ライフサイエンスコーパス: apical pole

1 orces to push the centrosome toward the cell apical pole.

2 ly by stimulation of membrane patches at the 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 deferens contain abundant V-ATPase in their apical pole and are responsible for acidifying the lumen

12 The initiation site of Ca(2+) wave at the apical pole and the pattern of wave propagation were ind

13 ral asymmetric localization to the merozoite apical pole and the posterior pole.

14 ion elicited a Ca2+ wave that started in the apical pole and then spread toward the base.

15 ear cells contain abundant V-ATPase in their apical pole, and an increase in their cell-surface V-ATP

16 pt base : surface gradient of APC within the apical pole/apical-lateral membranes at day 6.

17 nin, and bombesin signaling complexes at the apical pole are much more sensitive to stimulation than

18 ork highlights the importance of specialized apical pole disassembly for the repolarization of epithe

19 Initially, SpNK2.1 is restricted to the apical pole domain by beta-catenin-dependent processes o

20 GAC localizes to the apical pole in invasive stages of Toxoplasma gondii and

21 MLC-B localizes to the same extreme apical pole in the cell as MyoB, and the two proteins fo

22 gan as Ca2+ waves that were initiated at the apical pole, in the region of the type III InsP3 recepto

23 elicited local cytosolic Ca2+ spikes in the apical pole more than 15 microm away from the site of st

24 Gpbar1 is expressed at the apical pole of acinar cells and its genetic deletion is

25 and TLR4 are constitutively expressed at the apical pole of differentiated T84 cells.

26 ere phagocytized by mononuclear cells on the apical pole of epithelial cells.

27 g detected the H-K-ATPase exclusively on the apical pole of gastric parietal cells in Slc26a9(-/-) mi

28 es, mechanosensory structures located at the apical pole of hair cells in the inner ear.

29 upled dipeptide transporter localized at the apical pole of mouse small intestinal isolated enterocyt

30 of these proteins are also expressed at the apical pole of other epithelial cells, the parietal cell

31 he activation of beta1-integrins orients the apical pole of polarized cysts via a mechanism that requ

32 Arf1 was localized both at the apical pole of proximal tubule epithelial cells, but als

33 n, TIP39 and tuftelin immunolocalized to the apical pole of secretory ameloblasts (Tomes' processes)

34 at highest levels by endodermal cells at the apical pole of the body column just inferior to the base

35 a result of increased ligand release at the apical pole of the cell.

36 It does not block membrane retrieval at the apical pole of the hair cells, nor does it elicit the ex

37 polarization, and CLDN1 relocalized from the apical pole of the lateral cell membrane to the lateral

38 rocess effacement, nephrin dislocates to the apical pole of the narrowed filtration slits and also th

39 port proteins and channels must occur at the apical pole of the parietal cell.

40 y act to stimulate membrane insertion at the apical pole of these cells.

41 esent primarily in transport vesicles at the apical pole of tracheal epithelial cells, predicting tha

42 As the apical pole of transition stage embryos shows both morph

43 id-phase dextran are cointernalized from the apical poles of Madin-Darby canine kidney cells, they en

44 he most responsive complexes confined to the apical pole, probably to restrict the Ca2+ signals to th

45 e role of the cytoskeleton in supporting the apical pole remodeling, which appears to be necessary fo

46 In the apical pole there is a common early activation site for

47 elease sites in the granule-rich area in the apical pole to the basal part of the cell containing the

48 demonstrate that TLRs are positioned at the apical pole where they are poised to monitor the sensiti

49 ceptors and the Ca2+ release channels in the apical pole, whereas the other postulates long distance