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1 ryl-cholinesterase, nor of the high-affinity choline transporter.
2 -dependent, hemicholinium-3 (HC-3)-sensitive choline transporter.
3 icholinium-3 (HC-3)-sensitive, high affinity choline transporter.
4 and that snf-6 encodes a novel acetylcholine/choline transporter.
5  increases in the levels of the highaffinity choline transporter.
6 ion and proposes SLC25A48 as a mitochondrial choline transporter.
7 on of Slc44a1 as the primary oligodendrocyte choline transporter.
8 e presynaptic sodium-dependent high-affinity choline transporter 1 (CHT), which is known to be mutate
9 relatively unique in their expression of the choline transporter 1 (CHT1), which exhibits high-affini
10 ding SLC5A7, which encodes the high-affinity choline transporter 1 (CHT1).
11 se (AChE), choline acetyltransferase (ChAT), choline transporter 1 (CHT1, SLC5A7), vesicular acetylch
12 psis thaliana, 29.6% identity with the yeast choline transporter and 23.4% identity with the yeast UG
13 an increased expression of the high-affinity choline transporter and especially the muscarinic M2 rec
14 th in vivo and in vitro that FLVCR2 is a BBB choline transporter and is responsible for the majority
15 r presynaptic targeting of the high-affinity choline transporter and synaptic transmission.
16                          The activity of the choline transporter and the hemicholinium-3 binding were
17       identified SLC25A48 as a mitochondrial choline transporter, and its loss-of-function mutations
18 cle spindle afferents with the high-affinity choline transporter antagonist hemicholinium-3 similarly
19 cell-based assays to reveal that MFSD7c is a choline transporter at the blood-brain barrier (BBB).
20 r-like proteins-1 and -2 (CTL1 and CTL2) are choline transporter at the plasma membrane and mitochond
21  cerevisiae expresses a single high affinity choline transporter at the plasma membrane, encoded by t
22 gans encodes a high-affinity plasma-membrane choline transporter believed to be rate limiting for ace
23                    Osmotic activation of the choline transporter BetT promotes the uptake of external
24  or SLC49A1) was recently determined to be a choline transporter but is not highly expressed at the b
25 mpared with evidence from NP rats, increased choline transporter capacity [as indicated by maximum tr
26 rom choline transported by the high-affinity choline transporter (CHT) and reduced ACh content relati
27 riation in the gene encoding the presynaptic choline transporter (CHT) has been linked to attention-d
28                            The high-affinity choline transporter (CHT) is a protein integral to the f
29  sodium-dependent, hemicholinium-3-sensitive choline transporter (CHT) is believed to sustain acetylc
30 ion in SLC5A7, which encodes the presynaptic choline transporter (CHT), a critical determinant of syn
31 expression and activity of the high-affinity choline transporter (CHT), a molecule that mediates the
32 etyltransferase (ChAT) and the high-affinity choline transporter (ChT), as measured by reverse transc
33 on of the basal forebrain increased cortical choline transporter (CHT)-mediated choline transport in
34 nce indicating plastic mechanisms regulating choline transporter (CHT)-mediated high-affinity choline
35 ne transporter (VAChT) and the high-affinity choline transporter (CHT).
36 ARV), glutamic acid decarboxylase (GAD), and choline transporter (CHT).
37  be sustained by a hemicholinium-3-sensitive choline transporter (CHT).
38 a membrane, hemicholinium-3-sensitive (HC-3) choline transporter (CHT).
39 s on the functional capacity of the neuronal choline transporter (CHT).
40 rt of choline via the neuronal high-affinity choline transporter (CHT; SLC5A7) is essential for choli
41 cular ACh transporter, and the high-affinity choline transporter CHT1.
42 oline transporter (VAChT), the high-affinity choline transporter (CHT1) and ChAT.
43 onal uptake of choline via the high affinity choline transporter (CHT1) is essential for cholinergic
44                Sodium-coupled, high-affinity choline transporters (CHTs) are inhibited by 3-morpholin
45 to preserve choline and phosphatidylcholine, choline transporter deficiency was implicated in impaire
46 dhood-onset neurometabolic disease caused by choline transporter deficiency with autosomal recessive
47 ies with mutants deficient in BetT and other choline transporters demonstrated that BetT was responsi
48  the presence of multiple known and putative choline transporters encoded within its genome.
49 evealed that changes were not due to altered choline transporter expression, but rather due to increa
50 ntiporter belonging to the betaine/carnitine/choline transporter family of secondary transporters.
51 cantly reduced, but not completely abrogated choline transporter function.
52 vs. placebo), 14-16 SNPs within the cellular choline transporter gene solute carrier family 44 member
53                     Here, we reported that a choline transporter gene, CTL1, controls ionome homeosta
54              The recent cloning of the human choline transporter (hCHT) has allowed its expression in
55  underscore the essential role played by the choline transporter in sustaining acetylcholine neurotra
56 the hypothesis that an increased capacity of choline transporters in the right medial prefrontal cort
57               The presynaptic, high-affinity choline transporter is a critical determinant of signall
58                We present details of how the choline transporter is a major regulator of phosphatidyl
59 , which labels the presynaptic high-affinity choline transporter, is responsive additionally to nerve
60                               Characterizing choline transporter-like 1 (CTL1) as a new regulator of
61 tern blotting techniques, we have identified choline transporter-like 1 (CTL1) as a putative complexi
62                                          The choline transporter-like 1 (CTL1) protein is localized t
63  show that Small kernel 10 (Smk10) encodes a choline transporter-like protein 1 (ZmCTLP1) that facili
64  Lys90Metfs*18) in the SLC44A1 gene encoding choline transporter-like protein 1.
65                                          The choline transporter-like protein 1/solute carrier 44A1 (
66 pig peptides identical to sequences in human choline transporter-like protein 2 (CTL2).
67 stitution in the first extracellular loop of choline transporter-like protein 2, a member of the chol
68  direct evidence that anti-HNA-3a recognizes choline transporter-like protein 2.
69 1 encodes a member of a poorly characterized choline transporter-like protein family in plants and an
70  transporter-like protein 2, a member of the choline transporter-like protein family of membrane glyc
71                      The CTL1 gene encodes a choline transporter-like protein with an expression patt
72    The solute carriers 44A (SLC44A) known as choline transporter-like proteins-1 and -2 (CTL1 and CTL
73  to transport choline, and the proportion of choline transporters localized in the membrane of synapt
74 a broad clinical phenotype due to homozygous choline transporter missense mutations.
75 l outcomes arising from different classes of choline transporter mutation with distinct disease proce
76 aptic terminals to acquire the high-affinity choline transporter necessary for high-frequency transmi
77 deoxyglucose PET, and they overexpressed the choline transporter organic cation transporter 3.
78 he trafficking of the Caenorhabditis elegans choline transporter orthologue revealed deficits in tran
79       Quantitative analysis of high-affinity choline transporter rates as a function of inhibitor and
80 tide polymorphisms, rs2771040(G)) within the choline transporter SLC44A1 increase risk for choline de
81 ted by nicotinic acetylcholine receptors and choline transporters, such nanocapsules can effectively
82 ly conserved within the APC (amine-polyamine-choline) transporter superfamily.
83 ive frameshift mutation at the C-terminus of choline transporter that was associated with significant
84 report describes the relative roles of three choline transporters, the ABC transporter CbcXWV and two
85                Given the localization of the choline transporter to synaptic vesicles, we propose tha
86 ergic, activity-triggered delivery of silent choline transporters to the plasma membrane, in which no
87 molar conditions whereas BetT3 was the major choline transporter under hyperosmolar conditions.
88 itions, as BetT1 and CbcXWV were the primary choline transporters under hypo-osmolar conditions where
89            When POTS cells were treated with choline, transporter was up-regulated, and uptake of cho
90 uld directly interact with the high-affinity choline transporter which may impair steady-state and on