ライフサイエンスコーパス: long axes

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1 nds of circumferential rotation around their long axes.

2 ve a 3-fold rotational symmetry around their long axes.

3 dye di-8-ANEPPS, and stimulated along their long axes.

4 urface with a 60 degrees angle between their long axes.

5 ed in situ and after realignment along their long axes.

6 Rafts of hundreds of cells with their long axes aligned in parallel enlarge as individual cell

7 h induces a global realignment of interphase long axes along the direction of extension, this is suff

8 e. rotate about 115 degrees around their own long axes) and the mean relative axial displacement from

9 n coincident to the nanostructure and noodle long axes, and the resulting nanostructures show evidenc

10 These cells rolled about their long axes as they moved forward, following a right-hande

11 two PMI molecules are displaced along their long axes by one phenyl group (~4.3 A).

12 differences in conjugation both along their long axes (by the number of fused benzene or thiophene r

13 ed opacity of similar dimensions, with their long axes directed vertically.

14 he peptide molecules are oriented with their long axes normal to the bilayer (the "picket fence" orie

15 r, consistently match the orientation of the long axes of aligned and tightly packed polysaccharide f

16 illation over very short distances along the long axes of minicells, supporting the importance of geo

17 but significant radial distortions along the long axes of SWNTs.

18 chromophore's long axis is aligned with the long axes of the adjacent base pairs, maximizing intermo

19 ght due to preferential extinction along the long axes of the aligned grains.

20 w electronic transitions polarized along the long axes of the dimers.

21 The angle between long axes of the Fabs was 115 degrees, the most acute an

22 mpared to propagation at right angles to the long axes of the fibers, propagation along the long axis

23 axes of hydroxyapatite are aligned with the long axes of the fibers.

24 filament-like structures oriented along the long axes of the fibrils.

25 or Cy5 attached by 3-atom tethers, with the long axes of the fluorophore and the terminal basepair a

26 A key finding is that the long axes of the intercalated benzo[a]pyrenyl rings in t

27 helial cleavage plane angles relative to the long axes of the major retinal vessels during anaphase w

28 entated along the c axis and parallel to the long axes of the microribbons was observed in vitro.

29 ack in similar triclinic unit cells with the long axes of the molecules nearly perpendicular to the s

30 nsert loop are masked by rhoGDI and that the long axes of the two proteins are in parallel in the het

31 to lipid in an antiparallel manner, with the long axes of their helical repeats running perpendicular

32 rimers are predominantly arranged with their long axes oriented radially, and the width of the high m

33 her of two distinct orientations, with their long axes parallel or perpendicular to the direction of

34 cero-3-phosphocholine (POPC), lie with their long axes parallel to aqueous-lipid interfaces.

35 ching direction, but not in cells with their long axes parallel to stretch.

36 ile, beads predominantly migrated with their long axes parallel to the direction of motion, mimicking

37 fic manner, specifically in cells with their long axes perpendicular to the stretching direction, but

38 cTnI-cTnT(198-298) component lie with their long axes roughly parallel to one another with a relativ

39 gen-bonding substituents along the molecular long axes tunes properties such as hyperpolarizability,

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