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1 all target spot appeared in a corner of each polygon.
2 e sets is represented as a circle inside the polygon.
3 epresents multiple datasets as vertices in a polygon.
4 eduction was the primary pathway in degraded polygons.
5 o the differences in the shapes of the fused polygons.
6 ntact) to flat- and high-centered (degraded) polygons.
7 is region exhibit bulk flow features without polygons.
8 ection the most likely explanation for these polygons.
9 e same variant by computing intersections of polygons.
10 and evaluate the yield of new self-assembled polygons.
11 ing, and then converting, new self-assembled polygons.
12 a fixed equilibrium distribution of cellular polygons.
13 raphs, bar graphs, histograms, and frequency polygons.
14 significant depletion of hexagons and larger polygons.
15 face of the region is divided into irregular polygons about 20-30 kilometres in diameter, whose centr
16 Our AFM imaging resolves clathrin lattice polygons and provides height deformation in quantitative
18 5%) bird species based on geographical range polygons and then used Bayesian phylogenetic analyses to
20 ubules forms new three-way junctions and new polygons, and junction sliding and ring closure leads to
21 sted so far, composed of several fused water polygons, and showed 50-fold affinity enhancement with r
22 t polygons to 7 nmol m(-2) s(-1) in degraded polygons, and stable isotope signatures of CH4 and DIC s
26 tial coverage, as determined by their convex polygon area, was reduced in eyes with severe glaucoma.
30 te number, territory (the area of the convex polygon bounding the skeleton and cell body), and Polari
31 self-assembly and the shape of the obtained polygons can be controlled simply by changing the ratio
33 uality, few-layer antimonene monocrystalline polygons can be synthesized on various substrates, inclu
34 her sensitivity in the organic-rich soils of polygon center and trough than the relatively drier ridg
36 ter polygon, flat-center polygon, low center polygon, coalescent low center polygon, polygon trough,
37 he synthesis of stable, multicomponent fused polygon complexes in which coordination-driven self-asse
41 th geomorphic change from low to high center polygons, cumulatively resulting in an estimated negativ
42 ific subset of actin filaments localizing to polygons defined by ER sheets and tubules and describe a
43 ferences of particular cells among different polygon displays were correlated across reversed contras
46 llations that are created by placing regular polygons edge-to-edge around a vertex to fill the plane.
47 d of ten classes; drained slope, high center polygon, flat-center polygon, low center polygon, coales
48 e been proposed to explain this terrain, but polygons formed from thermal contraction (analogous to i
51 ssellation of the Euclidean plane by regular polygons has been contemplated since ancient times and p
53 croscopy reveal that the obtained antimonene polygons have buckled rhombohedral atomic structure, con
54 s controllably converted into an alternative polygon, have been achieved through the reaction between
55 gh positions of water-saturated low-centered polygon in Barrow Environmental Observatory, Barrow AK,
56 in measurement of a structural variant as a polygon in the plane, and identifies measurements suppor
60 shows that a good correlation exists between polygon interior angles and angles formed by the edges o
62 self-assembled Pt(II)-pyridyl metal-organic polygon is controllably converted into an alternative po
63 that a stereotyped distribution of cellular polygons is conserved in proliferating tissues among met
65 agmentation, defined by the mean diameter of polygons, is strictly governed by mechanical properties
66 thelia of mammalian skin, cells of irregular polygon-like shapes pack into complex, nearly flat two-d
68 ined slope, high center polygon, flat-center polygon, low center polygon, coalescent low center polyg
71 tion of a cross section of each motif with a polygon (n-gon, n=4, 8, 16) shows that a good correlatio
72 ed polyhedron of one sheet composed of plane polygons of finite size, and in which all the vertices a
73 ) distances and anion positioning versus the polygon opposing tetrazine rings are in agreement with D
74 to perform multiple tasks are arranged in a polygon or polyhedron (line, triangle, tetrahedron and s
75 al view holds that girih (geometric star-and-polygon, or strapwork) patterns in medieval Islamic arch
76 l files 1, 3, 4] and synthetic dataset using polygons, our methods tackled three aforementioned tasks
77 s chemical analyses of martian soil from the polygon-patterned northern plains of the Vastitas Boreal
78 n, low center polygon, coalescent low center polygon, polygon trough, meadow, ponds, rivers, and lake
79 ual objects, approximated by two-dimensional polygons representing cellular interfaces, in which each
81 In proteomaps, each protein is shown as a polygon-shaped tile, with an area representing protein a
83 hills of of water ice along the edges of the polygons) suggest that its N2 ice is about ten kilometre
85 dividual dendrites measured as convex hulls (polygons that enclose all branches passing through a she
86 owth of few-layer antimonene monocrystalline polygons, their atomical microstructure and stability in
87 1 such polyhedra have faces that are regular polygons; these polygons are equilateral triangles and s
88 hout disrupting the underlying metallacyclic polygons, thus producing eight different poly[2]pseudoro
89 decreased from 64 nmol m(-2) s(-1) in intact polygons to 7 nmol m(-2) s(-1) in degraded polygons, and
92 ination-driven self-assembled supramolecular polygons (triangles and rectangles) has been achieved us
93 nter polygon, coalescent low center polygon, polygon trough, meadow, ponds, rivers, and lakes, to det
94 , oxidation, and surface emissions in Arctic polygon tundra, across a wet-to-dry permafrost degradati
95 an overriding restriction: the frequency of polygon types correlates with the distribution of cell a
96 n ice, this layer is organized into cells or polygons, typically about 10 to 40 kilometres across, th
97 s by considering the distribution of Voronoi polygons (VP) generated from planar capillary locations
98 as observed when the number of adjuvants per polygon was increased, demonstrating the advantage of sh
101 age dominated CH4 production in low-centered polygons, while CO2 reduction was the primary pathway in
103 scaffold, like vesicle coats, is composed of polygons with vertices and edges forming a membrane-prox
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