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1 ith an IC(50) of 590 nM but does not inhibit prohormone convertase 2.
2 man prohormone convertase 7 but not by mouse prohormone convertase 2.
4 In Drosophila melanogaster, the homolog of prohormone convertase 2, dPC2 (amontillado), is required
5 nin levels in these brain regions shows that prohormone convertase 2 is important for cholecystokinin
8 mozygous for a deletion in the gene encoding prohormone convertase 2 (PC2) are generally healthy but
9 hermore, VHS-GAT-GFP-overexpression disrupts prohormone convertase 2 (PC2) autocatalytic cleavage, pr
10 og of the vertebrate neuroendocrine-specific Prohormone Convertase 2 (PC2) gene, and showed that amon
11 small-molecule prohormone convertase 1/3 or prohormone convertase 2 (PC2) inhibitors have been descr
14 s two domains, a 21-kDa protein required for prohormone convertase 2 (PC2) maturation and a carboxyl-
16 ese enzymes are evolutionarily related, only prohormone convertase 2 (PC2) requires 7B2 for activatio
17 Here, gene-targeted mice producing defective prohormone convertase 2 (PC2) were used to examine the p
18 7B2 is required for the production of active prohormone convertase 2 (PC2), an enzyme involved in the
19 ein 7B2 has been implicated in activation of prohormone convertase 2 (PC2), an important neuroendocri
23 he cDNA revealed that it corresponded to the prohormone convertase-2 (PC2) gene, which is involved in
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