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1 ddition, they are associated with erbB-1 and erbB-4 receptors.
2 ) associates physically with the full-length ErbB-4 receptor and functionally with the ErbB-4 cytopla
3 nd-dependent receptor trafficking, activated ErbB-4 receptors are subject to proteolytic cleavage inv
4 ctivity, however, does not act on the native ErbB-4 receptor before the metalloprotease-mediated clea
5 R analysis that expression of the ErbB-2 and ErbB-4 receptors, but not ErbB-1 or ErbB-3, is deregulat
6 ly regulates heregulin signaling through the ErbB-4 receptor by the activation of a selective proteol
9 ced receptor trafficking between the EGF and ErbB-4 receptors, EGF and heregulin have equivalent capa
14 ozyme strategy to achieve down-regulation of ErbB-4 receptors in various breast cancer cell lines.
15 ssays that intramembrane cleavage of APP and ErbB-4 receptor is not impaired by the Abeta42-lowering
16 binding to NIH 3T3 cells overexpressing the ErbB-4 receptor is rapidly decreased by 12-O-tetradecano
19 we show that activation of astrocytic erbB-2/erbB-4 receptors plays a significant role in the process
26 er cells revealed that the expression of the ErbB-4 receptor was completely abrogated by ribozyme tre
27 analyzed the heregulin-responsive wild-type ErbB-4 receptor, which does not mediate the rapid intern
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