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1 h and cell survival in a GFL-sensitive mouse pheochromocytoma cell line.
2 ator for RET activation in PC12 cells, a rat pheochromocytoma cell line.
3 quired for NGF-mediated survival in the PC12 pheochromocytoma cell line.
4 oxia (6 h, 1% O(2)) in the oxygen-responsive pheochromocytoma cell line.
5 We observed this effect in PC12W cells (rat pheochromocytoma cell line) and R3T3 cells (mouse fibrob
6 T2) receptor-induced apoptosis in PC12W (rat pheochromocytoma cell line) cells that express abundant
12 system, sGC regulation was examined in a rat pheochromocytoma cell line (PC12) exposed to nerve growt
14 e recombinant human alpha1 I domain, the rat pheochromocytoma cell line (PC12), and the rat glioma Ru
16 ction of neuronal differentiation of the rat pheochromocytoma cell line, PC12 cells, by nerve growth
22 perform studies in a continuous chromaffin (pheochromocytoma) cell line, such as PC12, although such
23 kin 5 promote neurite extension of the PC-12 pheochromocytoma cell line; this effect is abolished by
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