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1 h the core of cytochrome bc complexes can be labyrinthine.
2                   MVS is ideal for prolonged labyrinthine activation because it mimics constant head
3 es, hexagonally packed cylinders, spots, and labyrinthine and lamellar patterns.
4 ly, Arnt(-/-) placentas show greatly reduced labyrinthine and spongiotrophoblast layers, and increase
5 ms, with increased calcification and reduced labyrinthine area.
6 he ultrastructural organization of the blood labyrinthine barrier (BLB) was investigated in the human
7                       Fractones consisted of labyrinthine BL projecting from SEL blood vessels to ter
8 ental defects included significantly reduced labyrinthine branching morphogenesis, widespread penetra
9 ts, having flattened twisting processes with labyrinthine cavities communicating with the extracellul
10                                        While labyrinthine cells are present in the mutant Tfeb placen
11 calize to the ND at the entry point into the labyrinthine channels and, like their vertebrate counter
12 l constraints on regeneration, forming fused labyrinthine channels containing epithelial cells reprog
13  and to reduced passage of proteins into the labyrinthine channels for uptake by endocytosis, suggest
14 gh an SD-like nephrocyte diaphragm (ND) into labyrinthine channels that are active sites of endocytos
15                             Twelve bilateral labyrinthine-defective (LD) subjects and twelve normal h
16         These defects include the failure of labyrinthine development, the dilation of maternal blood
17 spongiotrophoblast layers, and a decrease in labyrinthine development.
18 uch as stroke may masquerade as a peripheral labyrinthine disorder and conversely benign conditions s
19 trate this approach by imaging ferrimagnetic labyrinthine domains in a Gd/Fe multilayer with perpendi
20 (26):11676-11681, where the two enantiomeric labyrinthine domains of the gyroid are connected to the
21 m, with the minority components also forming labyrinthine domains whose geometry and topology changes
22 nd naturally occurring ionic currents in the labyrinthine endolymph fluid.
23 y the role of Igf2 in the development of the labyrinthine exchange membrane and its functional conseq
24                             Patients lacking labyrinthine function did not.
25 and dynamic physicochemical conditions, with labyrinthine habitats composed of particles.
26 RI sequences for internal auditory canal and labyrinthine imaging, review the relevant anatomy, and d
27 ycosylated and subsequently localized to the labyrinthine ingrowths of the transfer cell walls.
28  were composed almost entirely of cells with labyrinthine ingrowths; these also were present in fossi
29                               In addition to labyrinthine inputs, the majority of neurons in this reg
30                                  Thus, cross-labyrinthine interactions appear to play important roles
31 inol/quinone (Q/QH2) transfer emphasizes the labyrinthine internal structure of the complex, includin
32 ignificant reduction in the thickness of the labyrinthine layer of the placenta is observed in LBP-1a
33 eads to a failure to correctly elaborate the labyrinthine layer of the placenta.
34 s restricted to the pituitary and hCS to the labyrinthine layer of the placenta.
35 l structural improvement was observed in the labyrinthine layer that was disrupted in the SOCS3-defic
36          Defects in the morphogenesis of the labyrinthine layer were observed as early as 11.5 dpc.
37 ormation, and the formation of the placental labyrinthine layer.
38 al defects that alter the development of the labyrinthine layer.
39                    Computational modeling of labyrinthine lymphatic vasculature supported the observa
40 rophoblast marker Mash2 and decreases in the labyrinthine markers Tfeb and Gcm1.
41 interface, (ii) a discoid shape, and (iii) a labyrinthine maternofetal interdigitation.
42  of an acoustic metasurface based on tapered labyrinthine metamaterials.
43 lar microstructure and the slip-hindering of labyrinthine microstructure further enhances the strengt
44 e in-situ formation of a nano-scale lamellar/labyrinthine negative thermal expansion (NTE) phase with
45 ithelial sheet of ectoderm gives rise to the labyrinthine network of cells that constitutes the funct
46 ng valley polarization, which we infer to be labyrinthine or otherwise highly intricate, with feature
47  metasurface design approach with perforated labyrinthine path coil structure to manipulate the acous
48                            The medium in the labyrinthine path coils in this design is air, but not l
49 within the (111) drives the formation of the labyrinthine pattern and the associated topological defe
50 Pb(Zr(0.4)Ti(0.6))O(3) results in a maze, or labyrinthine pattern, featuring meandering stripe domain
51 romagnet, resulting in formation of a glassy labyrinthine pattern.
52 d inhibitor morphogens for stripe, spot, and labyrinthine patterns and confirm the model predictions
53 joined together, they can form aperiodic and labyrinthine patterns.
54 ditional mesophases such as the disconnected labyrinthine phase and the mixed bimeron-skyrmion phase,
55 sing the temperature, this highly degenerate labyrinthine phase undergoes an inverse transition where
56                           Striking circular, labyrinthine, polygonal, and striped patterns of stones
57 n and the remaining mutants did not have the labyrinthine portion of the placenta.
58 ef review we discuss new insights into these labyrinthine relationships.
59 l (suprainiac and nuchal torus) and temporal labyrinthine (semicircular canal) morphology with the Ne
60  of the placenta to vascularize and form the labyrinthine spongiotrophoblast.
61 tion, and electron ptychography, we reveal a labyrinthine structure comprising coexisting monoclinic
62  the form of complex stackable cisternae and labyrinthine structures adjoining the PM at junctional c
63 on by combining the hybrid metastuctures and labyrinthine structures.
64 nta without affecting differentiation of the labyrinthine syncytiotrophoblasts.
65        The mature striatum is divided into a labyrinthine system of striosomes embedded in a surround
66  data provide proof of concept of inducing a labyrinthine topology to treat SL.
67 zed exclusively to the apical surface of the labyrinthine trophoblast around maternal blood sinuses,
68 h their physiological inhibitor HAI-1 to the labyrinthine trophoblast cells in proximity to basement
69 vels in the embryo but at high levels in the labyrinthine trophoblast cells of the placenta.
70 ), a transcription factor critical for mouse labyrinthine trophoblast development.
71  cells and chorionic plate, and later in the labyrinthine trophoblast of the chorioallantoic placenta
72 ctoderm of the chorion, and subsequently the labyrinthine trophoblast of the chorioallantoic placenta
73 gene expression occurred specifically in the labyrinthine trophoblast of the mouse placenta, which co
74 ranscript (P0) specifically expressed in the labyrinthine trophoblast of the placenta leads to reduce
75 mice and rats with predominant expression in labyrinthine trophoblast.
76 ctional zone, and decreased proliferation of labyrinthine trophoblasts.
77  dpc in ectoplacental cone, giant cells, and labyrinthine trophoblasts.
78 at the BL located at the pial surface formed labyrinthine tube-like structures enclosing numerous fib
79 scribe the proposed metamaterial with hybrid labyrinthine units, which reveals the mechanism of coexi
80 nfers placental insufficiency with decreased labyrinthine vascularization, yielding no viable offspri
81 the use of an anti-uPARAP gapmer to induce a labyrinthine vasculature and attenuate SL formation.
82 ulated cell superimposition in vitro and the labyrinthine vasculature in vivo with attenuated SL.
83 t mice, induction of SL led to a distinctive labyrinthine vasculature, defined herein by twisted and
84 sruption of the maternal allele in mice, the labyrinthine volume was increased in a manner consistent
85 staining for ET-1 receptors in the placental labyrinthine zone in hypoxic compared to normoxic dams.
86 centomegaly with specific defects within the labyrinthine zone involved in maternal-fetal nutrient tr
87                                          The labyrinthine zone of the placenta is diminished in Plk2(
88 th an increase in the volume fraction of the labyrinthine zone responsible for nutrient exchange, whe
89 , as were the volume and surface area of the labyrinthine zone responsible for placental nutrient tra
90 rea of the fetal blood vessel network in the labyrinthine zone, suggesting that Acer2 deficiency resu
91 aternal vasculature in the junctional and/or labyrinthine zones in E12.5 placentas.