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   1 activation of PI3K/Akt and p38 MAPK, but not MEK kinase.                                             
     2 hat is independent of both Mcs4 and the Wak1 MEK kinase.                                             
     3                           Raf is a candidate MEK kinase.                                             
     4 ctors and, in turn, activates its substrate, MEK kinase.                                             
     5 ulates Ras GTP-loading and activates Raf and MEK kinases.                                            
     6 m components of the MAPK pathway, B-Raf, and MEK kinases.                                            
     7  TPA induced the association of PKCbeta with MEK kinase 1 (MEKK-1), an upstream effector of the SAPK/
     8 e we show that nuclear c-Abl associates with MEK kinase 1 (MEKK-1), an upstream effector of the SEK1-
  
  
  
    12 o activate this pathway; a dominant-negative MEK kinase 1 (MEKK1) blocks activation of SAPK by NIK.  
  
  
  
  
  
  
  
  
    21     Targeted disruption of the gene encoding MEK kinase 1 (MEKK1), a mitogen-activated protein kinase
  
    23 -GTPase activating protein, RAB35), kinases (MEK kinase 1 and 4, PKC, MLCK, cyclin G-associated kinas
    24  activation by expression of kinase-inactive MEK kinase 1(MEKK1) or dominant-negative IkappaB (DeltaI
    25 aspase 3 are inhibited in cells deficient in MEK kinase 1, an upstream activator of JNK in reovirus-i
    26 The mitogen-activated protein kinase kinase (MEK) kinase 1 (MEKK1) mediates activin B signals require
  
  
  
    30 fluorescence imaging demonstrate that T cell MEK kinase 2 (MEKK2) is translocated to the T cell/antig
  
    32 domain-containing adaptor protein that binds MEK kinase 2 (MEKK2), a mitogen-activated protein kinase
  
  
    35 rgeted mutation of the active site lysine of MEK kinase 4 (MEKK4) produces a kinase-inactive MEKK4 pr
  
  
  
  
    40 itogen-activated protein kinase kinase (MAPK/MEK) kinase and phosphatidylinositol-3 (PI3) kinase, res
    41    Spa2p interacts with Ste11p (MAPK kinase [MEK] kinase) and Ste7p (MEK) of the mating signaling pat
  
  
  
    45 otentiated by signalling through the Ras-Raf-MEK kinase cascade and inhibited by a direct interaction
  
    47 on of Ras activation, negative regulation of MEK kinase (e.g. Raf) activities, and up-regulation of d
  
  
  
  
  
    53 , demonstrating that beta2AR stimulation and Mek kinase inhibition are required for ARA-211 antitumor
  
  
  
  
    58 ated protein kinase (MAP kinase)/ERK kinase (MEK) kinase inhibitor SL327, but not with the nonblood-b
  
  
  
    62 In this study, we cloned a full-length human MEK kinase (MEKK) 2 cDNA from Jurkat T-cells and demonst
  
    64 mammalian p65PAK protein kinases), Ste11 [an MEK kinase (MEKK) or MAPK kinase (MEK) kinase], Ste7 (ME
  
  
  
  
  
  
    71  this study, we investigated the role of the MEK kinase (MEKK)1/ERK/p90 ribosomal S6 kinase (RSK)1-de
    72 ivated/extracellular response kinase kinase (MEK) kinase (MEKK) is a serine-threonine kinase that reg
    73  with a dominant-negative MAP kinase kinase (MEK kinase, MEKK-1), confirming that HBx stimulates the 
    74 Nck-interacting kinase, acts upstream of the MEK kinase MEKK1 to activate the c-Jun N-terminal kinase
    75 cascade, activates NHE1 through a Cdc42- and MEK kinase (MEKK1)-dependent mechanism that is independe
  
  
    78 tified a developmentally regulated, putative MEK kinase (MEKKalpha) that contains an F-box and WD40 r
  
  
    81 t PTP3, suppressed growth defects due to the MEK kinase mutation, BCK1-20, and the MEK mutation, MKK1
  
  
    84 s fully compensated by other Raf proteins or MEK kinases or that its role in MEK/ERK activation is hi
    85 af-MEK-MAPK pathway with PD98059, or the Ras-MEK kinase-p38 pathway with SB203580 had no effect on ra
    86 tivity also was observed between the LPS and MEK kinase pathways, indicating that mutual antagonism c
  
  
    89 mains (in order): leucine-rich repeats, Ras, MEK kinase, Ras guanine nucleotide exchange factor N-ter
    90 an unidentified protein kinase A-insensitive MEK kinase, rather than Raf-1, to regulate ERK activity.
    91 Our results show that B-Raf was the critical MEK kinase required for M phase activation of the MAPK p
    92 In addition, U0126 (a selective inhibitor of MEK kinase responsible for ERK phosphorylation) blocked 
    93  Ste11 [an MEK kinase (MEKK) or MAPK kinase (MEK) kinase], Ste7 (MEK or MAPK kinase), and the transcr
    94 aused by deletion of BCK1, a gene encoding a MEK kinase that functions in a mitogen-activated protein
    95  that the mixed lineage kinases (MLK1-4) are MEK kinases that reactivate the MEK/ERK pathway in the p
    96 eam of Wak1, a homolog of the SSK2 and SSK22 MEK kinases, which transmits the stress signal to the Wi
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