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1 1d-null background, restoring granulation in juxtaglomerular cells.
2 to eliminate AGB labeling of mitral cells or juxtaglomerular cells.
3 ey cell line that models certain features of juxtaglomerular cells.
4 ors, expressed in renal proximal tubules and juxtaglomerular cells.
5 he adult under physiologic stress, the adult juxtaglomerular cell always possessed characteristics of
6 uggest that the MSC may be the origin of the juxtaglomerular cell and provide insight into novel unde
7 mplified odor-evoked activity in a subset of juxtaglomerular cells and attenuated glutamate release f
8 express the transgene appropriately in renal juxtaglomerular cells and secrete hREN into the circulat
9  that microRNAs maintain the renin-producing juxtaglomerular cells and the morphologic integrity and
10 a positive correlation between the number of juxtaglomerular cells and the number of granule cells de
11 ary to maintain the number of renin-positive juxtaglomerular cells and the plasticity of arteriolar s
12 n, renin protein remained localized to renal juxtaglomerular cells and was appropriately regulated by
13  tuned molecular receptive range compared to juxtaglomerular cells, and their odorant response profil
14 al cells, projection neurons; granule cells, juxtaglomerular cells, and tyrosine hydroxylase-containi
15                                              Juxtaglomerular cells are highly specialized myoepitheli
16 luR4 in the olfactory bulbs, specifically in juxtaglomerular cell bodies and their processes.
17 ivity-dependent labeling of mitral cells and juxtaglomerular cells but not of tyrosine hydroxlase-pos
18 stimulation of the renin-angiotensin system, juxtaglomerular cells contained rhomboid protogranules w
19 , interstitial inflammation, and an elevated juxtaglomerular cell count were noted at 20 to 30 wk aft
20                                      A lower juxtaglomerular cell count with focal cytoplasmic vacuol
21 tion of Dicer severely reduced the number of juxtaglomerular cells, decreased expression of the renin
22 ncluding mitral and tufted cells (M/TCs) and juxtaglomerular cells, form glomerular modules, which re
23 ion, deletion of Vhl shifts the phenotype of juxtaglomerular cells from a renin- to erythropoietin-se
24  a functional Ren1d gene are devoid of renal juxtaglomerular cell granules and exhibit an altered mac
25 s, which are reminiscent of renin-producing (juxtaglomerular) cells in the mammalian afferent arterio
26                 In vivo, LXRs colocalized in juxtaglomerular cells, in which LXR(alpha) was specifica
27 yer and are isolated from other glomeruli by juxtaglomerular cells; in addition, the compartmental pa
28 various stages of maturity, and suggest that juxtaglomerular cells maintain properties of both smooth
29    HREN protein production was restricted to juxtaglomerular cells of the kidney, and its expression
30 nin is synthesized in high quantities in the juxtaglomerular cells of the kidney, but little or none
31      COUP-TFII colocalized with renin in the juxtaglomerular cells of the kidney, which are the main
32  whether there was a correlation between the juxtaglomerular cell response and the response of the su
33                                              Juxtaglomerular cells showed similar excitatory odorant
34 ting the effect of ACEI and ARB in mice with juxtaglomerular cell-specific deficiency of the AC-stimu
35  renin expression and secretion is the renal juxtaglomerular cell, where its expression is tightly re
36 s typified by the activity of relatively few juxtaglomerular cells, which often occur in foci, and a

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