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1 al localization, with a stark absence at the basal membrane.
2  of caveolae-derived vesicles from apical to basal membrane.
3  control RPTC was limited exclusively to the basal membrane.
4 thelial trafficking, and exocytosis from the basal membrane.
5 red hepatocytes surrounded by a laminin-rich basal membrane.
6 primarily at the junction of the lateral and basal membrane.
7 branes and prominent in stress fibers on the basal membrane.
8 nd alpha 8 expression was accentuated at the basal membrane.
9 ellular tube to the leading filopodia of the basal membrane.
10 d upregulated immune markers adjacent to the basal membrane.
11 cal adhesions (FAs) that attach cells to the basal membrane.
12 systems for L-tryptophan in brush border and basal membranes.
13 on with less distribution on the lateral and basal membranes.
14 ontacts are reinforced along the lateral and basal membranes.
15                                    Thickened basal membrane(76.6%) and mesangial proliferation (53.5%
16  R252A (or R252E) mutants showed much higher basal membrane affinity and enzyme activity and faster s
17 m accounts for the fibrous topography of the basal membrane and allows for easy modulation of fiber s
18 ntified junctions that stabilize the forming basal membrane and enable basal cell closure.
19 e formation of junctions between the forming basal membrane and the yolk plasmalemma.
20  of ICAM-1 and caveolin-1 to the endothelial basal membrane and transmigrated through transcellular p
21 f specific cargoes to the apical, lateral or basal membranes and organize the cytoskeleton and intern
22 plan of any animal, possessing no organs, no basal membrane, and only four different somatic cell typ
23 a(+) transport, relocalization of CBI to the basal membrane, and the disappearance of CBI from the ap
24 population of epithelial cells, localizes to basal membranes, and specifically associates with elemen
25  ordered at the apical membranes compared to basal membranes, and that an inverse situation occurred
26 chanisms of net amino acid efflux across the basal membrane (BM) of the placental syncytiotrophoblast
27 encing pH-sensitive microelectrodes near the basal membrane by approximately 65% and 85% respectively
28 othelial growth factor (VEGF) secretion from basal membrane by inhibiting IGF-1 signaling and VEGF re
29 nction of LIN-2 is to localize LET-23 to the basal membrane domain of vulval precursor cells.
30 tion proteins (such as LET-23) to either the basal membrane domain or the cell junctions, and that mi
31 e show that TJ-mediated separation of apical-basal membrane domains is established prior to equilibra
32  shootwards (apical) (rather than rootwards (basal)) membrane domains.
33 on and bound to various extracellular matrix/basal membrane (ECM/BM) components, including collagen t
34 ity was required for contraction but not for basal membrane extension.
35 specifically on the microvilli of hepatocyte basal membranes, facing the space of Disse, where lipopr
36 t and inhibited by >90% by reduced pH in the basal membrane-facing solution.
37 ctivities and actomyosin cytoskeleton impact basal membrane fluctuations in adherent cells.
38 ding edge in human wounds, where it formed a basal membrane for endothelial cells and assisted neovas
39                                 We show that basal membrane function can be substituted in vitro by e
40 erent proliferative forms of anti-glomerular basal membrane (GBM) GN in rats were induced and whole c
41 splayed highly polarized localization at the basal membrane in the hypocotyl and root.
42 The channel was localized on the lateral and basal membranes in crypt cells.
43 ely expressed in neurons and is polarized to basal membranes in intestinal epithelial cells.
44 ial epithelial cells; reduced density of the basal membrane; lower density of keratocytes, increased
45 e lung where the protein concentrates in the basal membrane of alveolar Type I epithelial cells.
46 FNA2 human hearing loss, is expressed in the basal membrane of cochlear outer hair cells where it may
47     Unexpectedly, Lamc2 was deposited in the basal membrane of endothelial cells in blood vessels for
48 emidesmosome, the anchoring structure in the basal membrane of epithelial cells.
49 nsity lipoprotein receptors expressed on the basal membrane of hepatocytes.
50 lectively imaging dynamic processes near the basal membrane of live cells.
51 mains based on lipid-phase separation in the basal membrane of our cultured nonstimulated cells, and
52 ession of fibronectin and collagen IV in the basal membrane of pancreatic ducts and of cell clusters
53 that the IL-6 receptor was restricted to the basal membrane of Paneth cells both in vitro and in vivo
54 ressed tagged Inx7a localizes to the nascent basal membrane of the forming cells in wild-type eggs.
55 smic vesicles, and tubular extensions of the basal membrane of the invaded cells.
56 ptide OATP2B1 (SLCO2B1) are expressed in the basal membrane of the placental syncytiotrophoblast.
57        The isoform MCT3 is restricted to the basal membrane of the retinal pigment epithelium where i
58 ial in the testicular environment, where the basal membranes of adjacent polarized Sertoli cells form
59 O-1, were mislocalized along the lateral and basal membranes of fiber cells.
60 s expression co-localized with Col-IV in the basal membranes of juxtaposed endothelial cells.
61  method for studying dynamics at or near the basal membranes of living cells.
62 fficients of CD14 and TLR2 on the apical and basal membranes of macrophages using two fluorescence-ba
63 use eye, MFRP is localized to the apical and basal membranes of RPE and ciliary epithelium (CE).
64  prestressed mesh parallel to the apical and basal membranes of the cell.
65 (SGTP1 and SGTP4) and localized SGTP1 to the basal membranes of the tegument and the underlying muscl
66 e atypical cadherin Fat2 recruits the WRC to basal membranes of tricellular contacts where a new type
67      Polycystin-1 is highly expressed in the basal membranes of ureteric bud epithelia during early d
68 alysis revealed that XKir6.1 is localized to basal membranes on the blastocoel roof and cell-cell jun
69 pe or IP(3)R-knockout cells did not increase basal membrane permeability, but resulted in a substanti
70 tion of these and other findings is that the basal membrane possesses two systems, one of which is si
71  augments synaptic drive by depolarizing the basal membrane potential close to the action potential t
72  current contributed to the more depolarized basal membrane potential observed in VP neurons in the h
73 A, induces the receptor to distribute to the basal membrane, promotes cell proliferation, and alters
74 , that bound to various extracellular matrix/basal membrane proteins and was required for full virule
75 uced levels of several myelin-associated and basal membrane proteins compared with those of wild-type
76 escued the gland migration, lumen length and basal membrane protrusion defects and partially rescued
77 face is severely impaired, resulting in long basal membrane protrusions but little net movement or br
78  cells, and promotes extension of actin-rich basal membrane protrusions in the distal cells.
79 te, to downregulate E-cadherin and to extend basal membrane protrusions.
80 urfaces but was able to infect cells through basal membranes, replicate, and spread into surrounding
81 decrease in total iron transfer across their basal membrane seen in the mucosal block.
82 duals with the T594 M variant showed similar basal membrane slope conductance, compared with the wild
83  membrane and interacts genetically with the basal membrane-specific proteoglycan, Col18a1, pointing
84                 This transformation requires basal membrane-stimulated integrin signaling that coordi
85 ingival overgrowth, resulting in compromised basal membrane structure and increased interactions betw
86                                    Disrupted basal membrane structure in gingival overgrowth tissues
87 ly faster in the apical membrane than in the basal membrane, suggesting diffusion hindrance by the ad
88 sion, and peristromal lamina separation from basal membrane surfaces, as compared with control indexe
89 ntrolled by the stiffness of the lateral and basal membrane surfaces.
90                                       In the basal membrane, the diffusion coefficients obtained from
91                                              Basal membrane transport of L-tryptophan is more complex
92 lear evidence that two systems contribute to basal membrane transport since BCH is (in sodium-free me
93                       The disruption of pial basal membranes underlying the heterotopias and poor org
94                     However, staining at the basal membrane was weak.
95 asion to bronchial epithelium, and thickened basal membrane were found in same biopsy specimen.
96 eir mitochondria are highly localized at the basal membrane where EEC vesicle secretion occurs.
97  is mostly cytosolic and concentrated at the basal membrane, whereas galectin-3 tends to be concentra
98 ized to the apical membrane and TNFR1 to the basal membrane, whereas IFN-gammaR1 was detected on both
99 contracted, the myosin ring moved toward the basal membrane with ZO-1 and Rho-kinase.
100 uctural actin (DCSA), extends from apical to basal membranes, with frequent attachments.
101 an immunologic reaction against conjunctival basal membrane zone (BMZ) antigens.

 
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