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1 KCC2), Wnk1, Stk39 (SPAK), and Slc14a2 (UT-A urea transporter).
2 inity, small molecule inhibitors of the UT-B urea transporter.
3 an antibody to the rat vasopressin-regulated urea transporter.
4 odium channel (ENaC), aquaporin-2 (AQP2) and urea transporters.
5 ithout the inverted repeat of mammalian-type urea transporters.
6 concentration by stimulating aquaporin-2 and urea transporters.
7 t there are at least four different rat UT-A urea transporters.
8 cted with a reporter construct driven by the urea transporter-A promoter, in which the nitric oxide d
9 onor S-nitroso-N-acetylpenicillamine reduces urea transporter-A reporter activity under isotonic and
10 g the inner medullary collecting duct (IMCD) urea transporter A1 (UT-A1) and urea transporter A3 (UT-
12 ease in inner medulla aquaporin-2 (AQP2) and urea transporter A1 (UT-A1) in GD rats as compared with
13 G treatment significantly up-regulated renal urea transporter A1 and promoted its trafficking to apic
14 f TonEBP/NFAT5 target genes ClC-K1, Barttin, urea transporter-A1, and aquaporin 2 that are required f
15 ncomitantly, expressions of ClC-K1, Barttin, urea transporter-A1, and aquaporin 2 were significantly
16 oride channel 1 and its subunit Barttin, the urea transporter-A1, and the water channel aquaporin 2,
17 duct (IMCD) urea transporter A1 (UT-A1) and urea transporter A3 (UT-A3) have very low levels of urea
18 after prolonged fasting in late winter, when urea transporter abundance in gut tissue and urease gene
19 ys also had decreased expression of the UT-A urea transporter and collectrin, which is involved in ap
20 tein expression of renal sodium chloride and urea transporters and aquaporins in hypothyroid rats (HT
21 ions by analyzing experimental structures of urea transporters and proteins crystallized in the prese
23 olecular evidence for facilitated and active urea transporters, and integrative studies of their acut
24 ne-concentrating ability is reduced; and (c) urea transporters are expressed in non-renal tissues, an
25 the effect of adrenal steroids on the UT-A1 urea transporter because it is involved in the urine-con
26 discovers phospholipids associating with the urea transporters by combining structural observations,
27 isition of unique adaptive traits, such as a urea transporter, Ca(2+) :H(+) antiporter, mannosyl-3-ph
28 rea transporters, UT-A and UT-B, and several urea transporter cDNA isoforms have been cloned from hum
29 ransporters, UT-A and UT-B, encoding several urea transporter cDNA isoforms in humans, rodents, and s
31 echanism of dietary salt excretion relies on urea transporter-driven urea recycling by the kidneys an
32 e expression of solute carriers, such as the urea transporters encoded by Slc14a2, as well as aquapor
35 present the 2.3 A structure of a functional urea transporter from the bacterium Desulfovibrio vulgar
36 These insights improve our understanding of urea transporter function at a molecular level and provi
39 ating mechanism, we deleted 3 kb of the UT-A urea transporter gene containing a single 140-bp exon (e
40 rs, the molecular biology of the facilitated urea transporter gene families and cDNAs, and integrativ
44 owing to its high polarity, and specialized urea transporters have evolved to achieve rapid and sele
45 otide variation in the kidney-specific human urea transporter, HUT2, is associated with variation in
46 orter UT-B has been proposed to be the major urea transporter in erythrocytes and kidney-descending v
48 eviously characterized vasopressin-regulated urea transporter in the apical membrane of the terminal
49 le of inner medullary collecting duct (IMCD) urea transporters in the renal concentrating mechanism,
50 creased urea and a corresponding increase in urea transporters in the renal medulla as the result of
52 lusions can be made: (1) The collecting duct urea transporter is present in at least two forms (97 an
58 e, and Northern analysis showed no change in urea transporter mRNA abundance in either inner medullar
59 hypothesis that the abundance of the apical urea transporter of the inner medullary collecting duct
62 ng the concept that phloretin-sensitive IMCD urea transporters play a central role in medullary urea
64 There was no change in vasopressin-regulated urea transporter protein in the inner medullary base, an
66 s, including studies of uremic rats in which urea transporter protein is upregulated in liver and hea
67 proaches to perform integrative studies into urea transporter protein regulation, both in normal anim
68 lies and cDNAs, and integrative studies into urea transporter protein regulation, both in the kidney
70 ntibodies have been generated to many of the urea transporter proteins, and several novel findings ha
71 antibodies have been generated to the cloned urea transporter proteins, and the use of these antibodi
76 tified significantly increased levels of the urea transporter SLC14A1 in the OVT73 striatum, along wi
77 carrier family 14 member 1 gene, SLC14A1, a urea transporter that regulates cellular osmotic pressur
79 for the existence of facilitated and active urea transporters, the molecular biology of the facilita
83 Abundant slc14a1 expression, encoding the urea transporter UT-A, suggests a significant role in th
85 on coefficient in Xenopus oocytes expressing urea transporter UT-B (former name UT3), suggesting that
87 is study, we present the structures of human urea transporters UT-A and UT-B to characterize them at
98 cloning of two gene families for facilitated urea transporters, UT-A and UT-B, encoding several urea
103 n knockout mice indicate a critical role for urea transporters (UTs) in the urinary concentrating mec
104 m, the kidney epithelia contain facilitative urea transporters (UTs) that allow rapid equilibration b
105 ucidate the physiological role of the latter urea transporter, we have isolated the rat homologue (UT