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1 tes that are devoid of hemoglobin, so-called erythrocyte ghosts.
2 blocked falcipain-2-induced fragmentation of erythrocyte ghosts.
3 ceable binding of cytochalasin B to GLUT1 in erythrocyte ghosts.
4 e during the fusion of the Sendai virus with erythrocyte ghosts.
5 itide-metabolizing enzymes present in turkey erythrocyte ghosts.
6 ne lipids was investigated in resealed human erythrocyte ghosts.
7                                    In turkey erythrocyte ghosts, agonist-stimulated PIP2 hydrolysis i
8       (3) Resealing of the loop peptide into erythrocyte ghosts alters membrane morphology and stabil
9 ndocyanine green (ICG) dye is sequestered in erythrocyte ghosts and autologously re-injected to allow
10                           Phosphorylation of erythrocyte ghosts and purified PMCA by pp60(src) also r
11        Next, B cells were enriched with D(+) erythrocyte ghosts and sorted as single cells.
12 ere fabricated from hemoglobin-depleted mice erythrocyte-ghosts and doped with Indocyanine Green (ICG
13 helix insertion, the release of calcein from erythrocyte ghosts, and hemolysis of erythrocytes was mu
14 usion zone diameter in pairs of electrofused erythrocyte ghosts as a model for cell fusion.
15  PEOOH, PSOOH, SMOOH) using photoperoxidized erythrocyte ghosts as model donors and freshly prepared
16  stacked among smaller human erythrocytes or erythrocyte ghosts by sequential centrifugation at 700 g
17 o encapsulate indocyanine green (ICG) dye in erythrocyte ghost cells at a concentration that produced
18  investigated by measuring sugar uptake into erythrocyte ghosts containing or lacking ATP and glycoly
19 ith this activity from detergent extracts of erythrocyte ghosts depleted of cytoskeleton.
20                   As previous studies in the erythrocyte ghost have shown that polyamines can alter f
21 ceable binding of cytochalasin B to GLUT1 in erythrocyte ghosts in a competitive manner, with a Ki of
22 e transfer of ascorbate-derived electrons in erythrocyte ghosts is dependent in part on alpha-tocophe
23        Rupture by cell swelling should yield erythrocyte ghosts; membrane fusion is inhibited by inne
24 of known oligomeric state, the anisotropy of erythrocyte ghost membranes at 37 degrees C is consisten
25 on X-100 micelles, unilamellar liposomes, or erythrocyte ghost membranes increased in the following o
26  membrane Ca-ATPase (PM-Ca-ATPase) in native erythrocyte ghost membranes or a peptide (C25W) that has
27 Triton X-100-soluble and -insoluble pools in erythrocyte ghost membranes or when expressed in culture
28 sentative fluorescent chelators across human erythrocyte ghost membranes was investigated.
29 one PM-Ca-ATPase polypeptide chain in native erythrocyte ghost membranes.
30 s of CaM bound to the PM-Ca-ATPase in native erythrocyte ghost membranes.
31 erated in [(14)C]Ch-labeled donor membranes [erythrocyte ghosts or unilamellar DMPC/Ch (1.0:0.8 mol/m
32                        Release did not yield erythrocyte ghosts, positive-curvature amphiphiles did n
33 rn analysis of the Na pump from mature human erythrocyte ghosts, purified by ouabain column chromatog
34 ion of 3-O-methylglucose uniport in resealed erythrocyte ghosts requires cytosolic ATP and/or glutath
35 ar vesicles made of human, sheep, and rabbit erythrocyte ghosts rich in 24:1 SM and CHO, showed no la
36 o intact senescent erythrocytes, the remnant erythrocyte ghost shells were prone to recognition and b
37 nonagglutinable LUVs); (ii) photoperoxidized erythrocyte ghosts/SUVs or vice versa; and (iii) SUVs/mi
38                              This study uses erythrocyte ghosts to characterize the reversible cytopl
39    In this study, we labeled lipid symmetric erythrocyte ghosts with 125INA and DiO.