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 devoid of hemoglobin, so-called erythrocyte ghosts.

4 d dextrans from the interior of resealed RBC ghosts.

5 human erythroid precursor cells and red cell ghosts.

6 DA) was studied in bovine chromaffin granule ghosts.

7 including acellular capillaries and pericyte ghosts.

8 olecules associated with pigments in melanin ghosts.

9 lative to that observed using nonperoxidized ghosts.

10 ipain-2-induced fragmentation of erythrocyte ghosts.

11 ng of cytochalasin B to GLUT1 in erythrocyte ghosts.

12 ungal cells and are therefore called melanin ghosts.

13 study rhodamine phalloidin-labeled red cell ghosts.

14 rly inhibited the increased uptake in heated ghosts.

15 uptake in swollen ghosts but not in shrunken ghosts.

16 es but do assemble empty peroxisome membrane ghosts.

17 fusion of the Sendai virus with erythrocyte ghosts.

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

19 ere modified in tests with isolated membrane ghosts.

20 iterated acellular capillaries, and pericyte ghosts.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

36 reen (ICG) dye is sequestered in erythrocyte ghosts and autologously re-injected to allow direct visu

37 ed from hemoglobin-depleted mice erythrocyte-ghosts and doped with Indocyanine Green (ICG).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

69 demonstrate evidence of honorary authors or ghost authors.

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

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

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

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

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

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

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

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

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

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

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

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

82 chimeric Env proteins were cocultivated with Ghost CCR5 cells.

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

84 Furthermore, GHOST cell infection assays and blocking experiments wit

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

102 ary widely in size and eventually generating ghost cells.

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

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

105 1 induced "outre" giant cells and hypoploid "ghost" cells.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

131 wing for spreading of progenitors throughout ghost fibers.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

153 involved in the formation of a pseudothermal ghost image.

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

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

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

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

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

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

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

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

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

163 relations in Gaussian light sources used for ghost imaging.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

181 A ghost lineage analysis indicates that available felid fo

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

183 assignment to Pi. mertii partially fills the ghost lineage between younger ornithischian records and

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

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

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

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

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

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

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

191 Ghost maculopathy is the phenomenon of an imaging artifa

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

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

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

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

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

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

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

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

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

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

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

203 uorescent chelators across human erythrocyte ghost membranes was investigated.

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

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

206 is machinery with other domains of life, our ghost model will be an important tool for the exploratio

207 rom an early divergent and currently extinct ghost modern human lineage.

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

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

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

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

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

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

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

215 We further revealed that the ghost of land use past plays an important role in modera

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

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

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

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

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

221 r a novel societal tipping point which is a 'ghost' of a nearby saddle-node bifurcation from dynamica

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

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

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

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

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

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

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

229 Here we present the first description of ghost orchid pollination, and describe novel remote came

230 Florida's endangered ghost orchid, Dendrophylax lindenii, has long been confi

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

232 s resulted from more recent admixture with a ghost population that lacked a Neanderthal ancestry comp

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

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

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

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

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

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

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

240 The ghost reflections reveal that polymerase tubes are forme

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

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 s of isolated melanized cell walls (melanin "ghosts") revealed that the pigments are strongly associa

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

248 escent erythrocytes, the remnant erythrocyte ghost shells were prone to recognition and breakdown by

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

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

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

252 or agonistic intraspecific competition (e.g. ghost shrimp, Caprella spp.; sea anemones, Actinia equin

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

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

255 In this paper, a ghost structure (GS) method is proposed to simulate the

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

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

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

259 Here, we present a membrane-permeabilized ghost system that enables the manipulation of intracellu

260 aminated with the elongation, streaking, and ghost tail artifacts.

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

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

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

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

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

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

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

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

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

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

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

272 These so-called "ghost tracks" comprise a rich archive of biomechanical a

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

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

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

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

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

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

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

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

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

282 en vessels with intact endothelial cells and ghost vessels.

283 f the previously engorged draining veins and ghost vessels.

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

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

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

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

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

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

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

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

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

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

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

295 en melanized and nonmelanized cells, melanin ghosts were relatively enriched in SEs and PPs.

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

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

298 nsistently, actomyosin rings in myo2-S1 cell ghosts were unstable and severely compromised in contrac

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

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