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1 at from mice lacking c-Mpl (c-Mpl(-/-)), the thrombopoietin receptor.
2 xamine the in vivo effects of eltrombopag, a thrombopoietin receptor agonist (TPO-RA), on platelet fu
3                                          The thrombopoietin receptor agonist eltrombopag has been sho
4                                     The oral thrombopoietin receptor agonist eltrombopag is approved
5                       Eltrombopag (ELT) is a thrombopoietin receptor agonist reported to decrease lab
6                                          The thrombopoietin receptor agonist romiplostim could be an
7                             Romiplostim is a thrombopoietin receptor agonist that increases platelet
8              Eltrombopag is a small molecule thrombopoietin receptor agonist that might be a new opti
9 RE), we aimed to assess eltrombopag, an oral thrombopoietin receptor agonist, for thrombocytopenia (g
10                         Eltrombopag, an oral thrombopoietin receptor agonist, increases platelet coun
11             We tested whether eltrombopag, a thrombopoietin receptor agonist, might be effective in i
12 P were randomly assigned to receive the oral thrombopoietin-receptor agonist eltrombopag (30, 50, or
13         Eltrombopag is an oral, non-peptide, thrombopoietin-receptor agonist that stimulates thrombop
14          Eltrombopag is a new, orally active thrombopoietin-receptor agonist that stimulates thrombop
15  immunosuppression, eltrombopag, a synthetic thrombopoietin-receptor agonist, led to clinically signi
16                The effects of eltrombopag, a thrombopoietin-receptor agonist, on platelet function in
17                       Eltrombopag is an oral thrombopoietin-receptor agonist.
18                                              Thrombopoietin receptor agonists (eltrombopag; romiplost
19 has changed with the advent of rituximab and thrombopoietin receptor agonists (TPO-RAs) as options fo
20  efficacy and safety, in particular, for the thrombopoietin receptor agonists and the occurrence of l
21                                              Thrombopoietin receptor agonists are reported to increas
22 ents respond to antithymocyte globulins, and thrombopoietin receptor agonists are under investigation
23                   Tier 1 options (rituximab, thrombopoietin receptor agonists, low-dose corticosteroi
24 templating pregnancy while on treatment with thrombopoietin receptor agonists, rituximab, or mycophen
25                           PURPOSE OF REVIEW: Thrombopoietin-receptor agonists (TPO-RAs) have been app
26        Stimulation of platelet production by thrombopoietin-receptor agonists (TPO-RAs) is an effecti
27  Combining an immunosuppressant therapy with thrombopoietin-receptor agonists may be a good strategy
28 combination of immunosuppressant therapy and thrombopoietin-receptor agonists that lasted for a media
29 ies of small peptides that bind to the human thrombopoietin receptor and compete with the binding of
30   More recently, activating mutations in the thrombopoietin receptor and in JAK2 exon 12 have been id
31 wn decreased megakaryocyte expression of the thrombopoietin receptor (c-mpl) in patients with polycyt
32    Here we describe a deletion mutant of the thrombopoietin receptor (c-mpl) that has completely lost
33 ematopoietic growth factors that bind to the thrombopoietin receptor, c-Mpl.
34                                            A thrombopoietin receptor derivative that brings the proli
35 growth factor receptor-1 (F36VFGFR1) and the thrombopoietin receptor (F36VMpl) induced a sustained ex
36 d to express a conditional derivative of the thrombopoietin receptor (F36Vmpl).
37 atic activating mutations in JAK2 and in the thrombopoietin receptor gene (MPL) in most patients with
38 al 5 to 10% have activating mutations in the thrombopoietin receptor gene (MPL).
39  a p.Lys39Asn amino acid substitution of the thrombopoietin receptor gene (p = 1.5 x 10(-11)).
40  a chemically induced dimerizer and modified thrombopoietin receptor has now allowed the expansion of
41 mutations of the erythropoietin receptor and thrombopoietin receptor have been identified in familial
42 e discovery of an activating mutation in the thrombopoietin receptor in JAK2-negative myelofibrosis a
43 lation of proteins and the expression of the thrombopoietin receptor in platelets from patients with
44  resultant mice were compared with a Mpl-/- (thrombopoietin receptor knockout) thrombocytopenic murin
45  expression of p21(Cip1), p27(Kip1), and the thrombopoietin receptor, known regulators of HSC self-re
46                    Reduced expression of the thrombopoietin receptor MpI is characteristic of polycyt
47          However, expression of the platelet thrombopoietin receptor MpI was markedly reduced or abse
48                           Endocytosis of the thrombopoietin receptor Mpl was impaired in Dnm2-null pl
49 e demonstrated that mutant CALR binds to the thrombopoietin receptor MPL, and that the positive elect
50 59457 (SB), a nonpeptidyl hydrazone class of thrombopoietin receptor (Mpl) agonist, revealed toxicity
51 5R/R938Q induced spontaneous growth of Ba/F3-thrombopoietin receptor (MPL) but not of Ba/F3-human rec
52                            Expression of the thrombopoietin receptor (Mpl) by platelets and megakaryo
53                   We have reported defective thrombopoietin receptor (Mpl) protein expression in MPD
54             Mutations of thrombopoietin, the thrombopoietin receptor (MPL), and the erythropoietin re
55 port here that amino acid substitutions in a thrombopoietin receptor (Mpl)--containing cell growth sw
56  a marked reduction in the expression of the thrombopoietin receptor, Mpl, in polycythemia vera (PV)
57                                          The thrombopoietin receptor, Mpl, is a member of the cytokin
58 nner in 1 of 3 genes: JAK2, CALR, or MPL The thrombopoietin receptor, MPL, is the key cytokine recept
59 telets, and their precursors all express the thrombopoietin receptor, Mpl, on their cell surface.
60 en OTT-MAL and an activating mutation of the thrombopoietin receptor myeloproliferative leukemia viru
61 tor, the erythropoietin receptor (EpoR), the thrombopoietin receptor, or the granulocyte colony-stimu
62            miR-28 exerts negative effects on thrombopoietin receptor signaling and platelet formation
63 scribed, somatic, activating mutation in the thrombopoietin receptor that is sensitive to down-stream
64 ombopag (EP) is a small-molecule, nonpeptide thrombopoietin receptor (TPO-R) agonist that has been ap
65 ts before (n = 10) and during treatment with thrombopoietin receptor (TPO-R) agonists (n = 9).
66                  Decreased expression of the thrombopoietin receptor (TPOR or MPL) on the cell surfac
67 ns participate in the activity states of the thrombopoietin receptor (TpoR), a type 1 cytokine recept
68                                 In the human thrombopoietin receptor (TpoR), a unique amphipathic RWQ
69 l, small-molecule, nonpeptide agonist of the thrombopoietin receptor (TpoR), being developed as a tre
70 ase 2 phosphorylation, initiated through the thrombopoietin receptor (TPOR/Mpl) activation, was affec
71 genic CALR mutants specifically activate the thrombopoietin receptor (TpoR/MPL).
72 omerize with several other tagged receptors (thrombopoietin receptor, transforming growth factor beta
73                                 Although the thrombopoietin receptor was discovered in 1991 and throm
74  this idea, the signaling domain of Mpl (the thrombopoietin receptor) was targeted to the plasma memb

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