ライフサイエンスコーパス: erythrocyte membrane

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

2 gnificant revision of accepted models of the erythrocyte membrane.

3 he general structural integrity of the human erythrocyte membrane.

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

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

6 the distribution of phospholipids across the erythrocyte membrane.

7 tein-protein interactions that stabilize the erythrocyte membrane.

8 tein-protein interactions that stabilize the erythrocyte membrane.

9 to traffic newly synthesized proteins to the erythrocyte membrane.

10 ated analogue appear to readily traverse the erythrocyte membrane.

11 ding the unique mechanical properties of the erythrocyte membrane.

12 most abundant integral proteins in the human erythrocyte membrane.

13 gen of P. yoelii that is associated with the erythrocyte membrane.

14 ules and other surface proteins of the human erythrocyte membrane.

15 erposed over the thermal fluctuations of the erythrocyte membrane.

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

17 e merozoite surface and also associated with erythrocyte membrane.

18 transient local membrane deformations in the erythrocyte membrane.

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

20 ions and antimalarial compounds at the host erythrocyte membrane.

21 tructures within the surface of the infected erythrocyte membrane.

22 evor expression impacts deformability of the erythrocyte membrane.

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

24 molecular-dynamics model for simulating the erythrocyte membrane.

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

26 loring parasite-induced modifications of the erythrocyte membrane.

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

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

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

30 and membrane skeletal associations in human erythrocyte membranes.

31 enotype and measured the PUFA composition of erythrocyte membranes.

32 n organize into complexes on other mammalian erythrocyte membranes.

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

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

35 erythrocyte glycoproteins (hEGP) from human erythrocyte membranes.

36 fluorescent phosphatidylcholine analog from erythrocyte membranes.

37 ymorphisms might influence CR1 clustering on erythrocyte membranes.

38 characterized in enzyme purified from human erythrocyte membranes.

39 ve the accumulation of free cholesterol from erythrocyte membranes.

40 ilitate phosphatidylcholine flip-flop across erythrocyte membranes.

41 al and architectural peculiarities of bovine erythrocyte membranes.

42 were cotranslated in the presence of rabbit erythrocyte membranes.

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

44 Stachylysin also formed pores in sheep erythrocyte membranes.

45 the stimulation of phospholipase C in turkey erythrocyte membranes.

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

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

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

49 oteomics identified PIEZO1 peptides in human erythrocyte membranes.

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

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

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

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

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

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

56 acity to stimulate phospholipase C in turkey erythrocyte membranes (agonist effect) and to inhibit ph

57 acity to stimulate phospholipase C in turkey erythrocyte membranes (agonist effect) and to inhibit ph

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

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

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

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

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

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

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

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

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

67 This protein, which was isolated from human erythrocyte membranes and from K562 (human erythroleukem

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

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

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

71 Rh protein was detected in mouse erythrocyte membranes and was comparable in size to huma

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

73 10-30 nN) are needed to penetrate the tensed erythrocyte membrane, and these forces increase exponent

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

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

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

77 re aggregated, all the major proteins of the erythrocyte membrane are constrained to coaggregate with

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 ion of 4.1N, a novel neuronal homolog of the erythrocyte membrane cytoskeletal protein 4.1 (4.1R).

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

102 4.1N is a neuronal selective isoform of the erythrocyte membrane cytoskeleton protein 4.1R.

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

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

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

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

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

108 At 8 wk, erythrocyte membrane DHA composition increased significa

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

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

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

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

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

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

115 t alleles was similar, Gsalpha expression in erythrocyte membranes from the affected patient was redu

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

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

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

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

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

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

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

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

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

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

126 The erythrocyte membrane is a composite structure consisting

127 The erythrocyte membrane is a newly appreciated platform for

128 1 clustering in knob-like protrusions on the erythrocyte membrane is critical for cytoadherence, howe

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

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

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

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

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

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

135 3 microm dinitrophenyl S-glutathione, across erythrocyte membranes is inhibited by multidrug resistan

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

154 Erythrocyte membrane poration occurs in relaxed cells, t

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

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

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

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

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

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

161 ross-stage immunity to Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP-1).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

183 the malarial variant antigen, P. falciparum erythrocyte membrane protein 1 (PfEMP1), and particularl

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

206 To examine the relationship between erythrocyte membrane protein 7.2b deficiency and the hem

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

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

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

210 Erythrocyte membrane protein genes serve as excellent mo

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

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

213 Human stomatin (band 7.2b) is a 31-kDa erythrocyte membrane protein of unknown function but imp

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

215 beta-Spectrin is an erythrocyte membrane protein that is defective in many p

216 Ankyrin 1, an erythrocyte membrane protein that links the underlying c

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

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

219 We recently identified a 35-kDa erythrocyte membrane protein, phospholipid scramblase, t

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

238 nsgenically engineered mice lacking specific erythrocyte membrane proteins.

239 .1-like calcium channel exists in the mature erythrocyte membrane, RBC membrane preparations were imm

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

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

242 The erythrocyte membrane's ability to withstand the stresses

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

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

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

246 4.2 (P4.2) is an important component in the erythrocyte membrane skeletal network that regulates the

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

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

249 Among the erythrocyte membrane skeletal proteins, ankyrin and prot

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

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

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

253 The human erythrocyte membrane skeleton consists of hexagonal latt

254 Spectrin of the erythrocyte membrane skeleton is composed of alpha- and

255 The erythrocyte membrane skeleton is the best understood cyt

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

275 onal movement of proteins in the unperturbed erythrocyte membrane, these experiments suggest that a c

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

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

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

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

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

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

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

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

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

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

286 have recently shown that C5b-6 binds to the erythrocyte membrane via an ionic interaction with siali

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 rnal and cytoplasmic surface proteins of the erythrocyte membrane which had been covalently labeled n

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