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   1 RS-1 renders it a poorer substrate for JAK1 (Janus kinase-1).                                        
     2 facitinib (CP-690,550), an oral inhibitor of Janus kinases 1, 2, and 3 with in vitro functional speci
     3 ase 2 study for the treatment of MF with the Janus kinase 1/2 (JAK1/2) inhibitor momelotinib (MMB) de
  
  
     6 agues report their results on the use of the Janus kinase 1/2 (JAK1/2) inhibitor ruxolitinib in murin
  
  
     9 ) transcription factor and the JAK1/2-STAT3 (Janus Kinase 1/2 - Signal Transducer and Activator of Tr
    10 n of STAT1 signaling with the small-molecule Janus kinase 1/2 inhibitor ruxolitinib in vitro and in v
  
  
  
    14 dogenously processed K(d)-restricted peptide Janus kinase-1(3)(5)(5)(-)(3)(6)(3) (~15,000 copies/cell
  
  
    17  treatment with tofacitinib citrate, an oral Janus kinase 1/3 inhibitor, resulted in significant repi
    18 validation of one of these candidates, Jak1 (Janus kinase 1), a tyrosine kinase of the nonreceptor ty
    19     In phase 2 studies, baricitinib, an oral Janus kinase 1 and 2 inhibitor, reduced disease activity
    20 helial cells by decreasing the expression of Janus kinase 1 and p48, two essential components of the 
    21 ptor and correlated with rapid and sustained Janus kinase 1 and tyrosine kinase (Tyk) 2 tyrosine phos
    22 mmac-dependent signal requires activation of Janus kinases 1 and 3 and is sensitive to wortmannin, im
    23 s found that IL-4-induced phosphorylation of Janus kinases 1 and 3, IL-4R alpha, signal transducer an
  
  
  
    27 nt inhibition of interleukin-6 activation of janus kinase-1, gp 130, the interleukin-6 receptor, STAT
    28 e interleukin-6 signaling pathway, including janus kinase-1, gp 130, the interleukin-6 receptor, STAT
    29    Finally, we determined that inhibition of Janus kinase 1, inhibition of Glycogen synthase kinase 3
    30 d that phosphorylation levels of IL-4Ralpha, Janus kinase 1, insulin receptor substrate 1, and insuli
    31 e intracellular domain of IL-4Ralpha induces Janus kinase 1 (Jak1) activation, STAT6 activation, and 
    32  we discovered that miR-373 directly targets Janus kinase 1 (JAK1) and IFN-regulating factor 9 (IRF9)
  
  
    35  PDGF stimulates tyrosine phosphorylation of Janus kinase 1 (JAK1) and the signal transducer and acti
  
    37 ng the IL-4Ralpha subunit and the associated Janus kinase 1 (Jak1) as common essential components.   
    38 f the FERM and SH2-like domains of the human Janus kinase 1 (JAK1) bound to a fragment of the intrace
    39 is required for H(2)O(2) responsiveness, and Janus kinase 1 (JAK1) is required for adequate basal sig
  
    41 enes encoding interferon-receptor-associated Janus kinase 1 (JAK1) or Janus kinase 2 (JAK2), concurre
    42 mutations, including activating mutations of Janus kinase 1 (JAK1), in 9.1% of patients and provides 
    43 ng the IL-2 receptor beta chain (IL-2Rbeta), Janus kinase 1 (Jak1), Jak3, signal transducer/activator
    44 ctivators of transcription 1 (STAT1), STAT3, Janus kinase 1 (Jak1), Shc, Grb2, Sos1, and HGF receptor
  
  
    47 IFN-gamma alone can activate NF-kappaB, by a Janus kinase-1-mediated, but Stat1-independent, mechanis
    48 nt mutations of either the Box1 motif (binds Janus kinase 1) or the signal transducer and activator o
    49  10 (IP-10), and the signaling intermediates Janus kinase 1, signal transducer and activator of trans
  
    51 rc, epidermal growth factor receptor (EGFR), Janus kinase 1, tyrosine kinases, and G-protein-coupled 
    52 mponent of IL-6 signal transduction pathway, janus kinase-1, was unchanged following either CLP or 2C
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