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1 ant role in regulating acid secretion in the kidney collecting duct.
2 L are coexpressed in epithelial cells of the kidney collecting duct.
3 ence exists for active urea transport in the kidney collecting duct.
4 ndent fibrotic signaling within cells of the kidney collecting duct.
5 water pores in principal cells that line the kidney-collecting duct.
6 he apical membrane of principal cells in rat kidney collecting ducts.
7 nes of barrier epithelia such as bladder and kidney collecting duct, a feature essential to barrier f
8                         PAR2 is expressed in kidney collecting ducts, a main site of control of Na(+)
9 agonist-stimulated Na(+) reabsorption in the kidney collecting duct, acting to enhance Na(+),K(+)-ATP
10 ateral plasma membrane of principal cells in kidney collecting duct, airway epithelium, and gastric p
11 lateral plasma membranes of epithelia in the kidney collecting duct, airways, stomach, and colon.
12  in the outer and inner medulla, in isolated kidney collecting ducts, and in cultured outer and inner
13 ulates the osmotic water permeability of the kidney collecting duct by inducing exocytotic insertion
14 e uptake of fluorescently loaded ECVs into a kidney collecting duct cell line (mCCDC11) and into prim
15 ly stimulated ENaC-mediated Na+ current in a kidney collecting duct cell line, although GILZ2 and GIL
16 undantly expressed in mouse kidney and mouse kidney collecting duct cells (mpkCCD14).
17           Deleting this gene specifically in kidney collecting duct cells prevents cilia formation an
18                 Here we showed that in mouse kidney collecting duct cells, claudin-4 functioned as a
19                                           In kidney collecting duct cells, filamentous actin (F-actin
20 ation induced by desmopressin stimulation of kidney collecting duct cells.
21 s as a result of an autoimmune insult on the kidney collecting duct cells.
22 D in association with autoantibodies against kidney collecting duct cells.
23 uaporin 2 (AQP2) water channel, expressed in kidney collecting ducts, contributes critically to water
24 wth of cysts generated by Madin-Darby canine kidney collecting duct-derived cells in three-dimensiona
25               Thus, talins are essential for kidney collecting duct development through mechanisms th
26 thelial sodium channel (ENaC) present in the kidney collecting duct, distal colon, and the lung is re
27 ased ENaC current in Fischer rat thyroid and kidney collecting duct epithelia.
28 ressed at the basolateral plasma membrane of kidney collecting-duct epithelial cells.
29 ostcapillary venules, the epithelial cell of kidney collecting ducts, lung alveoli, and the Purkinje
30                         In this study murine kidney collecting duct (mCCDC11) cells were used to demo
31  plasma membrane accumulation of AQP2 in rat kidney collecting duct principal cells in situ, and in s
32      We found that HDAC7 is expressed in the kidney collecting duct, supporting a potential role for
33  normally associated with the differentiated kidney collecting duct system including the water channe
34 ystic dilation of the cortical and medullary kidney collecting duct system, a phenotype resembling in
35 ishable from that in basolateral membrane of kidney collecting duct; the E-face showed corresponding
36 n cornea, oral mucosa, esophagus, intestine, kidney collecting ducts, ureter, bladder, urethra, and t
37 + absorption across epithelia, including the kidney collecting duct, where it plays a critical role i
38 rin 2 (AQP2) is a water channel found in the kidney collecting duct, where it plays a key role in con

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