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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 cated techniques including microperfusion of juxtaglomerular apparatus in vitro, micropuncture of kid
9 ated techniques, including microperfusion of juxtaglomerular apparatus in vitro, micropuncture of ren
10 s, and elevation of luminal succinate in the juxtaglomerular apparatus increases renin secretion, cau
11 erized by hypertrophy and hyperplasia of the juxtaglomerular apparatus of the kidneys, aldosteronism
12 duction was similar in the isolated perfused juxtaglomerular apparatus of wild-type (WT) and nitric o
13 buloglomerular feedback in isolated perfused juxtaglomerular apparatus preparations, although minor d
14 t generate paracrine chemical signals in the juxtaglomerular apparatus to control vital kidney functi
15                                          The juxtaglomerular apparatus was still able to respond to t
16        They are the central component of the juxtaglomerular apparatus which controls systemic blood
17 o signal the release of renin from the renal juxtaglomerular apparatus, especially during volume depl
18                      TGF operates within the juxtaglomerular apparatus, sensing changes in tubular fl
19             Olfr78 is expressed in the renal juxtaglomerular apparatus, where it mediates renin secre
20  populations of fibroblasts and cells of the juxtaglomerular apparatus.
21 cells that constitute a key component of the juxtaglomerular apparatus.
22 ad fewer or no renin-expressing cells in the juxtaglomerular apparatus.
23 soactive mediator within the confines of the juxtaglomerular apparatus.
24 s confirmed that BNZ affected TGF within the juxtaglomerular apparatus.
25 tive renin in afferent arterioles and in the juxtaglomerular apparatus.
26 he adult under physiologic stress, the adult juxtaglomerular cell always possessed characteristics of
27 uggest that the MSC may be the origin of the juxtaglomerular cell and provide insight into novel unde
28 luR4 in the olfactory bulbs, specifically in juxtaglomerular cell bodies and their processes.
29 aMP6f) to investigate Ca(2+) dynamics within juxtaglomerular cell clusters ex vivo and in vivo.
30         Ex vivo Ca(2+) imaging revealed that juxtaglomerular cell clusters exhibit robust and coordin
31 and intercellular Ca(2+) oscillations within juxtaglomerular cell clusters under physiological condit
32 and intercellular Ca(2+) oscillations within juxtaglomerular cell clusters, ex vivo and in vivo.
33 , interstitial inflammation, and an elevated juxtaglomerular cell count were noted at 20 to 30 wk aft
34                                      A lower juxtaglomerular cell count with focal cytoplasmic vacuol
35  a functional Ren1d gene are devoid of renal juxtaglomerular cell granules and exhibit an altered mac
36  whether there was a correlation between the juxtaglomerular cell response and the response of the su
37  renin expression and secretion is the renal juxtaglomerular cell, where its expression is tightly re
38 ting the effect of ACEI and ARB in mice with juxtaglomerular cell-specific deficiency of the AC-stimu
39             We generated mice expressing the juxtaglomerular cell-specific genetically encoded Ca(2+)
40 rogenic lineage that generates glutamatergic juxtaglomerular cells (JGCs) for the OB.
41 mplified odor-evoked activity in a subset of juxtaglomerular cells and attenuated glutamate release f
42 express the transgene appropriately in renal juxtaglomerular cells and secrete hREN into the circulat
43  that microRNAs maintain the renin-producing juxtaglomerular cells and the morphologic integrity and
44 a positive correlation between the number of juxtaglomerular cells and the number of granule cells de
45 ary to maintain the number of renin-positive juxtaglomerular cells and the plasticity of arteriolar s
46 n, renin protein remained localized to renal juxtaglomerular cells and was appropriately regulated by
47                                              Juxtaglomerular cells are highly specialized myoepitheli
48                                              Juxtaglomerular cells are sensors that control blood pre
49 ivity-dependent labeling of mitral cells and juxtaglomerular cells but not of tyrosine hydroxlase-pos
50 stimulation of the renin-angiotensin system, juxtaglomerular cells contained rhomboid protogranules w
51 ion, deletion of Vhl shifts the phenotype of juxtaglomerular cells from a renin- to erythropoietin-se
52 various stages of maturity, and suggest that juxtaglomerular cells maintain properties of both smooth
53    HREN protein production was restricted to juxtaglomerular cells of the kidney, and its expression
54 nin is synthesized in high quantities in the juxtaglomerular cells of the kidney, but little or none
55      COUP-TFII colocalized with renin in the juxtaglomerular cells of the kidney, which are the main
56                                              Juxtaglomerular cells respond to such threats by increas
57 lood pressure or extracellular fluid volume, juxtaglomerular cells secrete renin, initiating an enzym
58                                              Juxtaglomerular cells showed similar excitatory odorant
59  tuned molecular receptive range compared to juxtaglomerular cells, and their odorant response profil
60 al cells, projection neurons; granule cells, juxtaglomerular cells, and tyrosine hydroxylase-containi
61 tion of Dicer severely reduced the number of juxtaglomerular cells, decreased expression of the renin
62 ncluding mitral and tufted cells (M/TCs) and juxtaglomerular cells, form glomerular modules, which re
63                 In vivo, LXRs colocalized in juxtaglomerular cells, in which LXR(alpha) was specifica
64 is of frozen day 14 UUO kidney revealed rare juxtaglomerular cells, novel activated proximal tubule a
65 in-secreting kidney tumours that derive from juxtaglomerular cells, specialised smooth muscle cells t
66 s typified by the activity of relatively few juxtaglomerular cells, which often occur in foci, and a
67 1d-null background, restoring granulation in juxtaglomerular cells.
68 to eliminate AGB labeling of mitral cells or juxtaglomerular cells.
69 ey cell line that models certain features of juxtaglomerular cells.
70 ors, expressed in renal proximal tubules and juxtaglomerular cells.
71 yer and are isolated from other glomeruli by juxtaglomerular cells; in addition, the compartmental pa
72 s, which are reminiscent of renin-producing (juxtaglomerular) cells in the mammalian afferent arterio
73 creasing the reservoir of these cells in the juxtaglomerular compartment (JGC).
74 re observed in the glomerular layer (GL) and juxtaglomerular external plexiform layer (EPL) of salama
75 lt of acquired or congenital errors in renal juxtaglomerular function (the source of renin), angioten
76 entifies PIEZO2 as an essential regulator of juxtaglomerular granular cell calcium activity and renin
77  that PIEZO2 is expressed in renin-producing juxtaglomerular granular cells and is required for their
78 tenosis produces two differing responses - a juxtaglomerular hypertensive response and cortical renal
79 e vasculature and direct activation of renal juxtaglomerular (JG) cell renin production.
80 n of the von Hippel-Lindau protein (pVHL) in juxtaglomerular (JG) cells of the kidney suppresses reni
81 ha), controls renin synthesis and release by juxtaglomerular (JG) cells of the kidney, but may also h
82                                              Juxtaglomerular (JG) cells synthesize and release renin,
83            Normally, renin is synthesized by juxtaglomerular (JG) cells, a specialized group of myoep
84 een ORN axons, mitral/tufted cell dendrites, juxtaglomerular (JG) cells, and glial cells during the d
85               Renin is stored in granules in juxtaglomerular (JG) cells, located in the pole of the r
86 ized endocrine cells in the kidney, known as juxtaglomerular (JG) cells.
87 d and secreted into the circulation by renal juxtaglomerular (JG) cells.
88 eceptor subtype exclusively present in mouse juxtaglomerular (JG) cells.
89 neurons that are referred to collectively as juxtaglomerular (JG) cells: external tufted (ET), perigl
90 he olfactory receptor neurons (ORNs) and the juxtaglomerular (JG) neurons of the glomerular layer.
91   Expression of tyrosine hydroxylase (TH) by juxtaglomerular (JG) neurons of the olfactory bulb (OB)
92 ons terminate on dendrites of projection and juxtaglomerular (JG) neurons.
93 types of neurons collectively referred to as juxtaglomerular (JG) neurons.
94  IV, renin was restricted to the "classical" juxtaglomerular localization.
95                                              Juxtaglomerular neurons (JGNs) of the mammalian olfactor
96  mice expressing GFP in approximately 70% of juxtaglomerular neurons (JGNs), a population that underg
97      In the glomerular layer of adults, many juxtaglomerular neurons are IP3R immunoreactive [IP3R(+)
98               External tufted (ET) cells are juxtaglomerular neurons that spontaneously generate burs
99  group I mGluR agonists on one population of juxtaglomerular neurons, external tufted (ET) cells, whi
100 ated, in part, by the intrinsic neurons, the juxtaglomerular neurons.
101 in-expressing cells became restricted to the juxtaglomerular portion of the afferent arteriole.
102 li not containing renin cells at the typical juxtaglomerular position.
103 e activity of the renin-1d enzyme in a local juxtaglomerular renin-angiotensin system.
104 t adenosine is a required constituent of the juxtaglomerular signaling pathway.
105 hese oscillatory patterns may play a role in juxtaglomerular signaling.
106 FBP1 was most apparent in the glomerulus and juxtaglomerular space.
107 the juxtaglomerular afferent arteriole, in a juxtaglomerular structure probably representing the extr

 
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