ライフサイエンスコーパス: prolate

1 ers were clearly oblate and one was slightly prolate.

2 ost all (99.7%) of the corneas examined were prolate.

3 and vortex separation patterns for the model prolate agree with those observed in Nemopsis bachei.

4 ibution of the molecules, which changes from prolate (aligned) to oblate (anti-aligned) in 300 fs.

5 Corneal asphericity was less prolate among myopes than in emmetropes and hyperopes (P

6 Prolate and curtate cycloids are also traced by differen

7 The AbiA system inhibits both prolate and small isometric phages by interfering with t

8 New York) has been designed with a modified prolate anterior surface to compensate for the spherical

9 , and C = 752.7446(3) MHz, indicating a near-prolate asymmetric top molecule.

10 The cluster contains a prolate Au(8) core and four level-3 extended staple moti

11 Au-SR]4 motifs, interlocked and capping on a prolate Au8 core.

12 r has moderate but statistically significant prolate axial anisotropy (D( parallel)/D( perpendicular)

13 hape using a paddling mode of swimming and a prolate bell shape using jet propulsion.

14 Cubomedusae, which often possess large prolate bells and are thought to swim via jet propulsion

15 vitro assembly system was developed to study prolate capsid assembly of phage o29 biochemically, and

16 WT T4 has a prolate capsid characterized by triangulation numbers (T

17 68, belongs to the T4-like myoviruses, has a prolate capsid, a long contractile tail and infects Proc

18 formation of one-dimensional hydrogen bonded prolate chains directed along the [110] direction.

19 ata for pure RL micelles can be described by prolate core-shell structures with a core radius of 7.7

20 sample was -0.346 +/- 0.101, representing a prolate corneal shape.

21 anterior chamber depths were related to less prolate corneas among emmetropes and hyperopes, which is

22 Less prolate corneas were related to deeper anterior chamber

23 ccuracy when used for eyes with physiologic, prolate corneas.

24 minantly parallel to POPC/POPS 3:1 bilayers (prolate deformation) when at the same time it induces a

25 ablations that attempt to avoid reducing the prolate eccentricity of the average cornea as well as wa

26 ometries are well approximated by those with prolate ellipsoid heads.

27 Our findings indicate that the prolate ellipsoid model for the manganese-stabilizing pr

28 with hydrodynamic behaviour equivalent to a prolate ellipsoid of axial ratio 4.3 +/- 0.7:1 and mass

29 bout 65% of the mass and the other, a highly prolate ellipsoid of revolution consisting of about 35%

30 When modeled as a prolate ellipsoid of revolution, the hydrated DnaC prote

31 teine motifs (Cys-X-Cys or Cys-Xn-Cys) and a prolate ellipsoid shape containing single alpha- and bet

32 ine motifs (Cys-X-Cys or Cys-X(n)-Cys) and a prolate ellipsoid shape containing single alpha- and bet

33 Hydrodynamic modeling suggests an asymmetric prolate ellipsoid shape for gp59, consistent with its X-

34 em II, is a natively unfolded protein with a prolate ellipsoid shape.

35 hape of the monomeric form of proapoA-I is a prolate ellipsoid with an axial ratio of about 6:1.

36 it is argued that ocr is best described by a prolate ellipsoid with dimensions of 10.4 nm by 2.6 nm.

37 n in solution has the approximate shape of a prolate ellipsoid with semi-axes of 24, 43, and 89 A.

38 Assuming tapasin is a prolate ellipsoid, we calculated an apparent length of 2

39 Assuming CRT to be a prolate ellipsoid, we calculated an apparent length of 2

40 The ms-HDL particles are found to form a prolate ellipsoidal shape, with sizes consistent with ex

41 with lower degrees of polymerization have a prolate ellipsoidal shape.

42 es an open helical shape that wraps around a prolate ellipsoidal type I hexagonal lyotropic liquid cr

43 cking fractions: spheres <oblate ellipsoids <prolate ellipsoids <dimers <spherocylinders.

44 Elongation into prolate ellipsoids (rod-like) reduces sinking speed, and

45 e rod morphology and the formation of single prolate ellipsoids and pairs of prolate ellipsoids joine

46 on of single prolate ellipsoids and pairs of prolate ellipsoids joined by partial constrictions.

47 0-nm filaments, whereas the dimers generated prolate ellipsoids measuring 3-4 nm in diameter.

48 Results suggest that these proteins resemble prolate ellipsoids with radius of gyration (R(g)) of app

49 d on the long-range limit of flow around the prolate ellipsoids, as derived from equivalent Stokes sp

50 Average shapes are consistent with prolate ellipsoids.

51 facilitating slow magnetic relaxation in the prolate Er(III) ion.

52 h axially elongated f-electron charge cloud (prolate) has only recently received attention.

53 The prolate head of phi29 has 10 hexameric units in its cyli

54 Bacteriophage T4 capsid is a prolate icosahedron composed of the major capsid protein

55 protein and the scaffolding proteins into a prolate icosahedron of precise dimensions.

56 The head of bacteriophage T4 is a prolate icosahedron with one unique portal vertex to whi

57 Most corneas examined in this study were prolate in contour.

58 Clinical data demonstrate that this modified prolate IOL provides superior functional vision, similar

59 his work questions the theory that oblate or prolate lanthanides must be stabilized with the appropri

60 g and attachment through homoepitaxy to form prolate-like secondary structures.

61 Eventually, these prolate-like structures form mesocrystals by oriented at

62 The alphaLA-SDS complexes contain a prolate micelle with a core radius of 11-14 A and a shel

63 lso demonstrate that gp32DeltaB protein is a prolate monomer with an elongated A-domain protruding fr

64 studies indicate that the gp59 protein is a prolate monomer, consistent with the crystal structure a

65 ven inertia perturbations acting on a nearly prolate, non-hydrostatic Earth with an effective elastic

66 e periphery (+0.80 +/- 1.29 D), indicating a prolate ocular shape (longer axial length than equatoria

67 eters such as volume, sphericity, oblate and prolate of individual particle and distributions were co

68 city in the light distribution, suggesting a prolate or bipolar structure that develops as early as t

69 pe of the PFCR may vary, being a hemisphere, prolate or oblate hemispheroid, or hemi-ellipsoid, based

70 tructures of fibered isometric and fiberless prolate prohead phi29 particles at resolutions of 8.7 A

71 Novel prolate rhombohedra centered by Sc-Sc dimers are also ge

72 sists of condensed triacontahedral and novel prolate rhombohedral (PR) clusters.

73 The eye maintained a slightly prolate shape during growth.

74 ore elongated and also distorted into a more prolate shape in both the white and Chinese groups.

75 This prolate shape is consistent with the proposed idea that

76 latory true polar wander occurs owing to the prolate shape of the non-hydrostatic Earth.

77 The strongly prolate shape of the proposed Au(26) core is supported b

78 tubular section in normal heads leads to the prolate shape, with a more complex and variable geometry

79 spending medium, the vesicle always adopts a prolate shape.

80 associated with increased axial length and a prolate shape.

81 ren were both elongated and distorted into a prolate shape.

82 assembly nor affected the morphology of the prolate-shaped procapsid.

83 he short-axis images were transformed to the prolate spheroid coordinate system, and detection of the

84 l shape of silver nanoparticles changed to a prolate spheroid with the aspect ratio as high as 3.5 at

85 parameters fall within certain ranges: In a prolate spheroid, reticular buckles take over longitudin

86 f the deformation suggests a steeply dipping prolate-spheroid pressure source beneath the eastern cal

87 In this work, we leverage discrete prolate spheroidal sequences (a.k.a. Slepian sequences)

88 ction, we aggregate the cocoa particles into prolate spheroids in micrometers.

89 ctron microscopy of this dodecamer reveals a prolate structure with the protease chambers at the dist

90 icles which have the same geometry as either prolate T=3 Q=5 procapsids formed in vivo or previously

91 of a 10 A resolution cryo-EM map of an empty prolate T4 head shows how the dodecameric portal assembl

92 first three-dimensional reconstruction of a prolate, tailed phage, and its empty prohead precursor b

93 e, the vesicle undergoes a transition from a prolate to oblate ellipsoid at a critical frequency, whi