ライフサイエンスコーパス: rim

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

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

3 ain from the CR chondrite NWA 852 exhibits a rim structure only visible in chemical maps.

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

5 lae reach full diameter, and the growth of a rim encloses the space between adjacent surfaces of two

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

7 The perinuclear actin rim structure colocalized with INF2 on stimulation, and

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

9 ximately 1-keV H(+) ions, produces amorphous rims up to approximately 150 nm thick on the surfaces of

10 Silicates with amorphous rims are observed on interplanetary dust particles and o

11 ct water sealed in vesicles within amorphous rims produced by SW irradiation of silicate mineral grai

12 l findings, including a Greco-Italic amphora rim produced in Latium or Campania, provide a relative c

13 accounting for age, C/D area ratio, NFL, and rim area.

14 A binding channel between the inner pore and rim of the Hfq hexamer contribute to the selectivity of

15 Class I sRNAs depend on proximal and rim Hfq sites for stability and turn over rapidly.

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

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

18 aracterized by two main regions, "core" and "rim", which differ in terms of evolutionary conservation

19 ount, and increased numbers of oral sex and "rimming" partners increased the risk of incident oral HP

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

21 ractures and the destruction of the anterior rim of the vertebral body.

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

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

24 eps away from the catalyst tip with attached rims of the carbon cap generates the wall of the nanotub

25 r interpreted as remnants of an impact basin rim are shown in GRAIL data to be a part of this continu

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

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

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

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

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

31 nteracts with concave membrane necks and bud rims.

32 recognizes a novel epitope in the so-called "rim" domain of AT and exerts its neutralizing effect thr

33 ositive metallic cation and the carbonylated rim of CB[n], and the location of the latter in the seco

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

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

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

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

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

39 e expression and formation of actin cortical rim and continuous barrier.

40 climate that supplied moisture to the crater rim and transported sediment via streams into the lake b

41 ted antiquity of rocks comprising the crater rim.

42 or BMO-MRW (r = 0.546) than with either CSLO rim area (r = 0.321, P < 0.001) or horizontal rim area (

43 or BMO-MRW (r = 0.680) than with either CSLO rim area (r = 0.330, P < 0.001) or horizontal rim area (

44 thelium (RPE) progenitors near the optic cup rim.

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

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

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

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

49 , with only 1 study with more than mild dark-rim artifacts.

50 ith excellent image quality and minimal dark-rim artifacts.

51 ation strategy has been shown to reduce dark-rim artifacts in first-pass perfusion imaging.

52 that this is because it enables the dilated rims of cisternae (containing the aggregates) to move ac

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

54 ness, cup-to-disc area ratio, and optic disc rim area.

55 Disc-rim protein peripherin2/rds enters the OS following a rh

56 adjacent lamellae, thereby initiating a disk rim.

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

58 na through epithelial flow around the distal rims of the optic cup.

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

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

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

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

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

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

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

66 ociated with a fungal culture-positive donor rim.

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

68 tcomes of grafts with culture-positive donor rims.

69 ediated by the polarization-sensitive dorsal rim area (DRA) of their eye.

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

71 y of the Drosophila retina called the dorsal rim area (DRA) act as detectors for polarized light.

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

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

74 r preferential fluid pumping around the drop rim.

75 ith the effect of IOP in the model excluding rim area measurements.

76 s can be introduced at the calix[6]arene exo rim.

77 and 4 bearing squaramide moieties at the exo rim (p-squaramidocalixarenes).

78 MD of -5 dB), area under ROC curve (AUC) for rim area, average RNFL thickness, and average GCC thickn

79 eal center and the nasal and temporal foveal rims.

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

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

82 eroinferior labrum associated with a glenoid rim fracture.

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

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

85 LGMD1D muscle has rimmed vacuoles and inclusion bodies containing DNAJB6,

86 im area (r = 0.321, P < 0.001) or horizontal rim area (0.403, P < 0.001).

87 im area (r = 0.330, P < 0.001) or horizontal rim area (r = 0.482, P < 0.001).

88 rim measures from radial B-scans: horizontal rim area between BMO and inner limiting membrane within

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

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

91 endently associated with a slower decline in rim area.

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

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

94 If -OH or H2O is generated in rims on silicate grains, there are important implication

95 ngs on biopsies of affected muscles include 'rimmed' (autophagic) vacuoles, aggregation of various pr

96 ment of visual field loss when incorporating rim area loss in the same model with the effect of IOP i

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

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

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

100 In contrast, the interface rim is significantly enriched in polymorphisms, similar

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

102 itical for the formation of the disc/lamella rim in photoreceptor outer segments (OSs), but plays a d

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

104 ptor bearing three azido groups at the large rim was selectively monofunctionalized through an intram

105 ations show that the distal face and lateral rim of Hfq interact with three sites in the rpoS leader,

106 stimation of retinal nerve fiber layer loss, rim loss, vertical cup-disc ratio, disc hemorrhage, and

107 Lower rim amide linked 8-amino quinoline and 8-amino naphthale

108 phenylene-diimine-capped conjugate of lower rim 1,3-calix[4]arene (L) was synthesized, characterized

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

110 lizing methylimidazolium groups on the lower rim.

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

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

113 coordinates the formations of disk membrane rim region and OS PM.

114 Minimum rim measurements from SD-OCT are significantly better co

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

116 ean minimum rim width (BMO-MRW); and minimum rim area (BMO-MRA) optimized within sectors and then sum

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

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

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

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

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

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

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

124 membrane within the BMO plane; mean minimum rim width (BMO-MRW); and minimum rim area (BMO-MRA) opti

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

126 OCT) index, Bruch's membrane opening minimum rim width (BMO-MRW), addresses these deficiencies and ha

127 aphy, while Bruch's membrane opening-minimum rim width (BMO-MRW), BMO area (BMOA), and peripapillary

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

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

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

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

134 tional fashion through the calixarene narrow rim.

135 Adaptation of Ugi-4CR for the narrow-rim modification of calix[4]arene toward the synthesis o

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

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

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

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

140 ptic disc area, optic cup area, neuroretinal rim area, cup volume, rim volume, cup-disc area ratio, h

141 Global disc margin-based neuroretinal rim area (DMRA) was measured with confocal scanning lase

142 ntional optic disc margin-based neuroretinal rim measurements lack a solid anatomic and geometrical b

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

144 ctionally progressive glaucoma, neuroretinal rim loss, and DH.

145 stigate possible differences in neuroretinal rim distribution, vascular pattern, and peripapillary re

146 ociated with RBV shift included neuroretinal rim loss (OR, 21.9; 95% CI, 5.7-83.6; P< 0.001) and DH (

147 gression (2 graders), including neuroretinal rim loss, parapapillary atrophy progression, and disc he

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

149 HR], 5.737; P = .012), narrower neuroretinal rim width at baseline (HR, 2.91; P = .048), use of syste

150 athy defined by the presence of neuroretinal rim thinning, notching or excavation of the cup, cup-to-

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

152 characteristics related to the neuroretinal rim distribution, vascular pattern, peripapillary region

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

154 ed as clinically having healthy neuroretinal rims and an MRA analysis of within normal limits in all

155 ction appears to recruit UL97 to the nuclear rim both for disruption of the nuclear lamina and phosph

156 owever, PKC was not recruited to the nuclear rim, and its localization was not affected by the absenc

157 clear egress and recruit UL97 to the nuclear rim, are UL97 substrates.

158 that this region is retained at the nuclear rim.

159 nuous distribution of the NEC at the nuclear rim.

160 measured by CSLO was compared with 3 SD-OCT rim measures from radial B-scans: horizontal rim area be

161 y well explained by the observed behavior of rim-pores.

162 ng that proper targeting and distribution of rim proteins may require RDS.

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

164 Finally, the free energy landscape of rim-pore expansion/HD dilation may very well explain why

165 Secondary outcomes included modifications of rim area and cup-to-disc ratio.

166 well as the free energy along the pathway of rim-pore expansion, we derived a simple analytical free

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

168 The mean rate of rim area change in eyes that developed visual field loss

169 e model, each 0.01 mm(2)/year faster rate of rim area loss was associated with a 2.94 higher risk of

170 was used to evaluate the ability of rates of rim area loss in predicting visual field development, ad

171 nderestimated due to the frequent absence of rimmed vacuoles in the muscle biopsy.

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

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

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

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

176 , and confocal scanning laser ophthalmoscopy rim area (coefficient of variation 4.2%-7.6%).

177 ), regardless of their occurrence in core or rim residues.

178 nerve fiber layer loss, disc hemorrhage, or rim loss were most likely to lead to underestimation of

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

180 0 mM NaCl, pitting is initiated at the outer rim of the confined zone, while below 10 mM NaCl, pittin

181 Ubiquitin chains are bound along the outer rim of the helical trajectory, bridging adjacent subunit

182 macrophages and viable cells at their outer rim.

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

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

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

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

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

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

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

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

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

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

193 Importance: Although nevi with a peripheral rim of globules (peripheral globular nevi [PGN]) observe

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

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

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

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

198 contrast enhancement and a colocalized phase rim.

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

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

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

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

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

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

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

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

207 itable chiral "bouncer" molecule to the pore rim prevents the passage of the undesired enantiomer whi

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

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

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

211 Superior and posterior rim deficiencies are associated with procedural failure.

212 Superior and posterior rim deficiencies were more common in failed than in succ

213 Progressive rim area loss was highly predictive of the development o

214 ins is preserved even in the absence of RDS, rim, and lamella structures.

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

216 ass II sRNAs regulate mRNAs carrying UA-rich rim-binding sites.

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

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

219 Scoured rims of the headwalls, relict plunge pools, sediment-tra

220 ring interact with the primary and secondary rim hydroxyl residues, respectively, enhancing complex s

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

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

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

224 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

225 ubes, and acetabulae that form a deep socket rimmed by a robust lip of bone.

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

227 29.4% had wider nasal rims than the superior rims, 14.7% had narrower nasal rims than the temporal ri

228 7% had narrower nasal rims than the temporal rims, and 42.9% had thinner nasal RNFLs compared to the

229 nd is accompanied by gain of the tetraspanin rim protein, peripherin.

230 orrelated to both RNFL thickness and MD than rim measurements within the BMO plane or based on the cl

231 A multivariable model revealed that rim loss and DH, but not rate of functional change, were

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

233 ith the line energy of the rim-pore, and the rim-pore reaches its equilibrium size before reaching th

234 tory cells, and a subset of them, around the rim, also expresses an FMRFamide-like neuropeptide.

235 birefringent crystal, are arrayed around the rim.

236 d baskets ought to unfold their gates at the rim for permitting the passage of guests to/from their i

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

238 The Cys(228)-Cys(448) disulfide is at the rim of the active site and is only three residues distan

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

240 In particular, conserved loops at the rim of the central channel, which are in direct contact

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

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

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

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

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

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

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

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

249 at is enlarged by alpha9 dimerization 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 However, the rim protein prominin-1 exhibits altered trafficking and

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

254 NF2 depletion resulted in attenuation of the rim formation.

255 dvances our understanding of the role of the rim in cone OS morphogenesis.

256 the HD competes with the line energy of the rim-pore, and the rim-pore reaches its equilibrium size

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

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

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

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

261 nity has investigated in detail rocks on the rim of the Noachian age Endeavour crater, where orbital

262 mRNAs, after which an arginine patch on the rim promotes base pairing between their complementary se

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

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

265 by the thicker rims to partially release the rim-cap energy.

266 lipid metabolism and protein synthesis, the rim of the metastasis displayed increased cellular growt

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

268 within the interface core, as opposed to the rim (p<0.01).

269 r E37 strengthened RNA interactions with the rim of Hfq and increased annealing of non-specific or U-

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

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

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

273 centers increasing to high values near their rims.

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

275 core of specific tumors compared with their rims.

276 anosheets that are stabilized by the thicker rims to partially release the rim-cap energy.

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

278 he nuclear periphery, coincident with a thin rim of heterochromatin.

279 This rim-pore is characterized by a nontoroidal shape that ch

280 e accumulation within the surrounding tissue rim.

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

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

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

284 Some hot spots were observed near the tumor rim.

285 ore and efficient drug delivery to the tumor rim.

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

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

288 tion of four phosphonate groups at the upper rim of a calix[4]pyrrole-resorcin[4]arene hybrid scaffol

289 tectures through subtle changes of the upper rim substituents.

290 nalized with a carboxylic group at the upper rim was used to enhance selectivity toward analytes cont

291 4]arenes with orientable groups at the upper rim were thoroughly analyzed.

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

293 and at the 1,3-distal positions of the upper rim, effectively catalyzes the cleavage of 2-hydroxyprop

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

295 cup area, neuroretinal rim area, cup volume, rim volume, cup-disc area ratio, horizontal and vertical

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

297 y, 95.9%; PLR, 18.13; and NLR, 0.27), as was rim area (sensitivity, 68%; specificity, 98%; PLR, 33.3;

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

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

300 mes freely accessing the outer marginal zone rim of SIGN-R1(+) macrophages and F4/80(+) red pulp macr