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1 or H7, and blocked by HgCl2, an inhibitor of aquaporin 1.
2 I reporters based on the human water channel aquaporin 1.
3 of Na(+)/Pi cotransporter 2, claudin-2, and aquaporin 1.
4 nown structures of the KcsA K(+) channel and aquaporin 1.
5 orter and the proximal tubule water channel, aquaporin-1.
6 express proximal tubular markers megalin and aquaporin-1.
7 of water-only transport pathways mediated by aquaporin-1.
8 igation of the water-permeation mechanism of aquaporin-1.
9 ormed on the structures of the water channel aquaporin-1.
14 identified and characterized the A. gambiae aquaporin 1 (AgAQP1) protein that is homologous to AQPs
15 otein (GFAP) promoter driving the EGFP-AQP1 (Aquaporin-1, an MRI reporter) fusion gene were employed.
16 on related genes Rock1 and Rock2, as well as aquaporin 1 and beta2 adrenergic receptor in female mice
17 y which the knockdown of Rock1 and Rock2, or aquaporin 1 and beta2 adrenergic receptor in female mice
19 oroid plexus epithelial cells indicates that aquaporin 1 and claudin-1 both remain normally polarized
20 c resolution crystal structures of mammalian aquaporin 1 and the bacterial glycerol permease GlpF.
22 LIM-FRET) and identified interaction between aquaporin-1 and band 3 at a distance of 8 nm, within the
25 GFR difference was found to be augmented in aquaporin-1 and Na/H exchanger-3 knockout mice, suggesti
28 orins 3 and 8 in primitive erythroblasts and aquaporins 1 and 9 in adult definitive erythroblasts.
30 alpha-helical transmembrane domains (opsin, aquaporin 1, and a connexin) with their area obtained fr
31 e to those through the transmembrane protein aquaporin-1, and are practically independent of the leng
34 xpression of 2 angiogenesis-related markers, aquaporin 1 (AQP1) and cellular retinoic acid-binding pr
36 ed after the known mercury-sensitive site of aquaporin 1 (AQP1) and determined the X-ray crystal stru
38 ity map of deglycosylated, human erythrocyte aquaporin 1 (AQP1) determined at 4 A resolution in plane
42 rmine the roles of lipid composition and the aquaporin 1 (AQP1) water channel in altering CO2 flux ac
46 Na(+)/glucose cotransporter 1 (SGLT1) and of aquaporin 1 (Aqp1), a water channel, at the attachment s
47 cell SGLT1, a Na+/glucose cotransporter, and aquaporin 1 (AQP1), a water channel, to the attachment s
48 gulated by secretin-responsive relocation of aquaporin 1 (AQP1), a water-selective channel protein, f
49 Dex-treated rats had increased abundance of aquaporin 1 (AQP1), AQP3, and Na-K-2Cl co-transporter pr
55 e retinal pigment epithelium (RPE) expresses aquaporin-1 (AQP1) and components of the natriuretic pep
56 ility, sensitivity, and specificity of urine aquaporin-1 (AQP1) and perilipin-2 (PLIN2) concentration
57 uctance but not the water flux through human Aquaporin-1 (AQP1) channels and impairs AQP1-dependent c
63 w the convergent evidence demonstrating that aquaporin-1 (AQP1) facilitates water transport across en
64 er channel activity, several studies suggest Aquaporin-1 (AQP1) functions as a nonselective monovalen
65 cytes and liposomes containing water channel aquaporin-1 (AQP1) have suggested that AQP1 is able to t
66 The mammalian lung expresses water channel aquaporin-1 (AQP1) in microvascular endothelia and aquap
67 The mammalian lung expresses water channel aquaporin-1 (AQP1) in microvascular endothelia, AQP4 in
77 Prevention of cation permeation in wild-type aquaporin-1 (AQP1) is believed to be associated with the
80 nce is presented here that the water channel aquaporin-1 (AQP1) is present in the ZG membrane and par
84 igid body docking of the atomic model of the aquaporin-1 (AQP1) tetramer showed that the freeze-fract
91 known blockers of water permeability through aquaporin-1 (AQP1) water channels were mercurial reagent
95 orrelating with tumor growth inhibition, and Aquaporin-1 (AQP1), a water channel modulated in tumor c
96 sed a prototype adenoviral vector to express aquaporin-1 (AQP1), presumably in the ductal cell layer
106 efficacy of serotype 5, adenoviral-mediated aquaporin-1 cDNA transfer to a single previously irradia
108 mulations using this method are performed on aquaporin-1 channels in a lipid bilayer, resulting in a
110 wo groups was observed in cells labeled with aquaporin 1, cytokeratin 7, and a-smooth muscle actin.
111 wo groups was observed in cells labeled with aquaporin 1, cytokeratin 7, and alpha-smooth muscle acti
115 administration was traced to a reduction in aquaporin-1 expression in the kidney of LXRbeta(-/-) mic
117 onic anhydrase enzymes and the water channel Aquaporin-1 for targeting this subpopulation of platelet
118 activity until Agre and colleagues purified aquaporin-1 from human erythrocytes and reported its cDN
119 the osmotic-permeability regulation of human aquaporin 1 (hAQP1) expressed in Xenopus oocyte membrane
121 cient, recombinant adenovirus encoding human aquaporin-1 (hAQP1), the archetypal water channel, was c
122 tissue in diseased rats was vascularized by aquaporin-1(+) high endothelial venules and vascular cel
124 data indicate that the carboxyl terminus of aquaporin-1 is intracellular and that loops C and E are
125 imilarity between the pf values of SGLT1 and aquaporin-1 makes a transcellular pathway plausible, it
129 The water-selective pathway through the aquaporin-1 membrane channel has been visualized by fitt
130 MUTM-NEI/1 cells expressed mRNA for NCAM, aquaporin 1, myocilin/trabecular meshwork glucocorticoid
131 ls of the S3 segment of the proximal tubule, aquaporin 1-negative cells of the thin descending limb o
135 id-reconstituted two-dimensional crystals of aquaporin-1 preserved in vitrified buffer in the absence
137 in the exosomal sorting of the water channel aquaporin-1 represents a newly described mechanism by wh
138 cular volume, which is associated with lower aquaporin 1 that is important for cerebrospinal fluid se
139 on, RGS4 expression inhibited trafficking of aquaporin 1 to the plasma membrane in LLC-PK1 cells and
143 serted at sequential sites within TM2 of the aquaporin-1 water channel by in vitro translation of tru
144 induces the exocytic insertion of functional aquaporin-1 water channels (AQP1) into the apical membra
146 t analysis showed approximately 1.4 x 10(12) aquaporin-1 water channels/cm2 of capillary surface, whi
147 with the overexpression of the water channel aquaporin 1, which was prevented by reactive oxygen spec