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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 copper depletion or genetic perturbations to copper transport proteins.
6 arily accomplished through the Ctr family of copper transport proteins.
7 Env-pseudotyped MLV reporters, we identified copper transport protein 1 (CTR1) as a receptor that was
8 rsa, and the major copper influx transporter copper transport protein 1 (CTR1) has been shown to regu
9 s to nAg and Ag(+), expression levels of the Copper Transport Protein 2 (CTR2) indicated that Ag biou
10 tions between two Drosophila plasma membrane copper transport proteins and demonstrate that copper im
12 on of OsCOPT1, which encodes a high-affinity copper transport protein, as well as other copper-defici
13 3747, demonstrating that these mycobacterial copper transport proteins B (MctB) are essential for Cu
15 A widely conserved family of high affinity copper transport proteins (Ctr proteins) mediates copper
19 served that ctr4(+), a previously identified copper transport protein from the fission yeast Schizosa
20 Here, we propose that COPT2, a high-affinity copper transport protein, functions under copper and iro
21 e of Ctr4 and a putative human high affinity copper transport protein, hCtr1, suggests that they are
22 smin (CP), the major plasma anti-oxidant and copper transport protein, is synthesized in several tiss