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1 ates with the intracellular location of this copper transporter.
2 elta mutant, demonstrating its function as a copper transporter.
3 -6-phosphate receptor (CI-MPR) and the ATP7B copper transporter.
4 lasma membrane and is the primary Drosophila copper transporter.
5 tly demonstrated that SLC25A3 functions as a copper transporter.
6 atodes were found to have great diversity of copper transporters.
7 ecial structural and mechanistic features in copper transporters.
8 n in the colon are accompanied by changes in copper transporters.
9 e action of the Ctr1 family of high affinity copper transporters.
10  between the major copper influx transporter copper transporter 1 (CTR-1) and PD-L1 expression across
11  mitochondrial copper levels by upregulating copper transporter 1 (CTR1) and depleting mitochondrial
12                                    Mammalian copper transporter 1 (CTR1) is a high-affinity copper in
13                                        Human copper transporter 1 (CTR1) is overexpressed in a variet
14                                The mammalian copper transporter 1 (CTR1) is responsible for the uptak
15                                              Copper transporter 1 (Ctr1) is the main entry point for
16                                              Copper Transporter 1 (CTR1) plays a key role in copper u
17                        We show here that the copper transporter 1 (Ctr1) protein is a critical router
18                           Down-regulation of copper transporter 1 (CTR1) reduces uptake and sensitivi
19 le the transfer of copper from the universal copper transporter 1 (CTR1) uptake protein to all known
20         The major copper influx transporter, copper transporter 1 (CTR1), has now been shown to contr
21 age of the copper-binding ecto-domain of the copper transporter 1 (Ctr1).
22                                        Human copper transporter 1 (hCTR1) is a homotrimer of a 190-am
23                                        Human copper transporter 1 (hCTR1) is the major high affinity
24  cellular uptake of (64)Cu mediated by human copper transporter 1 (hCtr1) or simply due to nonspecifi
25               It has been claimed that human copper transporter 1 (hCTR1), the human high-affinity co
26                                    The human copper transporter 1 (hCTR1), the major transporter resp
27                                    The human copper transporter 1 (hCtr1), when heterologously overex
28 ions and immunohistochemistry study of human copper transporter 1 expression in the tumor tissues.
29 r xenografts expressing high levels of human copper transporter 1 were well visualized on the PET ima
30 ulated not only by the copper importer CTR1 (copper transporter 1) but also by the copper exporter AT
31  chelation or genetic knockdown of the CTR1 (copper transporter 1) copper channel alters the spatiote
32 at CCS can interact with human high affinity copper transporter 1.
33                           In eukaryotes, the copper transporter-1 (CTR1) is the primary high-affinity
34 show that overexpressing the copper and gold COPPER TRANSPORTER 2 (COPT2) in Arabidopsis increases th
35                                              Copper transporter 2 (CTR2) is one of the four copper tr
36 e structurally related, previously enigmatic copper transporter 2 (Ctr2).
37 antly, this interaction is specific for this copper transporter, a finding consistent with the observ
38   Both CTR1, a copper importer, and ATP7A, a copper transporter across membranes, were significantly
39      Copper enters cells through a dedicated copper transporter and is distributed to intracellular c
40 rindled) mice, which lack a functional ATP7A copper transporter and serve as a model for Menkes disea
41                We explored the role of known copper transporters and chaperones in delivering copper
42                                      Because copper transporters and chaperones regulate platinum dru
43                                 Mutations in copper transporters and chaperones that perturb mitochon
44  thought to counter with an up-regulation of copper transporters and efflux pumps.
45 er, these results indicate that cell-surface copper transporters and SOD1 are required for completion
46 lls express high levels of CTR1, the primary copper transporter, and additional chaperones that are r
47                     Because silencing of the copper transporter ATP7A also reduced cell migration, th
48       In this study, we demonstrate that the copper transporter ATP7A is necessary for the activity o
49 escribe the unexpected crosstalk between the Copper transporter ATP7A, autophagy, and VEGFR2 degradat
50 ially expressed genes such as lysyl oxidase, copper transporter ATP7A, EphB6, RUNX2 and a variant of
51 ntly, expression of Atox1 and its partner, a copper transporter ATP7A, is upregulated.
52  antioxidant enzymes that obtains copper via copper transporter ATP7A.
53   It was shown previously that an intestinal copper transporter (Atp7a) was co-regulated with iron tr
54 sease (WND) is caused by inactivation of the copper transporter ATP7B and copper accumulation in tiss
55 isease (WD) is caused by inactivation of the copper transporter Atp7b and copper overload in tissues.
56                  Pathogenic mutations in the copper transporter ATP7B have been hypothesized to affec
57                Inactivating mutations in the copper transporter Atp7b result in Wilson's disease.
58 tion is disrupted due to inactivation of the copper transporter ATP7B resulting in hepatic copper ove
59   Excretion of copper into bile requires the copper transporter Atp7b, which is deficient in Wilson d
60 lson disease, a disorder due to mutations in copper transporter ATP7B.
61 ological disorder caused by mutations in the copper-transporter, ATP7B.
62              Both proteins are high affinity copper transporters but share distinct enzymatic propert
63   The Menkes and Wilson genes are homologous copper transporters, but differences in their expression
64 he iron transport ligand transferrin and the copper transporter caeruloplasmin in the control of iron
65 ed in this screen encoding homologues of the copper transporter Ccc2, the copper chaperone Atx1, the
66  copper transporter (CTR1), an intracellular copper transporter (CCC2), and a putative transcription
67 derstanding of the structure and function of copper transporters, chaperones and cupro-proteins, coup
68 se genes are annotated, respectively, as two copper transporter (CopA and CopB) genes and a zinc-cadm
69 rexpression of the Arabidopsis high-affinity copper transporter COPT1 slightly increases endogenous i
70                                          The copper transporter (Ctr) family of integral membrane pro
71 opper is transported by three members of the copper transporter (Ctr) family, namely Ctr4, Ctr5, and
72  accumulation is associated with the loss of copper transporter Ctr1 from the plasma membrane and the
73                            The high-affinity copper transporter CTR1 is encoded by CTR1 (SLC31A1), a
74           We investigated the ability of the copper transporter CTR1 to control the accumulation of D
75  these were Cu/Zn-superoxide dismutase Sod1, copper transporter Ctr1, and copper chaperone Lys7, sugg
76 s associated with the down-regulation of the copper-transporter Ctr1 in the liver and appearance of a
77 del lesions and TrkB-dependent expression of copper transporter (CTR1) on glia cells during neuroinfl
78                                              Copper transporter (Ctr1) plays an important role in reg
79 s transport system include a plasma-membrane copper transporter (CTR1), an intracellular copper trans
80                            The high-affinity copper transporter (Ctr1; SCLC31A1) plays an important r
81 study was to determine the role of an influx copper transporter, CTR1, in the ototoxicity induced by
82    Here we demonstrate that two Cryptococcus copper transporters, Ctr1 and Ctr4, differentially influ
83 ose that cisplatin uptake is mediated by the copper transporter Ctr1p in yeast and mammals.
84 l results, a model is presented in which the copper transporter Ctr1p serves as a molecular target of
85 the Saccharomyces cerevisiae plasma membrane copper transporter Ctr1p, in response to a change in ext
86  for strains lacking either the cell surface copper transporter, Ctr1p, or the putative copper transp
87 ion, whereas extracellular yeast upregulated copper transporter CTR4.
88             Under low-copper conditions, the copper transporters Ctr4 and Ctr5 are maximally expresse
89     We have cloned genes for a high affinity copper transporter (Ctr4) and copper-sensing transcripti
90 ructed using the cryptococcal CUF1-dependent copper transporter, CTR4.
91 tant Wilson cDNAs were expressed in a Menkes copper transporter-deficient mottled fibroblast cell lin
92 rotein expression and localization of Ctr1p (copper transporter), Fet3p (multicopper oxidase involved
93 dant but structurally distinct Ctr1 and Ctr3 copper transporters from Saccharomyces cerevisiae.
94                              Thus, restoring copper transporter function is an essential therapeutic
95 ed binding region was upstream of a putative copper transporter gene (ctpB), and crp-deleted bacteria
96 ations Mac1 protein is rendered inactive for copper transporter gene transcription.
97 s characterized by analyzing the function of copper transporter genes in Arabidopsis thaliana.
98 udies using the sphingolipid hydroxylase and copper transporter genes, SCS7 and CCC2, respectively, s
99                               Novel zinc and copper transporters have been identified as well, mostly
100                         Therefore, these two copper transporters have opposite effects on DDP sensiti
101                   Here, we report that human copper transporter (hCtr) 1 plays an important role in t
102 ation to CDDP through up-regulation of human copper transporter (hCtr) 1, which is also a transporter
103                                    The human copper transporter hCTR1 is a homotrimer composed of a p
104 he biochemical characterization of the human copper transporter hCtr1, which is important for underst
105 l transport is mediated by the high affinity copper transporter hCTR1.
106                      The human high-affinity copper transporter (hCtr1) plays an important role in th
107 y that expression of the human high-affinity copper transporter (hCtr1) was transcriptionally up-regu
108 s, demonstrating abundant expression of this copper transporter in hippocampal neurons.
109 ggesting that this protein may function as a copper transporter in rat pinealocytes.
110 1p specifically delivers copper to the Ccc2p copper transporter in the Golgi.
111 e copper transporter, Ctr1p, or the putative copper transporter in the secretory pathway, Ccc2p.
112 d member of the conserved CTR/COPT family of copper transporters in Arabidopsis thaliana, COPT6.
113 R1, CTR2, CTR3, and COPT1, encoding CTR-type copper transporters in Chlamydomonas.
114 lta strain; these genes encode the two major copper transporters in laboratory yeast strains.
115 pper transporter 2 (CTR2) is one of the four copper transporters in mammalian cells that influence th
116           We have expressed hCTR1, the human copper transporter, in Sf9 cells using a baculovirus-med
117  entry route of platinum drugs, and that the copper transporter is not internalized in response to ex
118 targeted to the late endosomes and the ATP7A copper transporter is translocated to the PM by elevated
119 et of meningoencephalitis, expression of the copper transporters is induced and is critical for Crypt
120 ansporter 1 (hCTR1), the human high-affinity copper transporter, is the major entry pathway for cDDP
121 ome, these results also show that defects in copper transporter localization contribute to hypopigmen
122 tinum-containing drugs and suggest that this copper transporter may also transport DDP.
123                 Changes in the expression of copper "transporters" may be useful to monitor copper st
124 ngs reveal unique and opposing functions for copper transporters of the host and pathogen during infe
125 he role of other organs expressing the ATP7B copper transporter on metabolic and ultrastructural chan
126                      Cu-ATPases are membrane copper transporters present in all kingdoms of life.
127 ess AgNPs in association with membrane bound copper transporter proteins cause sequestration of coppe
128  distinct from that of RAN1, which encodes a copper transporter required for ethylene receptor functi
129 ast CTR1 gene, which encodes a high-affinity copper transporter, results in increased cisplatin resis
130  Here, the authors report that the lysosomal copper transporter SLC46A3 is induced by TCDD and underl
131 at overexpression of the human or mouse Ctr1 copper transporter stimulates copper uptake in mammalian
132 ithiocarbamate)-copper (CuET) can bypass the copper transporter system and inhibit the function of p9
133                            ATP7A is a faster copper transporter than Wilson disease protein as eviden
134                Human CTR1 is a high-affinity copper transporter that also mediates the uptake of the
135 riants in ATP7A, an evolutionarily conserved copper transporter that is crucial for normal brain deve
136                                   ATP7B is a copper transporter that traffics between the intracellul
137 s subunit of a plasma membrane high affinity copper transporter, the presence of additional subunits
138 ls copper modulates phosphorylation of a key copper transporter, the Wilson's disease protein (WNDP).
139 ome is abnormal AP-1-mediated trafficking of copper transporters; this abnormal trafficking results i
140 carboxyl-terminal tail induce release of the copper transporter to the axons or axonal membranes.
141 module found in all eukaryotic high affinity copper transporters to date, which is sufficient for cop
142 s brain cell types particularly enriched for copper transporter transcripts.
143          The functional significance of this Copper transporter was demonstrated by the finding that
144     The cue system employs an inner membrane copper transporter, whereas the cus system includes a tr
145                    Perturbation of the human copper-transporter Wilson disease protein (ATP7B) causes

 
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