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1 he topological orientation of the yeast Ctr1 copper transport protein.
2 compounds able to restore function to faulty copper transport proteins.
3  represses transcription of genes coding for copper transport proteins.
4 he CTR1 and CTR3-encoded membrane-associated copper transport proteins.
5 arily accomplished through the Ctr family of copper transport proteins.
6 Env-pseudotyped MLV reporters, we identified copper transport protein 1 (CTR1) as a receptor that was
7 rsa, and the major copper influx transporter copper transport protein 1 (CTR1) has been shown to regu
8 s to nAg and Ag(+), expression levels of the Copper Transport Protein 2 (CTR2) indicated that Ag biou
9 tions between two Drosophila plasma membrane copper transport proteins and demonstrate that copper im
10 sels is dramatically decreased whereas other copper transport proteins are not altered.
11 on of OsCOPT1, which encodes a high-affinity copper transport protein, as well as other copper-defici
12 3747, demonstrating that these mycobacterial copper transport proteins B (MctB) are essential for Cu
13   A widely conserved family of high affinity copper transport proteins (Ctr proteins) mediates copper
14              Studies in mice reveal that the copper transport protein Ctr1 is essential for intestina
15                          Moreover, knockdown copper transport protein, Ctr1, also inhibited CoCl2-ind
16  transported into cells by two high affinity copper transport proteins, Ctr1 and Ctr3.
17 served that ctr4(+), a previously identified copper transport protein from the fission yeast Schizosa
18 Here, we propose that COPT2, a high-affinity copper transport protein, functions under copper and iro
19 e of Ctr4 and a putative human high affinity copper transport protein, hCtr1, suggests that they are
20 smin (CP), the major plasma anti-oxidant and copper transport protein, is synthesized in several tiss
21                                     Atox1, a copper transport protein, was recently identified as a c

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