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1 ulae the keel is perforated by open windows (fenestrae).
2 , its snout and lower jaw show large cranial fenestrae.
3 arly signs of endothelial injury and loss of fenestrae.
4  morphology and ontogeny of the portulae and fenestrae.
5  cytoplasmic protrusions through endothelial fenestrae.
6 rentiated LSECs is the presence of permeable fenestrae.
7  networks were reduced and their SECs lacked fenestrae.
8 organelles and the diaphragms of endothelial fenestrae.
9  role in the passage of proteins through the fenestrae.
10 phragms and increased density of hypophyseal fenestrae.
11   We also collected data on the life span of fenestrae.
12 O mice had a significantly reduced number of fenestrae.
13  associated with a change in the diameter of fenestrae and can be interpreted as a component of the "
14 rocess leading to the formation of apertured fenestrae and channels are also described in fenestrated
15 Notch1(lox/lox) mice had reduced endothelial fenestrae and developed portal hypertension and hepatic
16                              Until recently, fenestrae and fenestrae-associated structures were mainl
17 entation, we map protein distribution at SPB fenestrae and interrogate protein-protein interactions w
18 ultures of LSECs prevented the loss of their fenestrae and maintained the expression levels of Gata4
19 ndothelial swelling with loss of endothelial fenestrae and occlusion of the capillary lumens.
20 to monitor the position, size, and number of fenestrae and sieve plates using four-dimensional AFM (X
21 ecognizes specifically the diaphragms of the fenestrae and the stomatal diaphragms of caveolae and tr
22        Loss of diaphragms did not affect the fenestrae and transendothelial channels formation but di
23 ion of the diaphragms of caveolae as well as fenestrae and transendothelial channels.
24 eticulum (ER) connects daughter cells across fenestrae, and as the cell plate matures, fenestrae cont
25 the ultrastructure of glomerular endothelial fenestrae appeared entirely normal.
26                                      Second, fenestrae are absent from cis cisternae, but are present
27                              When all of the fenestrae are closed, the new cell wall is complete.
28                                              Fenestrae are dynamic structures that can contract or di
29               We demonstrate that glomerular fenestrae are filled with dense negatively charged polys
30                                              Fenestrae are small pores in the endothelium of renal gl
31 e two structures separate to lie in distinct fenestrae as a bipolar spindle forms.
32 agms, and swollen endothelial cells with few fenestrae as revealed by transmission electron microscop
33                Until recently, fenestrae and fenestrae-associated structures were mainly investigated
34 though decades of studies have characterized fenestrae at the ultrastructural level, little is known
35  Through metaphase, the SPBs remain in their fenestrae, bound to the polar ends of spindle MTs; at ab
36                               Contraction of fenestrae by serotonin was inhibited by chelation of ext
37 e span, formation, and disappearance of LSEC fenestrae; by doing so, we also gathered evidence on thr
38            As anaphase proceeds, the nuclear fenestrae close, and the SPBs are extruded back into the
39 ss fenestrae, and as the cell plate matures, fenestrae contract, causing the plasma membrane (PM) to
40 rther stabilize nascent plasmodesmata during fenestrae contraction.
41 , little is known on the mechanisms by which fenestrae form.
42 eolae formation, glomerular endothelial cell fenestrae formation in vivo does not require caveolin-1,
43 ells (IOCs) autonomously deposit collagen at fenestrae, forming rigid, tension-resisting grommets.
44        We observed also the dawn and rise of fenestrae-forming centers and defenestration centers in
45                   The ER's presence prevents fenestrae fusion, forming plasmodesmata, whereas its abs
46                       The small sizes of the fenestrae have so far prohibited any functional analysis
47 d gain, particularly in relation to bars and fenestrae, have led to a variety of hypotheses concernin
48 examined by scanning electron microscopy for fenestrae in sieve plates.
49  architecture and the ordered arrangement of fenestrae in sieve plates.
50 s from the dermis to the epidermis via small fenestrae in the sub-epidermal collagen fibril layer; mo
51 toreceptors as they exit the retina, forming fenestrae in this new, laminin-rich BM.
52   Previous reports indicate that endothelial fenestrae in vitro can form by fusion of caveolae or cav
53 her formation of glomerular endothelial cell fenestrae in vivo similarly involves caveolae and caveol
54    These results suggest that contraction of fenestrae is associated with Ca2+ influx.
55                                          The fenestrae of liver sinusoidal endothelial cells (LSECs)
56 of VEGF and TGF-beta resulted in the loss of fenestrae on CP vasculature and thickening of the otherw
57 out the previous hypothesis that endothelial fenestrae represent fused caveolae, at least for glomeru
58 ull, including the antorbital and mandibular fenestrae, serrated teeth, and closed lower temporal bar
59                          This is mediated by fenestrae, specialized permeable pores in the endothelia
60           The number and distribution of the fenestrae suggest that they form at the edges of the med
61 mall upper and ventrally open lower temporal fenestrae, supporting the hypothesis of diapsid affiniti
62 ifferent pathways implemented in the loss of fenestrae that result in defenestrated LSECs.
63 ctural evidence on single laying and grouped fenestrae, thereby elucidating their dynamic nature from
64  cytosol, ions traverse one of four external fenestrae to enter the rotundal vestibule and then cross
65 ached MTs arise de novo over remaining large fenestrae to focus local growth to these regions.
66 hy, we mapped the transition from cell plate fenestrae to plasmodesmata.
67                              The response of fenestrae to serotonin was mimicked by addition of a Ca2
68 anelles implicated in vascular permeability: fenestrae, transendothelial channels, and caveolae.
69 lae and transendothelial channels as well as fenestrae upon PMA treatment.
70               The reduction in the number of fenestrae was associated with a change in the diameter o
71              Liver endothelial cells possess fenestrae, which are pores supported by a cytoskeleton r
72 tinct diapsids comprise an open framework of fenestrae (window-like openings) separated by bony strut
73 thelial cells, had CD31 immunoreactivity and fenestrae with diaphragms, but they had a branched pheno
74 ent of sieve plates affects the structure of fenestrae within them was recorded.
75 ct the prevailing concept that biogenesis of fenestrae would be PLVAP-dependent, and reveal previousl