ライフサイエンスコーパス: basket

1 nkey vs. rat) and morphology (chandelier vs. basket).

2 2, and Nup60 components of the inner nuclear basket.

3 periphery and at the edge of the nucleopore basket.

4 yer would assist another player in scoring a basket.

5 of incomplete information on the CI of crude baskets.

6 n calorimetry to investigate the affinity of basket 1 (470 A(3)) for trapping variously sized and sha

7 Presumably, a desolvation of basket 1 and OP guests permits the inclusion complexatio

8 In particular, gated basket 1 comprises a porphyrin "floor" fused to four pht

9 The amphiphilic basket 1 shows a greater affinity (DeltaG degrees approx

10 We prepared dual-cavity basket 1 to carry six (S)-alanine residues at the entran

11 We designed basket 1 to comprise a C3-symmetric hydrophobic cage (47

12 cal nanostructures consisting of dual-cavity basket 1, forming a curved monolayer of large unilamella

13 Upon the addition of an anionic guest to basket 1, however, there was no formation of nanoparticl

14 nerve agents, form inclusion complexes with baskets 1-3 (K = 6-2243 M(-1)).

15 We found that molecular baskets 1-3, with amino acids at their rim, undergo phot

16 ized and shaped alkenes 18-21 with catalytic baskets 12(in)-Mn(III)-1 and 14(out)-Mn(III)-1 in the pr

17 Importantly, catalytic basket 14(out)-Mn(III)-1 was capable of kinetically reso

18 roscopy and mass spectrometry, we found that basket 2 would entrap 1-Zn(II) in water to give equimola

19 yridylmethyl)amine (TPA) ligand, and concave baskets 2 and 3, having glycine and (S)-alanine amino ac

20 Moreover, C3 symmetric and enantiopure basket 3, containing (S)-alanine groups at the rim, was

21 to investigate the aggregation propensity of basket 3b in THF/water solution by UV-visible spectrosco

22 ndergo photoinduced decarboxylations to give baskets 4-6 forming a solid precipitate in water.

23 ed cells through a draper-myoblast city-Rac1-basket (also known as JNK)-dependent autophagy pathway.

24 g, a technique traditionally used for market basket analysis, to biomonitoring data from the 2009-201

25 The TREX-2 complex localizes to the NPC basket and affects gene-NPC interactions, transcription,

26 edominantly coexist in 2-tetrad antiparallel basket and hybrid-2 structures that are arranged in "bea

27 tions and identify the 2-tetrad antiparallel basket and hybrid-2 topologies as the structural targets

28 Basket and ivy cells showed distinct spike-timing dynami

29 upling between molecular layer interneurons (basket and stellate cells).

30 symmetric channel capped by a nucleoplasmic basket and structurally unique, cytoplasmic fibrils whos

31 lp2p are necessary components of the nuclear basket and that they also embed the NPC within a dynamic

32 For both the market basket and the field survey, the highest total arsenic w

33 els during mapping with the IntellaMap Orion basket and the Rhythmia system.

34 of 1200 multicompartment neurons [pyramidal, basket, and oriens-lacunosum moleculare (OLM) cells] gen

35 arious G-quadruplexes, including the hybrid, basket, and propeller folds.

36 Degeneration of Purkinje, basket, and stellate cells, changes in the morphology of

37 revealed a unique self-assembled structure: baskets are formed by curved and self-wrapped nanometer-

38 nplanarity of the amide bonds, and a unique "basket" arrangement of (S)-N(1-phenylethyl) side chains

39 Importantly, baskets assemble into a vesicular nanomaterial (DH appro

40 hippocampal interneurons are classified into basket, axo-axonic (chandelier), and bistratified cells.

41 Purkinje and basket neurons caused abnormal basket axon collateral branching and targeting to Purkin

42 n with Purkinje Nfasc is required for proper basket axon collateral outgrowth and targeting to Purkin

43 Basket axon collaterals synapse onto the Purkinje soma/a

44 and for maintaining stable contacts between basket axon terminals and the Purkinje AIS during pincea

45 To compare the utility of this Bayesian basket (BB) design with that of a balanced randomized, b

46 ropean species of an extinct tribe of pollen-basket-bearing apine bees, Electrapini, of early-middle

47 The basket binds small molecule guests with association cons

48 (including nest basket, small basket, large basket, bitufted, pyramidal, and Martinotti cells), we c

49 In stark contrast, disruptive alleles of Basket (Bsk), the Drosophila homologue of JNK, exacerbat

50 Basket, but not ivy, cells changed their firing rates du

51 Teaching chains produced more robust baskets, but neither teaching nor imitation were strictl

52 e pathway: Ecr, Shd, Broad; the Wnt pathway: basket, c-jun) that are countered by up-regulation in so

53 r the rotor core although the low-resolution basket catheter is prone to false detections and may inc

54 The study was performed using a 64-electrode basket catheter on the left ventricle endocardium and 54

55 rotor modulation (FIRM) with an endocardial basket catheter was used in all cases.

56 A 56-electrode sock and 64-electrode basket catheter were placed around the epicardium and in

57 atrial electrograms collected from a 64-pole basket catheter were used to construct phase maps and id

58 ormed bilaterally using the St Jude EnligHTN basket catheter.

59 ventricular arrhythmias, using 64-electrode basket catheters in both ventricles to map VF prior to p

60 We used 64-pole basket catheters to measure regional dynamic conduction

61 Two 64-electrode basket catheters were inserted, respectively, into the l

62 A specialized axonal ending, the basket cell "pinceau," encapsulates the Purkinje cell ax

63 Kv1.2 is also expressed in cerebellar basket cell (BC) axon terminals, where its blockade incr

64 interneuron, the cholecystokinin-expressing basket cell (CCKBC), is particularly well suited to inte

65 ts to pyramidal neurons from the parvalbumin basket cell (PVBC) class of GABAergic neurons.

66 pplied this approach to quantify parvalbumin basket cell (PVBC) inputs in area 9 of the dorsolateral

67 ited pyramidal cells, resulting in increased basket cell activation and gamma power.

68 resis of l-aspartate, an NMDAR agonist, onto basket cell axon collaterals had no effect on evoked IPS

69 n for functional innervation by CCK-positive basket cell axon terminals was confirmed by reduced freq

70 tic synapse formation impairs the process of basket cell axonal branching and bouton formation.

71 rmally densely clustered at the terminals of basket cell axons in the cerebellar cortex.

72 ease machinery to test for NMDAR activity in basket cell axons.

73 his review explores the dichotomy of the two basket cell classes, cholecystokinin- (CCK) and parvalbu

74 ange projection pattern in the definition of basket cell function.

75 bumin-expressing interneurons, including the basket cell network which is fundamental to gamma oscill

76 Basket cell synapses predominantly express beta2-subunit

77 s plasticity was observed at somatodendritic basket cell synapses, but not at distal dendritic stella

78 pyramidal cells caused loss of CCK-positive basket cell terminals in hippocampus and neocortex.

79 isually targeted patch-clamp recordings from basket cell terminals of mice harbouring an ataxia-assoc

80 PV-positive basket cell terminals were unaffected in mutant mice, de

81 Our results show that both basket cell types can powerfully regulate the activity i

82 Furthermore, calcium indicators in basket cell varicosities did not report any change in in

83 We find no evidence for functional NMDARs in basket cell varicosities.

84 ine the time course of release at inhibitory basket cell-Purkinje cell synapses and show that it is i

85 ators reveal that channel-sensor coupling at basket cell-Purkinje cell synapses is very tight, with a

86 ate is coreleased with GABA from hippocampal basket cell-synapses to act on NMDA receptors.

87 impaired inhibition in epileptic animals at basket cell-to-granule cell (BC-->GC) synapses, which no

88 In a rat model of temporal lobe epilepsy, basket cell-to-granule cell (BC-->GC) synaptic transmiss

89 ll (PC) inputs to Martinotti cells (MCs) and basket cells (BCs) in layer 5 of the developing mouse vi

90 essing (VIP) and parvalbumin-expressing (PV) basket cells (BCs) in mouse hippocampal CA1.

91 In cerebellum, basket cells (BCs) innervate the soma and axon initial s

92 ramidal neurons, chandelier cells (ChCs) and basket cells (BCs), are generally thought to have the sa

93 ound in the PFC, chandelier cells (ChCs) and basket cells (BCs), are thought to play different roles

94 f PV(+) neurons, chandelier cells (ChCs) and basket cells (BCs), has not been determined.

95 bumin (PV)-expressing perisomatic inhibitory basket cells (BCs), whereas BCs and HICAPs rarely target

96 uting of inhibitory cholecystokinin-positive basket cells (CCK(+) BCs), through enhanced inhibition o

97 cteristics of the cholecystokinin-expressing basket cells (CCK-BC).

98 isomatically projecting parvalbumin-positive basket cells (PVBCs) and distal dendritically projecting

99 deling, we found that parvalbumin-expressing basket cells (PVBCs) evoked greater inhibition in CA1 PC

100 eurons include chandelier cells (PVChCs) and basket cells (PVBCs), which innervate the axon initial s

101 lls at the gamma peak but lag at trough; (5) basket cells amplify theta rhythms; (6) ketamine alters

102 tage deflection at steady state) was 1.69 in basket cells and 0.23 in stellate cells.

103 pulations of neocortical inhibitory neurons: basket cells and Martinotti cells.

104 a26YFP mice, were anatomically identified as basket cells and PV bistratified cells in the stratum py

105 n neurons into three classes: bipolar cells, basket cells and radial cells, respectively.

106 inhibitory synapses made by CCK(+)VGlut3(+) basket cells and the inhibitory drive they exerted on py

107 number of direct neighbors to be ~4 for rat basket cells and ~1 for rat stellate cells.

108 , supporting the view that PV(+) fast-firing basket cells are more likely to exhibit class 2 excitabi

109 ced selective and powerful excitation of PV+ basket cells are not understood.

110 Parvalbumin-positive (PV+) fast-spiking basket cells are thought to play key roles in network fu

111 gment oscillations; (4) pyramidal cells lead basket cells at the gamma peak but lag at trough; (5) ba

112 ADAM11 spares spontaneous GABA release from basket cells at the perisomatic synapse yet eliminates u

113 ppressing neurotransmitter release in single basket cells can have completely opposite effects depend

114 sleep and quiet wakefulness, suggesting that basket cells coordinate cell assemblies in a behavioral

115 ng events, CCK2 receptors on neighboring PV+ basket cells couple to an unusual, pertussis-toxin-sensi

116 Basket cells did not contribute to gamma oscillations ge

117 The distinct spike timing of basket cells during oscillations in CA1 and CA2/3 sugges

118 We found that both stellate and basket cells engaged in synchronized waves of calcium ac

119 Fast-spiking, parvalbumin-expressing, basket cells express muORs, but circumstantial evidence

120 normal integration into cortical circuits of basket cells expressing CCK and vesicular glutamate tran

121 somatic inhibition of pyramidal neurons from basket cells expressing cholecystokinin (CCK(b) cells) a

122 During theta oscillations, CA2/3 basket cells fired on the same phase as putative pyramid

123 Area CA2/3 basket cells fired phase locked to both CA2/3 and CA1 ga

124 unitary synaptic connections between GCs and basket cells in acute cerebellar slices from wild-type a

125 d the spike timing of parvalbumin-expressing basket cells in areas CA2/3 of anesthetized rats in rela

126 dependent generation of fast oscillations by basket cells in CA1 and CA2/3.

127 ts suggest that normal integration of CCK(+) basket cells in cortical networks is key to support spat

128 ransmitter release, in mouse cortical single basket cells in slice cultures decreases the number of i

129 ctedly large dendritic arborization of CA2/3 basket cells in stratum lacunosum moleculare (33% of len

130 timing of identified parvalbumin-expressing basket cells in the CA1 hippocampus of anesthetized rats

131 The networks of PV basket cells in the DG are regulated by vesicular releas

132 Cortical basket cells innervate hundreds of pyramidal cell somata

133 scopic investigations to show that, although basket cells innervate the entire somato-denditic membra

134 of inhibitory control accomplished by single basket cells is also variable.

135 icient control of principal neuron firing by basket cells is critical for information processing in c

136 Thus, alterations in basket cells may underlie the cortical oscillation defic

137 As the innervation patterns of individual basket cells on their different postsynaptic partners sh

138 parvalbumin- and cholecystokinin-expressing basket cells onto pyramidal neurons.

139 scillations from intrinsic network dynamics: basket cells primarily generated gamma and amplified the

140 cholecystokinin- and parvalbumin-containing basket cells provide equally potent control of principal

141 Normally, hippocampal basket cells provide strong and reliable synaptic inhibi

142 In contrast, VIP-positive basket cells provided perisomatic inhibition to CA1 pyra

143 s generated around stratum pyramidale, where basket cells selectively innervate pyramidal cells with

144 , electrical communication is stronger among basket cells than among stellate cells.

145 tors are coexpressed in parvalbumin-positive basket cells that are critical for gamma oscillations.

146 particularly true for a major population of basket cells that express the neuropeptide cholecystokin

147 fast calcium-permeable AMPA receptors enable basket cells to respond rapidly, such that they promptly

148 Spike timing of basket cells tuned the phase and amplitude of gamma osci

149 to Martinotti cells, while leaving those to basket cells unaffected.

150 associated with sharp waves, firing of CA2/3 basket cells was phase locked only to local but not CA1

151 , parvalbumin- or cholecystokinin-expressing basket cells were found to be similar.

152 g interneuron groups; parvalbumin-expressing basket cells were one of the most active GABAergic cells

153 Er81 protein levels define a spectrum of FS basket cells with different properties, whose relative p

154 c acid neurons (i.e., parvalbumin-containing basket cells) in layer 3 of the DLPFC.

155 parvalbumin-expressing interneurons (mostly basket cells) in sector CA1/subiculum is sufficient to i

156 cular layer interneurons (MLIs, stellate and basket cells) of the cerebellar cortex are linked togeth

157 pal CA3 regions, parvalbumin (PV)-expressing basket cells, activated by ACh and glutamatergic agonist

158 ntly differed between parvalbumin-containing basket cells, axoaxonic cells, and type 1 cannabinoid re

159 ervate pyramidal neuron perisomatic regions (basket cells, BCs) were depolarized by muscarinic recept

160 kinin- (CCK) and parvalbumin (PV)-containing basket cells, beginning with differences at the level of

161 Parvalbumin-expressing basket cells, making GABAergic synapses onto cell bodies

162 (CCK) is able to selectively depolarize PV+ basket cells, making these cells sensitive biosensors fo

163 terneurons, which include the CCK-expressing basket cells, strongly suppressed inhibitory oscillation

164 Furthermore, in basket cells, these receptors were associated with parti

165 type 1 cannabinoid receptor (CB1)-expressing basket cells, which might explain their distinct recruit

166 modulation of CA3 and CA1 pyramidal cells by basket cells, which receive different inputs.

167 reciprocally connected parvalbumin-positive basket cells, which start ripple-frequency spiking that

168 Basket cells, whose axon terminals surround principal ce

169 arly fast-spiking parvalbumin-positive (PV+) basket cells.

170 ule cells (GCs) by parvalbumin (PV)-positive basket cells.

171 rent from the dendritic arborizations of CA1 basket cells.

172 are highly enriched in hilar mossy cells and basket cells.

173 gly, significantly later than downstream CA1 basket cells.

174 he synaptic output of parvalbumin-expressing basket cells.

175 parvalbumin- and cholecystokinin-expressing basket cells.

176 ly modulated, including parvalbumin-positive basket cells.

177 lso enhance the distinct network function of basket cells.

178 ctive cationic conductance to depolarize PV+ basket cells.

179 ucing inhibition in fast-spiking parvalbumin basket cells.

180 tly expressed in the terminals of cerebellar basket cells.

181 eurons, specifically of parvalbumin-positive basket cells.

182 r to require the involvement of fast-spiking basket cells.

183 We conducted a basket clinical trial to assess the feasibility of such

184 Our results support the concept of basket clinical trials where patients are matched with e

185 conditions preserved other artefacts such as baskets coated with a similar dark substance.

186 ersion of CI estimates is greatly reduced in baskets compared to single crudes (coefficient of variat

187 In this study, we show that the nuclear pore basket component Alm1 is required to maintain both the p

188 osed that the loops are too far apart in the basket conformation in Na(+) solution but close enough i

189 olution, whereas a potentially photoreactive basket conformation is favored in Na(+) solution.

190 od to obtain a family of catalytic molecular baskets containing a spacious cavity (~570 A(3)).

191 of pollen was acquired for metatibial pollen baskets (corbiculae) of the same bee taxa from a taxonom

192 -beta-strand barrels, to beta-sheet cups and baskets covered by alpha-helical lids, to multi-alpha-he

193 pirals to structures that resemble spherical baskets, cuboid cages, starbursts, flowers, scaffolds, f

194 Based on an average consumer basket, daily intake of nickel from vegetable fats is at

195 These include the enrichment design, the basket design, and the umbrella design.

196 Analyses comprised a 2-level basket designed to evaluate variations in outcome and wh

197 eters anomaly has also become a 'waste paper basket' diagnosis for anterior segment developmental ano

198 describe the construction of gated molecular baskets, discuss their mechanism of action in regulating

199 Basket electrodes were within 1 cm of 54% of left atrial

200 With molecular baskets embodying the second coordination sphere about m

201 ed a cavity-shaped architecture resembling a basket, endowed with a large intramolecular space ( appr

202 browse function, facetted navigation and a 'basket' feature to store genes or gene signatures of int

203 Whereas the dimensions of hybrid and basket folds allowed them to enter the protein vestibule

204 selective binding substrate for antiparallel basket G-quadruplexes, with features that make it a usef

205 and installing the distinctive acylglycine "basket handle" of salinamide.

206 he single-electron oxidative dimerization of basket-handle porphyrins (BHPs) with different coordinat

207 Chiral and achiral basket-handle porphyrins (BHPs) with different p-xylene

208 Strapped or "basket-handle" porphyrins have been investigated previou

209 If a basket has underlying characteristics significantly diff

210 led-coil Mlp/Tpr proteins of the NPC nuclear basket have specific functions in interactions with chro

211 , choosing different materials to make their baskets if the previous basket in the chain performed po

212 observations suggest a role for the nuclear basket in providing an interaction platform that keeps R

213 ood categories that represent the whole food basket in Switzerland, and including food waste treatmen

214 erials to make their baskets if the previous basket in the chain performed poorly.

215 procedure was captured in the device filter baskets in 30 (75%) patients and sent for histopathologi

216 m fractionation at 64 or 128 electrodes with baskets in left (n = 17) or both (n = 14) atria during s

217 amics of fluorescently tagged yeast clathrin baskets in the presence of purified Ssa1p and Swa2p.

218 ing step for transport occurs at the nuclear basket, in the central channel, or on the cytoplasmic fa

219 ired double-patch recordings from inhibitory basket interneurons connected to pyramidal neurons and u

220 GABAergic basket interneurons form perisomatic synapses, which are

221 ell genetics to knock out NCAM in individual basket interneurons in mouse cortical slice cultures, at

222 Recorded parvalbumin-expressing basket interneurons innervated somata and proximal pyram

223 that a complete blockade of GABA release in basket interneurons resulted in an opposite effect, a ce

224 initial segments, and parvalbumin-expressing basket interneurons, targeting somata, dendrites, and sp

225 in (PV) and cholecystokinin (CCK) expressing basket interneurons.

226 a2p cooperatively disassemble yeast clathrin baskets into fragments larger than the individual triske

227 (Basel Stent Kosten-Effektivitats Trial [BASKET]; ISRCTN75663024).

228 ifferent types (including nest basket, small basket, large basket, bitufted, pyramidal, and Martinott

229 that GstDnaB1-300 forms a tetramer with two basket-like architectures, a finding consistent with tho

230 solution but close enough in a two G-tetrad basket-like form 3 conformation that can form in K(+) so

231 te, receive teaching or emulate by examining baskets made by previous chain members.

232 s been reconstituted using neuronal clathrin baskets mixed with the purified chaperone ATPase 70-kDa

233 e AIS during pinceau organization, while the basket neuron Nfasc in combination with Purkinje Nfasc i

234 Loss of Nfasc in both Purkinje and basket neurons caused abnormal basket axon collateral br

235 pecific Nfasc functions in both Purkinje and basket neurons.

236 re, we describe the link between the nuclear basket nucleoporins (Tpr and Nup153) and chromatin organ

237 e and reinforces the view that the branchial basket of lampreys is probably derived.

238 The basket of the nuclear pore complex (NPC) is generally de

239 rved, which could be assigned to the nuclear basket of the pore and might correspond to a repositioni

240 omain, the inter-domain linker, and the beta-basket of the substrate binding domain.

241 Stimuli-responsive vesicles, containing baskets of type 1 in their bilayer membrane, are unique

242 The structural adaptivity of dual-cavity baskets of type 1 is unique and important for designing

243 ariation in out-of-pocket costs for a fixed "basket" of asthma medications across 37 employers, we es

244 ll as the production-weighted CI of groups ("baskets") of crude oils.

245 , and of TPR, the nucleoporin that forms the basket on the nuclear side of the nuclear pore complex.

246 We create two different 20 oil field baskets, one of which has typical emissions and one of w

247 st-spiking interneurons, which are typically basket or chandelier neurons; and somatostatin containin

248 perimental studies have suggested that gated baskets ought to unfold their gates at the rim for permi

249 ith the weak interaction between the nuclear basket protein (Mlp1 or Tpr) and RBPs are the minimum re

250 sttranslational modifications of the nuclear basket protein Nup60 and analyzed how they intervene to

251 formation and initiate their export, nuclear basket proteins could more easily capture and retain the

252 Deletion or mutation of the nuclear basket proteins MLP1/2 or the mRNA binding protein Nab2

253 vealed that cells lacking the Mlp1/2 nuclear basket proteins show AID-dependent genomic instability a

254 ontaining the intervention allocation from a basket; ratio 1:1), and the intervention sessions were g

255 trastructural observations indicate that the basket reduces chromatin crowding around the central tra

256 rtin-alpha/CAS complexes form in the nuclear basket region, at the termination of protein import, and

257 that only two aromatic walls of the occupied basket's cavity form C-H...pi contacts with the guest to

258 ced that neutral guests insert deep into the basket's cavity to change its shape and thereby promote

259 three of the aromatic walls of the occupied basket's cavity.

260 exes in addition to functional groups at the basket's rim play a role in the efficiency (up to 98%) b

261 risk assessment based on a 2014 U.S. market basket sample.

262 Basket samples yielded collagen and blood proteins of bo

263 These objects have a unique basket shape; they possess a cavity the depth and width

264 of the triangular trimer assemble to form a basket-shaped nonamer.

265 Furthermore, gated baskets should permit examining the benefit of controlli

266 These dual-cavity baskets show a strong pi --> pi* absorption at 241 nm (e

267 cal cells of different types (including nest basket, small basket, large basket, bitufted, pyramidal,

268 superior olive glycinergic synapse, and the basket/stellate cell-Purkinje GABAergic synapse in the c

269 erentially contributed to climbing-fiber and basket/stellate-cell synapse functions, such that inhibi

270 neuroligins increased the size of inhibitory basket/stellate-cell synapses but simultaneously severel

271 meres (which we show to form an antiparallel basket structure with a diagonal loop across one end), t

272 provides a rare example of an organic kagome basket structure, with S = 1/2 radical ion chains locate

273 y care, including the purpose and utility of basket studies, biostatistical considerations in trial d

274 "Basket studies," or histology-agnostic clinical trials i

275 es, in some cases with dramatic responses on basket studies.

276 A field and market basket study (~1300 samples) of locally grown fruits and

277 nwall and Devon), and as reference, a market basket study of similarly locally grown produce from the

278 e undertook a histology-independent phase 2 "basket" study of vemurafenib in BRAF V600 mutation-posit

279 Importantly, the stability of basket subsetOP complexes in addition to functional grou

280 s that the pharyngeal epithelium of the gill basket supports the development of T-like cells, suggest

281 Maturation of basket synapses in postnatal cortex is activity dependen

282 arker agnostic (BA) design and a traditional basket (TB) design that includes only biomarker-positive

283 These basket-tethered and membrane-tethered proteasomes, which

284 moiety, a redox-switchable triptycene-based basket that can completely sterically encapsulate a gues

285 ialized cuticular processes forming a dorsal basket that carry a dense trash packet.

286 there is a rate-limiting step in the nuclear basket that is potentially associated with the mRNA reco

287 ific NPC locations: binding sites on the NPC basket that reflect its eightfold symmetry and more abun

288 uced to <1 gCO2/MJ in our elevated emissions basket) through strategies that only require gathering a

289 Participants were tasked with building a basket to carry as much rice as possible using a set of

290 longer mRNAs spend more time in the nuclear basket to form a compact conformation and initiate their

291 ered by the mandatory public health services basket to private programmes; insufficient progress in r

292 This basket trial design was not feasible for many of the arm

293 lti-cohort, open-label, phase 1b KEYNOTE-012 basket trial.

294 uncontrolled n-of-1 trials, and umbrella and basket trials.

295 ves from well-defined ribbons to vesicles to baskets, upon simply decreasing the concentration of 1 i

296 ncreased caloric content of the general food basket was introduced to the Maela refugee camp in Thail

297 coefficient of variation = 0.2 for a typical basket when 50% of data is learned at random), and field

298 proteins (mRNPs) first encounter the nuclear basket where mRNP rearrangements are thought to allow ac

299 Mad1-Mad2 complexes tethered to the nuclear basket, which activate soluble Mad2 as a binding partner

300 4, 361 A(3)) is relegated to the exterior of basket Zn(II)-1.