ライフサイエンスコーパス: ghost

1 e cells, resulting in hollow spheres called "ghosts".

2 a-crystallin was incorporated into red cell 'ghosts'.

3 d dextrans from the interior of resealed RBC ghosts.

4 human erythroid precursor cells and red cell ghosts.

5 DA) was studied in bovine chromaffin granule ghosts.

6 including acellular capillaries and pericyte ghosts.

7 lative to that observed using nonperoxidized ghosts.

8 ipain-2-induced fragmentation of erythrocyte ghosts.

9 ng of cytochalasin B to GLUT1 in erythrocyte ghosts.

10 ungal cells and are therefore called melanin ghosts.

11 study rhodamine phalloidin-labeled red cell ghosts.

12 rly inhibited the increased uptake in heated ghosts.

13 uptake in swollen ghosts but not in shrunken ghosts.

14 es but do assemble empty peroxisome membrane ghosts.

15 fusion of the Sendai virus with erythrocyte ghosts.

16 ort of long-chain natural FA across red cell ghosts.

17 ere modified in tests with isolated membrane ghosts.

18 to the outer aqueous compartment of red cell ghosts.

19 ta plaques containing numerous neuronal cell ghosts.

20 lizing enzymes present in turkey erythrocyte ghosts.

21 iterated acellular capillaries, and pericyte ghosts.

22 orporated into resealed human red blood cell ghosts, (2,3)-trinitrophenyl-adenosine-triphosphate (TNP

23 so induced calcium fluxes in Bob-transfected Ghost (3) cells, whereas gp120 strains not activating HT

24 n in the CCR-5, CXCR-4, and CD4 coexpressing GHOST(3) cells was consistent with the inhibition of Tat

25 using GFP expressing human osteosarcoma T4 [GHOST(3)] cell lines expressing CD4 and CCR5 or CXCR4 co

26 se this effect can be mimicked with "melanin ghosts"; a mutant lacking melanin showed reduced platele

27 We introduce GHOST, a global pairwise network aligner that uses a nov

28 d, in saccular capillary aneurysms, pericyte ghosts, acellular capillaries, retinal hemorrhages, and

29 In turkey erythrocyte ghosts, agonist-stimulated PIP2 hydrolysis is initially

30 sealing of the loop peptide into erythrocyte ghosts alters membrane morphology and stability.

31 lated microvascular cell apoptosis; pericyte ghost and acellular capillary development was inhibited

32 oscopy demonstrated intense labelling of non-ghost and ghost tangles with PBB3 and AV-1451, while dys

33 a bead attached to a permeabilized spherical ghost and the force-extension relation was obtained from

34 Analysis of coreceptor utilization using GHOST and U87 cell lines revealed that all of the isolat

35 he SIVagm, and four of the SIVsm isolates in GHOST and U87 cells.

36 oximately 55-65%) formation of both pericyte ghosts and acellular capillaries in diabetic rats and ga

37 At 18 months duration, pericyte ghosts and acellular capillaries were quantitated in the

38 tin incorporation into filaments in resealed ghosts and fluorescence recovery after photobleaching (F

39 tion of sugar transport in resealed red cell ghosts and in GluT1 proteoliposomes.

40 Experiments with resealed ghosts and inside-out vesicles revealed that negatively

41 we determined catalytic activity in membrane ghosts and intact cells.

42 was similar to that of AE1 in red blood cell ghosts and kidney homogenate and therefore probably repr

43 ized by the presence of peroxisomal membrane ghosts and mislocalization of peroxisomal matrix protein

44 Phosphorylation of erythrocyte ghosts and purified PMCA by pp60(src) also resulted in u

45 B cells were enriched with D(+) erythrocyte ghosts and sorted as single cells.

46 on to produce isotopically enriched pigment "ghosts" and applied 2D (13)C-(13)C correlation solid-sta

47 Specifically, protein carryover ("ghosting") and recovery were examined.

48 hanged the morphology of insoluble remnants (ghosts) and decreased the degree of syneresis.

49 srupted the integrity of insoluble remnants (ghosts) and increased the degree of syneresis of the gel

50 scular cell apoptosis, formation of pericyte ghosts, and acellular capillaries were measured.

51 ion, the release of calcein from erythrocyte ghosts, and hemolysis of erythrocytes was much slower wh

52 numbers in the ganglion cell layer, pericyte ghosts, and numbers of degenerate capillaries, as well a

53 e had greater atrophic capillaries, pericyte ghosts, and permeability than controls.

54 BALB/c mice were immunized with melanin ghosts, and two immunoglobulin M MAbs to melanin were ge

55 on electron microscopy revealed that melanin ghosts are covered with roughly spherical granular parti

56 n, the kinetic constants of CAIX in membrane ghosts are very similar to our previous measurements for

57 of periods of time during scanning when the ghost arm was present against when it was not revealed a

58 movement, CSF pulsation/blood flow create a ghost artifact which can be reduced by patient immobiliz

59 Acquisition times were lower and N/2 ghosting artifacts were eliminated with SPACE.

60 ip angle evolutions (SPACE) sequence reduces ghosting artifacts while maintaining image quality and s

61 ost likely because of the elimination of N/2 ghosting artifacts.

62 images for each of the following parameters: ghosting artifacts; clarity of the mediastinum, cardiac

63 ants are generally about 2-3 fold larger for ghosts as compared to the lipid vesicles.

64 H, SMOOH) using photoperoxidized erythrocyte ghosts as model donors and freshly prepared LDL as an ac

65 In red blood cells (ghosts), ATP is sequestered within the cytoskeletal-memb

66 of honorary authors, 32 (9%) had evidence of ghost authors (most commonly a member of the Cochrane ed

67 journals); 93 articles (11%) had evidence of ghost authors (range, 7%-16% among journals); and 13 art

68 in large-circulation journals, articles with ghost authors in smaller-circulation journals were more

69 to report on the prevalence of honorary and ghost authors, contributions by authors listed in the by

70 and 9 (2%) had evidence of both honorary and ghost authors.

71 demonstrate evidence of honorary authors or ghost authors.

72 To determine the prevalence of honorary and ghost authorship in Cochrane reviews, how authorship is

73 tion of reviews had evidence of honorary and ghost authorship.

74 hod of choice for plasmid preparation, but ''ghost bands" of denatured supercoiled DNA can result if

75 hymocytes and lipid symmetric red blood cell ghosts bound beta2GPI.

76 wild-type human PFN1 increases the number of ghost boutons, active zone density, F-actin content, and

77 ting markedly increased K+ uptake in swollen ghosts but not in shrunken ghosts.

78 cells do not rupture immediately and exhibit ghosting, but slowly obtain a round shape before they bu

79 number of type 2 diabetes-enhanced pericyte ghosts by 62% (P < 0.05).

80 In the presence of cytosol, these membrane ghosts can move towards the minus-ends of microtubules.

81 Some cells entrapped in these ghost cartilages escape apoptosis, maintain DNA synthesi

82 egradation, resulting in the persistence of "ghost" cartilages with adverse effects on skeletal integ

83 Their round spermatids bear "ghost" CBs, whose architecture is greatly disrupted.

84 ich express the Gpr15 coreceptor for SIV, or Ghost CCR5 cells, which express CCR5, an alternate corec

85 chimeric Env proteins were cocultivated with Ghost CCR5 cells.

86 isolates was determined in three assays: the GHOST cell assay, a phytohemagglutinin-stimulated periph

87 Furthermore, GHOST cell infection assays and blocking experiments wit

88 In GHOST cell infection assays, all three ACH142 R5 HIV-1 c

89 Novel systems using Tat protein and the GHOST cell line were developed to test and quantitate th

90 e tested for single-cycle infectivity in the GHOST cell line.

91 Screening a panel of Ghost cell lines expressing diverse human chemokine rece

92 rom several clades could grow in the various GHOST cell lines, and their use of one or more corecepto

93 e form of ductal hyperplasia with 'squamoid' ghost cell nodules in young animals.

94 bstitution results in loss of GhoT toxicity, ghost cell production and membrane damage while retainin

95 with a comparable low level of p-eEF2 was a "ghost" cell.

96 e indocyanine green (ICG) dye in erythrocyte ghost cells at a concentration that produced maximum cel

97 CXCR4 expression was upregulated in Ghost cells coexpressing CXCR4 and CCR5 or CXCR4, CCR5,

98 d infect GHOST cells expressing CCR5 but not GHOST cells expressing any of nine other HIV coreceptors

99 ll three ACH142 R5 HIV-1 clones could infect GHOST cells expressing CCR5 but not GHOST cells expressi

100 The resulting ghost cells retain Na/K-ATPase activity.

101 ly higher number of CCR5- and CD4-expressing GHOST cells than the weaker chimeras.

102 system for B. bacteriovorus composed of prey ghost cells that are recognized and invaded by the preda

103 We used GHOST cells to map the coreceptor specificity and relati

104 panel of genetically engineered cell lines (GHOST cells) that express CD4, one of eight chemokine re

105 s ultimately survive, whereas others become "ghost" cells (no detectable Nissl substance) at 12-24 ho

106 At 12 hours, all "ghost" cells exhibited little or no p-eEF2 staining, alt

107 1 induced "outre" giant cells and hypoploid "ghost" cells.

108 In contrast, trypsin sealed inside red cell ghosts cleaves at K743, as does trypsin treatment of ins

109 each respective nutrient allow the growth of ghost colonies or microcolonies that give rise to full-s

110 eurysms, acellular capillaries, and pericyte ghosts compared with diabetic controls.

111 opment of acellular capillaries and pericyte ghosts compared with littermate control animals.

112 to 5 s-1, while the rate of binding, for the ghost concentrations used in this study (>50 microM phos

113 and aliphatic chains present in the melanin ghosts, consistent with metabolic use as a cellular nutr

114 The resultant bacterial ghosts contain cytoplasmic membrane within bacteria-shap

115 ic resonance cryoporometry indicated melanin ghosts contain pores with diameters between 1 and 4 nm,

116 MI, each of the parasites, IE cytosol and IE ghost contained 60-80-kDa PfP2 complexes, which resolved

117 brane fraction, which consisted of membrane "ghosts," contained most (50-60%) of marker enzyme activi

118 d by measuring sugar uptake into erythrocyte ghosts containing or lacking ATP and glycolytic intermed

119 es were consistent with those obtained using ghosts containing pyranine to detect intracellular acidi

120 mation of acellular capillaries and pericyte ghosts-continued to increase through the 18 months exami

121 more efficiently than did bees observing a "ghost" demonstration (ball moved via magnet) or without

122 nical stability of the membranes of resealed ghosts devoid of TM is grossly, but reversibly, impaired

123 Thus, preparations of membrane ghosts dimerized 57 +/- 6 nmol of ferriprotoporphyrin IX

124 actions of a social model than a non-social "ghost display", however the mechanism underlying this ef

125 cells, and into resealed chromaffin granule ghosts efficiently through passive diffusion.

126 lantation and cross-innervation in the brown ghost electric fish.

127 wed multiple cellular elements with nucleic "ghosts" embedded in a putative lipid matrix.

128 ned as a beta-pyranose moiety in the melanin ghosts even after exhaustive degradative and dialysis tr

129 rimarily bi-directionally oriented along the ghost fiber longitudinal axis, allowing for spreading of

130 We conclude that ghost fibers are autonomous, architectural units necessa

131 Re-orienting ghost fibers impacted myogenic progenitors' migratory pa

132 These changes were not present in ghost fibers which myosin had been removed, excluding di

133 mnants from injured skeletal muscle fibers, "ghost fibers," govern muscle stem/progenitor cell behavi

134 wing for spreading of progenitors throughout ghost fibers.

135 of actomyosin cycle in reconstituted single ghost fibres were investigated by polarized fluorescence

136 lose relative, Mohavea confertiflora (desert ghost flower), which differs from Antirrhinum in corolla

137 Kinetics for reverse transfer from LDL to ghosts followed the same trend, but rates were significa

138 or reduced type 1 diabetes-enhanced pericyte ghost formation by 87% and the number of type 2 diabetes

139 long with purified nuclear, cytoplasmic, and ghost fractions within a 3-h period of time without the

140 of STD can readily solve the problem of the ghost frequency, the perceived pitch of a harmonic compl

141 d unable to promote dimerization in membrane ghosts from erythrocytes of untreated, infected mice.

142 Lens fiber cell ghosts from mutant and wild-type mice were examined in t

143 membrane skeleton in sheared red blood cell ghosts from normal and diseased mice.

144 nto acetone or by aging erythrocyte membrane ghosts from untreated or chloroquine-treated, infected m

145 nked polygenes can give rise to an apparent "ghost" gene, mapped to an incorrect interval.

146 d were overlaid with either CEMx174 cells or Ghost Gpr15 cells, which express the Gpr15 coreceptor fo

147 to inhibit the fusion with CEMx174 cells or Ghost Gpr15 cells.

148 contents, and instead the persistent empty 'ghost-granule' may act as a conduit to which secondary g

149 loped and integrated into a life cycle model-GHOST (GreenHouse gas emissions of current Oil Sands Tec

150 after 24 months, the time at which pericyte ghosts had previously been observed to develop, and from

151 s, imaging of micropipette-deformed red cell ghosts has allowed an assessment of actin orientations a

152 As previous studies in the erythrocyte ghost have shown that polyamines can alter flip-flop of

153 nti-p45 IgG detected p45 in crude hepatocyte ghost homogenates and blocked vigorously 125I-Lf binding

154 ur approach to sponges, we discover distinct ghost Hox and ParaHox loci.

155 We call this second locus a "ghost" Hox locus, because it is homologous to the human

156 this phenomenon of "ghost maculopathy." The ghost image was present consistently on near-infrared re

157 This spot was termed the "ghost image" in this phenomenon of "ghost maculopathy."

158 involved in the formation of a pseudothermal ghost image.

159 spatial light modulator ghost imaging, i.e., ghost-image formation based on structured illumination r

160 sulting in reduced 3-month CDVA (12 eyes) or ghost images (6 eyes).

161 was successful in 13 eyes, whereas 1 eye had ghost images and was re-treated with topography-guided p

162 ed optical aberrations such as shadowing and ghost images in 22 tumors (59%), which encroached on the

163 Transient or persistent monocular ghost images or diplopia occurred in 10 of 178 eyes (5.6

164 nd appear relevant for the implementation of ghost imaging in the regime of low illumination.

165 photon-coincidence measurements employed in ghost imaging with a parametric downconverter source.

166 hniques, such as interaction-free imaging or ghost imaging, because now the photons used to illuminat

167 ord plays no role in spatial light modulator ghost imaging, i.e., ghost-image formation based on stru

168 ge object transparencies in a manner akin to ghost imaging.

169 ee to which quantum discord is necessary for ghost imaging.

170 relations in Gaussian light sources used for ghost imaging.

171 We show that a ghost-imaging configuration, where the image is obtained

172 atic moieties of solid C. neoformans melanin ghosts include cell-wall components derived from polysac

173 n on intact cells, resealed ghosts, unsealed ghosts, inside-out vesicles, and microsomes from HEK293

174 he red blood cell homologue of 4.1 (4.1R) in ghosts, inside-out vesicles, and Triton shell preparatio

175 age of DA from the channeling pathway to the ghost interior.

176 r to the release into the bulk medium of the ghost interior.

177 d with other recent approaches, we find that GHOST is able to recover larger and more biologically si

178 We show that the spectral signature used by GHOST is highly discriminative, whereas the alignments i

179 K+-Cl- cotransport in human red cell ghosts is inhibited by divalent inorganic cations, solub

180 therefore, that FA transport across red cell ghosts is reasonably well described by transport across

181 During spawning, male and female brown ghost knife fish modulate their electric organ discharge

182 ke activity in P-type afferents of the brown ghost knifefish, Apteronotus leptorhynchus.

183 The brain of the brown ghost knifefish, which uses electric fields to "see", pr

184 ho sporadically experiences a supernumerary 'ghost' left arm that occupies the previous position of t

185 r endothelial cells degenerated, providing a ghost-like record of pretreatment vessel number and loca

186 A ghost lineage analysis indicates that available felid fo

187 Combining principles of ghost lineage analysis with molecular divergence dates,

188 dira (pterosaurs and birds) and shortens the ghost lineage inferred at the base of Avemetatarsalia.

189 sly unrecognized approximately 30 to 45 Myr "ghost lineage" for these Gondwanan eutherians.

190 onkeys) and Hominoidea (apes), implying long ghost lineages for both clades.

191 Several ancient bee clades are identified as ghost lineages that have left little fossil evidence of

192 mphimedon is a result of secondary loss (the ghost locus hypothesis).

193 e the origin of sponges, thus confirming the ghost locus hypothesis, and highlight the need to analys

194 ed into the centers of washed-white red cell ghosts lying on a coverglass, the height of the microsph

195 Ghost maculopathy is the phenomenon of an imaging artifa

196 All eyes with ghost maculopathy were found to be pseudophakic with a p

197 lar hyper-reflective spot resembling that in ghost maculopathy, but corresponding SD OCT images were

198 med the "ghost image" in this phenomenon of "ghost maculopathy." The ghost image was present consiste

199 dimple regions of red blood cells and their ghosts may be responsible for their biconcave shape.

200 re by cell swelling should yield erythrocyte ghosts; membrane fusion is inhibited by inner-leaflet am

201 H(2) for the spherical saponin-permeabilized ghost membranes (where B is the bending modulus and H th

202 gomeric state, the anisotropy of erythrocyte ghost membranes at 37 degrees C is consistent with dimer

203 Ghost membranes in which approximately 4% of the Ch had

204 hus, long-chain FA transport across red cell ghost membranes is rate-limited by a combination of flip

205 -soluble and -insoluble pools in erythrocyte ghost membranes or when expressed in cultured COS cells

206 Mildly peroxidized ghost membranes transferred overall ChOOH and PLOOH to L

207 uorescent chelators across human erythrocyte ghost membranes was investigated.

208 Binding of FA to ghost membranes was well described by simple, nonsaturab

209 Treatment of ghost membranes with either Zn2+ or melittin, agents tha

210 nd, importantly, mature human red blood cell ghost membranes, both expressed the SK4 protein.

211 Using red cell ghost membranes, energy transfer distances were measured

212 lity of NP41 to highlight degenerated nerve "ghosts" months posttransection that are invisible to the

213 pression library from the silk glands of the ghost moth, Hepialus californicus, and characterized lig

214 equilibrium state in the presence of latent "ghost" multistable attractors.

215 Phonological errors in naming (e.g. GHOST named as 'goath') are commonly seen in persisting

216 In the Clear and Ghost native gels of the entire mitochondrial proteome,

217 PiB positive; these resembled extracellular 'ghost' NFT.

218 hat include membrane blebbing, appearance of ghost nuclei, cell swelling, and lysis.

219 ected visual acuity, monocular diplopia, and ghosting of images.

220 Analysis of chitin ghosts of chs mutant strains by shadow-cast transmission

221 g, an immunoreactive channel was detected in ghosts of human red blood cells, consistent with the exp

222 As a consequence, this channel acts like a "ghost" of the limit cycle destroyed in the critical tran

223 Structures similar to the melanin "ghosts" of melanized cryptococcal cells were isolated fr

224 ickle hemoglobin, using preparations of open ghosts (OGs) with intact cytoskeletons from sickle (SS)

225 te-of-the-art methods (IsoRank, MI-GRAAL and GHOST), on both synthetic networks and real-world biolog

226 her tethered to actin directly within a cell ghost or connected to actin from outside a cell via glyc

227 Also, deletion of ghoST or ghoT results in significantly greater initial g

228 dogs after either the appearance of pericyte ghosts or formation of microaneurysms.

229 14)C]Ch-labeled donor membranes [erythrocyte ghosts or unilamellar DMPC/Ch (1.0:0.8 mol/mol) liposome

230 infusion of stored RBC-derived supernatant, ghosts, or stroma-free lysate, does not produce these ef

231 idoglycan degradation and rounded prey cell "ghosts" persist after mutant-predator exit.

232 Gene flow may have occurred via unsampled 'ghost' populations rather than directly between the popu

233 Release did not yield erythrocyte ghosts, positive-curvature amphiphiles did not inhibit r

234 of the Na pump from mature human erythrocyte ghosts, purified by ouabain column chromatography, has a

235 ive plaques and tangle-filled extraneuronal (ghost) pyramidal neurons that were D2 mRNA-negative.

236 in the human osteosarcoma-derived cell line GHOST.R5, and human cyclin T1 restored provirus expressi

237 this effect, DBR1 shRNA was introduced into GHOST-R5X4 cells, followed by infection at a multiplicit

238 cells, these peroxisomal membrane remnants (ghosts) rapidly incorporated peroxisomal matrix proteins

239 The ghost reflections reveal that polymerase tubes are forme

240 rientations within 3Dpol tubes give rise to "ghost reflections" in diffraction patterns computed from

241 efficient and parallelized implementation of GHOST, released under the Apache 2.0 license, is availab

242 sed osmotic water permeability compared with ghosts resealed with albumin.

243 Red blood cell ghosts resealed with CAII demonstrated increased osmotic

244 idized acceptor membranes (DMPC liposomes or ghosts, respectively) at 37 degrees C was monitored by t

245 sis of the morphology of chitin in cell wall ghosts revealed two distinct forms of chitin microfibril

246 made of human, sheep, and rabbit erythrocyte ghosts rich in 24:1 SM and CHO, showed no lateral domain

247 ivity studies with bovine chromaffin granule ghosts show that 3'-hydroxy-MPP(+) is one of the best kn

248 Data from membrane ghosts show that the increase in activity at reduced pH

249 mine uptake into purified chromaffin granule ghosts showed IC50 values of approximately 37 nM for res

250 ited swelling-activated K+ uptake in control ghosts, similarly inhibited the increased uptake in heat

251 "Ghost" species hidden by taxa of hybrid origin may be mo

252 ble LUVs); (ii) photoperoxidized erythrocyte ghosts/SUVs or vice versa; and (iii) SUVs/mitochondria.

253 ed by more than 20-fold, and they appear as "ghosts": swollen, elongated, and with reduced optical co

254 In a SUV/ghost system at 37 degrees C, the rate constant for tota

255 ted by neurofibrillary pathology to become a ghost tangle.

256 eurofibrillary tangles, neuropil threads and ghost tangles was rare and likewise its distribution dif

257 onstrated intense labelling of non-ghost and ghost tangles with PBB3 and AV-1451, while dystrophic ne

258 on and increased RD3 was noted in late-stage ghost tangles.

259 stains pre-tangles, NFTs and extracellular 'ghost' tangles due to the recognition of hyperphosphoryl

260 y silver method in order to reveal NFTs and 'ghost' tangles, ii) single-stained with anti-APP, and ii

261 tal vitamins C+E, and the number of pericyte ghosts tended to be reduced.

262 experimental measurements on red blood cell ghosts that have been made permeable by treatment with s

263 stals leaves behind a crystal-shaped matrix "ghost" that is capable of precipitation of Ca oxalate in

264 Heating red cells or ghosts to 49 C denatures spectrin.

265 This study uses erythrocyte ghosts to characterize the reversible cytoplasmic membra

266 he presence of exogenous PITP, after washing ghosts to remove PITP before activation of PLC, enhanced

267 Exposure of membrane ghosts to sonication or cold significantly increased the

268 e.g. fluidity) were manipulated by preparing ghosts under different experimental conditions such as i

269 ransmembrane domain inserted into DiO-125INA-ghosts under the same conditions as intact VSV G.

270 actions of trypsin on intact cells, resealed ghosts, unsealed ghosts, inside-out vesicles, and micros

271 nd also yielded particles similar to melanin ghosts upon digestion, providing additional evidence tha

272 mutant Bdellovibrio which leaves prey-shaped ghosts upon predation.

273 DR, specifically the appearance of pericyte ghosts, vascular leakage, and microaneurysm formation.

274 Vibrio cholerae ghosts (VCG) are nontoxic, effective delivery vehicles w

275 ss of endothelial cells and the formation of ghost vessels are observed, findings that correlate with

276 The number of ghost vessels was negatively correlated with vascular de

277 , number of CD45+ leukocytes, and number of "ghost vessels" were determined in a masked fashion and e

278 f the previously engorged draining veins and ghost vessels.

279 tosensitized labeling of VSV G by DiO-125INA-ghosts was also observed at pH 5.5, 4 degrees C, in the

280 , the C(i)-to-C(o) ratio was retained in RBC ghosts, was not dependent on ATP or external cations, an

281 of both powdered and solvent-swelled melanin ghosts, was used to provide new molecular-level insights

282 , number of vessels visualized, and arterial ghosting were significantly lower for the postcontrast 2

283 The spherical ghosts were centrifuged onto a coated coverslip upon whi

284 Triton X-100 extracts of hepatocyte membrane ghosts were chromatographed on Lf-agarose, a 45-kDa poly

285 Red cell ghosts were created by lysing the red cells and removing

286 To this end, red-blood-cell ghosts were made by hypotonic hemolysis and then reconst

287 y cells, acellular capillaries, and pericyte ghosts were measured in control diabetic rats versus non

288 enerate (acellular) capillaries and pericyte ghosts were measured in control diabetic rats versus tho

289 y flushing with an iso-osmotic solution, the ghosts were observed to be mainly oriented in a flat ali

290 n that, during centrifugation, the spherical ghosts were oriented by a dense band in its equatorial p

291 articles with striking similarity to melanin ghosts were recovered after digestion of lung and brain

292 increase in uptake was reversed when swollen ghosts were shrunk even though denaturation of spectrin

293 s across resealed H(+)- and Li(+)-loaded RBC ghosts were significantly lower when a pH gradient was p

294 Intact erythrocytes and ghosts were studied to determine whether the principles

295 lesions (acellular capillaries and pericyte ghosts) were not significantly (P > 0.05) present at 3 m

296 mbers of degenerate capillaries and pericyte ghosts, while preventing the decreased retinal thickness

297 orm either membrane blebs (cell-attached) or ghosts (whole cell).

298 tudy, we labeled lipid symmetric erythrocyte ghosts with 125INA and DiO.

299 Treatment of nb/nb ghosts with the nonionic detergent C12E8 (octaethylene g

300 itized activation of VSV prebound to labeled ghosts with visible light resulted in VSV G labeling und