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

1 models that explain permeation properties of neurotransmitter transporters.

2 tes, is an excellent model for this class of neurotransmitter transporters.

3 ay translate into distinct surface levels of neurotransmitter transporters.

4 embrane proteins, including ion channels and neurotransmitter transporters.

5 echanism are probably conserved in the human neurotransmitter transporters.

6 n receptor (SNARE) components with vesicular neurotransmitter transporters.

7 kely to be the endocytic signal for all SLC6 neurotransmitter transporters.

8 arity to the other two families of vesicular neurotransmitter transporters.

9 des a protein homologous to sodium-dependent neurotransmitter transporters.

10 g of architecture and mechanism of mammalian neurotransmitter transporters.

11 TM6 in DAT and is found in a number of other neurotransmitter transporters.

12 other binding sites for glycine, or at other neurotransmitter transporters.

13 n related to mammalian Na(+)-, Cl(-)-coupled neurotransmitter transporters.

14 uated as inhibitors of presynaptic monoamine neurotransmitter transporters.

15 utations that alter functional properties of neurotransmitter transporters.

16 Thus VGAT is the first of a new family of neurotransmitter transporters.

17 , we present an application of this model to neurotransmitter transporters, a superfamily of proteins

18 Thus, we enhanced the neurotransmitter transporter activity of rigid nucleosid

19 Plasma membrane neurotransmitter transporters affect synaptic signaling

20 onstration of phosphorylation of a vesicular neurotransmitter transporter and a potential mechanism f

21 he first example of an interaction between a neurotransmitter transporter and PKC.

22 other pyridine-binding proteins, such as the neurotransmitter transporters and channels, is proposed.

23 ter (PROT) belongs to a large superfamily of neurotransmitter transporters and is expressed in region

24 In addition, the sorting of vesicular neurotransmitter transporters and other synaptic vesicle

25 sis studies performed with related mammalian neurotransmitter transporters and provides exciting sugg

26 roaches for examining the oligomerization of neurotransmitter transporters and sheds light on their d

27 hat a protein that is unrelated to any known neurotransmitter transporters and that was previously su

28 tions, derived homology models of eukaryotic neurotransmitter transporters, and substituted cysteine

29 Neurotransmitter transporters are critical for synaptic

30 Neurotransmitter transporters are ion-coupled symporters

31 Expression and activity of SLC6 neurotransmitter transporters are modulated by interacti

32 Plasma membrane neurotransmitter transporters are regulators of extracel

33 Neurotransmitter transporters are responsible for remova

34 Mounting evidence supports the idea that neurotransmitter transporters are subject to many forms

35 Although the neurotransmitter transporters are suggested to be primar

36 ied an orphan protein related to a vesicular neurotransmitter transporter as system N.

37 logies to classical Na+- and Cl(-)-dependent neurotransmitter transporters but display unusual featur

38 PMAT is not homologous to known neurotransmitter transporters but exhibits low homology

39 dings provide a mechanistic framework of how neurotransmitter transporters can operate as anion-selec

40 s in the Drosophila inebriated (ine)-encoded neurotransmitter transporter cause increased neuronal ex

41 Not only do neurotransmitter transporters contribute to the regulati

42 Neurotransmitter transporters couple the inward movement

43 Neurotransmitter transporters couple to existing ion gra

44 Plasma membrane neurotransmitter transporters determine in part the conc

45 ng five genes: ine, which encodes a putative neurotransmitter transporter; eag, which encodes a potas

46 ence similarity to the Na(+)/Cl(-)-dependent neurotransmitter transporter family were identified.

47 SERT is the first member of the neurotransmitter transporter family whose folding has be

48 a member of the SLC6 Na+- and Cl--dependent neurotransmitter transporter family whose function has r

49 a novel member of the Na(+)/Cl(-)-dependent neurotransmitter transporter family with the highest seq

50 d transporter GAT1, and other members of the neurotransmitter transporter family, is its regulated re

51 larity to members of the Na+/Cl(-)-dependent neurotransmitter transporter family.

52 ty with members of the Na+ and Cl(-)-coupled neurotransmitter transporter family.

53 Plasma membrane neurotransmitter transporters for monoamines, GABA, glyc

54 pecific mechanisms that discriminate between neurotransmitter transporters for surface expression and

55 h for and against Na(+)- and Cl(-)-dependent neurotransmitter transporters forming oligomers.

56 ntrast, little is known about the control of neurotransmitter transporter function by interacting pro

57 noaminergic perikarya, but also of monoamine neurotransmitter transporter function.

58 derate but biologically important changes in neurotransmitter transporter function.

59 Neurotransmitter transporters function in synaptic signa

60 Neurotransmitter transporters generate larger currents t

61 r beta(2), thyroid hormone receptor TRbeta), neurotransmitter transporters (glutamate/aspartate trans

62 The second transmembrane domain (TM2) of neurotransmitter transporters has been invoked to contro

63 Neurotransmitter transporters have long been known to re

64 siological investigations of plasma membrane neurotransmitter transporters have shown that carriers c

65 This is the first demonstration of an insect neurotransmitter transporter immunolocalization study.

66 uch on recent insights into the functions of neurotransmitter transporters in their physiological con

67 omain-containing protein PICK1 and monoamine neurotransmitter transporters in vitro and in vivo.

68 ntracellular loop of all Na+/Cl(-)-dependent neurotransmitter transporters, in conformational changes

69 turally related to the Na(+)-Cl(-)-dependent neurotransmitter transporters, including the dopamine tr

70 ertheless, single-channel events produced by neurotransmitter transporters indicate the functional an

71 nable to automation for the discovery of new neurotransmitter transporter inhibitors.

72 Uptake by Na(+)/Cl(-)-dependent neurotransmitter transporters is the principal mechanism

73 Neurotransmitter transporters limit transmitter concentr

74 he highly conserved subfamily of orthologous neurotransmitter transporters, lineage-specific, paralog

75 internalization motifs, suggesting that SLC6 neurotransmitter transporters may have evolved unique en

76 Neurotransmitter transporters may promote synapse specif

77 Vesicular neurotransmitter transporters must localize to synaptic

78 In LeuT, a prokaryotic homolog of neurotransmitter transporters, Na(+) stabilizes outward-

79 Plasmalemmal neurotransmitter transporters (NTTs) regulate the level

80 and pharmacological properties of eukaryotic neurotransmitter transporters obtained through structura

81 Neurotransmitter transporters of the SLC6 family of prot

82 A high density of neurotransmitter transporters on axons and presynaptic b

83 Vesicular neurotransmitter transporters package transmitter into t

84 Sodium-dependent neurotransmitter transporters participate in the clearan

85 Sodium-coupled neurotransmitter transporters play a key role in neurona

86 Neurotransmitter transporters play an important role in

87 Neurotransmitter transporters play important roles in re

88 their previously characterized targets, the neurotransmitter transporter proteins.

89 Plasma membrane neurotransmitter transporters rapidly traffic to and fro

90 Neurotransmitter transporters regulate synaptic transmit

91 nt drugs are G protein-coupled receptors and neurotransmitter transporters, respectively.

92 hrine transporter (NET) are sodium-dependent neurotransmitter transporters responsible for reuptake o

93 embers of a family of Na+- and Cl--dependent neurotransmitter transporters responsible for the rapid

94 Cocaine binds with high affinity to several neurotransmitter transporters, resulting in elevated neu

95 in transporter gene solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 (SLC6

96 Tin2 in the SLC6A4 (solute carrier family 6 [neurotransmitter transporter, serotonin], member 4) gene

97 inephrine, and dopamine-by directly blocking neurotransmitter transporters (SERT, NET, and DAT, respe

98 of LeuT, a bacterial homologue of mammalian neurotransmitter transporters, show a molecule of bound

99 Neurotransmitter transporters, targets of abused and the

100 d (GABA) transporter GAT-1 is a prototype of neurotransmitter transporters that maintain low synaptic

101 As is observed with other neurotransmitter transporters, the activity of EAAC1 is

102 plicated in the regulation of many different neurotransmitter transporters, this study provides the f

103 polarized epithelial cells stably expressing neurotransmitter transporters to analyze the sorting beh

104 However, the molecular architecture coupling neurotransmitter transporters to the endocytic machinery

105 differs from inhibitory mechanisms for some neurotransmitter transporters under similar conditions.

106 act to modulate the expression of glutamate neurotransmitter transporters via gene activation.

107 rter related to the family of biogenic amine neurotransmitter transporters was functionally expressed

108 Neurotransmitter transporters, which act to clear transm

109 rier properties, and it shares topology with neurotransmitter transporters with unknown structure and