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1 press both a nucleoside kinase as well as an equilibrative nucleoside transporter.
2 recently cloned dipyridamole-sensitive human equilibrative nucleoside transporter.
3 ine, but not other deoxynucleosides, through equilibrative nucleoside transporters.
4 permease is related in sequence to mammalian equilibrative nucleoside transporters.
6 s following uptake into activated T cells by equilibrative nucleoside transporter 1 (ENT1) and inhibi
8 s a consequence of ticagrelor inhibiting the equilibrative nucleoside transporter 1 (ENT1) on platele
10 ecently, a variant of adenosine transporter, equilibrative nucleoside transporter 1 (ENT1), was assoc
14 iation in the last extracellular loop of the equilibrative nucleoside transporter 1 (ENT1; also calle
15 Inhibitor and substrate interactions with equilibrative nucleoside transporter 1 (ENT1; SLC29A1) a
19 e whether the nucleoside transporters, human equilibrative nucleoside transporter 1 (hENT1) or human
20 nomolar concentrations specifically to human equilibrative nucleoside transporter 1 (hENT1) produced
21 H-Thymidine transport was dominated by human equilibrative nucleoside transporter 1 (hENT1) under bot
23 toxicity include the activities of the human equilibrative nucleoside transporter 1 (hENT1), deoxycyt
27 . falciparum, the most virulent species, the equilibrative nucleoside transporter 1 (PfENT1) represen
28 thase (TYMS), thymidine kinase 1 (TK-1), and equilibrative nucleoside transporter 1 (SLC29A1) in HCC
29 specific and FKBP-dependent inhibitor of the equilibrative nucleoside transporter 1 and is efficaciou
31 inding studies confirm that CBD binds to the equilibrative nucleoside transporter 1 with a Ki < 250 n
32 enzymes (connexin43, connexin37, pannexin-1, equilibrative nucleoside transporter 1, CD39, CD73, ecto
33 g an astrocytic adenosine transporter, ENT1 (equilibrative nucleoside transporter 1; Slc29a1), show n
34 ntine) is a clinically used vasodilator with equilibrative nucleoside transporters 1 and 2 (ENT1 and
37 brative nucleoside transporter family member equilibrative nucleoside transporter-1 (ENT1) in the reg
38 investigated the effect on tumor immunity of equilibrative nucleoside transporter-1 (ENT1), the major
41 raC-8C cells that are deficient in the human equilibrative nucleoside transporter-1, the IC(50) of Ge
42 eling and experimental studies revealed that equilibrative nucleoside transporter 2 (ENT2), but not E
48 ntracellular uptake depends predominantly on equilibrative nucleoside transporters after conversion o
50 studies demonstrate that the NBMPR-sensitive equilibrative nucleoside transporters are novel and unex
51 sine A2B receptor agonists and inhibition of equilibrative nucleoside transporters by dipyridamole ma
52 mercaptopurine riboside (NBMPR)-insensitive, equilibrative nucleoside transporter ei by functional co
54 the first to predict drug interactions with equilibrative nucleoside transporter (ENT) 1 and ENT2 us
55 rter (CNT) blocker phloridzin but not by the equilibrative nucleoside transporter (ENT) blocker dipyr
56 while requiring intracellular uptake via the equilibrative nucleoside transporter (ENT) ENT1 or the c
57 s a newly cloned transporter assigned to the equilibrative nucleoside transporter (ENT) family (SLC29
59 de Transporter 1 (PfENT1) is a member of the equilibrative nucleoside transporter (ENT) gene family.
60 cause lung injury via adenosine receptors or equilibrative nucleoside transporter (ENT)-dependent int
62 o the recently cloned human NBMPR-sensitive, equilibrative nucleoside transporter ENT1 and thus was d
64 anol-sensitive adenosine transporter, type 1 equilibrative nucleoside transporter (ENT1), drink more
65 the nitrobenzylthioinosine (NBMPR)-sensitive equilibrative nucleoside transporter (ENT1), incubation
66 adenosine signaling by inhibiting the type 1 equilibrative nucleoside transporter (ENT1), whereas chr
68 ble to penetrate into cells deficient in the equilibrative nucleoside transporter ENT2, and reconstit
70 entrative nucleoside transporters (CNTs) and equilibrative nucleoside transporters (ENTs) are importa
75 ards the intracellular compartment by way of equilibrative nucleoside transporters (ENTs), we hypothe
79 identifies three transport mechanisms of the equilibrative nucleoside transporter family by which nuc
80 the first demonstration that members of the equilibrative nucleoside transporter family can be elect
85 being imported into cells by members of the equilibrative nucleoside transporter family, NR is predo
93 ishmania donovani express two members of the equilibrative nucleoside transporter family; LdNT1 encod
94 1 receptors but required adenosine uptake by equilibrative nucleoside transporters followed by its (i
95 the hypothesis that human concentrative and equilibrative nucleoside transporters (hCNT1 and hENT1)
96 or DNA and correlating its uptake with human equilibrative nucleoside transporter (hENT1) levels, str
100 exposure of SKOV-3 cells to dipyridamole, an equilibrative nucleoside transporter inhibitor; APCP, a
101 onstrate that Fun26, a homolog of human ENT (equilibrative nucleoside transporter), localizes to the
102 enosine kinase, adenosine deaminase, and the equilibrative nucleoside transporter: mature receptors w
105 hich inhibits transport of adenosine through equilibrative nucleoside transporter, raised the measure
109 on of the adenosine transporter ENT1 (type 1 equilibrative nucleoside transporter), which provides pr