ライフサイエンスコーパス: ellipsoid

1 nal bundles, giving a stiff, low-DNA-density ellipsoid.

2 mCherry, reveals a discrete, dynamic helical ellipsoid.

3 t-based model that considers each cell as an ellipsoid.

4 ater than predicted from the fitted triaxial ellipsoid.

5 arrangement of subunits formed an elongated ellipsoid.

6 Average shapes are consistent with prolate ellipsoids.

7 xy-terminal domain reveal asymmetric, oblate ellipsoids.

8 on, a sill-like, circular chamber (an oblate ellipsoid) 1 km thick and 14 km in diameter would have a

9 a dimer of triads in the shape of an oblate ellipsoid 140 A diameter x 70 A.

10 ions of spheres mixed with a small number of ellipsoids also produce uniform deposition.

11 esicles of two distinct morphologies (sphere/ellipsoid and cylinder/arachoid), large unilamellar vesi

12 sual acuity (P = 0.019) with higher rates of ellipsoid and external limiting membrane defects (P < 0.

13 and (4) vitelliform deposits located between ellipsoid and interdigitation lines on SD-OCT.

14 or the shuttling of microtubules between the ellipsoid and myoid is the underlying force for the morp

15 which localizes to the junction between the ellipsoid and myoid, functions to shuttle microtubules f

16 54 is compartmentalized predominantly in the ellipsoid and outer segment compartments.

17 In C. elegans, spindles are initially ellipsoid and parallel to the cortex before shortening t

18 Inner segment ellipsoid and relative ellipsoid reflectivity were close

19 e model the cells as deformable viscoelastic ellipsoids and incorporate signal transduction and cell-

20 rphology and the formation of single prolate ellipsoids and pairs of prolate ellipsoids joined by par

21 Such zones include the myoid, ellipsoid, and the interdigitation zones.

22 ecular envelope of DEBS3 is a thin elongated ellipsoid, and the results of rigid-body modeling sugges

23 the larger particles were defective spheres, ellipsoids, and bacilliform cylinders, with regions of T

24 Thus, after the ellipsoids are carried to the air-water interface by the

25 Hydrodynamic models of ellipsoids are presented, and it is argued that ocr is b

26 asmic granular hyperreflectivity and rounded/ellipsoid aspects of keratocytes, presence of small intr

27 ergoes a transition from a prolate to oblate ellipsoid at a critical frequency, which the theory iden

28 d complete preservation of the inner segment ellipsoid band in 1 patient, with variable lateral exten

29 with the lateral extent of the inner segment ellipsoid band in the OCT image.

30 ent had mild disruption of the inner segment ellipsoid band on OCT and additional mild digit abnormal

31 ivity (defined as the ratio of inner segment ellipsoid band reflectivity on overall retinal reflectiv

32 Inner segment ellipsoid band reflectivity, global retinal reflectivity

33 -outer segment junction or the inner segment ellipsoid band was disrupted within 1 degrees to 4 degre

34 s subtle irregularities at the inner segment ellipsoid band were seen.

35 ere, prolate or oblate hemispheroid, or hemi-ellipsoid, based on these findings; three-dimensional fo

36 dimensional domains, traditionally viewed as ellipsoids because of their two-dimensional lenticular s

37 ystal structure, with the axial ratio of the ellipsoid being approximately 4.5 as compared to only ap

38 The ellipsoid body (EB) in the Drosophila brain is a central

39 creen in Drosophila, we identify a subset of ellipsoid body (EB) neurons whose activation generates s

40 ression in the mushroom bodies (MBs) and the ellipsoid body (EB) of the central complex.

41 r optic tubercle (AOTU) and bulb (BU) to the ellipsoid body (EB) of the central complex.

42 -protocerebral bridge gall (E-PG) neuron and ellipsoid body (EB) R2/R4m ring neuron circuits both neg

43 SLC5A11 acts on approximately 12 pairs of ellipsoid body (EB) R4 neurons to trigger the selection

44 One of these compartments is the ellipsoid body (EB), a structure formed largely by the a

45 ocerebral bridge (PB), fan-shaped body (FB), ellipsoid body (EB), and noduli (NO).

46 Distinct dopaminergic neurons also innervate ellipsoid body (EB), where DopR function modulates arous

47 g is also important for the formation of the ellipsoid body (EB), where it influences the pathfinding

48 Here, we show that ring neurons of the ellipsoid body (EB-RNs) display spontaneous morning and

49 d by the noduli (from P12h), and finally the ellipsoid body (from P24h).

50 ous second messengers establish a functional ellipsoid body and act as a short-term aid in orientatio

51 DALcl2, form the large-field neurons of the ellipsoid body and fan-shaped body, respectively.

52 Perturbations in both the ellipsoid body and the ventral nerve cord, two regions i

53 xpressed in 10-13 pairs of R4 neurons of the ellipsoid body in the brain and functioned in these neur

54 ts of thermo and optogenetic manipulation of ellipsoid body neurons important for ethanol-induced loc

55 identify two reciprocally connected sets of ellipsoid body neurons that form the heart of a serotoni

56 Furthermore, the ellipsoid body of the central complex and giant synapses

57 so-called 'ring neurons', projecting to the ellipsoid body of the central complex, are reported to b

58 s in the brain, the mushroom bodies, and the ellipsoid body of the central complex.

59 innervation in the protocerebral bridge and ellipsoid body of the central complex.

60 A new study shows that the gene termed ellipsoid body open influences multiple signals to regul

61 Inputs to the fan-shaped body and ellipsoid body responded both to visual stimuli and to a

62 neurons of the mushroom body and a subset of ellipsoid body ring neurons (R2) is required for this ch

63 Thermogenetic inactivation of ellipsoid body ring neurons reduced group activity where

64 gnals to regulate a competence factor in the ellipsoid body to support normal working memory.

65 nervate a ring-shaped structure known as the ellipsoid body(3,11,12).

66 morphological phenotype in R-neurons of the ellipsoid body, a component of the central complex.

67 The ellipsoid body, a doughnut-shaped part of the fly brain,

68 esponses of neurons whose dendrites tile the ellipsoid body, a toroidal structure in the centre of th

69 of central neurons that does not include the ellipsoid body, a well-known pre-motor neuropil, provide

70 rosophila brain, we show that neurons in the ellipsoid body, but not in the mushroom bodies, are nece

71 ual memory, including central neurons in the ellipsoid body, but not the mushroom bodies or the fan-s

72 obtained from 24 neurons associated with the ellipsoid body, fan-shaped body, and protocerebral bridg

73 evelopment of a central brain structure, the ellipsoid body, suggesting that Rx function in the brain

74 Dop1R1 inputs onto CX columnar ellipsoid body-protocerebral bridge gall (E-PG) neuron a

75 development of axonal connections within the ellipsoid body.

76 e characteristic shape of the fan-shaped and ellipsoid body.

77 erebral bridge, fan-shaped body, noduli, and ellipsoid body.

78 he brain with a reduction in the size of the ellipsoid body.

79 omer in a subset of neurons that include the ellipsoid body.

80 e protocerebral bridge, fan-shaped body, and ellipsoid body.

81 hydrostatic, synchronously rotating triaxial ellipsoid but is best fit by such a body orbiting closer

82 lly and with a new simulation algorithm that ellipsoids can randomly pack more densely-up to phi= 0.6

83 eriments and computer simulations that Janus ellipsoids can self-assemble into self-limiting one-dime

84 ogically relevant shapes, including spheres, ellipsoids, capped cylinders, and hourglasses.

85 ible elongation and contraction of the Janus-ellipsoid chains by ~36% and that on long timescales lea

86 Transient ellipsoid changes were evident in 26% of treated eyes, m

87 an uncoated Nb ellipsoid to 2700 Oe for a Nb ellipsoid coated with ~200 nm thick MgB2 thin film.

88 r the parameters of the 'singular isothermal ellipsoid' density profile, which is commonly used to mo

89 ough the recovery coefficients of sphere and ellipsoid differed by only 0.7%, a difference of 31.7% w

90 The ellipsoid dimensions/radii are 175 x 28 nm for multimers

91 metry is broken, leading to the formation of ellipsoids, discs, and bowls.

92 Increased surface area occurs in oblate ellipsoids (disk-like), which rarely occur.

93 obal minimum of the objective function to an ellipsoid domain whose principal axes follow an exponent

94 phila undergo elongation from a sphere to an ellipsoid during oogenesis.

95 of different engulfment behaviors with some ellipsoids engulfing faster than spheres, and that phago

96 KV) was measured using stereology (TKVs) and ellipsoid equation (TKVe).

97 ng 60 polyps of different shapes (spherical, ellipsoid, flat) and size groups (5-9 mm, 11-15 mm) was

98 Ellipsoid formula-derived PVs had slopes closest to one

99 readers from MR images by using the standard ellipsoid formula.

100 roleiomyoma volume was measured by using the ellipsoid formula.

101 analytical model of the thermal niche of an ellipsoid furred endotherm that accurately predicts fiel

102 d double-labeled, small (11.8 x 8.0 microm), ellipsoid ganglion cells within the ethmoid nerve region

103 Ellipsoids gave the best agreement with measured forces,

104 L + 0.28, with the theory of rotation of the ellipsoid giving L + 0.28 for 7/2-, slowly decreasing to

105 are well approximated by those with prolate ellipsoid heads.

106 The swimming cell was modeled as an ellipsoid in Stokes flow, propelled by viscous forces on

107 Importantly, PDX-derived ellipsoids in microchambers retained patterns of drug re

108 ained by the dimensions and positions of the ellipsoids in the neutron-derived R-C model as well as m

109 us mass, identified by a radiologist-defined ellipsoid, in which six Doppler vascularity measures wer

110 We show that stretching cells from round to ellipsoid increases stream formation.

111 symplectic embedding of one four-dimensional ellipsoid into another.

112 , functions to shuttle microtubules from the ellipsoid into the myoid during the course of myoid elon

113 tral recirculation zone with the shape of an ellipsoid is formed in the non-reacting flow field with

114 (2) This ellipsoid is radially confined within the cell cylinder.

115 The major principal axis of the Poinsot ellipsoid is taken to be determined by an unquantized nu

116 ovea to the location where the inner segment ellipsoid (ISe) band became undetectable was measured.

117 ium (RPE) band, grading of the inner-segment ellipsoid (ISe) band integrity, and presence of hyperref

118 PURPOSE; The integrity of the inner segment ellipsoid (ISe) band, previously called the inner segmen

119 nct categories: (1) continuous inner segment ellipsoid (ISe), (2) ISe disruption, (3) ISe absence, (4

120 ngle prolate ellipsoids and pairs of prolate ellipsoids joined by partial constrictions.

121 was a defect in both the myoid zone and the ellipsoid junction (n = 1).

122 It often presented with an intact ellipsoid layer and was associated with tractional epire

123 r nuclear layer, external limiting membrane, ellipsoid layer, and interdigitation zone.

124 isruption of the external limiting membrane, ellipsoid layer, and interdigitation zone; and, in some

125 f photoreceptor inner segment-outer segment (ellipsoid) layer on SD-OCT and reduced ERG amplitudes co

126 disruption confined to the photoreceptor and ellipsoid layers; such injuries were associated with a b

127 ong-ranged interparticle attractions between ellipsoids lead to the formation of loosely packed or ar

128 two Ca2+-binding lobes and forms a compact, ellipsoid-like complex.

129 f the proteins are characterized by flexible ellipsoid-like structures with maximum dimensions in the

130 Endocytosis generates spherical or ellipsoid-like vesicles from the plasma membrane, which

131 erm retinal healing with reappearance of the ellipsoid line and visual acuity improved from 20/100 be

132 a; stage 2 (2 patients [12%]), inner segment ellipsoid line disruption; stage 3 (5 patients [29%]), p

133 Inner segment ellipsoid line loss generally correlated with the area o

134 developed bilateral focal foveal lesions and ellipsoid loss on spectral-domain OCT following peer-inf

135 actions: spheres <oblate ellipsoids <prolate ellipsoids <dimers <spherocylinders.

136 ncreasing packing fractions: spheres <oblate ellipsoids <prolate ellipsoids <dimers <spherocylinders.

137 To introduce an alternative 3D ellipsoid measuring technique that maximizes precision,

138 Mean measurement times for the ellipsoid method ranged from 4.6 to 5.2 minutes compared

139 Our findings indicate that the prolate ellipsoid model for the manganese-stabilizing protein is

140 e protein shape to a low-resolution triaxial ellipsoid model indicates that three discrete forms of t

141 software are myocardial sampling based on an ellipsoid model; use of the entire count profile between

142 85-A crystal structure of SleB(C) reveals an ellipsoid molecule with two distinct domains dominated b

143 e 'whisking' behavior, an approximately 8 Hz ellipsoid movement of the vibrissae, introduces a contex

144 strate that analysis of the minimum bounding ellipsoid of a coordination polyhedron provides a genera

145 drodynamic behaviour equivalent to a prolate ellipsoid of axial ratio 4.3 +/- 0.7:1 and mass of 27 kD

146 30% medullary compartment), a sphere, and an ellipsoid of equal volumes were 3D printed, filled with

147 pA hexamer in solution, modeled as an oblate ellipsoid of revolution, is very different from its crys

148 When modeled as a prolate ellipsoid of revolution, the hydrated DnaC protein has a

149 Here, we study the dynamics of triaxial ellipsoids of equivalent steric volume to proteins at di

150 increase of rOx immediately occurred in the ellipsoids of most photoreceptors.

151 for shapes like dimers, spherocylinders and ellipsoids of revolution.

152 form amorphous rounded vesicles to fibrillar ellipsoid organelles, during which they move from the pe

153 Experiments combined with ellipsoid packing models revealed that the mechanosensit

154 amphiphilic surfactant to afford asymmetric, ellipsoid particles.

155 based on theory for the covolume of triaxial ellipsoid particles.

156 function of distance between each globular, ellipsoid protein.

157 data "volume" for overlapped analytes (i.e., ellipsoids), provided there is sufficient chromatographi

158 microfluidic chambers, cancer cells grew as ellipsoids reaching millimeter-scale dimeters over the c

159 nal reflectivity, and relative inner segment ellipsoid reflectivity (defined as the ratio of inner se

160 e perimeters of annular lesions with loss of ellipsoid reflectivity and preserved RPE at the lesion c

161 Inner segment ellipsoid and relative ellipsoid reflectivity were closely correlated with cone

162 itation and emission, the mitochondrial-rich ellipsoid region of the cells shows strong fluorescence

163 egments, especially in the mitochondria-rich ellipsoid region.

164 Ellipsoids representing a 99% confidence interval surrou

165 to the outer limiting membrane and the cone ellipsoids, respectively, separated by the cone myoids.

166 The ellipsoids resulting from the partial anisotropic refine

167 ver, the distribution of anisotropic thermal ellipsoids revealed functionally important structure fle

168 ctures are addressed, including rods, tubes, ellipsoids, rings, and superellipsoids.

169 merical simulations of light scatter from an ellipsoid rounding up into a sphere.

170 hyperautofluorescent (hyperAF) rings with an ellipsoid shape and regular borders.

171 Abeta42 tetramers adopted an oblate ellipsoid shape and showed a significant increase in bet

172 tifs (Cys-X-Cys or Cys-Xn-Cys) and a prolate ellipsoid shape containing single alpha- and beta-domain

173 fs (Cys-X-Cys or Cys-X(n)-Cys) and a prolate ellipsoid shape containing single alpha- and beta-domain

174 amic modeling suggests an asymmetric prolate ellipsoid shape for gp59, consistent with its X-ray crys

175 suggest that the myopic eye tends toward an ellipsoid shape, rather than the globular shape of an em

176 ajority of the scatter plots have a similar, ellipsoid shape.

177 s a natively unfolded protein with a prolate ellipsoid shape.

178 ng and cell division is poorly understood in ellipsoid-shaped ovococcus bacteria, such as the human r

179 In ellipsoid-shaped ovococcus bacteria, such as the pathoge

180 st, we report here that GpsB is essential in ellipsoid-shaped, ovococcal Streptococcus pneumoniae (pn

181 e idea of representing protein surface as an ellipsoid shell.

182 lengths establish that the outer segment and ellipsoid signals originate from all-trans retinol and r

183 diffusion equations in idealized geometries (ellipsoids, spheres, and mushroom-shaped).

184 Ellipsoid spindles with flattened or pointed poles becam

185 parent LaMnO(3) phase, but the displacement ellipsoids suggest that incoherent distortions are signi

186 are associated with changes of the diffusion ellipsoid that are predominantly proportional along all

187 D geologic models of the lobes with triaxial ellipsoids that suitably represent the overall layers ar

188 vp increased from 2100 Oe for an uncoated Nb ellipsoid to 2700 Oe for a Nb ellipsoid coated with ~200

189 y of the iso-frequency surface from a closed ellipsoid to an open hyperboloid by use of artificially

190 ric field enhancement factor of an elongated ellipsoid to derive the energy distribution of electrons

191 In this work, we utilized Nb ellipsoid to simulate an inverse SRF cavity and investig

192 ystal structure of the hydroxylase and using ellipsoids to represent the reductase and protein B comp

193 particle size and shape from spheres through ellipsoids to toroids by varying the droplet composition

194 " non-attenuation-corrected as well as fixed-ellipsoid, uniform attenuation-corrected studies provide

195 Three CT volumetry techniques (modified ellipsoid volume [MELV], smart region of interest [ROI]

196 An alternative ellipsoid volume method is then proposed using these bou

197 Assuming tapasin is a prolate ellipsoid, we calculated an apparent length of 22.5 nm a

198 Assuming CRT to be a prolate ellipsoid, we calculated an apparent length of 29.8 nm a

199 analyzing data from experiments on colloidal ellipsoids, we show that facilitation plays a pivotal ro

200 A robust amount of rOx is produced in the ellipsoid when photoreceptors are exposed to blue light.

201 levels of rOx were observed in photoreceptor ellipsoids when cells were stained with DHF-DA.

202 f eight subunits, hydrodynamically an oblate ellipsoid, which binds DNA at chromosomal breakpoints.

203 and NAD+-binding domains are folded into an ellipsoid with a typical alpha/beta twisted open sheet s

204 the monomeric form of proapoA-I is a prolate ellipsoid with an axial ratio of about 6:1.

205 in structure that has an overall shape of an ellipsoid with dimensions 40 A x 26 A x 21 A and belongs

206 gued that ocr is best described by a prolate ellipsoid with dimensions of 10.4 nm by 2.6 nm.

207 e LDL from a sphere without partitions to an ellipsoid with partitions.

208 Pallas's shape is an ellipsoid with radii of 291 (+/-9), 278 (+/-9), and 250

209 ution has the approximate shape of a prolate ellipsoid with semi-axes of 24, 43, and 89 A.

210 nant role than target size for phagocytosis: Ellipsoids with an eccentricity of 0.954 and much smalle

211 and even approach phi approximately 0.74 for ellipsoids with other aspect ratios.

212 suggest that these proteins resemble prolate ellipsoids with radius of gyration (R(g)) of approximate

213 herent cultured cells approximates an oblate ellipsoid, with contralateral flattened surfaces facing

214 d 4) showed large errors only for sphere and ellipsoid (xSPECT, 23.4%; Flash3D, 21.6%).

215 Disruption of the ellipsoid zone (beta=0.699; P<0.001) and posterior hyalo

216 nization of the retinal inner layers (DRIL), ellipsoid zone (EZ) and external limiting membrane disru

217 oreceptor outer segment layer disrupting the ellipsoid zone (EZ) and interdigitation zone (IZ) (100%)

218 shment of the postoperative integrity of the ellipsoid zone (EZ) and the external limiting membrane (

219 Six eyes (10%) revealed a continuous ellipsoid zone (EZ) at 1 month, 18 eyes (30%) at 3 month

220 ized to 1 of 2 treatment groups METHODS: The ellipsoid zone (EZ) defect areas were measured on spectr

221 and (2) the "normalized" reflectivity of the ellipsoid zone (EZ) en face image.

222 BCVA), central subfield thickness (CST), and ellipsoid zone (EZ) integrity in macular edema (ME) pati

223 Measurement of the ellipsoid zone (EZ) line width and hyperautofluorescent

224 quantifying the progressive decrease of the ellipsoid zone (EZ) line width on spectral domain optica

225 toperative OCT images were analyzed using an ellipsoid zone (EZ) mapping platform to evaluate and qua

226 eserved autofluorescence (PAF) and preserved ellipsoid zone (EZ) on FAF and OCT images, respectively.

227 To determine a reliable method of using the ellipsoid zone (EZ) on optical coherence tomography (OCT

228 tion of external limiting membrane (ELM) and ellipsoid zone (EZ) were determined within the 1-mm cent

229 Ellipsoid zone (EZ) width (EZW) and outer nuclear layer

230 d visual acuity (BCVA), macular sensitivity, ellipsoid zone (EZ) width, and aqueous NAC were measured

231 e tomography (SDOCT) was used to measure the ellipsoid zone (EZ) width, which has been demonstrated t

232 nization of retinal inner layers (DRIL), and ellipsoid zone (EZ) within the central subfield (CSF).

233 ckness and presence of inner retinal layers, ellipsoid zone (EZ), and cystoid macular changes (CMCs).

234 ruption of external limiting membrane (ELM), ellipsoid zone (EZ), and interdigitation zone (IZ).

235 of change in the width of the inner segment ellipsoid zone (EZ; ie, inner/outer segment border) in t

236 thinning (approximately 7 mum/y) and loss of ellipsoid zone (in the range of 100 mum/y) in severe cas

237 ved (92.6% [5.8%]) vs absent (75.9% [12.6%]) ellipsoid zone (mean difference, 16.7%; 95% CI, 12.1% to

238 Intact ellipsoid zone (P = .0001) and external limiting membran

239 AF island size (P < .0001), length of foveal ellipsoid zone (P = .03), foveal thickness (P = .04), an

240 , exudation (P<0.001), and disruption of the ellipsoid zone (P<0.001) were associated with poorer BCV

241 Focal disruptions to the ellipsoid zone and external limiting membrane overlying

242 ffected eyes included discontinuation of the ellipsoid zone and hyperreflectivity underlying the reti

243 ated subretinal scar in 3 (19%), and loss of ellipsoid zone and outer nuclear layer in 3 (19%).

244 disease who had a focal preservation of the ellipsoid zone and outer nuclear layer in the fovea.

245 f RORA could be found, starting with loss of ellipsoid zone and subretinal deposits, followed by loss

246 as a fuzzy hyperreflective area between the ellipsoid zone and the interdigitation zone in the centr

247 eyes showed disruption of the photoreceptor ellipsoid zone and the interdigitation zone on SD-OCT, F

248 plexiform layer and the inner border of the ellipsoid zone and topographically corrected according t

249 The ellipsoid zone appeared intact in 13 eyes (81.2%).

250 ase duration (P < .001, 95% CI 5.4-9.1), and ellipsoid zone area declined exponentially at a rate of

251 pithelium (RPE) were the loss of the POS and ellipsoid zone associated with rod dysfunction.

252 Defects in the overlying ellipsoid zone band as seen by SD-OCT were associated wi

253 Mean time to resolution of ellipsoid zone changes was within 38 days.

254 Transient ellipsoid zone changes were noted in 26% of treated eyes

255 Mean ellipsoid zone defect (mum) reduced from 136 +/- 164 at

256 rtical size, external limiting membrane, and ellipsoid zone defect.

257 , RPE, or choroid were assessed and included ellipsoid zone discontinuity, outer nuclear layer (ONL)

258 Noted clinical and imaging features include ellipsoid zone disruption (100%), white fundus lesions (

259 orm layer involvement (5% vs 96%, P < .001), ellipsoid zone disruption (83% vs 3%, P < .001), RPE dis

260 s detachment was diagnosed by ultrasound and ellipsoid zone disruption (EZD) was determined by OCT, w

261 odegeneration as measured in the area of the ellipsoid zone disruption (or photoreceptor loss) measur

262 ariate analysis extent of DRIL (P = .03) and ellipsoid zone disruption (P < .001) correlated with bas

263 regression model with adjustment for CRT and ellipsoid zone disruption (P < 0.001).

264 d components of outer retinal atrophy (e.g., ellipsoid zone disruption), components of complete retin

265 kness, the occurrence of intraretinal cysts, ellipsoid zone disruption, and disorganization of retina

266 Length of ellipsoid zone disruption, external limiting membrane di

267 Six patients (67%) had foveal ellipsoid zone disruption, of which 1 had a hyporeflecti

268 al involvement, intraretinal cystoid spaces, ellipsoid zone disruption, RPE disruption, and choroidal

269 A few cases showed a suggestion of ellipsoid zone improvement.

270 D OCT images identified abnormalities of the ellipsoid zone in the central 7 degrees, while mfERG res

271 Ellipsoid zone integrity metrics significantly improved

272 zed pigmentary changes and on OCT imaging an ellipsoid zone interruption or outer nuclear layer chang

273 en age and both rate of constriction for the ellipsoid zone length and hyperautofluorescent outer ret

274 ections, thickness (from cube diagrams), and ellipsoid zone length.

275 The mean annual progression rates of ellipsoid zone line and hyperautofluorescent ring horizo

276 The length of the ellipsoid zone line was similar to the horizontal diamet

277 The ellipsoid zone line width and hyperautofluorescent ring

278 al diameter and vertical diameter along with ellipsoid zone line width from spectral-domain optical c

279 he intensity of inner segment/outer segment (ellipsoid zone line) reflectivity was reduced significan

280 ructurally by the en face OCT imaging of the ellipsoid zone loss appeared unchanged from baseline.

281 A hyporeflective gap in the photoreceptor ellipsoid zone on either side of this core shown in spec

282 al layers can occur with reappearance of the ellipsoid zone on OCT.

283 for the perifoveal loss of the photoreceptor ellipsoid zone on SD-OCT for affected and unaffected par

284 isis was detected in 5 eyes (31%), decreased ellipsoid zone reflectivity in 4 (25%), foveal retinal d

285 ss in moderate cases, but the breadth of the ellipsoid zone remained constant in both early and moder

286 36 eyes (92%) achieved U-shaped closure, and ellipsoid zone restoration was noted in 24 eyes (62%).

287 +/- 0.04), while Group 2 eyes showed broader ellipsoid zone than NIR-AF (R(2) = 0.60, slope 0.19 +/-

288 on of the external limiting membrane and the ellipsoid zone was associated with a decreased BCVA (P <

289 interdigitation zone was observed, while the ellipsoid zone was preserved.

290 Disruption of the ellipsoid zone was significantly correlated with VA in u

291 ter retinal layers (interdigitation zone and ellipsoid zone) terminated at a variable distance before

292 in AOSLO (punctate) and in SD OCT (prominent ellipsoid zone) was observed after regression of some SD

293 hypoautofluorescent on FAF and loss of RPE, ellipsoid zone, and external limiting membrane on SD OCT

294 oherence tomography of the disruption in the ellipsoid zone, and microperimetry when compared with ba

295 oss or disruption of the photoreceptor zone, ellipsoid zone, and retinal pigment epithelium (RPE, P <

296 s (8 eyes), including discontinuities of the ellipsoid zone, thinning of the central retina with incr

297 od-like extensions from islands of preserved ellipsoid zone.

298 dematous radial folds, and disruption of the ellipsoid zone.

299 tral macular thickness, and integrity of the ellipsoid zone.

300 had loss of retinal pigmented epithelium and ellipsoids zones, with or without subretinal material su