio

84 trated 1 or more foci of intramucosal signet ring cell gastric cancer in the examined specimen.

85 ), one in chain prenylated (cPta) and one in ring-closed prenylated pterocarpans (rPta), as character

86 yclizations of bis(vinyl boronate esters) or ring-closing metathesis reactions followed by complexati

87 Iron(III)-catalyzed carbonyl-olefin ring-closing metathesis represents a new approach toward

88 A highly efficient, Z-selective ring-closing metathesis system for the formation of macr

89 center, and the lactone moiety was formed by ring-closing metathesis.

90 ablish the E,Z-diene part, an ester-tethered ring-closing metathesis/base-induced eliminative ring op

91 c ring-opening of cyclobutene, electrocyclic ring-closing of Z-hexatriene, the [1,5]-H shift in Z-pen

92 , but support instead hydrogen-bond assisted ring-closing to prodrugs.

93 ility of in situ imine formation followed by ring-closing, but support instead hydrogen-bond assisted

94 The ring closure of domino protocol was highly stereoselecti

95 pine 6,6-dioxides it has been found that the ring closure of the zwitterion leading to the formation

96 Lewis acid catalyzed ring closure with a thiophene dialcohol in 2% ethanol-di

97 is photo-switchable following the reversible ring closure/opening of the central dithienylethene via

98 roduct merocyanine isomers, as well as their ring-closure reaction back to the spiropyran form.

99 This includes six C-C ring-closure steps that, through intramolecular Friedel-

100 ied it as chaperonin containing TCP1 or TCP1-Ring complex (CCT/TRiC chaperonin), a complex known to f

101 ace, recruits the MT nucleator gamma-tubulin ring complex (gamma-TuRC), and is sufficient to convert

102 The single-ring compound, vanillin, slightly slows down but cannot

103 taining either desmethyl- or oxa-lanthionine rings confirm that the precise geometry of these rings i

104 a common scaffold consisting of two aromatic rings connected by a linear or a cyclic spacer.

105 iously undescribed [4.4.0] and [5.3.0] fused-ring-containing products were obtained when santonin was

106 ely to be the major motor driving actomyosin ring contractility.

107 myo2-E1 also affects actomyosin ring contraction when rings isolated from permissive tem

108 Myp2p plays the dominant role in actomyosin ring contraction.

109 The difference in aromaticity between the rings contributes to the thermodynamic balance of the me

110 s with nonfullerene acceptors owning unfused-ring cores.

111 eraction and raise the possibility that Syt1 rings could pre-form on the synaptic vesicle to facilita

112 e (NMR) spectroscopic study of the chain and ring crystalline allotropes of Se as well as of amorphou

113 fused-ring benzazirine into a seven-membered ring cyclic ketenimine.

114 a new PET/CT system, the Discovery IQ with 5-ring detector blocks.

115 nal mucosal surface, we used a novel vaginal ring device comprising a silicone elastomer body into wh

116 sion in radial nerve cords, circumoral nerve ring, digestive system, tube feet and innervation of int

117 bulk experiments with a commercial rotating ring disk electrode.

118 by 2 point mutations (C62A/C65A) in the Pml RING domain.

119 er source coupled to a high-stability cavity-ring-down-spectroscopy setup.

120 he N-tier ring is pushed ahead by the C-tier ring during CMG translocation, opposite the currently ac

121 pressure balloon positioned across the valve ring during rapid ventricular pacing.

122 utenes is driven by the strain in the medium-ring (E,E)-1,3-diene intermediate.

123 ne ring after the cleavage of the piperazine ring (e.g., CIP product with m/z 280) is described for F

124 and this activity was dependent on both its RING E3 ligase and ADP-ribosylation factor (ARF) GTPase

125 DC34 that functions specifically with Cullin-RING E3 ligases, such as SCF (Skp1-Cullin-F-box).

126 The "FA core complex" contains the RING-E3 ligase FANCL and seven other essential proteins

127 Now a superior hydrogen-free 5/6/5 fused ring energetic material, 1,2,9,10-tetranitrodipyrazolo[1

128 enhancing nodules <3 mm in diameter without ring-enhancement or mass effect, and homogenous T2 signa

129 attack and (3) MRI spinal cord demonstrating ring-enhancement.

130 tom tunneling reaction involving spontaneous ring expansion of a fused-ring benzazirine into a seven-

131 rst examples where both cyclopropanation and ring expansion of arenes were rendered reversible.

132 pathway, the alkylidene ligand is lost, via ring expansion of the metallacyclobutane intermediate, l

133 es of arenes in thermally reversible Buchner ring expansion reactions, marking the first examples whe

134 uivalents of alkynes by coupling homoallylic ring expansion to yield the formal "6-endo" products wit

135 trogen ylide formation followed by azetidine ring expansion.

136 We identify SIAH2, a RING finger E3 ubiquitin ligase associated with the cell

137 ed phosphoproteomics, we have identified the RING finger E3 ubiquitin ligase RNF157 as a target at th

138 all nodule on the volar surface of his right ring finger.

139 tation of such piperidines is the piperidine ring flip and not nitrogen inversion or rotation about t

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

141 olytic P-ring and the structurally similar R-ring form the core complex that contains the proteolytic

142 apB provide additional positional cues for Z-ring formation and may help coordinate its assembly with

143 esuccinylase (DapE) facilitates functional Z ring formation by strengthening the Ter signal via ZapB.

144 These results suggest a path for aromatic ring formation in cold acetylene-rich environments such

145 Ring-forming AAA+ chaperones exert ATP-fueled substrate

146 a(15) N values from annual bone growth layer rings from dead-stranded animals, and then combined the

147 e strategy was also utilized for accessing 5-ring fused benzo[g]indolo[3,2-b]indole.

148 he fused and nonfused SMAs, we show that the ring-fusion introduces several beneficial effects on the

149 equired to function with GroES, and a single-ring GroEL variant GroEL(SR) forms a stable complex with

150 depends on the really interesting new gene (RING)-H2 interaction with the E2 enzyme UbcH5b in order

151 While substitution on the aromatic rings had comparatively little effect on quadricyclane l

152 ossessing highly functionalized cyclopentane rings has been developed employing soft ketone enolates

153 read use to forge bonds between two aromatic rings has enabled every branch of chemical science.

154 e bromodomain (BRD), CH2 (comprising PHD and RING), HAT, and ZZ domains at 2.4-A resolution.

155 oup substituted at the R-3 position on the C ring, have outstanding antioxidant activity.

156 hydroxylation of photo-oxidized heterocyclic rings, have been identified during photodegradation of S

157 yl side chain of the neomycin or paromomycin ring I, as part of the dioxabicyclooctane ring, into eit

158 ormation and constriction of the contractile ring in fission yeast.

159 rtance of the acetoxy functionality on the A-ring in its activity as a kappa-opioid receptor agonist.

160 aluate safety of IVT or an estradiol vaginal ring in patients with early-stage BC receiving an AI; se

161 n a regular array with dimensions matching a ring in the upper part of the complex.

162 between the toluene and the N-oxyl aromatic rings in the transition state structures.

163 lar hydroacylation has favored five-membered rings, in preference to four membered rings.

164 to homologous to E6AP C-terminus (HECT) and RING-in-between-RING (RBR) E3s.

165 the structural components of the contractile ring including filamentous actin (F-actin), myosin, and

166 to differently substituted (mainly on phenyl ring) indoles and 1-benzothiophenes from the reaction of

167 The (H2O)3Ne + H2O ring insertion barrier is sufficiently large, such that

168 in ring I, as part of the dioxabicyclooctane ring, into either the gauche-gauche or the gauche-trans

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

170 When the PYBs bind, the thiazolium ring is cleaved, but when the SCTs bind, ThDP is modifie

171 Therefore, the N-tier ring is pushed ahead by the C-tier ring during CMG trans

172 ol scaffold with fused tetrahydroquinoxaline rings is described.

173 s confirm that the precise geometry of these rings is essential for this synergistic activity.

174 ify the likelihood that the lumen of these c-rings is in a hydrated, potentially conducting state rat

175 rins can be stabilized if one of the pyrrole rings is replaced with a furan ring to afford stable oxa

176 assembling normal actomyosin rings, although rings isolated from myo2-E1-Sup1 are defective in ATP-de

177 lso affects actomyosin ring contraction when rings isolated from permissive temperature-grown cells a

178 Credible future tree ring isotope studies require explicit accounting for spe

179 zidines bearing a hydroxymethyl group at the ring junction were synthesized from a readily available

180 ving the RCM reaction to install the C18-C19 ring junction, was successful in assembling the macrolac

181 ical for a stable single-mode operation of a ring laser.

182 vide tight control of neddylation and cullin-RING-ligase activity in vivo.

183 omplex, regulates the activity of the cullin-RING-ligase type of ubiquitination E3s by promoting nedd

184 Casparian strips are ring-like lignin polymers deposited in the middle of ant

185 Overall, our data show that ring-like polymerization is an intrinsic property of Syt

186 compartment coherence between the middle and ring-little fingers tended to be higher as compared with

187 rine in either the 7 position of the steroid ring (LKM38) or the aliphatic tail (KK174), we mapped a

188 ort on a powerful extension of those modes, "ringing" mode, which more than doubles the number of non

189 Circumferentially within the ring, multiple proteins proximal to the membrane form cl

190 Using a ring network, we show how excitatory and inhibitory inte

191 nd to CA II via an interaction of the acidic ring nitrogen with the CA II active site zinc, as well a

192 udomigration of the substituent on the arene ring of arylglyoxals.

193 P synthase complex and specifically with the ring of c-subunits that constitute the membrane domain o

194 ation pathway lies between the core and gate ring of helices, distinct from the transporter pathway.

195 introduction of chlorine atoms on the indole ring of malbrancheamide differentiates it from other mem

196 samine sugar is attached to the macrolactone ring of MTM and PKM.

197 ct release complex, the reduced nicotinamide ring of the cofactor transiently enters the active site

198 more effective C-H...pi (between the phenyl ring of the EPK and the catalyst) and C-H...O interactio

199 hat contains all carbon atoms of the D and E ring of the natural product could be installed in three

200 he active site where it displaces the pterin ring of the THF product.

201 nthetic intermediate containing the EF and G rings of the target.

202 efficiency (W i ) reconstructions using tree rings often disregard developmental changes in W i as tr

203 omain (DBD) and discovered a novel hexameric ring oligomeric form.

204 a of aerosols at higher mass loadings, while ring-opened species (neither 5 nor 10 Si atoms/molecule)

205 ields of related diols that were oxidatively ring-opened to afford cyclopentane dialdehydes.

206 f iron-sulfur cluster cofactors in reductive ring opening and hydroxy-group elimination.

207 s, where the aldol condensation, cyclopropyl ring opening followed by cyclization took place in a sin

208 1,6-Anhydro ring opening gave suitable substrates for efficient synt

209 oselective desymmetrization catalysts in the ring opening of a variety of cyclic anhydrides.

210 -b]indoles via Lewis acid-catalyzed SN2-type ring opening of activated aziridines with indoles having

211 e readily synthesized through a nucleophilic ring opening of spiro[cyclopropane-1,3'-oxindoles] with

212 -closing metathesis/base-induced eliminative ring opening sequence was used.

213 nnelation results in increased retro-Bergman ring opening, allowing C(1)-C(5) cyclization to become a

214 enes upon acid-promoted cyclopropyl carbinol ring opening.

215 The ring-opening copolymerization of maleic anhydride and pr

216 A Bi(OTf)3-catalyzed ring-opening cyclization of (hetero)aryl cyclopropyl car

217 dates, switching off and on the nucleophilic ring-opening in a controlled manner.

218 The rate of living ring-opening metathesis polymerization (ROMP) of N-hexyl

219 istribution of grafts in polymers via living ring-opening metathesis polymerization (ROMP).

220 on of butadiene with ethylene, electrocyclic ring-opening of cyclobutene, electrocyclic ring-closing

221 onvenient low-cost method for regioselective ring-opening of donor-acceptor cyclopropanes with the Zn

222 produced commercially by the metal-catalyzed ring-opening polymerization of lactide.

223 ltaneously fast and selective for the living ring-opening polymerization of several common monomers,

224 he strained 3',5'-cyclic monomer can promote ring-opening polymerization to afford the resulting poly

225 ) chemistry, a novel C-N bond activation and ring-opening process is described for these increasingly

226 lfonamide is unprotected, the characteristic ring-opening reaction is completely silenced, which expl

227 the relevance of the protonation step in the ring-opening reactions of 1,3-benzoxazines with thiols i

228 ced, which explains that the majority of the ring-opening reactions reported in the literature invoke

229 The mechanism of ion-pairing, ring-opening, and catalyst deactivation have been studie

230 rted herein is an exceptional chemoselective ring-opening/C(sp(3) )-C(sp(3) ) bond formation in the c

231 hydrogen bonds between the oxazolidinedione ring oxygen and the CA II protein backbone.

232 of P. falciparum and arrest parasites at the ring phase of the asexual stage and also gametocytogensi

233 report the analysis of a concentric circular ring plasmonic optical antenna (POA) array using a simpl

234 o E6AP C-terminus (HECT) and RING-in-between-RING (RBR) E3s.

235 by water availability, as is evident in tree ring records.

236 on a 110 fs time scale is followed by corrin ring relaxation on a 260 fs time scale.

237 coustic pulse and the mechanical mode of the ring resonator is also studied.

238 itching the folding state of Miura-ori split-ring resonators.

239 the substrate phosphodianion and the ribosyl ring, respectively, and an 8.6 kcal/mol stabilization fr

240 ne Rh, regenerated instead with a six-carbon-ring retinal chromophore featuring a C(11)=C(12) double

241 Upon ring rotation, the protonated glutamate encounters the m

242 idoids share the exact five- to six-bicyclic ring scaffold of the Catharanthus iridoids.

243 promote epoxidation on opposite faces of the ring scaffold, evidence of competitive epoxidation pathw

244 roperties, the orientation of the pyrimidine ring seems to be a key parameter on the mubeta value due

245 ve complications were reported, except for 1 ring segment that had to be removed after 2 years owing

246 The ring-shaped cohesin complex orchestrates long-range DNA

247 The two ring-shaped hexamers are staggered, leading to a kinked

248 erating cell nuclear antigen (PCNA) adopts a ring-shaped structure to promote processive DNA synthesi

249 patients with myelodysplastic syndrome with ring sideroblasts (MDS-RS).

250 findings included hypoplasia with the double-ring sign, pallor, and increased cup-disc ratio in 5 pat

251 Ring size and adjacent steric hindrance modulate this hi

252 Lactams with various ring sizes and substituents at different positions all r

253 termolecular macrocycles with highly tunable ring sizes.

254 ion of the magnetic flux passing through the ring, so that they can be changed from diatropic ('aroma

255 nant monogenic locus, Prs, conferring Papaya ring-spot virus (PRSV) resistance in bottle gourd, to a

256 ery and that they mediate their effects on Z-ring stability during developmentally controlled cell di

257 sulfur-centered radical cation and a phenyl ring stabilized by the fibril framework.

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

259 hallenge due to their unique amalgamation of rings, stereocenters, and oxygenation.

260 o activate using transition metals; however, ring-strain release can provide the necessary thermodyna

261 ntres is increased by a factor of 4.5 in the ring structure with two parallel coupling paths as compa

262 onal groups, molecular weight, and number of ring structures, in addition to the volume of SOA formed

263 Persistent currents in non-molecular rings switch direction as a function of the magnetic flu

264 hesis vary widely among bacteria whereas the ring synthesis genes are highly conserved.

265 eaction to install the requisite tetracyclic ring system.

266 with unprecedented 6/11/5 and 6/6/7/5 fused ring systems when transiently co-expressed with a GFPP s

267 lin FtsZ polymerizes to form a discontinuous ring that drives bacterial cell division by directing lo

268 region, forms a large two-layered cytosolic ring that extensively interacts with the transmembrane c

269 e/thiosemicarbazone adduct is a medium-sized ring that forms rapidly and irreversibly without any cat

270 etion of GpsB prevents closure of the septal ring that in itself is PBP2x-dependent.

271 by constriction of an actomyosin contractile ring that is controlled by Rho-family small GTPases.

272 f Cu(2+) ions only at the center of single 6-rings that act not only as a catalytically active center

273 movement of FtsZ clusters around bacterial Z-rings that is powered by GTP hydrolysis and guides corre

274 ively listening to recorded sounds of a bell ringing, then actively striking the bell with a mallet,

275 ent cytokinesis by stabilizing the midcell Z-ring through a bundling-independent mechanism.

276 reoselective formation of the seven-membered ring through a Friedel-Crafts triflation and a late-stag

277 usly bind and bridge across two Dam1 complex rings through a tripartite interaction, each component o

278 f the pyrrole rings is replaced with a furan ring to afford stable oxasmaragdyrin.

279 ined mathematical model of the fission yeast ring to explore essential consequences of the recently d

280 ith linear connectivity of the fused benzene rings to those with cis- or trans-bent connectivities.

281 Seven-membered-ring trans-alkenes undergo rapid, uncatalyzed carboborat

282 o function with really interesting new gene (RING)-type E3s, thereby restricting it to homologous to

283 ntified FDH as a potential substrate for the RING-type ubiquitin ligase Keep on Going (KEG).

284 emonstrated an association with the Cullin-4-RING ubiquitin E3 ligase-4 (CRL4) complex, nucleosomes,

285 tial consequences of the recently discovered ring ultrastructure.

286 meric equilibrium, the corresponding pyrrole-ring unsubstituted indoles.

287 Data from animal studies and a ring vaccination clinical trial conducted in Guinea duri

288 INTERPRETATION: The results show that a ring vaccination strategy can be rapidly and safely impl

289 We did an open-label, cluster-randomised ring vaccination trial (Ebola ca Suffit!) in the communi

290 ease was reported in Guinea, and in response ring vaccination with the unlicensed rVSV-ZEBOV vaccine

291 oup to formaldehyde and reduces the pyrazine ring via an unusual tautomerizing demethylation reaction

292 central bis-spirocyclic tetrahydrothiophene ring was forged through the Stevens rearrangement of a s

293 g organic ligands with 1, 2, and 3 phenylene rings, we construct moisture-stable Ni-MOF-74 members wi

294 ws the appearance of fluorescent cytoplasmic rings when the prion domain is fused with GFP.

295 ssemble at midcell to form the cytokinetic Z-ring, which coordinates peptidoglycan (PG) remodeling an

296 In this study, we combined tree-ring width and basal area increment series from 40 tremb

297 We used tree-ring width data from a network of 110 forests in combina

298 lation of the C-3 position of the quinolinic ring with lithium diisopropylamide at -70 degrees C is e

299 scission occurs on both sides of the midbody ring with random order and that completion of the scissi

300 efficiently fusing large numbers of aromatic rings, yet such methods remain scarce.