ライフサイエンスコーパス: rim

1 neous (p = 0.0006), non-sparse (p < 0.0001), rim deposition within sparse tumors (p = 0.045), and per

2 s of subendocardial necrosis surrounded by a rim of fibrosis.

3 the joint surface, which was surrounded by a rim of high PF and intermediate MTT.

4 within the epiphyseal cartilage developed a rim calcification that originated from normal subjacent

5 (ii) Si and Al are mainly concentrated in a rim at the epidermis of the roots.

6 The rates of absolute rim area loss and percentage rim area loss in healthy an

7 ing TSPO in active lesions or chronic active rims are microglia/macrophages, our findings also emphas

8 on fronts and oscillatory zonings in altered rims of the materials, suggesting that corrosion of thes

9 Among rim+ lesions, susceptibility within the rim (20.04 +/- 1

10 ted with RNFL thickness (4.90, P < .001) and rim area (0.15, P < .001).

11 ed the changes in cup volume, disc area, and rim area on OCT.

12 ferences in lipid ordering in the centre and rim of the discs.

13 of forces per unit volume in the dimple and rim regions of the RBC.

14 rements of NMIIA densities at the dimple and rim validate our prediction that (a) membrane forces mus

15 pigment bearing cell types in the retina and rim region.

16 icking pathway for both disc (rhodopsin) and rim (PRPH2/ROM1) components of the OS.

17 of the algorithmic role of tumor in vein and rim arterial phase hyperenhancement improves the diagnos

18 leptomeningeal involvement, central vein and rim of lesions, microstructural abnormalities, iron accu

19 Degradation of the crater wall and rim probably supplied these sediments, which advanced in

20 The distance between the anterior rim of the acetabulum and the metaphysis measured 20.4 m

21 On multivariable analysis, deficiency of any rim, device >5 mm larger than ASD diameter, and weight:d

22 In addition to aortic rim deficiency, which was almost universal among erosion

23 ve susceptibility mapping were identified as rim+ lesions.

24 on at Izola mensa within the NW Hellas Basin rim.

25 nding to RNAP uses the residues in the beta' rim helices that contribute to the ppGpp binding site in

26 e bowls dominate, while pi-H bonding between rim and convex sides plays the important role in small m

27 y soil minerals to build a biomineralization rim, which can capture Zn.

28 for the ISNT rule not being obeyed for both rim and RNFL assessments.

29 ous eyes compared with healthy eyes for both rim area loss (-10.2x10(-3) vs. -2.8x10(-3) mm(2)/year,

30 tacked, but cisternal diameter is reduced by rim consumption.

31 on, to be ectopically expressed at the canal rim.

32 Aortic or superior vena cava rim deficiencies were more common in cases than in contr

33 microtopographic positions (polygon centers, rims, and troughs) along the permafrost degradation grad

34 In the circumscribed rim of high PF and intermediate MTT, which was only foun

35 tive processes, deconstructing the main core-rim diffusion profiles of multi-zoned crystals into diff

36 ues as low as 6.7 per thousand (maximum core-rim = 1.8 per thousand).

37 beneath a sedimentary cap rock at the crater rim.

38 ontaining methane is observed coating crater rims and walls as well as mountain tops, providing spect

39 e widespread, wind-eroded landscapes, crater rims eroded down by several hundred meters, pitted plain

40 ceptor) diminishes F-actin mainly at the cup rim, being consistent with its known localization.

41 Its localization at the high-curvature rim domains of outer segment disk membranes suggests tha

42 nctions directly to shape the high-curvature rim domains of the outer segment disk and suggests that

43 (P/rds), may contribute to the highly curved rim domains at disk edges.

44 ith a clear concave face and a highly curved rim.

45 n by the line tension acting on the detached rim of the lipid plug.

46 cup-to-disc area ratio, and lower optic disc rim area (P < 0.001 for all).

47 ally organized as ectopic incisures and disk rims.

48 etramer polymerization, localization at disk rims, interaction with GARP2, or the generation of membr

49 nning laser tomography for measurement of DM rim area (DM-RA) and with spectral domain optical cohere

50 Donor rim culture results were 3 times more likely to be posit

51 he incidence of positive corneoscleral donor rim fungal cultures after keratoplasty and to report cli

52 Detectable Candida growth in donor rim cultures, associated with a higher rate of post kera

53 primary outcome measures were positive donor rim fungal culture results and the development of postke

54 to determine the incidence of positive donor rim fungal cultures and clinical outcomes of all grafts

55 Positive donor rim fungal cultures are uncommon, but carry an unaccepta

56 ociated with a fungal culture-positive donor rim.

57 imycotic therapy when culture-positive donor rims are identified.

58 tcomes of grafts with culture-positive donor rims.

59 ct polarized light with a specialized dorsal rim area in their compound eye.

60 ster, photoreceptors R7 and R8 in the dorsal rim area (DRA) of the compound eye are specialized to de

61 d downstream of photoreceptors in the dorsal rim area (DRA), where linearly polarized skylight is det

62 ithin an area of the eye known as the dorsal rim, which detects the polarized sky pattern specificall

63 left-handed metallo-helicoid (H) with double rims.

64 which has a semicircular shape, an elevated rim, and a central pit.

65 No framework, an IHCC or ePTFE rim graft was used as framework.

66 6]arenes bearing adamantyl groups at the exo-rim form pseudorotaxanes with dialkylammonium axles pair

67 "target" aspect; Grade IIb present as a fine rim of external esophageal wall enhancement.

68 ion of Dlx5 and Lmo4, which are required for rim formation.

69 eal center and the nasal and temporal foveal rims.

70 s distinguish age-related rim area loss from rim area loss resulting from glaucoma.

71 ntified an increased risk of positive fungal rim culture results in tissue processed for endothelial

72 nal vessel density in GA regions, 500-mum GA rim regions, and non-GA regions to similar macular locat

73 Retinal vessel density in the GA rim region decreased in SVC and ICP but not in DCP.

74 eroinferior labrum associated with a glenoid rim fracture.

75 d with healthy eyes, the mean rate of global rim area loss was 3.7 times faster and the mean rate of

76 The mean rate of global rim area loss was significantly faster in progressing gl

77 Foxp3, Il10), whereas those in the granuloma rims associate with activated T cells and macrophages.

78 tis (sIBM) pathogenesis is unknown; however, rimmed vacuoles (RVs) are a constant feature.

79 hydrophobic central cavity and a hydrophilic rim on the GP, as observed for the m102.3-HeV co-crystal

80 sis lesions, characterized by a hyperintense rim of iron-enriched, activated microglia and macrophage

81 to validate that lesions with a hyperintense rim on quantitative susceptibility mapping from both rel

82 , and 43 chronic lesions with a hyperintense rim on quantitative susceptibility mapping were identifi

83 s evidence that suggests that a hyperintense rim on quantitative susceptibility measure within a chro

84 esion with hypointense core and hyperintense rim with or without contrast enhancement; and (2) "Motor

85 endently associated with a slower decline in rim area.

86 variate analysis, there was no difference in rim area rate before and after the endpoint (median diff

87 sceptibility (relative to CSF) was higher in rim+ (2.42 +/- 17.45 ppb) compared to rim- lesions (-14.

88 tivated microglia/macrophages, was higher in rim+ lesions compared to rim- lesions (P = 0.015).

89 This is consistent with an increase in rim tissue thickness and a more anterior position of the

90 dpoint was strongly linked to a reduction in rim area rate decline (8 x 10(-3) mm(2)/y for each addit

91 jects had wider nasal rims than the inferior rims, 29.4% had wider nasal rims than the superior rims,

92 h a well-defined periablational inflammatory rim, for IRE, the infiltrate penetrated the ablation zon

93 on, and two terpyridines (TPYs) in the inner rim for subsequent folding by selective intramolecular c

94 ired for RNA repair are located on the inner rim of each ring.

95 ng to multiple positive charges on the inner rim of helicoid, double-stranded DNA molecules (dsDNA) c

96 minal flexible half emanating from the inner rim of the upper hexon channel into the tegument layer.

97 (2)} units with lanthanide ions on the inner rim, giving the general formula {Mo(90)Ln(10)}.

98 and classified in four groups (interfacial, rim, allosteric, orthosteric) according to their propert

99 residing in both the tumor core and invasive rim regions, with the maximal levels found in the invadi

100 y weight), tumors showed a heavily iodinated rim surrounding the tumor having an average uptake of 2.

101 ), each with three (S)-glutamic acids at its rim, were found (NMR, ITC) to complex diammonium alkanes

102 aring diazonium functionalities at its large rim and carboxylic functions at its small rim, which is

103 t known case of the participation of lateral rim cells in a sub-retinal pigment shield in an insect e

104 s, the sub-retinal extensions of the lateral rim cells can be seen as a functional adaptation to mini

105 cell type, but by extensions of the lateral rim pigment cells that penetrate gaps in the BM.

106 ein sign, subpial demyelination and lesional rims), which are not included in the current multiple sc

107 ce of methoxy or propoxy groups at the lower rim were synthesized.

108 ough the upper rim and the through the lower rim.

109 lizing methylimidazolium groups on the lower rim.

110 a supramolecular co-assembly based on lower-rim dodecyl-modified sulfonatocalix[4]arene (SC4AD) and

111 Mean rim area, RNFL, and GC-IPL thickness were 1.31 mm(2) (st

112 Patients with a VF endpoint had a median rim area rate that was nearly 3 times worse than those w

113 Metal rims expelled during chondrule formation, but still atta

114 Minimum rim width (MRW), ganglion cell-inner plexiform layer thi

115 Minimum rim width, retinal nerve fiber layer and GCL thickness,

116 on strategies to calculate BMO-based minimum rim area led to significantly different results.

117 hour sector-wise optimized BMO-based minimum rim area was calculated independently.

118 ization used for calculating the BMO minimum rim area in spectral domain optical coherence tomography

119 -gMRA) and sector-wise optimized BMO-minimum rim area (BMO-MRA).

120 luding BMO-minimum rim width and BMO-minimum rim area.

121 average, superior, and inferior BMO-minimum rim width (BMO-MRW).

122 O)-based measurements, including BMO-minimum rim width and BMO-minimum rim area.

123 w objective assessment of cupping by minimum rim width at Bruch's membrane opening (MRW-BMO).

124 simultaneously optimized continuous minimum rim surface parameter between Bruch's membrane opening (

125 parameters (minimum rim area (MRA), minimum rim width (MRW), Bruch's membrane opening (BMO) area, me

126 ferences in Bruch's membrane opening minimum rim width (BMO-MRW) in spectral-domain optical coherence

127 Bruch membrane opening-minimum rim width (BMO-MRW) assessment offers a new diagnostic u

128 ters included BMO-globally optimized minimum rim area (BMO-gMRA) and sector-wise optimized BMO-minimu

129 MO-based neuroretinal rim parameter, minimum rim width (BMO-MRW), and RNFL thickness.

130 ulated the change in OCT parameters (minimum rim area (MRA), minimum rim width (MRW), Bruch's membran

131 Two neuroretinal parameters, minimum rim width and retinal nerve fiber layer thickness, in ad

132 %) in the central 1-mm circle (C(1)), 1.5-mm rim (R(1.5)), and 2.5-mm circle (C(2.5)) from the 3 x 3-

133 -mm and 6 x 6-mm scans and FD% in the 2.5-mm rim (R(2.5)) and 5-mm circle (C(5)) from the 6 x 6-mm sc

134 Finally, focused ablation within 5-mm rim of the prospective channel regions eliminated 18 of

135 obtained using protocols for which a sub-mm rim of tumor remained after ablation.

136 vered from the Ro 8-4304-insensitive mutant (rim) screen using a mutagenized chs3-2D population.

137 tional fashion through the calixarene narrow rim.

138 the superior rims, 14.7% had narrower nasal rims than the temporal rims, and 42.9% had thinner nasal

139 cifically, 10.9% of subjects had wider nasal rims than the inferior rims, 29.4% had wider nasal rims

140 han the inferior rims, 29.4% had wider nasal rims than the superior rims, 14.7% had narrower nasal ri

141 Mean BMO disc and neuroretinal rim (NRR) areas ranged from 0.94 to 4.06 mm(2) (mean 1.7

142 r quantification of a BMO-based neuroretinal rim parameter, minimum rim width (BMO-MRW), and RNFL thi

143 Likewise, the following neuroretinal rim parameters showed significant changes with trabecule

144 thickness parameter, the 3D MDB neuroretinal rim thickness parameter had uniformly equal or better di

145 cula in contrast to the minimum neuroretinal rim width (MRW) and peripapillary retinal nerve fiber la

146 p-to-disc ratio of 0.7 or more, neuroretinal rim notching, retinal nerve fiber layer defect, and bare

147 e examined the stability of OCT neuroretinal rim parameters after glaucoma surgery for ongoing detect

148 etinal nerve fiber layer and/or neuroretinal rim defects, and disc haemorrhages).

149 owing from blood vessels at the neuroretinal rim remains an issue.

150 We determined whether neuroretinal rim assessment based on Bruch's membrane opening (BMO),

151 1, nucleoporin 98 and nucleoporin 62 nuclear rim staining are observed in Purkinje cells of ATXN1[82Q

152 zer function from centromeres to the nuclear rim during myogenesis.

153 dElys localized to the nuclear rim in interphase cells, but during mitosis it was absen

154 The nuclear rim protein Amo1 has been proposed to tether the mating-

155 We identify the nuclear rim protein Amo1(NUPL2) as a factor required for the pro

156 that this region is retained at the nuclear rim.

157 s, cytoplasmic bodies, caps, central nuclei, rimmed fibers, and/or mild endomysial fibrosis.

158 oughout the expansive hyperintense border of rim+ lesions, which co-localized with iron containing CD

159 tramer chain formation for the continuity of rim formation during disk morphogenesis.

160 Exclusion of rim arterial phase hyperenhancement as a means of satisf

161 healthy and progressing eyes, the pattern of rim area loss and percentage rim area loss were similar,

162 Overall RNFL, average GCC and ONH rim volume were considered in the analysis.

163 were significantly lower P < .001) than ONH rim area (0.90 and 77%) and GCC thickness (0.91 and 55%)

164 pare their diagnostic abilities with the ONH rim area, peripapillary retinal nerve fiber layer (RNFL)

165 my resulted in anatomical changes to the ONH rim associated with reduced glaucomatous cupping.

166 eation and welding of gold seeds on the open rims of NCNCs enriched with nitrogen functionalities, as

167 e was noted to have an upper lateral orbital rim mass.

168 e cells throughout and spheres with an outer rim of viable cells but necrotic cells centrally.

169 pared with two terminal alkynes in the outer rim for polymerization, and two terpyridines (TPYs) in t

170 0 mM NaCl, pitting is initiated at the outer rim of the confined zone, while below 10 mM NaCl, pittin

171 captures 12-16 actin filaments on the outer rim of the helix.

172 macrophages and viable cells at their outer rim.

173 er of the CheY protein family to the outside rim of the C ring.

174 subdivided into catalysis promoted by the PA rim/cavity, PA-based nanomaterials, and PA-based polymer

175 in the D'' layer beneath the circum-Pacific rim.

176 Paramagnetic rim lesions, rare in other neurological conditions (52%

177 etic resonance imaging by their paramagnetic rims, and increasing evidence supports their association

178 ear, respectively; P < 0.001) and percentage rim area loss (-1.1% vs. -0.2%/year, respectively; P < 0

179 tes of absolute rim area loss and percentage rim area loss in healthy and progressing glaucomatous ey

180 the pattern of rim area loss and percentage rim area loss were similar, tending to be fastest in the

181 aster and the mean rate of global percentage rim area loss was 5.4 times faster in progressing glauco

182 tor expression measurement in periablational rim, serum, and distant tumor 24 hours to 7 days after a

183 ession and macrophages in the periablational rim (P < .05).

184 e pathways upregulated in the periablational rim after hepatic RFA, of which STAT3 was active in four

185 fy key expressed genes in the periablational rim after radiofrequency ablation (RFA) and their role i

186 nt spleen, the characteristic perifollicular rim marking the marginal zone (MZ), which is the interfa

187 Peritumoral-rim radiomic features were most relevant to both classif

188 ns with transient rim, those with persistent rim had less volume shrinkage and became more T1 hypoint

189 Pathologically, persistent rims corresponded to an iron-laden inflammatory myeloid

190 Growth along the phagophore rim marks the progress of both organelle expansion and u

191 In centripetal lesions, a phase rim colocalized with initial contrast enhancement.

192 contrast enhancement and a colocalized phase rim.

193 In later stages of MS, phase rim lesions continue to smolder, exerting detrimental ef

194 n early lesion evolution, a persistent phase rim in lesions that shrink least and become more T1 hypo

195 ve MS cases, the histopathology of the phase rim was determined.

196 For each lesion, time evolution of the phase rim, lesion volume, and T1 hypointensity were assessed.

197 In 12 of 22, this phase rim persisted after enhancement resolved.

198 No centrifugal lesions developed phase rims at any time point.

199 e is only valid for 37.0% of disc photograph rim assessments and 43.8% of RNFL measurements.

200 n of the apical membrane patches to the pore rim and the apparent area compressibility modulus, an in

201 on into the MOM and localization to the pore rim.

202 re readily resolved on the gold-covered pore rims of the PSMs and which are discussed in the context

203 obile domains that were attached to the pore rims and (ii) mobile, round-shaped lo domains within the

204 There was a higher incidence of positive rim cultures over the last 5 years of the analytic perio

205 independent dataset, the DSF model predicted rim area and mean sensitivity paired measurements more a

206 rids + piatnitzkysaurids), such as prominent rims around the anterior articular surfaces of cervical

207 d to help clinicians distinguish age-related rim area loss from rim area loss resulting from glaucoma

208 cytoskeletal fragments around the aperture's rim during the expansion phase results in parallel bundl

209 ddition to functional groups at the basket's rim play a role in the efficiency (up to 98%) by which O

210 We found that two regions of LukE's rim domain contribute to hemolysis, namely residues 57-7

211 Global and sectoral rim areas were measured using confocal laser scanning op

212 d a deep perinarial fossa defined by a sharp rim.

213 secondary outcome measures were significant: rim area, cup volume, or disc area.

214 identified at the middle/outer active sites rim, which could be targeted to increase the CAI isoform

215 ge rim and carboxylic functions at its small rim, which is post-functionalized with alkyne moieties.

216 volume (HR 1.30, 95% CI: 1.05-1.61), smaller rim volume (HR 1.25, 95% CI: 1.01-1.54), larger maximum

217 p area (HR 1.33, 95% CI: 1.08-1.64), smaller rim area (HR 1.33, 95% CI: 1.07-1.64), larger cup volume

218 th enhanced subduction near the southeastern rim of the AC.

219 veals that SCARB2 binds EV71 on the southern rim of the canyon, rather than across the canyon, as pre

220 or patterns including homogeneity, sparsity, rim, and peripheral deposition.

221 lular flow of tumour cells from the spheroid rim towards its core.

222 29.4% had wider nasal rims than the superior rims, 14.7% had narrower nasal rims than the temporal ri

223 7% had narrower nasal rims than the temporal rims, and 42.9% had thinner nasal RNFLs compared to the

224 electrochemical electron transfer across the rim of nanospheres, and the thermodynamics and kinetics

225 we report the composition of soil along the rim of a 450-m diameter fresh crater at the Chang'e-3 (C

226 Multiple histidine residues along the rim of the VISTA extracellular domain mediate binding to

227 Three distinct functional areas (the rim, hypoxic, and normoxic cores) were clearly discernib

228 Lack of proliferation at the rim and/or over-clearing of epithelial cells in the cent

229 Diabetic muscles collected at the rim of normal tissue surrounding the plane of dissection

230 further attenuated by charged Glu192 at the rim of S1 in thrombin, which is replaced by uncharged Gl

231 eractions with the Arg1173 side chain at the rim of the binding site.

232 ficity, including a glutamate residue at the rim of the channel entrance that appears to be positione

233 ow while the exocyst tethers vesicles at the rim of the division plane.

234 thanol is evaporating, preferentially at the rim of the drop because of the singularity there.

235 ects the hindering of the evaporation at the rim of the droplet by the nonvolatile oil meniscus, prev

236 itotic addition of new photoreceptors at the rim of the hemispheric retina, topological defects, call

237 o Lys to increase the positive charge at the rim of the interdomain region.

238 ration in a negatively curved annulus at the rim of the invagination.

239 ified by lesion-to-brain ratios (L/B) at the rim of the resection cavity (considered treatment-relate

240 Postoperative reactive changes at the rim of the resection cavity appear to be mild.

241 of 1.7 +/- 0.2 for (3)H-MET was noted at the rim of the resection cavity in the first week after surg

242 reactive changes in (18)F-FET uptake at the rim of the resection cavity within the first 2 wk after

243 ) and retinal progenitor cells (RPCs) at the rim of the retina, called the ciliary marginal zone (CMZ

244 ill exhibit BODIPY fluorescence right at the rim of these packages.

245 resorption, leaving behind the region at the rim to form a tube-shaped canal.

246 rotrusion by expanding Rac activation at the rim while suppressing expansion of the active Ras interi

247 sket 3, containing (S)-alanine groups at the rim, was found to transfer its static chirality to entra

248 at is enlarged by alpha9 dimerization at the rim.

249 g glycine and (S)-alanine amino acids at the rim.

250 the difference in the densities between the rim and the dimple regions of red blood cells and their

251 uring contractile-ring constriction, but the rim of the cleavage furrow is the main site for endocyto

252 es with arterial phase hyperenhancement, the rim pattern was more common among non-HCC malignancies t

253 TSPO and HLA-DR in active lesions and in the rim of chronic active lesion, relative to normal appeari

254 Special focus was given on the rim and tip regions of the zeolite ZSM-5 crystals.

255 nest in active termite mounds [3] or on the rim of degassing volcanoes, seemingly preferring such ha

256 otein interact with positive residues on the rim of Hfq, as has been recently proposed for a mechanis

257 hey also showed that residues located on the rim of the heptamer are required for optimal binding to

258 f arginines in a semi-conserved patch on the rim of the Hfq hexamer and correlates with the previousl

259 eroid core had an alkalinizing effect on the rim, producing therein a milieu conducive for growth.

260 ueous 1 muL samples can be injected onto the rim of the TiO2-coated glass wafer, before the entire wa

261 ensity must be larger in the dimple than the rim to produce the observed membrane curvatures.

262 e T1 hypointense over time suggests that the rim might mark failure of early lesion repair and/or irr

263 crystallography driven study shows that the rim of the interface of individual 14-3-3 complexes can

264 ivated microglia mapped most strongly to the rim of MS plaques.

265 isco-interacting residues located toward the rim of the hexamer were found to be less critical to Rca

266 en aging and GCL thickness compared with the rim or peripapillary RNFL may indicate that GCL thicknes

267 mong rim+ lesions, susceptibility within the rim (20.04 +/- 14.28 ppb) was significantly higher compa

268 ers, which assemble into long ribbons at the rims of the inner membrane cristae.

269 via interactions of the carboxylates at the rims with ammoniums on the guest.

270 ol of COPI budding and vesicle fusion at the rims.

271 ogen bonding networks are formed between the rims of CD and CB6 in a manner that is positively cooper

272 sitive to the activity of macrophages in the rims of white matter lesions.

273 seem to be passive and are often simply the rims of the indentation pockets arising from the turbule

274 the remaining DNA duplexes interact with the rims and serve as bridges between adjacent hexamers.

275 cular baskets 1-3, with amino acids at their rim, undergo photoinduced decarboxylations to give baske

276 irectional (up/down) allyl moieties on their rims is reported.

277 a = 633 nm, their (100) faces and thus their rims fluoresce brightly, while the pseudohexagonal faces

278 core of specific tumors compared with their rims.

279 that is associated with a constant-thickness rim of growing cells at the cluster edge, as well as the

280 retinal nerve fiber layer (RNFL) thickness, rim area, and ganglion cell-inner plexiform layer (GC-IP

281 e accumulation within the surrounding tissue rim.

282 her in rim+ (2.42 +/- 17.45 ppb) compared to rim- lesions (-14.6 +/- 19.3 ppb, P < 0.0001).

283 ages, was higher in rim+ lesions compared to rim- lesions (P = 0.015).

284 ared with centripetal lesions with transient rim, those with persistent rim had less volume shrinkage

285 ng in substantial overestimation of the true rim tissue thickness and underestimation of cup depth.

286 ations substantially lower in invasive tumor rim (intact BBB) compared to glioblastoma core (disrupte

287 [(18)F]BR-351 (11%) volumes along the tumor rim could be identified.

288 PDO3A)(H2O)] and dox release along the tumor rim, mirroring the TSL distribution pattern.

289 ore and efficient drug delivery to the tumor rim.

290 rpyridine (tpy) group installed at its upper rim.

291 cone conformation: passage through the upper rim and the through the lower rim.

292 4]arenes with orientable groups at the upper rim were thoroughly analyzed.

293 derivative (1H3)(2+), decorated at the upper rim with two guanidinium units and a phenolic hydroxyl i

294 n of rigid urea functionalities on the upper rim; and the introduction of the water-solubilizing meth

295 ature and essentially supported by the upper-rim (t)Bu groups of the ((t.Bu)ArO)(3)tacn(3-) ligand.

296 e possibly sourced from the Gale crater wall/rim/central peak.

297 ne 1c, bearing tert-butyl groups at the wide rim, was threaded by all of the cations under study (wit

298 .6, P < .001) and negatively associated with rim area (-0.02, P < .001).

299 AXL had a negative association with rim area (-0.05, P < .001).

300 tients with an endpoint (n = 59) had a worse rim area rate prior to the endpoint compared to those wi