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1 tion of the cell became thinner and remained biconcave.
2 d blood cell surface, with a bias toward the biconcave 'dimple'.
3 the nucleated normoblast stage to the mature biconcave discocyte, both the structure and mechanical p
4 s, resembling normal reticulocytes to smooth biconcave discocytes.
5 rticle adhesion, we find that HI between the biconcave discoid particles prompts the formation of lay
6    When the attached spheres were changed to biconcave discs by flushing with an iso-osmotic solution
7 spheres in hypo-osmotic solutions and smooth biconcave discs in iso-osmotic solutions.
8                                          The biconcave disk shape of the mammalian red blood cell (RB
9             Urea by itself did not alter the biconcave disk shape of the red cell; however, above thr
10 are asymmetric including pushpin-, star- and biconcave disk-like structures, as well as more complex
11 of the human red blood cell is known to be a biconcave disk.
12 ed cells in rouleau, immediately reverted to biconcave disks as they flipped onto a stack.
13 e fraction of the cells, f, were taken to be biconcave disks perfectly oriented relative to the flat
14 rsible shape transformations, from initially biconcave disks to elongated and folded geometries with
15    Here, we report the preparation of unique biconcave djurleite Cu1.94S nanoplatelets (NPls) from te
16 ascent murine reticulocytes that mature into biconcave erythrocytes in vitro should be useful in furt
17  hours, about 20% to 25% of the cells became biconcave erythrocytes.
18 dren, flat glenohumeral joints; 19 children, biconcave glenoid; and 17 children, pseudoglenoid.
19 oglenoid, -10 degrees for those with flat or biconcave glenoids, and 0 degrees for those with concent
20                                              Biconcave human red blood cells moved downward at low fo
21     Morphological deviations from the normal biconcave RBC shape are commonly associated with disease
22         All thrombi and emboli contained few biconcave red blood cells but many polyhedrocytes or rel
23                  Finally, we reveal that the biconcave red cell shape is highly stable under moderate
24 pted value of 2 x 10(-19) J to stabilize the biconcave shape against the cup shape.
25 BC shape, recent experiments reveal that RBC biconcave shape also depends on the contractile activity
26 d elasticity, can explain the red-blood-cell biconcave shape as well as other shapes that red blood c
27 Helfrich-Canham energy, we find that the RBC biconcave shape depends on the ratio of forces per unit
28 hey lose their ability to recover the normal biconcave shape in successive loading cycles of stretchi
29                           The formation of a biconcave shape is attributed to the assembly and migrat
30 ectrin-based membrane skeleton maintains the biconcave shape of erythrocytes, but whether spectrins a
31 r crossing IES and progressively acquire the biconcave shape of mature RBCs.
32  and thermal energies and also maintains the biconcave shape of RBCs.
33 membrane that are highly correlated with the biconcave shape of RBCs.
34 f the skeleton and confer the characteristic biconcave shape of red cells.
35  distinctive features, including small size, biconcave shape, extended lifespan (~115 days), and lack
36 diate-stage iRBCs) tend to flip due to their biconcave shape, whereas schizonts (late-stage iRBCs) te
37 nd their ghosts may be responsible for their biconcave shape.
38 , loss of surface area, and acquisition of a biconcave shape.
39  nuclei and organelles and assume a flexible biconcave shape.
40 onversion of ISCs formed in vivo back to the biconcave shape.
41 rin links are used to populate spherical and biconcave surfaces and intermediate shapes, and coarse-g
42 t, with flattening of the posterior glenoid; biconcave, with the humeral head in articulation with th