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1 rut pore size and controlled film width (via layering).
2 aracterized by a neocortex that has inverted layering.
3 the possible presence of complex, inner-core layering.
4 copically characterized by abnormal cortical layering.
5 ures, leading to a disruption of the desired layering.
6 or protein, is also required for neocortical layering.
7 ivity revealed a depth-decaying near-surface layering.
8 on of progenitors and neurons, but preserved layering.
9 ce are postnatal viable with normal cortical layering.
10 rface of the brain and disorganized cortical layering.
11  of one-, two- and three-dimensional tilings/layerings.
12 disorganization of this cell population with layering aberrations, severe granule neuron migration de
13 ient mice die soon after birth with neuronal layering abnormalities in the cerebral cortex, a consequ
14 B1; they died soon after birth with neuronal layering abnormalities in the cerebral cortex.
15 he adult brain does not result in additional layering abnormalities.
16                                This neuronal layering abnormality is due to defective neuronal migrat
17 mpared at various imaging depths (2-8 mm) by layering additional biologic tissues on top of the rats
18 e deficits observed in floxed dab1 mice with layering alterations in the hippocampus and neocortex.
19 thin the follicle epithelium leads to double layering and accumulation of actin and ZO-1 in between,
20 pha-helical proteins use amphipathic helical layering and bundling to form modular lipid-binding comp
21           This is followed by the successive layering and compaction of additional tongues to create
22 n time of only 15 days with the onset of HLE layering and differentiation observed.
23  of Lis1 and Ndel1 displayed severe cortical layering and hippocampal defects, but Lis1 mutants had m
24 ory cells contributes to defects in cortical layering and hypocellularity in the ventral LGN and amyg
25 , or both results in abnormalities in cortex layering and in trajectories of secondary axons.
26 contrast, canopy vertical complexity (canopy layering and shape) did not affect movement.
27 pressing Delta FGFR4a show disorganized cell layering and specifically lack photoreceptor cells.
28  appropriate development of cerebellar folia layering and structure.
29  the inner core has been inferred to possess layering and to be less anisotropic than at greater dept
30 e explained by changes in cell arrangements (layering) and in the size of the nuclei.
31 cortex retains its fundamental organization, layering, and input-output relations as it scales in vol
32 erinatal lethality, disorganized neocortical layering, and profound hippocampal cytoarchitectural dis
33  identify critical conditions to produce the layering, and relate the results quantitatively to doubl
34    The proposed PEC production process omits layering approaches currently employed for PEMs, reducin
35 ures, interfacial geometries, gradation, and layering are advantageous for penetration resistance, en
36 mal patterns of dendritogenesis and neuronal layering as determined by Golgi staining.
37 decoupled from layering, thereby eliminating layering as the driver for shear thinning.
38                                    Molecular layering at the lipid-nanotube interface is reported.
39                                              Layering at the liquid-solid interface plays an importan
40 natal mortality, disrupted cerebral cortical layering attributable to abnormal neuronal migration, la
41 mesh rotation, tilt angle (branch droop) and layering (branch overlap).
42  The forebrain not only showed disruption of layering, but also neurodegenerative changes accompanied
43   Here we test whether Cul5 regulates neuron layering by affecting Dab1 stability or other mechanisms
44 arge secreted protein that controls cortical layering by signaling through the very low density lipop
45 hese results show that Cul5 regulates neuron layering by stimulating Dab1 degradation and that Cul5 c
46 ellar cortical development (size, foliation, layering, cell number, and position), which proceeds to
47                            Although cortical layering, cytoarchitecture, and proteome were found to b
48 of active Dab1 protein and a unique cortical layering defect, characterized by excess migration and b
49          Pafah1b1(+/-) mice have hippocampal layering defects, whereas homozygous mutants are embryon
50 ell population and subsequently to extensive layering defects.
51 phalus and enhanced cortical and hippocampal layering defects.
52                                          The layering depth, however, is threefold greater than that
53         However the spacer peptide acts as a layering determinant during tube assembly.
54                                         Such layering differences between orders, and similarities am
55 ch spatial segregation caused by the smectic layering dramatically enhanced photopolymerization rates
56 s system, where it is important for cortical layering during development and survival of dopaminergic
57 w that, above a critical injection velocity, layering emerges over a time scale of minutes.
58 ons, including disarray of cerebral cortical layering, fusion of cerebral hemispheres and cerebellar
59 most abnormal (cell rounding, sloughing, and layering; grade 2) and HAF intensity profiles were highe
60      Several genes essential for neocortical layering have been identified in recent years, but their
61                      Cortical morphology and layering in adult Hdc KO mice were also preserved.
62 change might be responsible for the observed layering in Mars' polar deposits by modulating depositio
63 use disabled1 (mdab1) gene disturbs neuronal layering in the cerebral cortex, hippocampus and cerebel
64                                              Layering in the crater walls preserves evidence of ancie
65  surfaces that promote ice nucleation induce layering in the interfacial water, suggesting that the o
66 ads to permanent abnormalities of structural layering in the neocortex and hippocampus.
67 ensely packed and had distinct photoreceptor layering in the OCT images).
68 t temperatures below 5200 kelvin and lead to layering in the outer core if the concentrations of the
69                     We found no evidence for layering in the outer core in the travel times and wave
70 x, concomitant with an inversion of cortical layering in the rostral cortex.
71                                         Weak layering in tropical soils is hypothesized to decrease n
72 the brain revealed normal structure and cell layering, including normal cortical barrel fields; histo
73                           The extent of this layering increases with the volume fraction, or degree o
74                                     Cortical layering is a hallmark of the mammalian neocortex and a
75                                     Cortical layering is normal, but neurons are smaller than those i
76                 Our data imply that cortical layering is not a static process, but rather requires in
77                                 A pronounced layering is observed in the film, with the density exhib
78 e difficult to draw LB films, almost perfect layering is obtained due to the inability to convert fro
79                              This additional layering is thwarted when the PE conformation is constra
80                                      Retinal layering, key cell types, synaptic structure, and mGluR6
81  in epitaxial thin film form by sequentially layering La(1-x)Sr(x)MnO(3) and SrO unit cells aided by
82                        New work reveals that layering mathematical modeling on top of imaging may be
83          This is achieved through a cascaded layering of a network into functional subsystems, where
84 e identified a class-specific medial-lateral layering of axons in the central nervous system formed d
85                            To understand the layering of controls needed to poise this gene heritably
86 d abnormal angular features, iii) concentric layering of cristae membranes, iv) matrix compartmentali
87 idence of ice near the surface, has distinct layering of different materials, and has a mean density
88  provide constraints on studies of viscosity layering of Earth's mantle and guide further research in
89 tive phylogeography, have their roots in the layering of gene trees across geography, a paradigm that
90 are distinct and provide a genetic basis for layering of immune system development.
91                               Defects in the layering of Langmuir-Blodgett (LB) films can be eliminat
92 terial is developed utilizing a hierarchical layering of micro- and nanoscale silica lamellae to crea
93 s a glycoprotein that is critical for proper layering of neocortex during development as well as dyna
94 nvolve fusion of adjacent lobules, disrupted layering of neurons and glia, and fragmentation of the p
95 dels had a small forebrain with disorganized layering of neurons and nuclear shape abnormalities, sim
96                                              Layering of neurons in the cerebral cortex and cerebellu
97 ties resembling lissencephaly, with abnormal layering of neurons in the cerebral cortex and cerebellu
98 ogenesis is not detectably affected, but the layering of neurons in the cortex is inverted, and the f
99 omplex design developing and evolving by the layering of new patterns on pre-patterns is likely to be
100        This work demonstrates the successful layering of orthogonal logic gates, a design strategy th
101                          However, we observe layering of particles at the cell wall due to steric int
102 ling pathways and HOM-C genes, and uncover a layering of patterning systems that may reflect their ev
103      So far, NIMs have been realized through layering of resonant structures, such as split-ring reso
104 lity that is inherited from the depositional layering of sedimentary laminations, where the highest p
105 vaporation of small sample volumes that uses layering of silicone oil on solution surfaces but still
106                             Such interfacial layering of simple liquids has been theoretically predic
107 ptic cup formation, neural tube closure, and layering of the cerebral cortex.
108 the alpha3 integrin gene results in abnormal layering of the cerebral cortex.
109                             In addition, the layering of the corneal stroma is poorly formed or absen
110         Our data confirm that the outside-in layering of the dentate gyrus continues through adulthoo
111 elial repulsion, which prevents uncontrolled layering of the endothelium.
112 interpretation of these phenomena identifies layering of the fluid perpendicular to the shear gradien
113 tonotopic organization of cat ICC, reflect a layering of the frequency organization paralleling its a
114 ength nonhydrostatic geoid, we infer viscous layering of the mantle using a method that allows us to
115    We outline a unified model for inside-out layering of the neocortex, hinging on a new interpretati
116 nd Anchiornis make individual feathers weak, layering of the wing feathers may have produced a strong
117                    Heterostructures based on layering of two-dimensional (2D) materials such as graph
118 e findings are consistent with a sequential "layering" of cultural diversity in humans and chimpanzee
119  the developmentally ordered appearance (or "layering") of distinct hematopoietic stem cells (HSCs) t
120      This is perhaps best exemplified in the layering, or lamination, of the retinal inner plexiform
121 l positions to constitute the inside-outside layering order of cortical lamination.
122 y layered rocks, some of which have a strong layering-parallel foliation, confirm a long-held belief
123 usly that instead of the normal "inside-out" layering pattern of cortical neurons, cortical neurons a
124 the dentate gyrus is formed in an outside-in layering pattern that may extend through adulthood.
125 rphology, generating highly ordered periodic layering patterns.
126 g sites and C3G activation causes an unusual layering phenotype.
127                                          The layering proceeds radially inward from the outer surface
128 mechanism leading to the pinning and surface layering provides new insight into the role of alloying
129                                      Correct layering requires an extracellular protein, Reelin (Reln
130  Hence, our findings suggest that inside-out layering requires distinct functions of Reelin and p35/C
131            Age-depth relations from internal layering reveal a large region of rapid basal melting in
132 ion of hippocampal, cortical, and cerebellar layering reveals that the NFDNPVY sequence of Apoer2 is
133 15 K or approximately 30 K, depending on the layering sequence.
134 ing specific 2D building blocks and specific layering sequences of van der Waals heterostructures sho
135  of the trend of transition temperature with layering structure in the Ca-spaced compounds and to pre
136                                          The layering structure of a painting contains a wealth of in
137                     This unique hierarchical layering structure of graphene films provides great poss
138                       Surface-induced atomic layering, the hallmark of liquid metals, is also found b
139          This fragile smectic liquid crystal layering, the material with the simplest positional orde
140 ow that shear thinning can be decoupled from layering, thereby eliminating layering as the driver for
141 of an amorphous reaction intermediate if the layering thickness is less than 35 A.
142  the Reln gene, results in abnormal neuronal layering throughout several regions of the brain.
143 state made possible by spatial limitation of layering to a periodic array of nanoscale filaments.
144 us and does not necessarily require a global layering to have occurred at the time of the comet's for
145           Multiple healed rupture sites with layering were frequently found in segments with acute an
146 parable stratified graft with a 2- to 3-cell layering, which compared similarly to AM cultures.
147 te that the density variation induced by the layering will cause xenon, confined to an approximately
148 THF solution followed by crystallization via layering with hexane under N2.
149 id-solid phase transition producing regional layering, with the possibility of large-scale variations
150 e outer plexiform layer, cell body size, and layering within the inner nuclear layer and by the morph
151  into solution organize radial compositional layering within the tube wall, a mechanism studied on a

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