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1 n and activation, or phosphorylation, of the epidermal growth factor receptor kinase.
2 ow affinity of this radiotracer to wild-type epidermal growth factor receptor kinase.
3 wly developed, irreversible inhibitor of the epidermal growth factor receptor kinase.
4 Eps15 is a phosphorylation substrate of the epidermal growth factor receptor kinase.
5 ylated and thereby activated in vitro by the epidermal growth factor receptor kinase.
6 Lapatinib is a dual inhibitor of HER2 and epidermal growth factor receptor kinases.
7 activation by beta(3)AR depends upon Src and epidermal growth factor receptor kinase activities and i
13 tyrosine kinases, including JAK1, JAK3, HCK, epidermal growth factor receptor kinase, and insulin rec
15 13-residue peptide sequence (Y1173) from the epidermal growth factor receptor/kinase (EGFR) at which
16 Ischemic PC had no effect on the activity of epidermal growth factor receptor kinases, either at 5 or
17 ) for noninvasive detection of active mutant epidermal growth factor receptor kinase-expressing non-s
19 the FER kinase inhibitor crizotinib and the epidermal growth factor receptor kinase inhibitor canert
20 ortmannin (IC50 approximately 25 nmol/L) and epidermal growth factor receptor kinase inhibitor gefiti
24 r receptor, with local administration of the epidermal growth factor receptor kinase inhibitors AG147
27 holipase C-beta, protein kinase A, c-Src and epidermal growth factor receptor kinase pathways or inhi
28 e used purified Stat3 alpha, Stat3 beta, and epidermal growth factor receptor kinase produced in reco
29 t PV antibody binding leads to activation of epidermal growth factor receptor kinase, Src, p38 MAPK,
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