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1 embling interdigitated foot processes at the basal surface.
2 two distinct steps, acute and obtuse, on the basal surface.
3 a concomitant increase in actomyosin on the basal surface.
4 , where it restricts protein delivery to the basal surface.
5 nner by promoting dendritic retention on the basal surface.
6 otal internal reflection fluorescence on the basal surface.
7 urface directly displaced podosomes near the basal surface.
8 adial glia/progenitor fibers toward the pial/basal surface.
9 esulting in rearrangement of contacts on the basal surface.
10 dge surfaces of kaolinite rather than to the basal surfaces.
11 the middle surface bisecting the apical and basal surfaces.
14 ne RGCs retards process outgrowth toward the basal surface and impairs apical polarity and adherens j
16 but the cell nuclei are not polarized to the basal surface and no lumen formation occurs, indicating
17 in a Triton-X-100-insoluble structure at the basal surface and that the staining of this structure is
18 s and their mitotic spindles parallel to the basal surface and undergo symmetric cell divisions in wh
19 face between the Co and Mo atoms on the MoS2 basal surface and we ascribe the higher activity to the
21 calcium-binding protein that is found on the basal surfaces and in the extracellular matrix of cells
22 rovilli, an increase in actin bundles at the basal surface, and a reduction in cell height without an
26 to show that the CFTR+ cell line (S9) had a basal surface ATP concentration that could be detected w
27 ls, which retain contact with the apical and basal surfaces but where basolateral proteins (LGL) beco
28 atively that the electroactivity of the HOPG basal surface can be significantly lowered by the adsorp
30 ribbon (rib) gene disrupt this coupling: the basal surface continues to extend towards its normal tar
31 eous oscillations in the contraction of cell basal surfaces develop in a subset of follicle cells.
32 ations compromised NHE3 activity by reducing basal surface expression and/or loss of basal transport
33 ectrin by small interference RNA reduces the basal surface expression of alphahTRPC4 and prevents the
34 ecreased constitutive shedding and increased basal surface expression of c-Kit, with diminished apopt
36 E cells, together with a concomitant loss of basal surface expression of monocarboxylate transporter
38 sfer localized stress from the apical to the basal surface globally, resulting in rearrangement of co
39 ing from hydroxyl functional groups, whereas basal surfaces have a permanent negative charge arising
40 T84d) to DN32.D3 cells was greater along the basal surface in comparison with the apical surface.
42 alpha6beta4 integrin is localized on the basal surface in structures referred to as type II hemid
45 involvement of Tf in Fe transport across the basal surface, laser scanning confocal microscopy with 3
46 m cells biotinylated at either the apical or basal surface localized membrane 25- and 27-kDa heat sho
49 are large protein complexes organized at the basal surface of cells, which physically connect the ext
50 ement complex C5b-9 assembles rapidly on the basal surface of cultured primary porcine RPE cells but
51 The protein remains at high levels on the basal surface of ectoderm cells but is temporarily reduc
53 sory neurons can be positioned either at the basal surface of epidermal cells, or enclosed within epi
54 sal plane pyrolytic graphite (BPPG), and the basal surface of highly oriented pyrolytic graphite (HOP
56 l adhesion-like clusters of integrins on the basal surface of imaginal disc epithelia and junctional
57 elial cell biology, nutrient delivery to the basal surface of intestinal epithelial cell membranes ma
58 displayed reduced O-glycosylation along the basal surface of larval wing imaginal discs, which was r
59 s ligand VCAM-1, of polarized T cells at the basal surface of lymphatic but not blood vessel endothel
60 beta 4 integrin subunits are present at the basal surface of many epithelial cells and serve as rece
65 ase variants were able to transcytose to the basal surface of rat and human BMEC in a manner dependen
66 lization of these receptors to the apical or basal surface of RPE cells was determined with immunocyt
68 racellular matrix, the T cell adheres to the basal surface of the bronchial epithelial cell using alp
69 all-trans retinol (ROL) was delivered to the basal surface of the cultured RPE by serum retinol-bindi
71 bumin was segregated from transferrin at the basal surface of the epithelial cells and did not coloca
72 rane stained positively for laminin, and the basal surface of the epithelial cells stained positively
73 a 2, and alpha 3 integrins, whereas only the basal surface of the epithelial cells, where they are in
75 that alphaSMA-expressing cells appear at the basal surface of the future epithelial cleft prior to bi
80 lls intercalate by first wedging between the basal surface of the outer epithelium but only insert ap
82 demonstrated that CD46 was polarized to the basal surface of the RPE along with beta1 integrin, show
85 ucted by sequentially seeding the apical and basal surfaces of acellular dermis with cultured human k
87 unctions, thereby effecting its release from basal surfaces of an infected epithelium to the apical o
88 AR proteins localize to either the apical or basal surfaces of cells prior to blastocoel formation; w
89 mobility in adsorbed water films on external basal surfaces of clay is similar to that in the near-su
91 isappear, numerous filopodia extend from the basal surfaces of epithelial cells, the space between th
94 nts demonstrated that MCO1 is located on the basal surfaces of the digestive system and Malpighian tu
95 i of progenitors move between the apical and basal surfaces of the neuroepithelium in phase with thei
96 tory) system, the cell bodies and apical and basal surfaces of the tracheal epithelium normally move
97 ed that ICAM-1 was present on the apical and basal surfaces of umbilical vein endothelium in vitro an
99 ct with the extracellular matrix defines the basal surface, setting in motion E-cadherin-mediated cel
101 demonstrates definitively that the pristine basal surface supports fast ET, and that ET is not confi
102 investigated by imaging the response of the basal surface to localized force application over the ap
103 r in transmission of the FGF signal from the basal surface to the rest of the cell or in the apical c
104 asurements at different locations across the basal surface, unambiguously revealing it to be highly e
105 cular surface of polarized cells, apical and basal surfaces were infected with wild-type virus or a g
106 t and ceased as laminin 111 localized to the basal surface, whereas dissemination of carcinoma cells
107 ere more sensitive when CPE-treated on their basal surface, whereas Vero cells were more sensitive wh
108 Misshapen decreases integrin levels at the basal surface, which may facilitate detachment of each c
109 reactivity ratio of biotite edge surfaces to basal surfaces, while acetate does not impact this relat
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