ライフサイエンスコーパス: juxtaglomerular

1 expected presence of the BSC2 protein at the juxtaglomerular afferent arteriole, in a juxtaglomerular

2 Macula densa (MD) cells of the juxtaglomerular apparatus (JGA) are salt sensors and gen

3 t 20-28 h, while Thy 1-positive cells in the juxtaglomerular apparatus (JGA) were sequestered from th

4 of renal glomeruli producing renin in their juxtaglomerular apparatus and by four times wild-type nu

5 in the renin-secreting granular cells of the juxtaglomerular apparatus and the collecting duct.

6 ecretion is important for the maintenance of juxtaglomerular apparatus architecture.

7 and provide evidence for a new role for the juxtaglomerular apparatus in the maintenance of the mesa

8 erized by hypertrophy and hyperplasia of the juxtaglomerular apparatus of the kidneys, aldosteronism

9 duction was similar in the isolated perfused juxtaglomerular apparatus of wild-type (WT) and nitric o

10 buloglomerular feedback in isolated perfused juxtaglomerular apparatus preparations, although minor d

11 t generate paracrine chemical signals in the juxtaglomerular apparatus to control vital kidney functi

12 The juxtaglomerular apparatus was still able to respond to t

13 o signal the release of renin from the renal juxtaglomerular apparatus, especially during volume depl

14 TGF operates within the juxtaglomerular apparatus, sensing changes in tubular fl

15 Olfr78 is expressed in the renal juxtaglomerular apparatus, where it mediates renin secre

16 ad fewer or no renin-expressing cells in the juxtaglomerular apparatus.

17 soactive mediator within the confines of the juxtaglomerular apparatus.

18 s confirmed that BNZ affected TGF within the juxtaglomerular apparatus.

19 tive renin in afferent arterioles and in the juxtaglomerular apparatus.

20 he adult under physiologic stress, the adult juxtaglomerular cell always possessed characteristics of

21 uggest that the MSC may be the origin of the juxtaglomerular cell and provide insight into novel unde

22 luR4 in the olfactory bulbs, specifically in juxtaglomerular cell bodies and their processes.

23 , interstitial inflammation, and an elevated juxtaglomerular cell count were noted at 20 to 30 wk aft

24 A lower juxtaglomerular cell count with focal cytoplasmic vacuol

25 a functional Ren1d gene are devoid of renal juxtaglomerular cell granules and exhibit an altered mac

26 whether there was a correlation between the juxtaglomerular cell response and the response of the su

27 renin expression and secretion is the renal juxtaglomerular cell, where its expression is tightly re

28 ting the effect of ACEI and ARB in mice with juxtaglomerular cell-specific deficiency of the AC-stimu

29 mplified odor-evoked activity in a subset of juxtaglomerular cells and attenuated glutamate release f

30 express the transgene appropriately in renal juxtaglomerular cells and secrete hREN into the circulat

31 that microRNAs maintain the renin-producing juxtaglomerular cells and the morphologic integrity and

32 a positive correlation between the number of juxtaglomerular cells and the number of granule cells de

33 ary to maintain the number of renin-positive juxtaglomerular cells and the plasticity of arteriolar s

34 n, renin protein remained localized to renal juxtaglomerular cells and was appropriately regulated by

35 Juxtaglomerular cells are highly specialized myoepitheli

36 ivity-dependent labeling of mitral cells and juxtaglomerular cells but not of tyrosine hydroxlase-pos

37 stimulation of the renin-angiotensin system, juxtaglomerular cells contained rhomboid protogranules w

38 ion, deletion of Vhl shifts the phenotype of juxtaglomerular cells from a renin- to erythropoietin-se

39 various stages of maturity, and suggest that juxtaglomerular cells maintain properties of both smooth

40 HREN protein production was restricted to juxtaglomerular cells of the kidney, and its expression

41 nin is synthesized in high quantities in the juxtaglomerular cells of the kidney, but little or none

42 COUP-TFII colocalized with renin in the juxtaglomerular cells of the kidney, which are the main

43 Juxtaglomerular cells showed similar excitatory odorant

44 tuned molecular receptive range compared to juxtaglomerular cells, and their odorant response profil

45 al cells, projection neurons; granule cells, juxtaglomerular cells, and tyrosine hydroxylase-containi

46 tion of Dicer severely reduced the number of juxtaglomerular cells, decreased expression of the renin

47 ncluding mitral and tufted cells (M/TCs) and juxtaglomerular cells, form glomerular modules, which re

48 In vivo, LXRs colocalized in juxtaglomerular cells, in which LXR(alpha) was specifica

49 s typified by the activity of relatively few juxtaglomerular cells, which often occur in foci, and a

50 1d-null background, restoring granulation in juxtaglomerular cells.

51 to eliminate AGB labeling of mitral cells or juxtaglomerular cells.

52 ey cell line that models certain features of juxtaglomerular cells.

53 ors, expressed in renal proximal tubules and juxtaglomerular cells.

54 yer and are isolated from other glomeruli by juxtaglomerular cells; in addition, the compartmental pa

55 s, which are reminiscent of renin-producing (juxtaglomerular) cells in the mammalian afferent arterio

56 creasing the reservoir of these cells in the juxtaglomerular compartment (JGC).

57 re observed in the glomerular layer (GL) and juxtaglomerular external plexiform layer (EPL) of salama

58 lt of acquired or congenital errors in renal juxtaglomerular function (the source of renin), angioten

59 n of the von Hippel-Lindau protein (pVHL) in juxtaglomerular (JG) cells of the kidney suppresses reni

60 ha), controls renin synthesis and release by juxtaglomerular (JG) cells of the kidney, but may also h

61 Juxtaglomerular (JG) cells synthesize and release renin,

62 een ORN axons, mitral/tufted cell dendrites, juxtaglomerular (JG) cells, and glial cells during the d

63 Renin is stored in granules in juxtaglomerular (JG) cells, located in the pole of the r

64 ized endocrine cells in the kidney, known as juxtaglomerular (JG) cells.

65 d and secreted into the circulation by renal juxtaglomerular (JG) cells.

66 eceptor subtype exclusively present in mouse juxtaglomerular (JG) cells.

67 neurons that are referred to collectively as juxtaglomerular (JG) cells: external tufted (ET), perigl

68 he olfactory receptor neurons (ORNs) and the juxtaglomerular (JG) neurons of the glomerular layer.

69 Expression of tyrosine hydroxylase (TH) by juxtaglomerular (JG) neurons of the olfactory bulb (OB)

70 ons terminate on dendrites of projection and juxtaglomerular (JG) neurons.

71 types of neurons collectively referred to as juxtaglomerular (JG) neurons.

72 IV, renin was restricted to the "classical" juxtaglomerular localization.

73 Juxtaglomerular neurons (JGNs) of the mammalian olfactor

74 mice expressing GFP in approximately 70% of juxtaglomerular neurons (JGNs), a population that underg

75 In the glomerular layer of adults, many juxtaglomerular neurons are IP3R immunoreactive [IP3R(+)

76 External tufted (ET) cells are juxtaglomerular neurons that spontaneously generate burs

77 group I mGluR agonists on one population of juxtaglomerular neurons, external tufted (ET) cells, whi

78 ated, in part, by the intrinsic neurons, the juxtaglomerular neurons.

79 in-expressing cells became restricted to the juxtaglomerular portion of the afferent arteriole.

80 li not containing renin cells at the typical juxtaglomerular position.

81 e activity of the renin-1d enzyme in a local juxtaglomerular renin-angiotensin system.

82 t adenosine is a required constituent of the juxtaglomerular signaling pathway.

83 hese oscillatory patterns may play a role in juxtaglomerular signaling.

84 FBP1 was most apparent in the glomerulus and juxtaglomerular space.

85 the juxtaglomerular afferent arteriole, in a juxtaglomerular structure probably representing the extr