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1  within the cortical collecting duct and the connecting tubule.
2 y homologous nephron progenitor cell-derived connecting tubule.
3 f split-opened cortical collecting ducts and connecting tubules.
4 ion and K(+) secretion in principal cells of connecting tubule and collecting duct.
5 ted cells, a subtype of cells present in the connecting tubule and collecting ducts.
6 rin-dependent HCO(3)(-) secretion within the connecting tubule and cortical collecting duct, or gave
7 rption in distal tubule segments such as the connecting tubule and cortical collecting duct.
8 egments from the transition zone of the late connecting tubule and early cortical collecting duct dem
9 cell types of the nephron progenitor-derived connecting tubule and ureteric progenitor-derived collec
10 nit was more apically distributed within the connecting tubules and cortical collecting ducts of Pon3
11 he thick ascending limb of Henle's loop, the connecting tubule, and in some, but not all, cells of co
12 part of the distal convoluted tubule and the connecting tubule, and regulation results from the inter
13 ron, i.e., the distal convoluted tubule, the connecting tubule, and the cortical collecting duct.
14 n the late distal convoluted tubules (DCT2), connecting tubules, and collecting ducts.
15  from scRNA-seq pointed to proximal tubules, connecting tubules, and principal cells as likely cellul
16 ed syntaxin-4 mRNA in glomeruli, vasa recta, connecting tubules, and thin descending limbs of Henle's
17 cted rat cortical collecting ducts (CCD) and connecting tubules, but not in proximal tubules, medulla
18 e (segments S1-S3) and distal convoluted tub/connecting tubule cell sub-populations.
19 mmunofluorescence ANKRA is also expressed in connecting tubule cells and principal cells of collectin
20  gene expression, primarily in principal and connecting tubule cells and, to a lesser extent, in segm
21  B and non-A-non-B intercalated cells of the connecting tubule (CNT) and the cortical collecting duct
22 split-open distal convoluted tubule 2 (DCT2)/connecting tubule (CNT) from mice on NL or LS/LM diets.
23 beta1-subunit is also expressed in the renal connecting tubule (CNT), a segment of the aldosterone-se
24 I constituted 35% to 40% of all cells in the connecting tubule (CNT), cortical collecting duct (CCD),
25 dn1 double-knockout mice (DE(AC) ), and Edn1 connecting tubule/collecting duct-specific conditional k
26 studied four groups of mice: wild-type mice, connecting tubule/collecting duct-specific Dot1l conditi
27 sing Edn1, which encodes endothelin 1 in the connecting tubule/collecting duct.
28 bundance increased in principal cells of the connecting tubule/collecting ducts.
29             Pkd2 was highly expressed in all connecting tubules/collecting duct cell types and weakly
30 lower blood [K(+) ], more functional ENaC in connecting tubules/cortical collecting ducts, higher ami
31 absorption in the late distal convoluted and connecting tubules (DCT2/CNT) is initiated by Ca(2+) inf
32  AQP2 trafficking in cortical collecting and connecting tubules in parallel with an increase in urine
33 ed ASDN remodeling, involving a reduction in connecting tubule mass and attenuation of epithelial sod
34  most prominent in the distal convoluted and connecting tubules of the kidney.
35 rm the late distal convoluted tubule (DCT2), connecting tubule segments 1 and 2 (CNT1 and CNT2, respe
36 /NOTCH signaling, which expands the cortical connecting tubule with PCs and replaces acid-secreting a