ライフサイエンスコーパス: erythrocyte ghost

コーパス検索結果 (１語後でソート)

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1 blocked falcipain-2-induced fragmentation of erythrocyte ghosts.

2 ceable binding of cytochalasin B to GLUT1 in erythrocyte ghosts.

3 e during the fusion of the Sendai virus with erythrocyte ghosts.

4 itide-metabolizing enzymes present in turkey erythrocyte ghosts.

5 ne lipids was investigated in resealed human erythrocyte ghosts.

6 In turkey erythrocyte ghosts, agonist-stimulated PIP2 hydrolysis i

7 (3) Resealing of the loop peptide into erythrocyte ghosts alters membrane morphology and stabil

8 Phosphorylation of erythrocyte ghosts and purified PMCA by pp60(src) also r

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

10 helix insertion, the release of calcein from erythrocyte ghosts, and hemolysis of erythrocytes was mu

11 usion zone diameter in pairs of electrofused erythrocyte ghosts as a model for cell fusion.

12 PEOOH, PSOOH, SMOOH) using photoperoxidized erythrocyte ghosts as model donors and freshly prepared

13 stacked among smaller human erythrocytes or erythrocyte ghosts by sequential centrifugation at 700 g

14 o encapsulate indocyanine green (ICG) dye in erythrocyte ghost cells at a concentration that produced

15 investigated by measuring sugar uptake into erythrocyte ghosts containing or lacking ATP and glycoly

16 ith this activity from detergent extracts of erythrocyte ghosts depleted of cytoskeleton.

17 As previous studies in the erythrocyte ghost have shown that polyamines can alter f

18 ceable binding of cytochalasin B to GLUT1 in erythrocyte ghosts in a competitive manner, with a Ki of

19 e transfer of ascorbate-derived electrons in erythrocyte ghosts is dependent in part on alpha-tocophe

20 Rupture by cell swelling should yield erythrocyte ghosts; membrane fusion is inhibited by inne

21 of known oligomeric state, the anisotropy of erythrocyte ghost membranes at 37 degrees C is consisten

22 on X-100 micelles, unilamellar liposomes, or erythrocyte ghost membranes increased in the following o

23 membrane Ca-ATPase (PM-Ca-ATPase) in native erythrocyte ghost membranes or a peptide (C25W) that has

24 Triton X-100-soluble and -insoluble pools in erythrocyte ghost membranes or when expressed in culture

25 sentative fluorescent chelators across human erythrocyte ghost membranes was investigated.

26 one PM-Ca-ATPase polypeptide chain in native erythrocyte ghost membranes.

27 s of CaM bound to the PM-Ca-ATPase in native erythrocyte ghost membranes.

28 erated in [(14)C]Ch-labeled donor membranes [erythrocyte ghosts or unilamellar DMPC/Ch (1.0:0.8 mol/m

29 Release did not yield erythrocyte ghosts, positive-curvature amphiphiles did n

30 rn analysis of the Na pump from mature human erythrocyte ghosts, purified by ouabain column chromatog

31 ion of 3-O-methylglucose uniport in resealed erythrocyte ghosts requires cytosolic ATP and/or glutath

32 ar vesicles made of human, sheep, and rabbit erythrocyte ghosts rich in 24:1 SM and CHO, showed no la

33 nonagglutinable LUVs); (ii) photoperoxidized erythrocyte ghosts/SUVs or vice versa; and (iii) SUVs/mi

34 This study uses erythrocyte ghosts to characterize the reversible cytopl

35 In this study, we labeled lipid symmetric erythrocyte ghosts with 125INA and DiO.

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