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1 of Na(+)/Pi cotransporter 2, claudin-2, and aquaporin 1.
2 or H7, and blocked by HgCl2, an inhibitor of aquaporin 1.
3 I reporters based on the human water channel aquaporin 1.
4 nown structures of the KcsA K(+) channel and aquaporin 1.
5 orter and the proximal tubule water channel, aquaporin-1.
6 of water-only transport pathways mediated by aquaporin-1.
7 igation of the water-permeation mechanism of aquaporin-1.
8 ormed on the structures of the water channel aquaporin-1.
13 identified and characterized the A. gambiae aquaporin 1 (AgAQP1) protein that is homologous to AQPs
15 c resolution crystal structures of mammalian aquaporin 1 and the bacterial glycerol permease GlpF.
16 LIM-FRET) and identified interaction between aquaporin-1 and band 3 at a distance of 8 nm, within the
19 GFR difference was found to be augmented in aquaporin-1 and Na/H exchanger-3 knockout mice, suggesti
22 orins 3 and 8 in primitive erythroblasts and aquaporins 1 and 9 in adult definitive erythroblasts.
24 alpha-helical transmembrane domains (opsin, aquaporin 1, and a connexin) with their area obtained fr
25 e to those through the transmembrane protein aquaporin-1, and are practically independent of the leng
28 ed after the known mercury-sensitive site of aquaporin 1 (AQP1) and determined the X-ray crystal stru
29 ity map of deglycosylated, human erythrocyte aquaporin 1 (AQP1) determined at 4 A resolution in plane
33 rmine the roles of lipid composition and the aquaporin 1 (AQP1) water channel in altering CO2 flux ac
37 Na(+)/glucose cotransporter 1 (SGLT1) and of aquaporin 1 (Aqp1), a water channel, at the attachment s
38 cell SGLT1, a Na+/glucose cotransporter, and aquaporin 1 (AQP1), a water channel, to the attachment s
39 gulated by secretin-responsive relocation of aquaporin 1 (AQP1), a water-selective channel protein, f
40 Dex-treated rats had increased abundance of aquaporin 1 (AQP1), AQP3, and Na-K-2Cl co-transporter pr
46 e retinal pigment epithelium (RPE) expresses aquaporin-1 (AQP1) and components of the natriuretic pep
47 ility, sensitivity, and specificity of urine aquaporin-1 (AQP1) and perilipin-2 (PLIN2) concentration
51 er channel activity, several studies suggest Aquaporin-1 (AQP1) functions as a nonselective monovalen
52 cytes and liposomes containing water channel aquaporin-1 (AQP1) have suggested that AQP1 is able to t
53 The mammalian lung expresses water channel aquaporin-1 (AQP1) in microvascular endothelia and aquap
54 The mammalian lung expresses water channel aquaporin-1 (AQP1) in microvascular endothelia, AQP4 in
63 Prevention of cation permeation in wild-type aquaporin-1 (AQP1) is believed to be associated with the
66 nce is presented here that the water channel aquaporin-1 (AQP1) is present in the ZG membrane and par
70 igid body docking of the atomic model of the aquaporin-1 (AQP1) tetramer showed that the freeze-fract
77 known blockers of water permeability through aquaporin-1 (AQP1) water channels were mercurial reagent
81 sed a prototype adenoviral vector to express aquaporin-1 (AQP1), presumably in the ductal cell layer
90 efficacy of serotype 5, adenoviral-mediated aquaporin-1 cDNA transfer to a single previously irradia
92 mulations using this method are performed on aquaporin-1 channels in a lipid bilayer, resulting in a
97 administration was traced to a reduction in aquaporin-1 expression in the kidney of LXRbeta(-/-) mic
99 onic anhydrase enzymes and the water channel Aquaporin-1 for targeting this subpopulation of platelet
100 activity until Agre and colleagues purified aquaporin-1 from human erythrocytes and reported its cDN
101 the osmotic-permeability regulation of human aquaporin 1 (hAQP1) expressed in Xenopus oocyte membrane
103 cient, recombinant adenovirus encoding human aquaporin-1 (hAQP1), the archetypal water channel, was c
104 tissue in diseased rats was vascularized by aquaporin-1(+) high endothelial venules and vascular cel
106 data indicate that the carboxyl terminus of aquaporin-1 is intracellular and that loops C and E are
107 imilarity between the pf values of SGLT1 and aquaporin-1 makes a transcellular pathway plausible, it
110 The water-selective pathway through the aquaporin-1 membrane channel has been visualized by fitt
111 MUTM-NEI/1 cells expressed mRNA for NCAM, aquaporin 1, myocilin/trabecular meshwork glucocorticoid
113 id-reconstituted two-dimensional crystals of aquaporin-1 preserved in vitrified buffer in the absence
115 in the exosomal sorting of the water channel aquaporin-1 represents a newly described mechanism by wh
116 on, RGS4 expression inhibited trafficking of aquaporin 1 to the plasma membrane in LLC-PK1 cells and
120 serted at sequential sites within TM2 of the aquaporin-1 water channel by in vitro translation of tru
121 induces the exocytic insertion of functional aquaporin-1 water channels (AQP1) into the apical membra
123 t analysis showed approximately 1.4 x 10(12) aquaporin-1 water channels/cm2 of capillary surface, whi
124 with the overexpression of the water channel aquaporin 1, which was prevented by reactive oxygen spec
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