ライフサイエンスコーパス: bowl

1 evels comparable to those of the 1930s 'dust bowl'.

2 encoding a MAPK), 14-3-3epsilon, and bowel (bowl).

3 attached to the interior carbon atom of the bowl.

4 ytic priming; K95 lies deeper in the chalice bowl.

5 uctures by destabilizing the nuclear protein Bowl.

6 l density to appear both above and below the bowl.

7 in which the Cs+ cation resides in the calix bowl.

8 ptor-binding site sequestered in the chalice bowl.

9 closed assembly that forms the bottom of the bowl.

10 flush and placement of the liver in the ice-bowl.

11 the zinc-finger proteins Drumstick (Drm) and Bowl.

12 regating Lines away from nuclearly localized Bowl.

13 ing the electron-rich cavity of the aromatic bowl.

14 nker caps a hydrophobic area adjacent to the bowl.

15 ntain as keeping a marble near the base of a bowl.

16 l from the Hyd-Lin complex, thus stabilizing Bowl.

17 ts the conformer distribution toward perfect bowls.

18 g to the formation of ellipsoids, discs, and bowls.

19 s(+) ions sandwiched between two corannulene bowls.

20 ndpaper) encountered before they reached the bowls.

21 ivalent to smoking 365 joints or filled pipe bowls.

22 cting in synergy with CsF, yielded molecular bowl 1syn in a moderate 30% yield.

23 ne 7 has been investigated to give molecular bowl 1syn in a stereoselective fashion.

24 ble (4.5:1) ratio, in favor of the molecular bowl 1syn.

25 ming algorithms from the Kaggle Data Science Bowl 2017 public competition: grt123, Julian de Wit and

26 )day(-1) through daily consumption of half a bowl (65g) of breakfast cereal and four slices of toaste

27 Lines binds directly to Bowl and decreases Bowl abundance.

28 One site, together with the Ca(2+) bowl, accounts for all physiological regulation of BK ch

29 Here, we show that Bowl accumulates in the PE from early stages of wing dev

30 ly, we show that Drm and Lines also regulate Bowl accumulation and consequent patterning in the epith

31 ting drm expression, while Wingless inhibits Bowl accumulation by repressing drm expression anterior

32 Conversely, Drm allows Bowl accumulation in drm-expressing cells by inhibiting

33 Together, lines and bowl act as a binary switch to generate a stable Notch s

34 or tennis facilities, indoor ice arenas, and bowling alleys were higher than at traditional fitness c

35 groups to the corannulene core flattens the bowl and affects the solid-state packing.

36 otein-protein interactions between Lines and Bowl and between Drm and Lines regulate the steady-state

37 Lines binds directly to Bowl and decreases Bowl abundance.

38 omains engage ESCRT-III substrates above the bowl and help transfer them into the bowl to be pumped t

39 Thus, we provide evidence that bowl and lines act as a binary switch to subdivide the w

40 of Hsp31 mutants, we show that although both bowl and linker-loop-shielded residues participate in su

41 r of the slo1 high-affinity sensors (calcium bowl and RCK1 Asp362/Asp367) is required for ethanol to

42 decreased Ca(2+) activation for both Ca(2+) bowl and RCK1 Ca(2+) sites, suggesting that both high-af

43 of the recent multiyear drought or the Dust Bowl and the 1950s droughts will become the new climatol

44 y, whereas antibodies against the GP chalice bowl and the fusion loop require FcgammaR engagement for

45 open assembly that defines the sides of the bowl and the lower ring forming a closed assembly that f

46 t these theories and explore new hypotheses; Bowles and Choi have developed one such model.

47 property rights (lending further support to Bowles and Choi's original proposal).

48 We have replicated the model of Bowles and Choi, and used the FIO method to identify com

49 The work of Boyd, Richerson, Fehr, Gintis, Bowles and their collaborators has long included the the

50 erein, we report a system of interconverting bowls and cages that are able to respond to various sele

51 acellular C terminus, including the 'calcium bowl' and the RCK domain, is not necessary for the calci

52 udes a high-affinity Ca(2+)-binding site (Ca bowl) and contains similar secondary structural elements

53 partic amino acids that is known as the Ca2+ bowl, and is located within the second of the tandem RCK

54 Further, we show that drm, bowl, and lin are required for patterning of the hindgut

55 hat the defect in hindgut elongation in drm, bowl, and lin mutants is due, in large part, to the requ

56 transcriptional regulators, drumstick (drm), bowl, and lines (lin), are required to establish normal

57 The genes drumstick, bowl, and lines (which encode putative transcriptional r

58 signaling molecules regulated by drumstick, bowl, and lines, in particular of the JAK/STAT activator

59 on the symmetry axis above the cavity of the bowl, and the binding of six extended Vta1p monomers cau

60 many tissues, lines acts antagonistically to bowl, and we found that this is true for hub specificati

61 can open with 0, 1, 2, 3, or 4 functional Ca-bowls, and that each subunit with a functional Ca-bowl c

62 Unique structures (bowls, arcades of hooks, cones at the cell ends, two lay

63 Thus, Drm, Lines, and Bowl are components of a molecular regulatory pathway th

64 odd, sob, drm, and bowl are expressed in a segmental pattern in the develop

65 ee Ca(2+) binding sites including the Ca(2+) bowl are mapped onto the structure based on mutagenesis

66 is true for hub specification, establishing bowl as a positively acting factor in the development of

67 ypes, HF-lesioned pigeons consistently chose bowls associated with one of the training stimuli.

68 On test trials, pigeons chose the bowl at the correct location in the room if either the c

69 have revealed the presence of a hydrophobic bowl at the Hsp31 dimer interface and shown that the lin

70 ania, Italy) and preserved in their original bowls at the Naples National Archaeological Museum (Ital

71 The 2018 Data Science Bowl attracted 3,891 teams worldwide to make the first a

72 e trained to discriminate between two reward bowls based on a stimulus (rough/smooth sandpaper) encou

73 intake was measured by weighing the feeding bowl before and after meals, and breast milk intake was

74 ncapsulate only the smallest (G1), while the bowl binds all of them.

75 le popcorn bags, natural plates, compostable bowls, biodegradable boxes, bagasse containers and eco-f

76 ns holding between them (apples contained in bowls, bowls supported by tables).

77 = 3.682 angstrom) and cannot undergo bowl-to-bowl (BTB) inversion below 373 K in toluene.

78 Bowl c-B was further used to synthesize a series of hete

79 (a))(4)] cage (o-C) and a [Pd(2)(c-L(a))(3)] bowl (c-B) were obtained, respectively.

80 The flexible microenvironment within the bowl causes an induced fitting to occur as the reagent a

81 Commercial toilet bowl cleaning tablets were examined in laboratory system

82 expands into distal and proximal regions in bowl clones.

83 rene adopts a boat conformation in 1-4 and a bowl conformation in 5 and 6.

84 The calculations also revealed that the bowl constriction is necessary for the aromatic arms to

85 , and that each subunit with a functional Ca-bowl contributes a stepwise increase to both the coopera

86 The severe drought of the 1930s Dust Bowl decade coincided with record-breaking summer heatwa

87 a long-standing history of chewing on toilet bowl deodorizing cakes.

88 The smaller size CNB1 has a deeper bowl depth ( d = 4.997 angstrom) than CNB2 ( d = 3.682 a

89 ction from which an empirical correlation of bowl depth and inversion barrier that follows a quartic

90 lowed for a study correlating the structure (bowl depth) and the energy of bowl inversion.

91 d to access bond lengths, bond angles, and a bowl depth.

92 ries of corannulene derivatives with varying bowl depths has allowed for a study correlating the stru

93 In this bowl-digging task, rats encounter two equal value learni

94 approaches to the treatment of inflammatory bowl disease and intestinal infections and to new immuni

95 mutations increase the risk for inflammatory bowl disease and the severity of graft-versus-host disea

96 s, pi-pi bonding between convex sides of the bowls dominate, while pi-H bonding between rim and conve

97 or sumanene on Ag(111) that both bowl-up and bowl-down conformations can be stabilized.

98 in the CTL group could win vouchers in prize-bowl drawings, but HIV care behaviors were not incentivi

99 reproduce the anomalous features of the Dust Bowl drought.

100 the US associated with the Great Plains Dust Bowl drought.

101 lead to maize losses equivalent to the Dust Bowl drought.

102 n the instrumental record including the Dust Bowl drought.

103 The "Dust Bowl" drought of the 1930s was highly unusual for North

104 based tool, we tested on a 2018 Data Science Bowl (DSB) competition dataset, three users obtained DSB

105 to prioritise surfaces closest to the toilet bowl during peak exposure periods, thereby promoting hea

106 anges experienced in utero in America's Dust Bowl during the Great Depression to unusually detailed i

107 s and the most severe drought since the Dust Bowl era of the 1930s, resulting in substantial economic

108 ral regions comparable to those of the "dust bowl" era and inexorable sea level rise.

109 trained to find food hidden in 1 of 4 color bowls (feature cues) located next to a landmark beacon (

110 rgets the zinc finger-containing oncoprotein Bowl for ubiquitin-mediated degradation, with Lin functi

111 ta-strand IV to the II-III loop, and a broad bowl from helix A to helix C.

112 functions as a pseudosubstrate by displacing Bowl from the Hyd-Lin complex, thus stabilizing Bowl.

113 om a small plastic cup, from a large plastic bowl, from a large plastic bowl with a guidewire and its

114 ranched pathway downstream of Notch in which Bowl functions to direct hub cell assembly in parallel t

115 tterns; in contrast, the less-tightly linked bowl gene is expressed in a distinctly different pattern

116 The bowl gene is therefore required for the elaboration of p

117 h signaling, which induces expression of the bowl gene, the product of which represses ap.

118 t lists of RNA 3D structures provided by the Bowling Green State University RNA group, R3D Align conn

119 e hypothesis to reconcile these data is that bowl has a role at an earlier stage in tarsal developmen

120 For example, a bowl has the affordance of holding water, but a sieve do

121 l Ca(2+)-regulatory site, termed the 'Ca(2+) bowl', has been located to the large cytosolic carboxy t

122 the intrinsic properties of redox-active pi-bowls, has been prepared.

123 For surface-adsorbed pi bowls, however, only conformations with the bowl opening

124 turn, Dl signals asymmetrically to stabilize Bowl in adjacent distal cells.

125 This is accomplished both by outcompeting Bowl in binding to Lines and by redistributing Lines to

126 nes protein destabilizes the nuclear protein Bowl in ectodermal structures.

127 Conversely, the activation of bowl in the DP (by removal or inhibition of lines functi

128 Broad inhibition of Bowl in the PE resulted in the replacement of the PE wit

129 ion to positional disorder of the C(40)H(50) bowls in the solid-state structure, has prevented the ac

130 s that catalyse nanowire growth as a 'mixing bowl', in which growth materials are sequentially suppli

131 revealed the preservation of the corannulene bowl inside the prepared rigid matrix, which offers the

132 ulting compounds (1 and 2) display a bowl-to-bowl inversion at room temperature.

133 molecule corannulene undergoes rapid bowl-to-bowl inversion at room temperature.

134 ten the bowl, thus causing a decrease in the bowl inversion barrier.

135 epening of the bowl, thus an increase in the bowl inversion barrier.

136 d by dynamic NMR analysis, showing a bowl-to-bowl inversion energy (DeltaG()) of 16.7 kcal mol(-1), w

137 A bowl-to-bowl inversion for a C70 fragment in solution was invest

138 the planar transition state for the bowl-to-bowl inversion of (ethyl)corannulene (which accelerates

139 The transition state structure for bowl-to-bowl inversion of 1 is planar (D(2)(h)()) and lies 30.9

140 nted structural phase transition involving a bowl inversion of one-third of the molecules.

141 Catalysis of the bowl-to-bowl inversion processes that pertain to corannulene is

142 ations suggest that SubPcs undergo a bowl-to-bowl inversion that was shown to be dependent on the axi

143 ne bridge with a cis-cyclohexane (preventing bowl inversion) and replacing one urea function with a f

144 e racemization rate constant for the bowl-to-bowl inversion, k(rac) = 7.1 x 10(-6) s(-1), corresponds

145 the structure (bowl depth) and the energy of bowl inversion.

146 Bowl-inversion barriers around DeltaG(double dagger) = 1

147 We also show that the Ca bowl is an essential element for the Ca(2+)-induced rear

148 s) and, like its close relative Odd-skipped, Bowl is produced in response to Notch signalling at a su

149 Ca(2+), the affinity of Ba(2+) to the Ca(2+) bowl is reduced about fivefold, and coupling of binding

150 One site, termed the Ca(2+) bowl, is embedded within the second RCK domain (RCK2; re

151 ing and, in particular, the work of Choi and Bowles [J.-K.

152 Conversely, ectopic bowl leads to a reduction in bric-a-brac2, with a concom

153 For instance, contorting PDIs into bowls leads to high-efficiency singlet fission materials

154 sized; X-ray crystallography showed a chiral bowl-like conformation with each urea hydrogen-bonded to

155 The latter guests are bound within the bowl-like cup of the C4P in a ball-and-socket binding mo

156 ed in pericentral hepatocytes resulting in a bowl-like distribution in marked contrast with that of t

157 Lastly, we demonstrate that the as-derived bowl-like mesoporous carbon particles manifest enhanced

158 Bowl-like mesoporous carbon particles with radially orie

159 anisotropic assembly approach to synthesize bowl-like mesoporous polydopamine particles with diamete

160 external structures were revealed, including bowl-like objects decorating the outer membrane, arcades

161 ies are transferred to nanostructures with a bowl-like shape matching the viral spherical surface.

162 The ATPase domains of Vps4p form a bowl-like structure composed of stacked hexameric rings.

163 determining region (CDR) structures with a "bowl-like" conformation in CDR-H2 that tightly and speci

164 y different from the future permanent, 'dust-bowl-like' megadrought conditions, lasting decades to a

165 The Ca(2+) bowl, located within the second RCK domain, forms an EF-

166 Compared with previous estimates for Ca(2+) bowl-mediated activation by Ca(2+), the affinity of Ba(2

167 ently developed method to reexamine Choi and Bowles' model under a much broader range of conditions t

168 ich five consecutive Asp residues of the "Ca-bowl" motif are changed to Asn, reduces (45)Ca(2+)-bindi

169 al of these genes have altered expression in bowl mutant cells.

170 ntation, and thus appear to act redundantly, bowl mutant clones do perturb leg development.

171 Specifically, bowl mutant clones result in a failure of joint formatio

172 However, despite the fact that bowl mutant clones result in fusion of tarsomeres, Bowl

173 We therefore investigated the effects of bowl mutations on the expression of leg 'gap' genes that

174 re trained to find food located in a colored bowl, near a landmark beacon, in a constant room locatio

175 ly important mutations cluster near the Ca2+ bowl, near the "flexible interface" between RCK domains,

176 moved by itself but chose the correct color bowl next to the beacon if they were moved together.

177 (3) a beta-turn, sitting in the middle of a bowl of alpha-helix residues.

178 ace, such as breakfast cereals floating in a bowl of milk or bubbles at the surface of a soft drink,

179 The Dust Bowl of the 1930s was the driest and hottest for agricul

180 assembly of the C38H14-buckybowl, a fragment bowl of the C70 fullerene, has been studied with scannin

181 A bowl of ~100 to 150 g cooked GR (50 g dry weight) can pr

182 The Cauvery Delta, the 'Rice Bowl' of India follows a time-tested cultivation pattern

183 pressure differentials, then was poured into bowls open to the OR 2 environment before injection into

184 bowls, however, only conformations with the bowl opening pointing away from the surface have been ob

185 of the molecules are oriented such that the bowl opening points down.

186 Isolated molecules adsorb bowl opening-up with the center C6 ring parallel to the

187 ameworks with the intrinsic properties of pi-bowls opens a new avenue for preparing redox-active mate

188 All subjects (100%) had a so-called bowl or convex shape to the choroid-sclera junction, and

189 ect location in the room if either the color bowl or the beacon was moved by itself but chose the cor

190 ent age in current users) multiplied by pipe-bowls or cigars per day.

191 ect that was either a conceptual match (e.g. bowl) or mismatch (e.g. wood).

192 at was classed as optimistic if it chose the bowl ordinarily associated with the high value reward.

193 between groups (F(ST) ) produced by Choi and Bowles' original model is much greater than empirical es

194 Many became grossly enlarged, bowling-pin-shaped cells having up to 80-fold-increased

195 r than what has been reported for the double-bowl polyurethane foam PAS.

196 d onto National Surgical Adjuvant Breast and Bowl Project protocol C-04.

197 Hedgehog promotes Bowl protein accumulation by promoting drm expression, w

198 utant clones result in fusion of tarsomeres, Bowl protein is only found at the t1/tibial and t5/preta

199 While the Sob and Bowl proteins each contain five tandem fingers, the Odd

200 ome-host interactions before and after small bowl radiation injury may eventually allow prediction of

201 h-affinity Ca(2+)-binding site (the "calcium bowl") reduced the Ca(2+) and abolished the Mg(2+) depen

202 al reasons: (a) its sequence similarity with bowl required for Drosophila hindgut development; (b) it

203 ts with a mutation to disrupt a key site (Ca-bowl) required for activation by low concentrations of C

204 parotomy for 2 patients (with necrotic small-bowl resection for 1 of these patients).

205 We find that mutations in bowl result in similar phenotypes to Notch, causing fusi

206 ehind the toilet and 0.15 m above the toilet bowl rim, which is where bioaerosol sampling occurred.

207 Regioselective functionalization of the bowl's rim was then finally achieved either via consecut

208 Bowles, Science 318, 636-640].

209 pheral B atom by Al in B(12)(-), which has a bowl shape with a B(9) outer ring and an out-of-plane in

210 Our X-ray and cryo-EM structures reveal a bowl-shape composite outer beta-wall, which houses a cen

211 mined by the complementary shape between the bowl-shape of the cavity and the shape of the ligand.

212 The stable bowl-shape stomatocyte morphology is ideal for the speci

213 A bowl-shaped a,a,a,a-tetraalkynyl calix[4]pyrrole and dik

214 py has revealed that the Piezo1 structure is bowl-shaped and capable of inducing membrane curvature v

215 (4-) )](2-) , illustrate a record ability of bowl-shaped and highly charged corannulene to provide al

216 ions indicate that the 8-ring aggregates are bowl-shaped and highly fluxional, compared to the 12-rin

217 nt of two groups of orthogonal reactivity in bowl-shaped as-indaceno[3,2,1,8,7,6-pqrstuv]picene (Idpc

218 lows the methyl group to be installed in the bowl-shaped azatricyclic structure; this crucial reactio

219 esidue Ser205, contributes to formation of a bowl-shaped binding site for ubiquitin.

220 A bowl-shaped calix[4]arene with its exciting host-guest c

221 al carceplex can be assembled by linking two bowl-shaped calix[4]arenes via four dimetal units, (DAni

222 The molecular structures of bowl-shaped carbocations 1 and 2 crystallized as salts w

223 uces greater distortion of the unsubstituted bowl-shaped cavitand than radial substitution.

224 a nanocontainer, which is built up from six bowl-shaped cavitands that are connected together with 1

225 The cation is situated in the bowl-shaped cavity of calix[4]arene.

226 The small bowl-shaped CNB1 demonstrates selective encapsulation of

227 molecular properties of two fully conjugated bowl-shaped CNBs (CNB1/CNB2), in which six/eight cyclope

228 g additional trimer contacts and filling the bowl-shaped concavity observed at the tip of the DEN-2 s

229 The fused bowl-shaped corannulene provides these porphyrins with a

230 a structural motif based on a C(3)-symmetric bowl-shaped core, on which three substituted amino acids

231 Dimerization leads to a large, bowl-shaped crevice, which might be involved in vivo in

232 The data for tripeptide amides fit bowl-shaped curves; an example is N-t-Boc-Val-Pro-Arg-7-

233 for hydroxycobalamin is located in a shallow bowl-shaped depression at the C-terminal end of the beta

234 erosion that, on Earth, are characterized by bowl-shaped depressions several tens of centimetres acro

235 YdaH is a bowl-shaped dimer with a solvent-filled basin extending

236 xistence of five-membered rings results in a bowl-shaped geometry, as revealed by X-ray crystallograp

237 sisting of 12-fold gp14 adaptor ring, 8-fold bowl-shaped gp15, and 4-fold gp16 tip.

238 At 1200 degrees C, the bowl-shaped hydrocarbon 1 rearranges to the planar isome

239 macrocycle-templating strategies to isolate bowl-shaped metallocavitands, and highlights interesting

240 Here, the synthesis of a bowl-shaped molecule is described and evidence of its re

241 atrylene analogues (CTVs) are supramolecular bowl-shaped molecules known for their ability to complex

242 Metal detector: a bowl-shaped nanomolecule (see picture; S yellow, C gray,

243 It is made possible by the familiar, bowl-shaped pelvis, whose short, wide iliac blades curve

244 Bowl-shaped pi-conjugated compounds offer the possibilit

245 efficient bottom-up strategy toward a novel bowl-shaped polycyclic aromatic hydrocarbons (PAH) C34 w

246 calibrated heretofore against X-ray data for bowl-shaped polycyclic aromatic hydrocarbons (PAHs).

247 The particles were based on bowl-shaped polymer vesicles, or stomatocytes, assembled

248 at high molecular coverage, the formation of bowl-shaped porphyrins occurs, along with transmetalatio

249 tal, solvent-exposed position into the flat, bowl-shaped S2' pocket.

250 talysts are dirhodium complexes that adopt a bowl-shaped shape on formation.

251 In this design, we constructed biodegradable bowl-shaped stomatocytes encapsulating the enzymes gluco

252 We report here the bowl-shaped structure of angiostatin kringles 1-3, the f

253 The bowl-shaped structure of methylene-bridged indenocorannu

254 The bowl-shaped structure was unambiguously determined by X-

255 ), furnishing a planar-chiral, atropisomeric bowl-shaped structure whose stereochemical stability ari

256 Prc forms a monomeric bowl-shaped structure with a lid-like PDZ domain connect

257 concave encapsulation of a metal ion by two bowl-shaped sumanenyl anions in [Cs(C21 H11(-) )2 ](-) w

258 The bowl-shaped surface near the FMN-binding site is likely

259 heptameric MSL1 channel contains an unusual bowl-shaped transmembrane region, which is reminiscent o

260 The transporter is a bowl-shaped trimer with a solvent-filled extracellular b

261 l molecular structures show that PIEZO1 is a bowl-shaped trimer with extended arms.

262 lassifying the contour and shape as concave (bowl-shaped) or inflective (S-shaped contour with >/=1 i

263 tuted heteroacepentalenides leads to chiral, bowl-shaped, 10 pi aromatic species.

264 All molecules are bowl-shaped, and the pentalene isomers, 2 and 4, are mos

265 rises exclusively from binding at the Ca(2+)-bowl site.

266 ty of merging the intrinsic properties of pi-bowls, specifically corannulene derivatives, with the ve

267 The structure exhibits a highly ordered bowl stacking that is unusual for corannulenes with acyc

268 ing between them (apples contained in bowls, bowls supported by tables).

269 ancet, and an object held a blood collection bowl, supported the hypothesis that it could be a mediev

270 helping to differentiate IBD from irritable bowl syndrome and for monitoring disease activity.

271 C was stabilized by increasing the starting bowl temperature (before a standard linear increase in t

272 355) provide the framework for the "aromatic bowl" that serves as a trimethylamine-binding site in TM

273 expressed odd-cognate genes, sob and bowel (bowl), that encode proteins with highly conserved C2H2 z

274 es regulate the steady-state accumulation of Bowl, the downstream effector of this pathway.

275 Bowl, then, acts cell-autonomously, together with one or

276 the peri positions causes a deepening of the bowl, thus an increase in the bowl inversion barrier.

277 peri positions are repulsive and flatten the bowl, thus causing a decrease in the bowl inversion barr

278 ove the bowl and help transfer them into the bowl to be pumped through the center of the dodecameric

279 unctioning as a substrate adaptor to recruit Bowl to Hyd for ubiquitination.

280 oss proximal leg segments, lines antagonizes bowl to promote Dl expression by relief-of-repression.

281 dicate that odd and sob are more likely than bowl to share overlapping developmental roles, some func

282 NB2 ( d = 3.682 angstrom) and cannot undergo bowl-to-bowl (BTB) inversion below 373 K in toluene.

283 The resulting compounds (1 and 2) display a bowl-to-bowl inversion at room temperature.

284 curved molecule corannulene undergoes rapid bowl-to-bowl inversion at room temperature.

285 estigated by dynamic NMR analysis, showing a bowl-to-bowl inversion energy (DeltaG()) of 16.7 kcal mo

286 A bowl-to-bowl inversion for a C70 fragment in solution wa

287 bilizing the planar transition state for the bowl-to-bowl inversion of (ethyl)corannulene (which acce

288 The transition state structure for bowl-to-bowl inversion of 1 is planar (D(2)(h)()) and li

289 Catalysis of the bowl-to-bowl inversion processes that pertain to corannu

290 T calculations suggest that SubPcs undergo a bowl-to-bowl inversion that was shown to be dependent on

291 The racemization rate constant for the bowl-to-bowl inversion, k(rac) = 7.1 x 10(-6) s(-1), cor

292 ocess and empirical models suggest that Dust-Bowl-type droughts today would have unprecedented conseq

293 ologies composed of spike-, hemisphere-, and bowl-type subunit nanotopographies, respectively, the ra

294 In addition, we explore the coexisting bowl-up and -down conformations with respect to host-gue

295 re we show for sumanene on Ag(111) that both bowl-up and bowl-down conformations can be stabilized.

296 Active halogens persisted in toilet bowl water for >24 h.

297 m a large plastic bowl, from a large plastic bowl with a guidewire and its sheath, from a large plast

298 ack of woven gauze, and from a large plastic bowl with a large cotton towel) were tested at different

299 idewire and its sheath, from a large plastic bowl with a stack of woven gauze, and from a large plast

300 site and that Mg(2+) can bind to the calcium bowl with less affinity than Ca(2+).

301 DFT calculations predict that 5 exists as a bowl, with all six substituents intramolecularly H-bonde

302 only objects and features (red apples, glass bowls, wooden tables), but also relations holding betwee