ライフサイエンスコーパス: erythrocyte membrane

1 ce of a member of this family, EAAT3, on the erythrocyte membrane.

2 molecular-dynamics model for simulating the erythrocyte membrane.

3 te-derived STEVOR proteins from the infected erythrocyte membrane.

4 loring parasite-induced modifications of the erythrocyte membrane.

5 ponents of the import channel located on the erythrocyte membrane.

6 d in binding to full-length ankyrin-R in the erythrocyte membrane.

7 ms the core of a multiprotein complex in the erythrocyte membrane.

8 Ad5, leading to close juxtaposition with the erythrocyte membrane.

9 gnificant revision of accepted models of the erythrocyte membrane.

10 he general structural integrity of the human erythrocyte membrane.

11 eceptor for dematin and adducin in the human erythrocyte membrane.

12 , also called the junctional complex, in the erythrocyte membrane.

13 the distribution of phospholipids across the erythrocyte membrane.

14 tein-protein interactions that stabilize the erythrocyte membrane.

15 tein-protein interactions that stabilize the erythrocyte membrane.

16 to traffic newly synthesized proteins to the erythrocyte membrane.

17 ated analogue appear to readily traverse the erythrocyte membrane.

18 ding the unique mechanical properties of the erythrocyte membrane.

19 most abundant integral proteins in the human erythrocyte membrane.

20 erposed over the thermal fluctuations of the erythrocyte membrane.

21 omplement receptor type 1 (CR1, CD35) on the erythrocyte membrane.

22 e merozoite surface and also associated with erythrocyte membrane.

23 transient local membrane deformations in the erythrocyte membrane.

24 complexes on the inner surface of the human erythrocyte membrane.

25 ions and antimalarial compounds at the host erythrocyte membrane.

26 tructures within the surface of the infected erythrocyte membrane.

27 evor expression impacts deformability of the erythrocyte membrane.

28 oteomics identified PIEZO1 peptides in human erythrocyte membranes.

29 and membrane skeletal associations in human erythrocyte membranes.

30 enotype and measured the PUFA composition of erythrocyte membranes.

31 n organize into complexes on other mammalian erythrocyte membranes.

32 zyme complexes on the inner surface of human erythrocyte membranes.

33 gella's ability to promote pore formation in erythrocyte membranes.

34 erythrocyte glycoproteins (hEGP) from human erythrocyte membranes.

35 fluorescent phosphatidylcholine analog from erythrocyte membranes.

36 characterized in enzyme purified from human erythrocyte membranes.

37 ymorphisms might influence CR1 clustering on erythrocyte membranes.

38 ve the accumulation of free cholesterol from erythrocyte membranes.

39 ilitate phosphatidylcholine flip-flop across erythrocyte membranes.

40 al and architectural peculiarities of bovine erythrocyte membranes.

41 were cotranslated in the presence of rabbit erythrocyte membranes.

42 e and not to the parasitophorous vacuolar or erythrocyte membranes.

43 Stachylysin also formed pores in sheep erythrocyte membranes.

44 the stimulation of phospholipase C in turkey erythrocyte membranes.

45 ss) by sequential rupture of the vacuole and erythrocyte membranes.

46 at is so integral to its role in stabilizing erythrocyte membranes.

47 d under analogous conditions on intact human erythrocyte membranes.

48 oteins ZIP8 and ZIP10 were detected in human erythrocyte membranes.

49 ember of the large and diverse P. falciparum erythrocyte membrane 1 (PfEMP1) protein family.

50 terize adhesion across Plasmodium falciparum erythrocyte membrane 1 (PfEMP1) proteins in the 3D7 para

51 ar gene family encodes Plasmodium falciparum erythrocyte membrane 1 (PfEMP1) proteins that act as vir

52 -domain protein p55 and glycophorin C at the erythrocyte membrane, a similar complex comprising CASK

53 for ameliorating some of the consequences of erythrocyte membrane abnormalities.

54 acity to stimulate phospholipase C in turkey erythrocyte membranes (agonist effect) and to inhibit it

55 PP kindreds identified numerous mutations in erythrocyte membrane alpha-spectrin (SPTA1).

56 s, stevor and Pfmc-2TM, also localize to the erythrocyte membrane, although it is not known if they u

57 several proteins that are inserted into the erythrocyte membrane, although none of these proteins ha

58 to a reduction in protein 4.2 content of the erythrocyte membrane and hemolytic anemia.

59 Here, we use primaquine to perturb the erythrocyte membrane and induce detergent-free buoyant v

60 es not appear to affect transport across the erythrocyte membrane and is, therefore, not involved in

61 constitute the two major tethers between the erythrocyte membrane and its spectrin skeleton.

62 vement of lipids other than PS and PE in the erythrocyte membrane and suggests that the flippase has

63 was determined by separation of parasite and erythrocyte membranes and determination of enzyme marker

64 ed BKV binding to and interaction with human erythrocyte membranes and determined that this interacti

65 ersibly oxidized GAPDH accumulated in stored erythrocyte membranes and supernatants through storage d

66 dence that PDI is present in human and mouse erythrocyte membranes and that selective blockade with m

67 chanism can explain the action of sPLA(2) on erythrocyte membranes and that temperature and calcium l

68 ng and skeletal binding protein of the human erythrocyte membrane) and have examined the impact of th

69 mport system, likely between the PVM and the erythrocyte membrane, and that this transportation proce

70 10-30 nN) are needed to penetrate the tensed erythrocyte membrane, and these forces increase exponent

71 migrated with the slower TM major species in erythrocyte membranes, and hTM5b comigrated with the fas

72 solated cdb3-PO4 (but not cdb3) to band 3 in erythrocyte membranes; and (v) phosphorylation-induced b

73 emoglobin at the early trophozoite stage and erythrocyte membrane ankyrin and protein 4.1 at the late

74 the MCs in the transport of proteins to the erythrocyte membrane are summarized.

75 of 45-kDa has been isolated from the porcine erythrocyte membrane as a major protein antigen recogniz

76 at have provided insights into properties of erythrocyte membranes as well as parasite mechanisms tha

77 IA by polyunsaturated fatty acid content of erythrocyte membranes (as a percentage of total lipids)

78 Band 3, the major protein of the human erythrocyte membrane, associates with multiple metabolic

79 h sickle cell disease (SCD) manifest loss of erythrocyte membrane asymmetry with PS exposure, we have

80 The cytoplasmic domain of erythrocyte membrane band 3 (cdb3) serves as a center of

81 The cytoplasmic domain of erythrocyte membrane band 3 (cdb3) serves as a center of

82 ic constitutive model of the red blood cell (erythrocyte) membrane based on recently improved charact

83 Rh5 and Ripr are positioned parallel to the erythrocyte membrane before membrane insertion.

84 parum parasites and structurally investigate erythrocyte membranes, both during and after P. falcipar

85 DCytb was also found in guinea pig erythrocyte membranes but not in erythrocyte membranes f

86 roteins may associate not only in the mature erythrocyte membrane, but also during their posttranslat

87 o hydrolyze lipids in fluid regions of human erythrocyte membranes, but primarily when those regions

88 ormation of domains of ordered lipids within erythrocyte membranes by interacting directly with the i

89 (unlike stomatin) is fully extractable from erythrocyte membranes by NaOH, pH 11.

90 TM in elevating the mechanical stability of erythrocyte membranes by stabilizing the spectrin-actin-

91 We demonstrate erythrocyte membrane cholesterol levels modulate the pre

92 We reported an erythrocyte membrane-coated nanogel (RBC-nanogel) system

93 Using erythrocyte membrane-coated nanoparticles and staphyloco

94 zeta potential, and protein contents of the erythrocyte membrane-coated nanoparticles were verified

95 Here we show that human erythrocyte membranes contain a cytochrome b(561) (Cyt b

96 Absorption spectroscopy showed that human erythrocyte membranes contain an Asc-reducible b-type Cy

97 Erythrocyte membranes contain up to 27% sphingomyelin.

98 at the mechanism of the interaction with the erythrocyte membrane could be different for the two prot

99 Plasmodium falciparum ends with the ruptured erythrocyte membrane curling outwards, buckling, evertin

100 the 4.1G and 4.1N proteins, homologs of the erythrocyte membrane cytoskeletal protein 4.1.

101 investigate the effect of the storage on the erythrocyte membrane deformability and morphology.

102 Current models of the erythrocyte membrane depict three populations of band 3:

103 challenged since there is recent evidence of erythrocyte membrane-derived cholesterol in plaques.

104 The amount of erythrocyte membrane-derived cholesterol is also suggest

105 These results reveal a novel mechanism of erythrocyte membrane destabilization that could contribu

106 At 8 wk, erythrocyte membrane DHA composition increased significa

107 Erythrocyte membranes dose-dependently enhanced calcific

108 shment of proper mechanical integrity of the erythrocyte membrane during erythropoiesis.

109 bound to nor translocated through the intact erythrocyte membrane during parasite development, but fl

110 ved in parasite-induced modifications of the erythrocyte membrane during parasite development.

111 metocytes undergo remarkable shifts in their erythrocyte membrane elasticity, which may allow them to

112 Lysed erythrocyte membranes enhanced calcification to a simila

113 The significance of erythrocyte membrane fatty acids (EMFAs) and their ratio

114 bic acid, 25-hydroxyvitamin D [25(OH)D], and erythrocyte membrane fatty acids following birth until I

115 eous self-assembly of haemoglobin-containing erythrocyte membrane fragments on the surface of preform

116 Previous studies suggest that erythrocyte membranes from intraplaque hemorrhage into t

117 guinea pig erythrocyte membranes but not in erythrocyte membranes from the mouse or rat.

118 ed by extracting it into acetone or by aging erythrocyte membrane ghosts from untreated or chloroquin

119 lylactosamine structures associated with the erythrocyte membrane glycoprotein, band 3 (detected by s

120 The activity induced by hypotonic stress in erythrocyte membranes had the pH dependence, ion depende

121 Proteins of the erythrocyte membrane have served as the prototypes of ho

122 bilayer distribution of phospholipids in the erythrocyte membrane have significant physiologic conseq

123 also alters the mechanical properties of the erythrocyte membrane in a concentration-dependent manner

124 of products from pir members to the infected erythrocyte membrane in the rodent malaria parasite P.ch

125 radable polymeric nanoparticles with natural erythrocyte membranes, including both membrane lipids an

126 N, H(2)V(V)O(4)(-) and the ligands cross the erythrocyte membrane independently, with dhp the uptake

127 the stimulation of phospholipase C in turkey erythrocyte membranes induced by 30 nM 2-MeS-ADP in the

128 alcification model, and in vivo after murine erythrocyte membrane injection into neointimal lesions o

129 ortant role for HNF1A in the preservation of erythrocyte membrane integrity, calcium homeostasis, and

130 The erythrocyte membrane is a composite structure consisting

131 The erythrocyte membrane is a newly appreciated platform for

132 1 clustering in knob-like protrusions on the erythrocyte membrane is critical for cytoadherence, howe

133 ly the compartmentalization of Hb within the erythrocyte membrane is disrupted.

134 tering of Complement Receptor 1 (CR1) in the erythrocyte membrane is important for immune-complex tra

135 As the presence of KAHRP at the erythrocyte membrane is necessary for cytoadherence in v

136 ology of the band 3 (AE1) polypeptide of the erythrocyte membrane is not fully established despite ex

137 oposed that the high level of cholesterol in erythrocyte membranes is a protective mechanism to guard

138 ith Kd = 14 nM; (iii) binding of cdb3-PO4 to erythrocyte membranes is inhibited both by antibodies ag

139 3 microm dinitrophenyl S-glutathione, across erythrocyte membranes is inhibited by multidrug resistan

140 nd that a limiting step in the hydrolysis of erythrocyte membranes is the ability of phospholipids to

141 Spectrin (Sp), a key component of the erythrocyte membrane, is routinely stretched to near its

142 efficient at introducing IpaB and IpaC into erythrocyte membranes, it is possible that IpaD is respo

143 ve giant unilamellar vesicles (GUVs) made of erythrocyte membrane lipids (erythro-GUVs) when exposed

144 n hematopoietic stem cells, reduced elevated erythrocyte membrane LysoPC content and circulating AA l

145 s impaired leading to significantly elevated erythrocyte membrane lysophosphatidylcholine (LysoPC) co

146 Lower concentrations of n-3 PUFAs or ALA in erythrocyte membranes may be good predictors for cogniti

147 We investigated the concept that erythrocyte membrane microparticles (MPs) concentrate ce

148 interact with microbial membrane models over erythrocyte membrane models, correlating well to previou

149 xamined the impact of these modifications on erythrocyte membrane morphology, deformability, and stab

150 In a nested case-control study, erythrocyte membrane n-3 content was higher in fish-oil

151 irect, quantitative measure of the impact of erythrocyte membranes on the homogeneous nucleation proc

152 We have measured the effect of erythrocyte membranes on the rate of homogeneous nucleat

153 ociations between n-3 PUFA concentrations in erythrocyte membrane or plasma and cognitive function in

154 ment-sensitive probe, laurdan, revealed that erythrocyte membrane order decreases systematically with

155 Here we define the reversible changes in erythrocyte membrane organization that underpin this bio

156 In sickle cell disease (SCD), loss of erythrocyte membrane phospholipid asymmetry occurs with

157 Through natural selection, some erythrocyte membrane polymorphisms are likely to have re

158 Erythrocyte membrane poration occurs in relaxed cells, t

159 throcytic merozoites and the inner aspect of erythrocyte membranes, preventing the rupture of infecte

160 the effects of seven other divalent ions on erythrocyte membrane properties.

161 cid product-to-precursor ratios derived from erythrocyte membrane proportions, and T2D risk.

162 These var genes encode P. falciparum erythrocyte membrane protein (PfEMP)1 variants with dist

163 Continual variation of the P. falciparum erythrocyte membrane protein (PfEMP1) antigens displayed

164 ated by members of the variant P. falciparum erythrocyte membrane protein 1 (PfEMP-1) family and resi

165 Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) antigens mediate

166 s report, we show that Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) binds ICAM-1.

167 the parasite adhesion receptor P. falciparum erythrocyte membrane protein 1 (PfEMP1) clusters.

168 egion 1 (CIDR1) domains of the P. falciparum erythrocyte membrane protein 1 (PfEMP1) developed antibo

169 ified isolates and recombinant P. falciparum erythrocyte membrane protein 1 (PfEMP1) domains to quant

170 is associated with the type of P. falciparum erythrocyte membrane protein 1 (PfEMP1) expressed on the

171 The Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) family is a high

172 ntal sequestration of IEs is a P. falciparum erythrocyte membrane protein 1 (PfEMP1) family member en

173 Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) family members m

174 ingle and unique member of the P. falciparum erythrocyte membrane protein 1 (PfEMP1) family named VAR

175 The Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) family of antige

176 BLs) and the large and diverse P. falciparum erythrocyte membrane protein 1 (PfEMP1) family of cytoad

177 related group A subset of the P. falciparum erythrocyte membrane protein 1 (PfEMP1) family of IE adh

178 The Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) family proteins

179 antigenically variant Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) family.

180 the variant surface Ag Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) is a key compone

181 Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) is an important

182 Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) is expressed on

183 Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) mediates parasit

184 Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) mediates the bin

185 gen 2-CSA (VAR2CSA), a Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) protein family m

186 larly IgG specific for Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) proteins on the

187 py gene family encodes Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) variant antigens

188 related with antibodies to the P. falciparum erythrocyte membrane protein 1 (PfEMP1) variant gene fam

189 rotein family in Plasmodium falciparum named erythrocyte membrane protein 1 (PfEMP1), encoded by var

190 Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1), expressed on P.

191 The exported virulence protein, P falciparum erythrocyte membrane protein 1 (PfEMP1), is responsible

192 The variant antigen Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1), present on the

193 P. falciparum erythrocyte membrane protein 1 (PfEMP1), the major eryth

194 st work to date has focused on P. falciparum Erythrocyte Membrane Protein 1 (PfEMP1), two other multi

195 antigens (VSAs), including the P. falciparum erythrocyte membrane protein 1 (PfEMP1).

196 throcytes, such as the Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1).

197 ily of variant proteins called P. falciparum erythrocyte membrane protein 1 (PfEMP1).

198 ession of the variant antigen, P. falciparum erythrocyte membrane protein 1 (PfEMP1).

199 cular endothelium, mediated by P. falciparum erythrocyte membrane protein 1 (PfEMP1).

200 surface protein family Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1).

201 hesion proteins of the Plasmodium falciparum-erythrocyte membrane protein 1 class on the infected ery

202 sera was observed, suggesting P. falciparum erythrocyte membrane protein 1 expression.

203 ns encoding individual Plasmodium falciparum-erythrocyte membrane protein 1 structural domains.

204 s analysis shows that specific P. falciparum erythrocyte membrane protein 1 types are linked to cereb

205 r virulence-associated group A P. falciparum erythrocyte membrane protein 1 variants and identifies t

206 um falciparum var gene/PfEMP1 (P. falciparum erythrocyte membrane protein 1) family that bind EPCR, i

207 its variant surface proteins (P. falciparum erythrocyte membrane protein 1) to evade the host immune

208 The var gene family encodes P. falciparum erythrocyte membrane protein 1, different versions of wh

209 dictive of protection included P. falciparum erythrocyte membrane protein 1, merozoite surface protei

210 Plasmodium falciparum erythrocyte membrane protein 3 (PfEMP3) is a parasite-de

211 We identified Erythrocyte membrane protein band 4.1-like 5 (Epb41l5) a

212 fy the first barrier element described in an erythrocyte membrane protein gene and indicate that exon

213 tion of the regulatory elements that control erythrocyte membrane protein gene expression have import

214 Erythrocyte membrane protein genes serve as excellent mo

215 g, and genomic organization in regulation of erythrocyte membrane protein genes, we performed chromat

216 f the membrane-spanning alpha-helix from the erythrocyte membrane protein glycophorin A (GPA).

217 contain both KAHRP and the parasite-derived erythrocyte membrane protein PfEMP1.

218 hese studies strongly suggest that extensive erythrocyte membrane protein phosphorylation and ubiquit

219 h include factor VIIa, Plasmodium falciparum erythrocyte membrane protein, and a specific variant of

220 ermined that domain III of AMA1 binds to the erythrocyte membrane protein, Kx, and that the rate of i

221 bellar ataxia-35; and loss of the structural erythrocyte membrane protein, protein 4.2, leads to here

222 arge and diverse protein family P falciparum erythrocyte membrane protein-1 (PfEMP-1) and involves di

223 omain of the large and diverse P. falciparum erythrocyte membrane protein-1 (PfEMP-1) family, when ex

224 es with the altered display of P. falciparum erythrocyte membrane protein-1 (PfEMP-1), the parasite's

225 ease depends on the variant of P. falciparum erythrocyte membrane protein-1 as well as its amount and

226 host polymorphism that affects P. falciparum erythrocyte membrane protein-1 display is hemoglobin C,

227 Steps by which P. falciparum erythrocyte membrane protein-1 is exported to the parasi

228 Clonal expression of a single P. falciparum erythrocyte membrane protein-1 variant on the surface of

229 riable surface antigens named "P. falciparum erythrocyte membrane protein-1" encoded by the var multi

230 cytoadherence ligand, PfEMP-1 (P. falciparum erythrocyte membrane protein-1), correlates with these f

231 Interference with P. falciparum erythrocyte membrane protein-1-mediated phenomena appear

232 Plasmodium falciparum erythrocyte membrane protein-1-mediated sequestration of

233 ncode variable adhesins termed P. falciparum erythrocyte membrane protein-1.

234 riant surface antigens such as P. falciparum erythrocyte membrane protein-1.

235 s avidly and reversibly to band 3, the major erythrocyte membrane protein.

236 hrocytes from mice lacking each of the major erythrocyte membrane proteins were examined for GE local

237 Important gene networks encoding erythrocyte membrane proteins, surface receptors, and he

238 standing of the regulation of genes encoding erythrocyte membrane proteins, we have identified and ch

239 y mutant human erythrocytes, missing various erythrocyte membrane proteins.

240 nsgenically engineered mice lacking specific erythrocyte membrane proteins.

241 .1-like calcium channel exists in the mature erythrocyte membrane, RBC membrane preparations were imm

242 ikely to be involved in functions related to erythrocyte membrane remodeling and enucleation.

243 onally efficient coarse-grained model of the erythrocyte membrane reveals that restructuring and cons

244 Erythrocyte membranes (RMs) were used to coat the BPQDs,

245 The erythrocyte membrane's ability to withstand the stresses

246 malaria parasites perforate their enclosing erythrocyte membrane shortly before egress.

247 ly related Cyts b(561), immunoblots of human erythrocyte membranes showed only the duodenal cytochrom

248 rocyte protein 4.1) defines the nodes of the erythrocyte membrane skeletal network and is inseparable

249 ctrin, F-actin, and protein 4.1R defines the erythrocyte membrane skeletal network, which governs the

250 this group, has been shown to interact with erythrocyte membrane skeletal protein spectrin.

251 Among the erythrocyte membrane skeletal proteins, ankyrin and prot

252 ecific target genes including those encoding erythrocyte membrane skeleton (EMS) proteins.

253 Spectrin is the major component of the erythrocyte membrane skeleton and exists as a 526 kDa al

254 -1) provides the primary linkage between the erythrocyte membrane skeleton and the plasma membrane.

255 The human erythrocyte membrane skeleton consists of hexagonal latt

256 The erythrocyte membrane skeleton is the best understood cyt

257 ange and provides an attachment site for the erythrocyte membrane skeleton on the cytoplasmic domain.

258 l lattice structure, resembling the expanded erythrocyte membrane skeleton structure, in the somatode

259 As key components of the erythrocyte membrane skeleton, spectrin and ankyrin spec

260 res of striated muscle myofibrils and in the erythrocyte membrane skeleton.

261 an actin-binding and bundling protein of the erythrocyte membrane skeleton.

262 Protein 4.1R was first identified in the erythrocyte membrane skeleton.

263 ith band 3 and the concomitant regulation of erythrocyte membrane stability, and (3) release of ATP f

264 spectrin/actin-binding peptide critical for erythrocyte membrane stability, is modulated by the diff

265 spectrin/actin-binding peptide critical for erythrocyte membrane stability.

266 e spectrin-actin-binding domain critical for erythrocyte membrane stability.

267 so associated with a substantial increase in erythrocyte membrane stiffness and/or viscosity.

268 These include contributing to erythrocyte membrane structural integrity, transport of

269 ha-spectrin, which in turn leads to abnormal erythrocyte membrane structure and function.

270 cin caused classical physical changes to the erythrocyte membrane such as morphological alterations (

271 uring spontaneous inside-out vesiculation of erythrocyte membranes suggests that the parasite co-opts

272 ained molecular dynamics (CGMD) model of the erythrocyte membrane that explicitly describes the phosp

273 elease that features a biochemically altered erythrocyte membrane that folds after pressure-driven ru

274 hospholipid translocation across vesicle and erythrocyte membranes; that is, they act as synthetic tr

275 t available and accessible, making the human erythrocyte membrane the favored target.

276 tly normal protein composition of the mutant erythrocyte membrane, the retention of the spectrin-acti

277 oxide generation at the inner surface of the erythrocyte membrane, thus coupling the release of oxyge

278 or and Pfmc-2TM families are exported to the erythrocyte membrane, thus supporting the hypothesis tha

279 the ankyrin-band 3 linkage destabilized the erythrocyte membrane to a lesser degree than complete de

280 duces an increase in the permeability of the erythrocyte membrane to monovalent ions.

281 permeabilization and eventual rupture of the erythrocyte membrane to release the parasites.

282 accompanied by relocation of actin from the erythrocyte membrane to the Maurer's clefts.

283 The principal bridge connecting the erythrocyte membrane to the spectrin-based skeleton is e

284 ional model of the junctional complex in the erythrocyte membrane, to explore the effect of Sp unfold

285 gens stabilize sialylated glycan clusters on erythrocyte membranes uniquely for each blood type, gene

286 ned amounts of cholesterol were removed from erythrocyte membranes using methyl-beta-cyclodextrin.

287 ng enclosed beneath the lipid bilayer in the erythrocyte membrane) via a nonstiff, and thus efficient

288 -cohort study, omega-3 fatty acid content of erythrocyte membranes was also inversely associated with

289 To investigate the nanomechanics of the erythrocyte membrane we developed a hybrid model that co

290 values of the model parameters for Band 3 in erythrocyte membranes, we are able to estimate the value

291 a lower ratio of arachidonic acid to EPA in erythrocyte membranes were associated with a higher cogn

292 However, the osteoinductive effects of erythrocyte membranes were reduced in human arterial smo

293 sembly of a glycolytic enzyme complex on the erythrocyte membrane which is associated with a shift in

294 oskeletal system is the inner surface of the erythrocyte membrane, which provides an erythrocyte with

295 ior to insertion of the SLS complex into the erythrocyte membrane, which resulted in formation of a t

296 eviously described as clustered in the human erythrocyte membrane, which was thought to be necessary

297 EM, is distinct from that in the surrounding erythrocyte membrane, with a structure at the apex that

298 nditions results in reduced integrity of the erythrocyte membrane, with formation of exocytic microve

299 nt of the necrotic core, the accumulation of erythrocyte membranes within an atherosclerotic plaque m

300 Our theoretical modeling demonstrates that erythrocyte membrane wrapping alone, as a function of me