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1 ers were clearly oblate and one was slightly prolate.
2 ost all (99.7%) of the corneas examined were prolate.
3 microscopy, we have determined structures of prolate 12 procapsids and isometric SaPIbov5 procapsids.
4 and vortex separation patterns for the model prolate agree with those observed in Nemopsis bachei.
5 ibution of the molecules, which changes from prolate (aligned) to oblate (anti-aligned) in 300 fs.
6                 Corneal asphericity was less prolate among myopes than in emmetropes and hyperopes (P
7                                              Prolate and curtate cycloids are also traced by differen
8                The AbiA system inhibits both prolate and small isometric phages by interfering with t
9  New York) has been designed with a modified prolate anterior surface to compensate for the spherical
10 , and C = 752.7446(3) MHz, indicating a near-prolate asymmetric top molecule.
11                       The cluster contains a prolate Au(8) core and four level-3 extended staple moti
12 Au-SR]4 motifs, interlocked and capping on a prolate Au8 core.
13 r has moderate but statistically significant prolate axial anisotropy (D( parallel)/D( perpendicular)
14 hape using a paddling mode of swimming and a prolate bell shape using jet propulsion.
15       Cubomedusae, which often possess large prolate bells and are thought to swim via jet propulsion
16 vitro assembly system was developed to study prolate capsid assembly of phage o29 biochemically, and
17                                  WT T4 has a prolate capsid characterized by triangulation numbers (T
18 68, belongs to the T4-like myoviruses, has a prolate capsid, a long contractile tail and infects Proc
19 s, drugs, and steroid derivatives within its prolate cavity.
20 formation of one-dimensional hydrogen bonded prolate chains directed along the [110] direction.
21 le in the formation and stabilization of the prolate cluster.
22 ata for pure RL micelles can be described by prolate core-shell structures with a core radius of 7.7
23  sample was -0.346 +/- 0.101, representing a prolate corneal shape.
24 1.3-7.0; P = .011), compared to spherical or prolate corneas (Q value <= 0).
25 anterior chamber depths were related to less prolate corneas among emmetropes and hyperopes, which is
26                                         Less prolate corneas were related to deeper anterior chamber
27 ccuracy when used for eyes with physiologic, prolate corneas.
28 minantly parallel to POPC/POPS 3:1 bilayers (prolate deformation) when at the same time it induces a
29 d pointed towards emission from an extremely prolate-deformed state with a dominant s(1/2) proton com
30 ablations that attempt to avoid reducing the prolate eccentricity of the average cornea as well as wa
31 atic volume by marking out dimensions of the prolate ellipsoid formula from two orthogonal images of
32 ometries are well approximated by those with prolate ellipsoid heads.
33               Our findings indicate that the prolate ellipsoid model for the manganese-stabilizing pr
34  with hydrodynamic behaviour equivalent to a prolate ellipsoid of axial ratio 4.3 +/- 0.7:1 and mass
35 bout 65% of the mass and the other, a highly prolate ellipsoid of revolution consisting of about 35%
36                            When modeled as a prolate ellipsoid of revolution, the hydrated DnaC prote
37 teine motifs (Cys-X-Cys or Cys-Xn-Cys) and a prolate ellipsoid shape containing single alpha- and bet
38 ine motifs (Cys-X-Cys or Cys-X(n)-Cys) and a prolate ellipsoid shape containing single alpha- and bet
39 Hydrodynamic modeling suggests an asymmetric prolate ellipsoid shape for gp59, consistent with its X-
40 em II, is a natively unfolded protein with a prolate ellipsoid shape.
41 hape of the monomeric form of proapoA-I is a prolate ellipsoid with an axial ratio of about 6:1.
42 it is argued that ocr is best described by a prolate ellipsoid with dimensions of 10.4 nm by 2.6 nm.
43 n in solution has the approximate shape of a prolate ellipsoid with semi-axes of 24, 43, and 89 A.
44                        Assuming tapasin is a prolate ellipsoid, we calculated an apparent length of 2
45                         Assuming CRT to be a prolate ellipsoid, we calculated an apparent length of 2
46     The ms-HDL particles are found to form a prolate ellipsoidal shape, with sizes consistent with ex
47  with lower degrees of polymerization have a prolate ellipsoidal shape.
48 es an open helical shape that wraps around a prolate ellipsoidal type I hexagonal lyotropic liquid cr
49 cking fractions: spheres <oblate ellipsoids <prolate ellipsoids <dimers <spherocylinders.
50                              Elongation into prolate ellipsoids (rod-like) reduces sinking speed, and
51 e rod morphology and the formation of single prolate ellipsoids and pairs of prolate ellipsoids joine
52  large aspect ratios such as oblate and long prolate ellipsoids are found to exhibit very long alignm
53 on of single prolate ellipsoids and pairs of prolate ellipsoids joined by partial constrictions.
54 0-nm filaments, whereas the dimers generated prolate ellipsoids measuring 3-4 nm in diameter.
55 Results suggest that these proteins resemble prolate ellipsoids with radius of gyration (R(g)) of app
56 d on the long-range limit of flow around the prolate ellipsoids, as derived from equivalent Stokes sp
57           Average shapes are consistent with prolate ellipsoids.
58 facilitating slow magnetic relaxation in the prolate Er(III) ion.
59 ributions of rotational bands in 51 deformed prolate even-even nuclei in the 152 A 250 mass region [F
60 also confirmed the presence of an unexpected prolate geometry based on an elongated T = 4 capsid with
61 ng and emission from the aligned effectively prolate grains.
62 h axially elongated f-electron charge cloud (prolate) has only recently received attention.
63  seven structural proteins assembling into a prolate head and a short non-contractile tail.
64                                          The prolate head of phi29 has 10 hexameric units in its cyli
65 rate, whereas those with dorsoventrally more prolate headshields exhibit maximum hydrodynamic efficie
66                 Bacteriophage T4 capsid is a prolate icosahedron composed of the major capsid protein
67  protein and the scaffolding proteins into a prolate icosahedron of precise dimensions.
68            The head of bacteriophage T4 is a prolate icosahedron with one unique portal vertex to whi
69     Most corneas examined in this study were prolate in contour.
70 Clinical data demonstrate that this modified prolate IOL provides superior functional vision, similar
71 his work questions the theory that oblate or prolate lanthanides must be stabilized with the appropri
72 g and attachment through homoepitaxy to form prolate-like secondary structures.
73                            Eventually, these prolate-like structures form mesocrystals by oriented at
74          The alphaLA-SDS complexes contain a prolate micelle with a core radius of 11-14 A and a shel
75 lso demonstrate that gp32DeltaB protein is a prolate monomer with an elongated A-domain protruding fr
76  studies indicate that the gp59 protein is a prolate monomer, consistent with the crystal structure a
77 ven inertia perturbations acting on a nearly prolate, non-hydrostatic Earth with an effective elastic
78 e periphery (+0.80 +/- 1.29 D), indicating a prolate ocular shape (longer axial length than equatoria
79 eters such as volume, sphericity, oblate and prolate of individual particle and distributions were co
80 : oblate thermal ellipsoids below 60 meV and prolate ones above 60 meV.
81 city in the light distribution, suggesting a prolate or bipolar structure that develops as early as t
82 pe of the PFCR may vary, being a hemisphere, prolate or oblate hemispheroid, or hemi-ellipsoid, based
83 tructures of fibered isometric and fiberless prolate prohead phi29 particles at resolutions of 8.7 A
84                                        Novel prolate rhombohedra centered by Sc-Sc dimers are also ge
85 sists of condensed triacontahedral and novel prolate rhombohedral (PR) clusters.
86                The eye maintained a slightly prolate shape during growth.
87 ore elongated and also distorted into a more prolate shape in both the white and Chinese groups.
88                                         This prolate shape is consistent with the proposed idea that
89                      This is indicative of a prolate shape of choroidal contour at CIB and COB.
90                     We further show that the prolate shape of phi29's capsid is possible due to conca
91 latory true polar wander occurs owing to the prolate shape of the non-hydrostatic Earth.
92                                 The strongly prolate shape of the proposed Au(26) core is supported b
93 P and explain the observed dependence of the prolate shape on SP.
94 namics is characterized by a rapid oblate-to-prolate shape transformation of the electron gas, and pe
95 tubular section in normal heads leads to the prolate shape, with a more complex and variable geometry
96 spending medium, the vesicle always adopts a prolate shape.
97 associated with increased axial length and a prolate shape.
98 ren were both elongated and distorted into a prolate shape.
99                                         Soft prolate-shaped microgels at the air-water interface offe
100  assembly nor affected the morphology of the prolate-shaped procapsid.
101  we find that we can distinguish oblate- and prolate-shaped protein complexes by using the CCS, molec
102 Ss have higher volumetric cell densities and prolate shapes.
103 he short-axis images were transformed to the prolate spheroid coordinate system, and detection of the
104 ged polymer microparticles, characterized by prolate spheroid shape, at silica and gold sensors was i
105 l shape of silver nanoparticles changed to a prolate spheroid with the aspect ratio as high as 3.5 at
106  parameters fall within certain ranges: In a prolate spheroid, reticular buckles take over longitudin
107                       Using a semi-classical prolate-spheroid model, we quantify the transition frequ
108 f the deformation suggests a steeply dipping prolate-spheroid pressure source beneath the eastern cal
109 nvalues of the self-adjoint extension of the prolate spheroidal operator reproduce the UV behavior of
110           In this work, we leverage discrete prolate spheroidal sequences (a.k.a. Slepian sequences)
111 ction, we aggregate the cocoa particles into prolate spheroids in micrometers.
112 odes were configured as either ellipsoids or prolate spheroids in patterns given by the Cantor dust f
113 ctron microscopy of this dodecamer reveals a prolate structure with the protease chambers at the dist
114          All Intacs were implanted using the Prolate system console and instrumentation from Addition
115 icles which have the same geometry as either prolate T=3 Q=5 procapsids formed in vivo or previously
116 of a 10 A resolution cryo-EM map of an empty prolate T4 head shows how the dodecameric portal assembl
117  first three-dimensional reconstruction of a prolate, tailed phage, and its empty prohead precursor b
118 rects the assembly of 12 helper capsids from prolate to isometric.
119 e, the vesicle undergoes a transition from a prolate to oblate ellipsoid at a critical frequency, whi

 
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