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1 and fusion during the secretory cycle of the gastric parietal cell.
2 e membrane trafficking and acid secretion in gastric parietal cells.
3 uter medullary collecting duct (OMCD) and in gastric parietal cells.
4 ing tubulovesicles to the apical membrane of gastric parietal cells.
5 dney outer medullary collecting duct and the gastric parietal cells.
6 tly expressed on the basolateral membrane of gastric parietal cells.
7 tially distributed to the apical membrane of gastric parietal cells.
8 egulators, IQGAP1 and IQGAP2, are present in gastric parietal cells.
9 that contain the H,K-ATPase in unstimulated gastric parietal cells.
10 ows for activation of polarized secretion in gastric parietal cells.
11 bly blocking ATP4A, a P-type H+/K+ ATPase in gastric parietal cells.
12 SCAR) located on the basolateral membrane of gastric parietal cells.
13 ly identified one such protein in studies of gastric parietal cells.
14 roton pump responsible for acid secretion by gastric parietal cells.
15 entified a 78 kDa AKAP which was enriched in gastric parietal cells.
16 and membrane remodeling processes typical of gastric parietal cells.
18 polarized distribution of actin isoforms in gastric parietal cells and association of gastric ezrin
20 ts demonstrate that ezrin is a major AKAP in gastric parietal cells and may function to tether type I
21 apical membrane-cytoskeletal interactions in gastric parietal cells and thereby causes hypochlorhydri
22 /K(+) ATPase characteristic of the mammalian gastric parietal cell, and the molecular mechanisms of a
23 se bearing a transgenic TCR specific for the gastric parietal cell antigen, H(+)K(+)-ATPase, to induc
24 AQP1 in intrahepatic cholangiocytes, AQP4 in gastric parietal cells, AQP3 and AQP4 in colonic surface
26 dney collecting duct, airway epithelium, and gastric parietal cells, as well as in astrocytes and ske
27 iously, AKAP120 was identified from a rabbit gastric parietal cell cDNA library; however, a monoclona
30 of acid-secreting cells similar to mammalian gastric parietal cells has been identified by a unique u
32 H-K-ATPase exclusively on the apical pole of gastric parietal cells in Slc26a9(-/-) mice, in contrast
36 The H,K-adenosine triphosphatase (ATPase) of gastric parietal cells is targeted to a regulated membra
40 ed the MHC class II molecule presentation of gastric parietal cell (PC)-specific H(+)/K(+)-ATPase, wh
41 2A), zinc transporter 8, thyroid peroxidase, gastric parietal cells (PCAs), tissue transglutaminase,
42 tamoxifen leads to apoptosis of >90% of all gastric parietal cells (PCs) and metaplasia of zymogenic
43 te that Hip1r is abundantly expressed in the gastric parietal cell, predominantly localizing with F-a
44 These mice develop autoantibodies to the gastric parietal cell proton pump, H/K ATPase, and aberr
46 H+/K(+)-ATPase is the proton pump in the gastric parietal cell that is responsible for gastric ac
48 of Trpml1 and its role in acid secretion by gastric parietal cells were analyzed using biochemical,
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