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1 ular layer and varying flow loss in the deep vascular plexus.
2 he formation of an adequate and stable brain vascular plexus.
3 graphy and, to a lesser extent, in the inner vascular plexus.
4  to influence the maturation of the coronary vascular plexus.
5 re prominent alterations in the deep retinal vascular plexus.
6 ile severely impairing formation of the deep vascular plexus.
7 rticularly during formation of the secondary vascular plexus.
8 nd ventrally from the surrounding perineural vascular plexus.
9 se each lobular area of the choriocapillaris vascular plexus.
10 efects in the reorganization of the yolk sac vascular plexus.
11 s early angiogenic remodeling of the primary vascular plexus.
12 e retinal postcapillary venules of the inner vascular plexus.
13 nt and in angiogenic remodeling of the early vascular plexus.
14 yos revealed normal formation of the primary vascular plexus.
15 units with capillaries in 2 of the 3 retinal vascular plexuses.
16 entation and highly branched organization of vascular plexuses.
17 larged vascular sinuses rather than branched vascular plexuses.
18 tterning of the superficial and deep retinal vascular plexuses.
19 ll motion are observed during formation of a vascular plexus: (1) global tissue deformations that pas
20 heet-like medial translocation of the entire vascular plexus; (3) structural rearrangements, such as
21  incomplete formation of the retinal primary vascular plexus, absence of the deep plexi, and persiste
22 ailed to localize at the leading edge of the vascular plexus and at vascular branchpoints.
23 gamma3-null (Lamc3(-/-)) retinal superficial vascular plexus and consequently the vascular branching
24 e expression of specific genes in the entire vascular plexus and retina.
25 s led to a central amalgamation of the inner vascular plexus and the deep vascular plexus, which appe
26           Mechanisms of stabilization of the vascular plexus and the role of mechanotransduction in t
27 ls, along the central-peripheral extent of a vascular plexus, and among different vascular laminae.
28 opodial extension, growth of the superficial vascular plexus, and astrocyte remodeling.
29 iate, but failed to organize normally into a vascular plexus, and smooth muscle cells did not differe
30 , adhered to the newly formed subventricular vascular plexus, and then divided into daughter cells.
31                Mechanisms that stabilize the vascular plexus are not well understood.
32 al cells in the lung, including those in the vascular plexus around the airways.
33 of BEVs at the leading edge of the advancing vascular plexus as measured by the decrease in luminal t
34          Branching of vessels in the primary vascular plexus, as well as appropriate localization of
35     This progressively extended to the outer vascular plexus at day 9 pi.
36  began at day 8 pi and extended to the outer vascular plexus at day 9 pi.
37  at the growing front and stalk cells in the vascular plexus behind the front.
38 matched, with a mean proportion of the inner vascular plexus being 95.3% (95% CI, 92.2%-97.8%) vs 4.7
39 ring angiogenic sprouting of the superficial vascular plexus but also showed impaired vessel branchin
40 ss of capillary density in the inner retinal vascular plexus but many more prominent alterations in t
41 n animal models of bile duct and peribiliary vascular plexus damage.
42 sions and Relevance: By presenting 3 retinal vascular plexuses distinctly, PR-OCTA reveals capillary
43 icial vascular plexus (SVP) and deep retinal vascular plexus (DVP).
44 heless, development of an organized yolk sac vascular plexus failed in Yap-/- embryos.
45  same areas of altered inner and absent deep vascular plexus flow signal.
46 tion to altered inner plexus and absent deep vascular plexus flow.
47 egation of angioblasts to form the primitive vascular plexus, followed by the proliferation, differen
48 ls, whose absence results in delayed nascent vascular plexus formation and under-development of the c
49 130a enhancement were mirrored by changes in vascular plexus formation around the terminal airways.
50 topic expression along the notochord induces vascular plexus formation at midline.
51 tochord ablation in quail embryos results in vascular plexus formation at midline.
52  reduces radial endothelial migration during vascular plexus formation in a gene dose-dependent manne
53 itic mesoderm and neural tube also supported vascular plexus formation, indicating that the neural tu
54 d three dimensional (3D) architecture of the vascular plexus forming at the regenerating wound tissue
55    Correlation among pericyte coverage, deep vascular plexus growth, and hypoxia after LeTx treatment
56 eart, form through remodeling of an immature vascular plexus in a process triggered and shaped by blo
57                    Formation of the coronary vascular plexus in Gpc3-deficient embryos was delayed co
58 uperficial vascular plexus included the deep vascular plexus in the central macula for all 3 instrume
59  which presomitic mesoderm explants formed a vascular plexus in the presence of added VEGFA.
60 ects in remodeling of the primitive coronary vascular plexuses in the Cx43 KO heart.
61 ers revealed the presence of 2 to 4 distinct vascular plexuses in the retina, depending on location r
62 o vessel formation, in the initial embryonic vascular plexus, in the growing blood vessels during ang
63 ion slab designed to isolate the superficial vascular plexus included the deep vascular plexus in the
64  embryos, endothelial cells formed a primary vascular plexus indicative of intact vasculogenesis but
65                              Maturation of a vascular plexus is a critical and yet incompletely under
66 at formation of a VEGF-directed, intra-islet vascular plexus is required for development of islet inn
67 anatomical deficiencies, including lack of a vascular plexus, leading to slower vascularization after
68 y, extent of hypoxia, and growth of the deep vascular plexus network.
69 rization, vascularization of the peribiliary vascular plexus (PBVP), and constriction of hepatic arte
70 l(s) that direct formation of the perineural vascular plexus (PNVP) that encompasses the neural tube
71  the subsequent formation of the peri-neural vascular plexus (PNVP), a vascular network that surround
72 eased endothelial cell maturation, disrupted vascular plexus remodeling and lack of later stages of v
73           Development and stabilization of a vascular plexus requires the coordination of multiple si
74 ngineered genetically were able to recruit a vascular plexus, showing that the neural tube is the sou
75  also observed a profusion of large coronary vascular plexuses subepicardially.
76  following the establishment of a functional vascular plexus such as in models of wounding or tumour
77 ouse that endocardial cells form a primitive vascular plexus surrounding the liver bud and subsequent
78 nd fractal dimension (FD) at the superficial vascular plexus (SVP) and deep retinal vascular plexus (
79 ng this model, we show that a subventricular vascular plexus (SVP) extends through a hindbrain germin
80 cula, an area where the superficial and deep vascular plexuses terminate.
81                                          The vascular plexus that is initially formed is then remodel
82 pment begins with the formation of a primary vascular plexus that is rapidly remodeled by angiogenesi
83 und in trunk vessels, such as the perineural vascular plexus, the cardinal vein, and presumptive inte
84                            The inner retinal vascular plexus, the outer plexus, and deeper vascular i
85 ual angioblasts coalesce to form the primary vascular plexus through a process called vasculogenesis.
86 assively into the brain parenchyma from pial vascular plexuses to meet metabolic needs of growing neu
87 mography angiography (OCTA) blur the retinal vascular plexuses together and limit visualization of th
88 ntation, studies of the superficial and deep vascular plexuses using manufacturer-recommended default
89 cans and the proportion of the inner retinal vascular plexus vs the outer retinal capillary plexus as
90  endothelium of retinal venules of the inner vascular plexus was first observed at day 6 pi.
91                           The inner and deep vascular plexus were analyzed in relation to cystoid mac
92                           The inner and deep vascular plexus were analyzed in relation to structural
93 from endothelial cells that form a primitive vascular plexus which recruits smooth muscle cells to fo
94 on of the inner vascular plexus and the deep vascular plexus, which appeared to be in a state of decl
95 ity and vascular coverage in the superficial vascular plexus, while severely impairing formation of t

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