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1 tein (SAP) kinases p46/54 SAP kinase and p38 SAP kinase.
8 arkedly activated the MAP kinases, ERK-1 and SAP kinase (JNK), which are substrates for MEK-1 and SEK
9 kinases; Erks) and stress-activated protein (SAP) kinases mediate cellular responses to a wide variet
10 the stress-mediated activation of the JNK-1 SAP kinase or RK/p38 in vivo, or to inhibit nuclear sign
11 er components of the pathway mediated by the SAP kinase p38 change their cellular location on activat
13 nhibitor (PD98059) the basal activity of the SAP kinase pathway was enhanced twofold, and the ability
14 of a 1 Gy radiation exposure to activate the SAP kinase pathway was increased approximately sixfold 6
16 tivities of protein kinase A and the MAP and SAP kinase pathways may represent one physiological mech
17 n (MAP) kinase and stress activated protein (SAP) kinase pathways, and induced p21(Cip-1/WAF1) via a
18 rmacologic assessment of Erk/MAP kinase, Jnk/SAP kinase, PI 3-kinase, protein kinase C, and the Src-r
21 ccurs upon PHX and results in an increase in SAP kinase versus MAP kinase signaling by catecholamines
22 ely 60% identical to that of the other three SAP kinases which contain a TGY motif in their activatio
23 ctivity of MAP and stress-activated protein (SAP) kinases, which results in decreased insulin signali
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