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1 so expressed in thick ascending limb and the macula densa.
2 marily adjusting transport downstream of the macula densa.
3 ortant in its highly specialized role in the macula densa.
4 helial cells of the thick ascending limb and macula densa.
5 ck ascending limb of Henle's loop and of the macula densa.
6 , with the most pronounced expression in the macula densa.
7 old in the cortical thick ascending limb and macula densa.
8 immunoreactive COX-2 expression inthe cTALH/macula densa.
9 r upregulation of NOS1beta expression in the macula densa affects sodium excretion and salt-sensitive
10 onship between (a) NaCl concentration at the macula densa and (b) glomerular filtration rate or glome
11 at tubular epithelial cells located near the macula densa and associated with the renal arterioles ex
13 a is a primary NOS1 isoform expressed in the macula densa and regulates the tubuloglomerular feedback
14 nal cortex, COX-2 expression is localized to macula densa and surrounding cortical thick ascending li
15 ocalized to cTALH cells in the region of the macula densa, and that dietary salt restriction increase
17 lar elements involves ATP release across the macula densa basolateral membrane through a maxi-anion c
18 These results indicate that AngII stimulates macula densa basolateral Na/H exchange via AT1 receptors
19 p38 stimulates COX-2 expression in cTALH and macula densa by transcriptional regulation predominantly
21 activity or expression we clonally derived a macula densa cell line (MMDD1 cells) from SV-40 transgen
28 rabbit kidney, the intracellular pH (pHi) of macula densa cells was measured with fluorescence micros
29 neuronal isoform of nitric oxide synthase in macula densa cells, reduces the constrictor effect of ad
31 trated marked accumulation of elastin in the macula densa, collecting ducts, and pelvicalyceal epithe
33 In summary, these results demonstrate that macula densa COX-2 expression is oppositely regulated by
35 ice had decreased hyperfiltration, decreased macula densa cyclooxygenase-2 expression, decreased albu
36 al delivery of fluid yet does not activate a macula densa-dependent fall in SNGFR because it blunts t
38 lar epithelial cells at the perimeter of the macula densa exhibit spontaneous oscillations in intrace
40 ty NKCC2B contributes to salt absorption and macula densa function in the low NaCl concentration rang
43 luminal chloride [Cl(-)] at the level of the macula densa increases renin production and secretion, w
44 sed by a change in NaCl concentration at the macula densa, is likely initiated by the generation of a
45 that ATP consumed in active transport by the macula densa leads to formation of adenosine, which caus
46 Because of the presence of NKCC2A in the macula densa, maximum tubuloglomerular feedback response
50 nd G(olf) colocalize in renal tubules and in macula densa (MD) cells which modulate glomerular filtra
51 of neuronal nitric oxide synthase (nNOS) in macula densa (MD) cells, experiments were performed in a
53 TGF) depends on Na-K-2Cl co-transport in the macula densa (MD), but it is less clear whether Na,K-ATP
55 and/or cellular uptake of L-arginine limits macula densa nitric oxide generation and actions on tubu
63 lar cells that were within 100 microm of the macula densa plaque using four-dimensional multiphoton m
64 the thick ascending loop of Henle (TALH) and macula densa, providing the error signal for tubuloglome
65 Reducing luminal NaCl concentration in the macula densa region of the nephron stimulates renin secr
66 ited by changes in NaCl concentration in the macula densa region of the nephron, thereby serving as a
68 we discuss recent advances in understanding macula densa sensing and suggest these cells, in additio
69 tubuloglomerular feedback through increased macula densa sodium and chloride delivery, leading to af
72 tracellular calcium dynamics in cells of the macula densa, the observation was made that tubular epit
73 interrupt distal tubular fluid flow past the macula densa, thus minimizing tubuloglomerular feedback-
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