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1 per examined area (glomerulus, proximal, and distal tubules).
2 orption through sodium channels in the renal distal tubule.
3 progenitors, and then subsequently marks the distal tubule.
4 e of inclusions from epithelial cells of the distal tubule.
5 sorption and potassium secretion in the late distal tubule.
6  for FGF23-dependent FGFR activation, in the distal tubule.
7 at this regulation likely takes place in the distal tubule.
8 e sodium chloride cotransporter (NCC) in the distal tubule.
9 )(-) reabsorption in the proximal tubule and distal tubule.
10  liver and splenic macrophages and in kidney distal tubules.
11 disappeared except for a small population of distal tubules.
12 tion, and impaired autophagy in proximal and distal tubules.
13 tors lacking beta-catenin failed to form the distal tubules.
14  significantly greater than that observed in distal tubules.
15 tch inhibition to generate both proximal and distal tubules.
16 alized to tricellular tight junctions of the distal tubules.
17 idin-encoding Hamp1 and hepcidin staining in distal tubules.
18 ximal tubules and represses the formation of distal tubules.
19 fic for the collecting ducts and a subset of distal tubules.
20 e collecting ducts and both the proximal and distal tubules.
21  retention occurs mainly in the proximal and distal tubules.
22 e in a more oxidized state than those in the distal tubules.
23 TPase, was lower in proximal tubules than in distal tubules.
24 ules, but potential was better maintained in distal tubules.
25 (3)(-) reabsorption in both the proximal and distal tubules.
26 d bicarbonate transport by both proximal and distal tubules.
27 ne or more of the sodium transporters of the distal tubule (a site for fine tuning of sodium balance)
28 genous endothelins as mediators of increased distal tubule acidification induced by dietary acid.
29 ace epithelium and is induced throughout the distal tubule after administration of LPS.
30                       In the amphibian early distal tubule aldosterone activates the Na(+)-H+ exchang
31 is through greater delivery of sodium to the distal tubule and activation of tubuloglomerular feedbac
32 -derived organoids differentiate into TFA2B+ distal tubule and CDH1+ connecting segment progenitors,
33 ntrolling Na(+) reabsorption along the renal distal tubule and collecting duct (CD).
34 secretion of buffered protons (mainly in the distal tubule and collecting duct).
35 fusion where the new nephron plumbs into the distal tubule and establishes blood filtrate drainage.
36  we show that mecom is necessary to form the distal tubule and to restrict both proximal tubule forma
37 ats: lithium reabsorption in the superficial distal tubules and amiloride-sensitive lithium reabsorpt
38 t E12.5 and epithelial cells of proximal and distal tubules and collecting ducts at E17.5 and P0 mous
39 3 widened in I/R-injured kidneys from normal distal tubules and collecting ducts to dilated proximal
40 d expression of 24p3R in apical membranes of distal tubules and collecting ducts, but not of proximal
41           Histology revealed cystogenesis in distal tubules and collecting ducts, decreased ciliogene
42 ult mouse kidney, NPN protein was located in distal tubules and collecting ducts.
43 ional deletion of LRRC8A in proximal but not distal tubules and constitutive deletion of LRRC8D cause
44 uired at high levels during nephrogenesis in distal tubules and later exclusively in thick ascending
45 viral load (pvl), showing preference for the distal tubules and medulla.
46 protein expression in the renal proximal and distal tubules and significantly increased PGI2, not PGE
47  injury, HB-EGF is produced predominantly in distal tubules and that endogenous HB-EGF may be an impo
48  the renal cortex (specifically proximal and distal tubules) and sustained beyond 2 months post injec
49 ssion in the proximal tubule, loop of Henle, distal tubule, and collecting duct and suggest that unde
50 tributes importantly to acidification in the distal tubule, and that it plays a major role in limitin
51 lus, proximal tubules, thick ascending limb, distal tubules, and collecting ducts.
52  intense staining of crescents, proximal and distal tubules, and interstitial mononuclear cells.
53 gments, including cortical collecting ducts, distal tubules, and loop of Henle.
54  such as the proximal tubule, loop of Henle, distal tubules, and podocytes, using extracellular matri
55 the epithelial layers of the loops of Henle, distal tubules, and the collecting ducts of the kidney a
56                  The insulin receptor in the distal tubule appears to modulate BP, but the role of th
57 tuft plus Bowman's capsule, 10X for proximal/distal tubule, arteries and afferent arterioles, and 40X
58 sal medium, differentiated into proximal and distal tubules as well as endothelium, as highlighted by
59 ts derived from either collecting tubules or distal tubules but not from proximal tubules, which corr
60 lls, mesangial cells, endothelial cells, and distal tubules but not proximal tubules.
61   We estimated the diameters of proximal and distal tubules by the minor axis of oval tubular profile
62 d greater furosemide-induced calciuresis and distal tubule calcium transport pathways were enhanced.
63 way, lending support to the novel finding of distal tubule cell apoptosis in patients with FSGS.
64 bules of Drosophila, we show that a specific distal tubule cell regulates both tissue architecture an
65 ptors on the luminal surface of proximal and distal tubule cells and on afferent and efferent arterio
66 cently tagged PTH1Rs, we show that in kidney distal tubule cells and rat osteosarcoma cells, which la
67 l tubule progenitors express cadherin-6, the distal tubule cells express E-cadherin, whereas the glom
68  cells transiently transfected with 24p3R or distal tubule cells internalized submicromolar concentra
69 noreactivity in the descending thin limb and distal tubule cells was located in the Golgi apparatus a
70 cant conservation in podocytes, proximal and distal tubule cells, and divergence in cellular composit
71 member of the WNK kinase family expressed by distal tubule cells, interacts with WNK4 and WNK1 to reg
72 confirmed an abnormality of proximal but not distal tubule cells, marked in sustained ARF but not in
73 icantly shorter cilia formed on proximal and distal tubule cells.
74 , apoptosis was evident in both proximal and distal tubule cells.
75 crease the fluid and electrolyte load to the distal tubule, consistent with a role of MD nNOS in tubu
76 nal free light chains with uromodulin in the distal tubules, defining light chain cast nephropathy.
77 es in both the proximal (proximal SNGFR) and distal tubules (distal SNGFR).
78 xpression of WNK1-S and WNK4 is strongest in distal tubule, dropping sharply in collecting duct and w
79 luding FGFR1, and alpha-Klotho in the kidney distal tubule (DT), leading to increased sodium retentio
80 rominent expression by maturing proximal and distal tubules during development, but with a more prono
81 ical membrane of the diluting segment (early distal tubule, EDT) of the frog are involved in the regu
82                           The Xenopus laevis distal tubule epithelial cell line A6 was used as a mode
83  5 (TRPV5) channel on the apical membrane of distal tubule epithelial cells.
84 preciable hypertrophy and hyperplasia of the distal tubule epithelium of the nephron, resembling salt
85 oliferating cells were found in proximal and distal tubule epithelium throughout the cortex, and the
86                              Notably, S1 and distal tubules exhibited similar metabolic profiles desp
87 re the concentration of bicarbonate in early distal tubule fluid and to measure distal bicarbonate re
88                            In collections of distal tubule fluid, TF/P were 2.8 +/- 0.3 [-/-] and 4.4
89                  In the kidney, proximal and distal tubules had markedly higher mtDNA levels compared
90                    Bosentan had no effect on distal tubule HCO3 or H+ secretion in control animals.
91                                       In the distal tubule, however, calcium is reabsorbed by channel
92     Fractional lithium delivery to the early distal tubule in low-K+ rats (0.31 +/- 0.01) was similar
93 cterized as podocytes, proximal tubules, and distal tubules in an additional 10 days.
94 ed that HB-EGF was produced predominantly in distal tubules in kidneys injured either by ischemia/rep
95  basolateral plasma membrane of proximal and distal tubules in rat kidney, where many G protein-coupl
96 of phosphorylated S6 protein in proximal and distal tubules in T2Di(+) patients confirmed changes in
97 ximal tubules and represses the formation of distal tubules in the mammalian nephron, we show that in
98 +/+, during free-flow collections from early distal tubules (influence of MD intact, 7 +/- 0.7 versus
99 ion of the collecting duct, proximal tubule, distal tubule, interstitial cells, and rarely glomerular
100 egulated, and those in the loop of Henle and distal tubule lineages were downregulated.
101 olocalization experiments using proximal and distal tubule markers confirmed that EBV DNA and the CD2
102 zation of FGFR1 and Klotho suggests that the distal tubule may be an effector site of FGF23.
103 approaches were used to evaluate the role of distal tubule NHE2 in compensating for the proximal defe
104  secretion and increased H+ secretion in the distal tubule of animals given dietary acid.
105                        The epithelium of the distal tubule of the nephron shows striking hypertrophy
106 red for terminal differentiation of the late distal tubule of the Xenopus pronephros and regulates re
107 analyses demonstrated jagged-1 expression in distal tubules of kidneys from normal mice or contralate
108 ally distinct WNK bodies were evident in the distal tubules of mice subjected to dietary potassium lo
109 d increased H+ secretion in in vivo-perfused distal tubules of rats fed dietary acid as (NH4)2SO4.
110 rter (NCC) mediated salt reabsorption in the distal tubules of the kidney.
111 wn to be required for the differentiation of distal tubule precursors into early stage distal convolu
112  of these factors colocalized with tfap2a in distal tubule precursors.
113 hymosin-B4 in zebrafish altered proximal and distal tubule pronephros growth suggesting a possible ro
114 ateral potassium channel of the proximal and distal tubules, respectively.
115                 Microperfusion of live renal distal tubules reveals that they are impermeable to wate
116 ere, we generated mice lacking mTORC2 in the distal tubule (Rictorfl/fl Ksp-Cre mice), which were via
117 responsible for differentiation of the first distal tubule segment.
118 or kidney function and endothelial cells and distal tubule segments for blood pressure pathogenesis.
119 alance between K secretion and absorption in distal tubule segments such as the connecting tubule and
120 i was measured in single microperfused early distal tubule segments using the fluorescent probe 2',7'
121 egions that include a series of proximal and distal tubule segments, which are comprised of intercala
122  and alpha-Klotho expression in proximal and distal tubule segments.
123 age minor axis diameter in oval proximal and distal tubules separately and by cortex depth in patient
124 tex depth or by glomeruli versus proximal or distal tubule size.
125 ses in medullary blood flow and decreases in distal tubule sodium reabsorption that offset acute rise
126 lly, normal lithium clearance suggested that distal tubule sodium reabsorption was not downregulated
127 he low NaCl diet, fenoldopam decreased renal distal tubule sodium transport but did not cause natriur
128 ed with the inhibition of renal proximal and distal tubule sodium transport.
129 ced in structure and/or coiling whereas more distal tubule structure was unaffected.
130 luminal bicarbonate load is presented to the distal tubule, such as in NHE3 null mice.
131  Ccnd1 and Tuba1a/b was detected in immature distal tubules, suggesting cell cycle regulation may be
132                In vivo microperfusion of rat distal tubules suggests that a significant fraction of b
133 ytoskeletal alterations in live proximal and distal tubules that arise at the onset of severe IRI.
134 dium retention shifted from the proximal and distal tubules to the collecting system.
135 natriuresis by inhibiting renal proximal and distal tubule transport, but on a low NaCl diet the incr
136 rolling sodium excretion at the level of the distal tubules via activation of the apical epithelial s
137 ractional lithium delivery to the end of the distal tubule was increased slightly (to 0.15 +/- 0.02;
138 orption of fluid or chloride up to the early distal tubule was not different between nNOS -/- and +/+
139 lcium channel TRPV5, normally present in the distal tubule, was expressed in Xenopus oocytes.
140 r markers specifically expressed in the late distal tubule were absent in xBic-C-MO-injected embryos.
141 segment, whereas concentrations in the early distal tubule were markedly lower.
142                                              Distal tubules were present but in reduced numbers, and
143 d in all nephron segments, especially in the distal tubule, where it correlated with an increase in s
144 cells differentiate into mature proximal and distal tubules, whereas expression of the related Pax8 p
145 large pleomorphic nuclei in the proximal and distal tubules with mild interstitial inflammation, mini
146 his study, the cortical thick ascending limb-distal tubule, with attached glomerulus, was isolated an

 
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