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1 ranscript for the major LPA-producing enzyme autotaxin.
2 r A7, angiopoetin 1, endothelial lipase, and autotaxin.
3 and a species homolog of the human cytokine autotaxin.
4 oach is illustrated with the results against autotaxin, a phospholipase implicated in cardiovascular
5 phosphonate (16c) mimicked LPA in inhibiting autotaxin, a secreted lysophospholipase D that produces
7 osphatidic acid (LPA), a lipid by-product of autotaxin activity, is involved in cancer, vascular defe
8 fied mechanism by which galectin-3 regulates autotaxin and assign a novel role for NFAT1 during melan
10 These data indicate that elevated levels of autotaxin and soluble markers of immune activation durin
13 expression of the autocrine motility factor autotaxin, as determined by Affymetrix gene chip, real-t
16 r in EOC ascites, is an enzymatic product of autotaxin (ATX) and phospholipase A(2) (PLA(2))enzymes.
17 ented here identify the extracellular factor autotaxin (ATX) as a novel upstream signal modulating HD
18 program of forming joints, we used GDF-5 and Autotaxin (Atx) as joint tissue specific markers, and So
20 r3 or inhibition of the LPA-producing enzyme autotaxin (ATX) in pregnant mice leads to HB-EGF and COX
37 ramatically (approximately 100-fold) encodes Autotaxin (ATX), a secreted tumor motility-promoting fac
38 udy describes the identification and role of autotaxin (ATX), a secretory protein and a major source
41 l evidence implicated the lysophospholipase, autotaxin (ATX), and its product, lysophosphatidic acid
42 d by the enzymatic activity of extracellular autotaxin (ATX), binds LPA receptors, resulting in an ar
43 clear factor of activated T cells 2 (NFAT1), autotaxin (ATX), lysophosphatidic acid (LPA), and beta-c
44 ial for the motility stimulating activity of autotaxin (ATX), one member of the exophosphodiesterase
51 acid (LPA), a potent neuronal activator, and autotaxin (ATX; ectonucleotide pyrophosphatase/phosphodi
52 mal models express significant quantities of autotaxin (ATX; ENPP2), a lysophospholipase D that catal
54 with itch severity and, in combination with autotaxin, distinguished pregnant women with itch that w
55 profiling identified the protumorigenic gene autotaxin (ENPP2) to be downregulated after silencing ga
57 Here we report that galectin-3 regulates autotaxin expression at the transcriptional level by mod
58 nd that the alpha6beta4 integrin potentiates autotaxin expression through the upregulation and activa
59 ng sites in the promoter region of the mouse autotaxin gene (ATX, ENPP2), which we were able to verif
61 s including osteoprotegerin, syndecan-2, and autotaxin have been refined from the general locations p
63 grin alpha6beta4-dependent overexpression of autotaxin in MDA-MB-435 cells is mediated by NFAT1, but
65 ibitors (bile salts) into potent competitive Autotaxin inhibitors that do not interact with the catal
73 gated LPA-stimulated vascular Akt signaling, autotaxin/LPA-driven phosphorylation of Akt and cyclin D
78 y a novel pathway in which LPA production by autotaxin/lysoPLD regulates murine hemostasis and thromb
79 s and thrombosis and suggest that binding of autotaxin/lysoPLD to activated platelets may provide a m
80 ating interferon-free HCV treatment and that autotaxin may be causally linked to immune activation du
84 wo consensus NFAT binding sites found in the autotaxin promoter strongly and specifically bind NFAT1
88 mice increased levels in the vessel of both autotaxin, the lysophospholipase D enzyme responsible fo
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