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1 ormation of the capillary endothelium in the renal medulla.
2 d in the pancreas, spleen, renal cortex, and renal medulla.
3 HDAC) inhibitor, MS275, was delivered to the renal medulla.
4 elatively low (<10%) in the renal cortex and renal medulla.
5 to demonstrate accurate drug delivery to the renal medulla.
6 membrane alterations primarily involving the renal medulla.
7 renal senescence and safeguards cells in the renal medulla.
8 nd of COX-1 in COX-1>COX-2 mice in the inner renal medulla.
9 s enriched in the renal cortex and 11 in the renal medulla.
10 e abundant in the renal cortex and 72 in the renal medulla.
11 otential role of Id4 in the formation of the renal medulla.
12 n ambient tonicity normally occurring in the renal medulla.
13 g II)-mediated decrease of blood flow in the renal medulla.
14 thesis of COX2-dependent vasodilators in the renal medulla.
15  these exo-miRs was significantly altered in renal medulla.
16 reased in the renal cortex as well as in the renal medulla.
17  within the kidney, and atrophy of the inner renal medulla.
18 tions from the renal cortex but not from the renal medulla.
19 echanism and the structural integrity of the renal medulla.
20 ts in a state of relative hypoxia within the renal medulla.
21 1), an enzyme whose function is important in renal medullas.
22 - 65 (standard deviation) and 31 msec +/- 6; renal medulla, 1702 msec +/- 205 and 60 msec +/- 21; ren
23 ngiotensin II receptor AT2 expression in the renal medulla (63.3 +/- 12.1 versus 19.5 +/- 44.2 x 10(4
24                                 Cells in the renal medulla adapt to the stress of hypertonicity (hype
25 ere generated without respiratory gating and renal medulla and collecting system were more resistant
26  is present in collecting duct cells in both renal medulla and cortex and in thin descending limbs of
27  protein expression was also observed in the renal medulla and cortex of Heph/Cp KO mice.
28  different wall thicknesses were used in the renal medulla and cortex to reproduce the inhomogeneous
29                               Mean FA of the renal medulla and cortex was significantly higher in gro
30  expression between the renal cortex and the renal medulla and greatly expands the known differential
31 s of [3H]ouabain binding to slices of rabbit renal medulla and high resolution quantitative autoradio
32 activity on organic osmolyte accumulation in renal medulla and in cultured mouse renal medullary inte
33 a2 assembles with beta1-Na+,K+-ATPase in the renal medulla and in distal colon.
34   STZ rats showed upregulation of PRR in the renal medulla and preferential distribution of PRR on th
35 ption factor, is abundantly expressed in the renal medulla and regulates many oxygen-sensitive genes
36 s examined, it was specifically localized to renal medulla and retinal pigmented epithelial cells, an
37 exhibited decreased iron accumulation in the renal medulla and significant attenuation of the renal i
38 is underscored by the necrotic injury of the renal medulla and subsequent renal failure that results
39 ) in membranes from cultured IMCD cells, rat renal medulla, and freshly isolated IMCD cells.
40                         In contrast, thymus, renal medulla, and regions of the brain and gut expresse
41 is dissociated from the relatively preserved renal medulla, and the earliest effect on excretory func
42 /PGE(2) or Wnt/beta-catenin signaling in the renal medulla, and their involvement in the regulation o
43 ney tissue, in the cortex or adjacent to the renal medulla; and in liver tissue, with and without met
44 s in the number of inflammatory cells in the renal medulla are BP dependent.
45                   The collecting tubules and renal medulla are derived from Pax2-positive ureteric bu
46 ponding increase in urea transporters in the renal medulla as the result of increased protein intake
47 ressed in bacteria, yeast, and the mammalian renal medulla because their expression is best understoo
48 the urine-concentrating mechanism within the renal medulla causes fluctuations in extracellular osmol
49 were found to be significantly higher in the renal medulla compared to the cortex.
50 rate passes through the nephron and into the renal medulla, electrolytes, water, and urea are reabsor
51 is of renographic findings, renal cortex and renal medulla enhancement curves and normalized enhancem
52                             FA values in the renal medulla exhibit a good correlation with renal func
53 ude that TonEBP is a master regulator of the renal medulla for cellular protection against high osmol
54 ns were also inhibited by 70% and 61% in the renal medulla from decoy rats.
55                          TonEBP protects the renal medulla from the deleterious effects of hyperosmol
56 onclude that (i) Pax2 is expressed in normal renal medulla, (ii) its expression is regulated there by
57                                          The renal medulla in most AQP1/AQP3 null mice by age 4 weeks
58  or scrambled ODNs were transfected into the renal medulla in uninephrectomized Sprague-Dawley rats.
59 rt and aorta, but >1000 genes altered in the renal medulla, including those regulating the endogenous
60 gnaling cascades independently of RAS in the renal medulla, including Wnt/beta-catenin signaling, cyc
61        Urea, in concentrations unique to the renal medulla, increases transcription and protein expre
62 ction in the hyperosmolar environment of the renal medulla is a complex process that requires selecti
63  accumulation of compatible osmolytes in the renal medulla is catalyzed by the sodium/myo-inositol co
64 urvival in the hypertonic environment of the renal medulla is dependent on the intracellular accumula
65                                 However, the renal medulla is devoid of classic lymphatics.
66  Due to local hypoxia and hypertonicity, the renal medulla is subject to extreme oxidative stress.
67 ic stress, which naturally occurs within the renal medulla, is elevated under the setting of SCT.
68 ble kinase (Sgk1), which is expressed in the renal medulla, is regulated by extracellular tonicity.
69                                          The renal medulla maintains salt and water balance and is pr
70 e unique extracellular osmolality within the renal medulla modulates a specific gene expression patte
71 nation is that the methylamines found in the renal medulla, namely glycerophosphocholine and betaine,
72  mRNA levels were significantly lower in the renal medulla of Agtr1(A)(-/-) and Agtr1(A/B)(-/-) than
73  periureteric bud capillaries in the nascent renal medulla of embryonic mice.
74 e increased in both the renal cortex and the renal medulla of endotoxemic rats.
75 NOS levels were significantly greater in the renal medulla of female rats compared with male rats (35
76 NOS levels were significantly greater in the renal medulla of female rats compared with male rats (67
77 pression were significantly decreased in the renal medulla of Heph/Cp KO mice, while the expression o
78  mild decrease in AQP-2 protein level in the renal medulla of heterozygous CBS mice.
79 lphaENaC-encoding mRNA was attenuated in the renal medulla of mice with disruption of the Per1 gene,
80             The abundance of TNFalpha in the renal medulla of SS rats, but not the salt-insensitive c
81                                          The renal medulla produces concentrated urine through the ge
82 eptor-2 agonist, dDAVP, was delivered to the renal medulla resulting in a significant increase in wat
83 ynamics during reperfusion contribute to the renal medulla's susceptibility to ischemic injury.
84 aller in other parts of the body than in the renal medulla, similar mechanisms operate throughout, yi
85 1, mRNA levels increase significantly in the renal medulla, specifically in renal medullary interstit
86 e of biophysical and paracrine events in the renal medulla that integrate the vascular and tubular re
87 ssed on the endothelium of vasa recta in the renal medulla, the lymph node subcapsular and medullary
88                                       In the renal medulla, there was significant phosphorylation of
89                   Vascular congestion of the renal medulla-trapped red blood cells in the medullary m
90            Adenosine is generated within the renal medulla under hypoxic conditions and is known to i
91 ynthesis/response pathway in the renal inner renal medulla undermines the homeostatic response to a H
92   The abundance of TNFalpha receptors in the renal medulla was significantly higher in SS rats than S
93  shows a marked increase in apoptosis in the renal medulla where hypertonicity normally prevails.
94         Cyclooxygenase-2 is expressed in the renal medulla where inhibition causes fluid retention an
95 II and ET in plasma, right atrium, lung, and renal medulla which was further localized to cardiomyocy