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1 ly by stimulation of membrane patches at the apical pole.
2 orces to push the centrosome toward the cell apical pole.
3  signaling proteins, including GPCRs, at the apical pole.
4 t calcium-dependent membrane uptake at their apical pole.
5 ited preferential entry and release from the apical pole.
6 nd why the waves are always initiated at the apical pole.
7  proteins next to the plasma membrane at the apical pole.
8 s the type III receptor was localized to the apical pole.
9   Basal acidification was slower than at the apical pole.
10 li with associated glycocalyx located at the apical pole.
11 half of those divisions happen away from the apical pole.
12 ntrating several secretory organelles at the apical pole.
13  deferens contain abundant V-ATPase in their apical pole and are responsible for acidifying the lumen
14    The initiation site of Ca(2+) wave at the apical pole and the pattern of wave propagation were ind
15 ral asymmetric localization to the merozoite apical pole and the posterior pole.
16 ion elicited a Ca2+ wave that started in the apical pole and then spread toward the base.
17 ear cells contain abundant V-ATPase in their apical pole, and an increase in their cell-surface V-ATP
18 pt base : surface gradient of APC within the apical pole/apical-lateral membranes at day 6.
19 nin, and bombesin signaling complexes at the apical pole are much more sensitive to stimulation than
20 helial glandular architecture with an inward apical pole delineating a luminal cavity.
21 ork highlights the importance of specialized apical pole disassembly for the repolarization of epithe
22      Initially, SpNK2.1 is restricted to the apical pole domain by beta-catenin-dependent processes o
23                         GAC localizes to the apical pole in invasive stages of Toxoplasma gondii and
24          MLC-B localizes to the same extreme apical pole in the cell as MyoB, and the two proteins fo
25 gan as Ca2+ waves that were initiated at the apical pole, in the region of the type III InsP3 recepto
26 llular redistribution of PKA activity to the apical pole, increased CFTR phosphorylation, and establi
27  elicited local cytosolic Ca2+ spikes in the apical pole more than 15 microm away from the site of st
28                   Gpbar1 is expressed at the apical pole of acinar cells and its genetic deletion is
29 and TLR4 are constitutively expressed at the apical pole of differentiated T84 cells.
30 ere phagocytized by mononuclear cells on the apical pole of epithelial cells.
31 g detected the H-K-ATPase exclusively on the apical pole of gastric parietal cells in Slc26a9(-/-) mi
32 es, mechanosensory structures located at the apical pole of hair cells in the inner ear.
33 upled dipeptide transporter localized at the apical pole of mouse small intestinal isolated enterocyt
34  of these proteins are also expressed at the apical pole of other epithelial cells, the parietal cell
35 he activation of beta1-integrins orients the apical pole of polarized cysts via a mechanism that requ
36               Arf1 was localized both at the apical pole of proximal tubule epithelial cells, but als
37 n, TIP39 and tuftelin immunolocalized to the apical pole of secretory ameloblasts (Tomes' processes)
38 at highest levels by endodermal cells at the apical pole of the body column just inferior to the base
39  a result of increased ligand release at the apical pole of the cell.
40 mples revealed annexin A13 expression at the apical pole of the Eustachian tube epithelium as well as
41  It does not block membrane retrieval at the apical pole of the hair cells, nor does it elicit the ex
42 polarization, and CLDN1 relocalized from the apical pole of the lateral cell membrane to the lateral
43 rocess effacement, nephrin dislocates to the apical pole of the narrowed filtration slits and also th
44 port proteins and channels must occur at the apical pole of the parietal cell.
45 y act to stimulate membrane insertion at the apical pole of these cells.
46 esent primarily in transport vesicles at the apical pole of tracheal epithelial cells, predicting tha
47                                       As the apical pole of transition stage embryos shows both morph
48 id-phase dextran are cointernalized from the apical poles of Madin-Darby canine kidney cells, they en
49 he most responsive complexes confined to the apical pole, probably to restrict the Ca2+ signals to th
50 e role of the cytoskeleton in supporting the apical pole remodeling, which appears to be necessary fo
51                                       In the apical pole there is a common early activation site for
52 elease sites in the granule-rich area in the apical pole to the basal part of the cell containing the
53  demonstrate that TLRs are positioned at the apical pole where they are poised to monitor the sensiti
54 ceptors and the Ca2+ release channels in the apical pole, whereas the other postulates long distance