ライフサイエンスコーパス: basket

1 dents in round 3 were included in the final "basket".

2 best to avoid 'putting all your eggs in one basket'.

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

4 periphery and at the edge of the nucleopore basket.

5 ontaining the intervention allocation from a basket.

6 ent CPSF6 clustering adjacent to the nuclear basket.

7 of incomplete information on the CI of crude baskets.

8 ons, but not varicose CGRP+ fibers and CGRP+ baskets.

9 Few NOS+ varicosities occurred in baskets.

10 nthase and their relationship with calbindin baskets.

11 re removed using stone retrieval balloons or baskets.

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

13 obtaining multigram quantities of molecular basket 1 (syn) in overall 11% yield, using inexpensive c

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

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

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

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

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

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

20 Two molecular baskets 1(6-), each with three (S)-glutamic acids at its

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

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

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

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

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

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

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

28 unoreactivity and association with calbindin baskets, a finding that may have significant functional

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

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

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

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

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

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

35 nule cells and molecular layer interneurons (basket and stellate cells).

36 The primary complication of ML is basket and stone impaction, which can lead to complicati

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

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

39 gns (including multi-arm, multistage trials, basket and umbrella studies and research from big data s

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

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

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

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

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

45 he nerve cell bodies surrounded by calbindin baskets belong to motor neurons and ascending interneuro

46 The basket binds small molecule guests with association cons

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

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

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

50 d refinement will likely be needed, but this basket can be used immediately to guide ongoing monitori

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

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

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

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

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

56 ormed bilaterally using the St Jude EnligHTN basket catheter.

57 ation maps were acquired with a 64-electrode basket catheter.

58 le, 63+/-9 years) were recorded with 64-pole basket catheters and simultaneous 57-lead body surface E

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

60 uide atrial fibrillation (AF) ablation using basket catheters recently showed high rates of AF termin

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

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

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

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

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

66 teral formation and hypertrophy of GABAergic basket cell axonal processes, could be compensatory resp

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

68 Selective depletion of basket cell GABAergic neurotransmission increases the fr

69 compare how the lack of stellate cell versus basket cell GABAergic neurotransmission sculpts the firi

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

71 SD95 and GAD67 unexpectedly mark patterns of basket cell pinceaux that map onto Purkinje cell functio

72 uit features he exemplified using cerebellar basket cell projections.

73 Basket cell synapses predominantly express beta2-subunit

74 ions suggest that subcellular alterations at basket cell synapses rather than chandelier cell synapse

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

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

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

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

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

80 T2) mouse conditional allele, we reveal that basket cell zones comprise different sizes of pinceaux.

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

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

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

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

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

86 re, we find that excessive GABA release from basket cells (BCs) attenuates the firing frequency of Pu

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

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

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

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

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

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

93 mp and 2-photon laser scanning microscopy of basket cells (BCs), we found that classical excitatory p

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

95 ltage-gated sodium currents were impaired in basket cells (BCs).

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

99 nvestigated GABAergic parvalbumin-expressing basket cells (pvBCs) in layer 2/3 (L2/3) in human neocor

100 decrease in excitatory synaptic drive to PV basket cells (PVBCs) likely underlies reduced function.

101 a 46% spike rate reduction during SWRs in PV basket cells (PVBCs), while PV bistratified and axo-axon

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

103 tions at two subtypes of PV(+) interneurons: basket cells and chandelier cells.

104 ich primarily affected Purkinje cells (PCs), basket cells and climbing fibres, in individuals with ET

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

106 large decrease in intrinsic excitability of basket cells and oriens-lacunosum moleculare interneuron

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

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

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

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

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

112 Basket cells did not contribute to gamma oscillations ge

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

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

115 Axons of surviving NeuroD2-deficient basket cells follow irregular trajectories and their inh

116 Basket cells form dense inhibitory plexuses that wrap Pu

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

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

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

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

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

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

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

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

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

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

127 Particularly, basket cells might serve as target for innovative therap

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

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

130 By contrast, parvalbumin (PV)-expressing basket cells originate mostly from the rostral MGE, wher

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

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

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

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

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

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

137 struct a terminal differentiation program in basket cells that regulates targeted axon growth and inh

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

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

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

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

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

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

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

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

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

147 yramidal cells, parvalbumin-positive (PV(+)) basket cells, and an unidentified class of anti-SWR inte

148 (+) interneurons in addition to the expected basket cells, and their extensive circuit innervation pr

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

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

151 hibitory neuron, parvalbumin-expressing (PV) basket cells, have selectively reduced activity in a mod

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

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

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

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

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

157 tly expressed in the terminals of cerebellar basket cells.

158 eurons, specifically of parvalbumin-positive basket cells.

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

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

161 rent from the dendritic arborizations of CA1 basket cells.

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

163 required for the terminal differentiation of basket cells.

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

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

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

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

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

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

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

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

172 oth in the neuropil and forming pericellular baskets contacting somata of pyramidal cells.

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

174 This surgical basket could allow a more standardized assessment of a c

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

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

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

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

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

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

181 urs or multiple myeloma were included in the basket dose-expansion cohort (12 non-small-cell lung can

182 For the basket dose-expansion phase, eligible patients had advan

183 In the basket dose-expansion phase, we evaluated antitumour act

184 tre, open-label, phase 1 dose-escalation and basket dose-expansion study at the Royal Marsden Nationa

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

186 ry artery and branches, either a circular or basket electrophysiology catheter was placed in the righ

187 With molecular baskets embodying the second coordination sphere about m

188 onalization with beta-cyclodextrin molecular baskets enables loading and delivery of diverse chemical

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

190 8]) of 26 response-evaluable patients in the basket expansion achieved objective responses.

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

192 led CGRP+ varicosities were most abundant in baskets, followed by CALR+ varicosities, with a high deg

193 s data suggests that the unique cation-free "basket" formed by the Fmoc-G-PNA conjugate can serve as

194 ges, such as fashioning a hook to retrieve a basket from a tube, remarkably difficult?

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

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

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

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

199 If a basket has underlying characteristics significantly diff

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

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

202 ss signaling factor JNK, encoded by the gene basket in Drosophila.

203 ligase highwire and c-Jun N-terminal kinase basket in olfactory receptor neurons weaken the sleep-pr

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

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

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

207 In conclusion, CGRP+ baskets in mouse colon are formed by intrinsic enteric n

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

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

210 GABAergic basket interneurons form perisomatic synapses, which are

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

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

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

214 half (48%) of nerve cell bodies inside CGRP+ baskets lacked both NOS and CALR, while two overlapping

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

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

217 hedral fivefold symmetry axis, and forming a basket-like pentamer helix bundle.

218 We have recently reported specialized basket-like structures, immunoreactive for calbindin, th

219 The latter formed dense, basket-like varicosity clusters (CGRP+ baskets) that env

220 romone-responsive lcPNs appeared to exhibit "basket-like" dendritic arborizations in two MGC compartm

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

222 d 98% of the time a provider reviewed our in-basket messages.

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

224 Degron (AID) system to distinguish roles of basket nucleoporins NUP153, NUP50 and TPR.

225 A final basket of 32 procedures representing diseases categories

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

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

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

229 ion on the industrial composition and export baskets of national economies.

230 Enabled by more facile access to molecular baskets of type 1 (syn), a range of recognition studies

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

232 ons based on a larger number of TH-positive "baskets" of fibers around neurons in this region and gre

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

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

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

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

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

238 that fusing a DNA binding domain to the NPC basket protein Nup1 reduces telomere relocalization to n

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

240 vestigate the role of the major nuclear pore basket protein, TPR, in regulating mRNA and lncRNA nucle

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

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

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

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

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

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

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

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

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

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

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

252 Basket samples yielded collagen and blood proteins of bo

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

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

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

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

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

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

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

260 as a PV showing a cation-sensitive/dependent basket structure for an alternative endosomal egress.

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

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

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

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

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

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

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

268 In this open-label, phase 2 basket study, patients were enrolled from 32 hospitals a

269 MyPathway is an ongoing, phase 2a, multiple basket study.

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

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

272 Maturation of basket synapses in postnatal cortex is activity dependen

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

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

275 CALR+ and CGRP+ varicosities colocalized in baskets than in circular muscle.

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

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

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

279 ense, basket-like varicosity clusters (CGRP+ baskets) that enveloped myenteric nerve cell bodies.

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

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

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

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

284 r AF electrograms were analyzed from 64-pole baskets to reconstruct activation times, map propagation

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

286 ntre, Rare Oncology Agnostic Research (ROAR) basket trial in patients with BRAF(V600E)-mutated rare c

287 ial is a multicentre, open-label, phase 1/2, basket trial of durvalumab and olaparib in solid tumours

288 ts referred for various indications (i.e., a basket trial) excluding the 2 main classic indications:

289 In this single-arm, open-label, phase 2 basket trial, we recruited patients from 26 hospitals in

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

291 and treatment will be the design of adaptive basket trials that combine histopathology and genetic pr

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

293 erates vesicles of a predominantly hexagonal-basket type; larger and with faster kinetics than in oth

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

295 Baskets were characterized further by triple labeling wi

296 reting epithelium of the larval shell of the basket whelk Tritia (also known as Ilyanassa).

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 applicable list of surgical procedures, or "basket", which could represent a health system's capacit

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