ライフサイエンスコーパス: equilibrative nucleoside transporter

1 press both a nucleoside kinase as well as an equilibrative nucleoside transporter.

2 recently cloned dipyridamole-sensitive human equilibrative nucleoside transporter.

3 permease is related in sequence to mammalian equilibrative nucleoside transporters.

4 Erythrocyte equilibrative nucleoside transporter 1 (eENT1) levels ar

5 They import purines via equilibrative nucleoside transporter 1 (ENT1) homologs.

6 s a consequence of ticagrelor inhibiting the equilibrative nucleoside transporter 1 (ENT1) on platele

7 Overexpression of equilibrative nucleoside transporter 1 (ENT1) or concent

8 ecently, a variant of adenosine transporter, equilibrative nucleoside transporter 1 (ENT1), was assoc

9 s RBV uptake by preventing the expression of equilibrative nucleoside transporter 1 (ENT1).

10 iation in the last extracellular loop of the equilibrative nucleoside transporter 1 (ENT1; also calle

11 Inhibitor and substrate interactions with equilibrative nucleoside transporter 1 (ENT1; SLC29A1) a

12 We identified the human equilibrative nucleoside transporter 1 (hENT1) as the mo

13 The human equilibrative nucleoside transporter 1 (hENT1) is an imp

14 We have previously shown that the human equilibrative nucleoside transporter 1 (hENT1) is expres

15 e whether the nucleoside transporters, human equilibrative nucleoside transporter 1 (hENT1) or human

16 nomolar concentrations specifically to human equilibrative nucleoside transporter 1 (hENT1) produced

17 H-Thymidine transport was dominated by human equilibrative nucleoside transporter 1 (hENT1) under bot

18 toxicity include the activities of the human equilibrative nucleoside transporter 1 (hENT1), deoxycyt

19 The expression of human equilibrative nucleoside transporter 1 (hENT1), thymidin

20 cells expressing thymidine kinase and human equilibrative nucleoside transporter 1 (hENT1).

21 The Plasmodium falciparum Equilibrative Nucleoside Transporter 1 (PfENT1) is a mem

22 CBD inhibited adenosine uptake via equilibrative nucleoside transporter 1 and synergistical

23 inding studies confirm that CBD binds to the equilibrative nucleoside transporter 1 with a Ki < 250 n

24 enzymes (connexin43, connexin37, pannexin-1, equilibrative nucleoside transporter 1, CD39, CD73, ecto

25 ntine) is a clinically used vasodilator with equilibrative nucleoside transporters 1 and 2 (ENT1 and

26 We stably transfected the cloned human equilibrative nucleoside transporters 1 and 2 (hENT1 and

27 brative nucleoside transporter family member equilibrative nucleoside transporter-1 (ENT1) in the reg

28 lism by potently and directly inhibiting the equilibrative nucleoside transporter-1 (ENT1).

29 Low expression of human equilibrative nucleoside transporter-1 (hENT1) may resul

30 raC-8C cells that are deficient in the human equilibrative nucleoside transporter-1, the IC(50) of Ge

31 (3)H-FMAU transport was dominated by human equilibrative nucleoside transporter 2.

32 Here, we found that mice lacking the equilibrative nucleoside transporter 3 (ENT3) developed

33 ntracellular uptake depends predominantly on equilibrative nucleoside transporters after conversion o

34 Equilibrative nucleoside transporters are a unique famil

35 studies demonstrate that the NBMPR-sensitive equilibrative nucleoside transporters are novel and unex

36 sine A2B receptor agonists and inhibition of equilibrative nucleoside transporters by dipyridamole ma

37 mercaptopurine riboside (NBMPR)-insensitive, equilibrative nucleoside transporter ei by functional co

38 Equilibrative nucleoside transporters encompass two cons

39 rter (CNT) blocker phloridzin but not by the equilibrative nucleoside transporter (ENT) blocker dipyr

40 while requiring intracellular uptake via the equilibrative nucleoside transporter (ENT) ENT1 or the c

41 s a newly cloned transporter assigned to the equilibrative nucleoside transporter (ENT) family (SLC29

42 Transporters of the equilibrative nucleoside transporter (ENT) family promot

43 de Transporter 1 (PfENT1) is a member of the equilibrative nucleoside transporter (ENT) gene family.

44 o the recently cloned human NBMPR-sensitive, equilibrative nucleoside transporter ENT1 and thus was d

45 anol-sensitive adenosine transporter, type 1 equilibrative nucleoside transporter (ENT1), drink more

46 the nitrobenzylthioinosine (NBMPR)-sensitive equilibrative nucleoside transporter (ENT1), incubation

47 adenosine signaling by inhibiting the type 1 equilibrative nucleoside transporter (ENT1), whereas chr

48 ng to a novel isoform of the NBMPR-sensitive equilibrative nucleoside transporter (ENT1).

49 ble to penetrate into cells deficient in the equilibrative nucleoside transporter ENT2, and reconstit

50 entrative nucleoside transporters (CNTs) and equilibrative nucleoside transporters (ENTs) are importa

51 Equilibrative nucleoside transporters (ENTs) are polytop

52 Consistent with the notion that equilibrative nucleoside transporters (ENTs) terminate a

53 Equilibrative nucleoside transporters (ENTs) translocate

54 ards the intracellular compartment by way of equilibrative nucleoside transporters (ENTs), we hypothe

55 ignaling is terminated by its uptake through equilibrative nucleoside transporters (ENTs).

56 e occurred by translocation of adenosine via equilibrative nucleoside transporters (ENTs).

57 identifies three transport mechanisms of the equilibrative nucleoside transporter family by which nuc

58 the first demonstration that members of the equilibrative nucleoside transporter family can be elect

59 Permeases of the equilibrative nucleoside transporter family mediate the

60 Previous studies have implicated the equilibrative nucleoside transporter family member equil

61 Permeases belonging to the equilibrative nucleoside transporter family promote upta

62 The first mammalian examples of the equilibrative nucleoside transporter family to be charac

63 LdNT2 is a member of the equilibrative nucleoside transporter family, which posse

64 ituted gate operates in other members of the equilibrative nucleoside transporter family.

65 PfNT2 is, like PfNT1, a member of the equilibrative nucleoside transporter family.

66 but exhibits low homology to members of the equilibrative nucleoside transporter family.

67 s that is homologous to other members of the equilibrative nucleoside transporter family.

68 substantial homology to other members of the equilibrative nucleoside transporter family.

69 topology similar to members of the mammalian equilibrative nucleoside transporter family.

70 ishmania donovani express two members of the equilibrative nucleoside transporter family; LdNT1 encod

71 1 receptors but required adenosine uptake by equilibrative nucleoside transporters followed by its (i

72 the hypothesis that human concentrative and equilibrative nucleoside transporters (hCNT1 and hENT1)

73 or DNA and correlating its uptake with human equilibrative nucleoside transporter (hENT1) levels, str

74 The human equilibrative nucleoside transporter (hENT1) protein tra

75 s thymidine kinase gene (hsv-tk) and a human equilibrative nucleoside transporter (hENT1).

76 The human equilibrative nucleoside transporter, hENT1, which is se

77 exposure of SKOV-3 cells to dipyridamole, an equilibrative nucleoside transporter inhibitor; APCP, a

78 onstrate that Fun26, a homolog of human ENT (equilibrative nucleoside transporter), localizes to the

79 enosine kinase, adenosine deaminase, and the equilibrative nucleoside transporter: mature receptors w

80 Equilibrative nucleoside transporters of the SLC29 famil

81 Equilibrative nucleoside transporters play essential rol

82 hich inhibits transport of adenosine through equilibrative nucleoside transporter, raised the measure

83 The rat equilibrative nucleoside transporter (rENT1) was reveale

84 ENT1 is an equilibrative nucleoside transporter that enables trans-

85 on of the adenosine transporter ENT1 (type 1 equilibrative nucleoside transporter), which provides pr