ライフサイエンスコーパス: afferent arteriole

1 bular capillaries, and 0.85 for arteries and afferent arterioles).

2 ricted to the juxtaglomerular portion of the afferent arteriole.

3 are arranged as clusters at the tip of each afferent arteriole.

4 lotho(-/-) mice, which was present up to the afferent arterioles.

5 (JG) cells, located in the pole of the renal afferent arterioles.

6 d granulated cells located in the glomerular afferent arterioles.

7 d not induce significant vasoconstriction of afferent arterioles.

8 st pronounced in the most distal part of the afferent arterioles.

9 arcuate arteries and to the beginning of the afferent arterioles.

10 reased the diameters of the interlobular and afferent arterioles.

11 in preglomerular microvessels, predominantly afferent arterioles.

12 creases in diameters of the interlobular and afferent arterioles.

13 ing (juxtaglomerular) cells in the mammalian afferent arterioles.

14 n by transducing TGF-mediated signals to the afferent arteriole, a function that is independent of ni

15 trations, PAF dilates isolated microperfused afferent arterioles (Af-Art) via nitric oxide (NO).

16 Renal afferent arterioles (Aff) from angiotensin II (AngII)-in

17 mpairs acetylcholine-induced vasodilation of afferent arterioles (Aff) in AngII-induced hypertension

18 O2-) mediates enhanced contractions of renal afferent arterioles (Aff) of angiotensin II (Ang II)-inf

19 n constitutive accumulation of HIF-2alpha in afferent arterioles and glomerular cells and HIF-1alpha

20 ited impairments in the myogenic response of afferent arterioles and in renal blood flow autoregulati

21 e the recruitment of immunoreactive renin in afferent arterioles and in the juxtaglomerular apparatus

22 e smooth muscle cells, freshly isolated from afferent arterioles and interlobular arteries averaging

23 cture consisting of the nephron, glomerulus, afferent arteriole, and efferent arteriole.

24 10X for proximal/distal tubule, arteries and afferent arterioles, and 40X for peritubular capillaries

25 ed glomerular filtration rate, hyalinosis of afferent arterioles, and striped cortical tubulo-interst

26 effect on diameters of the interlobular and afferent arterioles at concentrations up to 1 microM.

27 st, 5,6-EET constricted the interlobular and afferent arterioles by 16 +/- 3% (N = 6) and 21 +/- 3% (

28 reased the diameters of the interlobular and afferent arterioles by 18 +/- 2% (N = 10) and 20 +/- 3%

29 preferentially vasoconstricts the glomerular afferent arterioles by depleting endothelial nitric oxid

30 wild-type littermate controls, an attenuated afferent arteriole constrictor response to endothelin-1

31 dministration of 10 muM S1P, the diameter of afferent arterioles decreased to 35%+/-5% of the control

32 With iodixanol, afferent arteriole diameters were significantly reduced

33 +]i responses to 40 mM K+ were suppressed in afferent arterioles from diabetic rats (delta = 63+/-5 n

34 In perfused afferent arterioles from mouse kidney, adenosine and the

35 Afferent arterioles from rats and P2X1 KO mice were exam

36 (3 to 300 microM) had virtually no effect on afferent arterioles from sham rats; however, this K(ATP)

37 bar and arcuate arteries in the fetus to the afferent arterioles in the adult was observed.

38 e of the BSC2 protein at the juxtaglomerular afferent arteriole, in a juxtaglomerular structure proba

39 I-ANG II binding studies on freshly isolated afferent arterioles indicated that ANG II receptor densi

40 at the constriction response to adenosine in afferent arterioles is mediated by A1AR coupled to a PTX

41 In afferent arterioles isolated by microdissection from Sha

42 In contrast with LacZ-positive cells in the afferent arterioles, LacZ-positive cells in the glomerul

43 elective labeling of renin cells along renal afferent arterioles of adult mice.

44 -type numbers of renin-producing cells along afferent arterioles of the glomeruli rather than by up-r

45 damide (1 microM) vasodilates juxtamedullary afferent arterioles perfused in vitro; the vasodilation

46 explain the increased tone and reactivity in afferent arterioles perfused with iodixanol.

47 Diameters of interlobular and afferent arterioles preconstricted with 0.5 microM norep

48 AngII causes constriction of the afferent arteriole primarily by stimulation of calcium e

49 alpha1-resistant/alpha2-resistant mice, and afferent arteriole responsiveness again was confirmed by

50 TGF-induced vasoconstriction of the afferent arteriole results from the enhanced effect of s

51 he functional connection between tubules and afferent arterioles (so-called tubuloglomerular feedback

52 Adenosine induces vasoconstriction of renal afferent arterioles through activation of A1 adenosine r

53 ubule perfusate confirmed the ability of the afferent arteriole to contract in the presence of ouabai

54 The contractile response of isolated afferent arterioles to adenosine was normal in e-5'NT/CD

55 seven types of renin distribution along the afferent arterioles were identified.

56 highly expressed near the glomerulus, in the afferent arteriole, where it may also dilate renal arter

57 s the glomerular filtration rate by dilating afferent arterioles while constricting efferent arteriol

58 ype 1B (AT(1B)) subtypes in freshly isolated afferent arterioles, while there was very little AT2 rec