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1 ibly degraded by the highly conserved enzyme sphingosine-1-phosphate lyase.
2 and demonstrate that inhibiting the enzyme, sphingosine-1-phosphate lyase 1 (SPL), has neuroprotecti
3 he expression of sphingosine kinase 1 and 2, sphingosine-1-phosphate lyase 1, and sphingosine-1-phosp
4 otein kinase type I-beta regulatory subunit, sphingosine-1-phosphate lyase 1, centaurin beta 1, prote
5 hingosine-1-phosphate receptor-1 (S1PR1) and sphingosine-1-phosphate lyase-1 (SPL1) in splenocytes wa
7 eatment of mice with FTY720 inhibited tissue sphingosine-1-phosphate lyase activity within 12 h, wher
11 osphate was stable in the presence of active sphingosine-1-phosphate lyase, demonstrating that the ly
12 iotropic effect, which is due to the loss of sphingosine-1-phosphate lyase, establishes sphingolipids
15 ian cell fate decisions, a recombinant human sphingosine-1-phosphate lyase fused to green fluorescent
18 Additionally, we demonstrate that the human sphingosine-1-phosphate lyase gene is regulated by a GAT
19 isruption in Dictyostelium discoideum of the sphingosine-1-phosphate lyase gene, which encodes the en
22 neumophila translocates the effector protein sphingosine-1 phosphate lyase (LpSpl) to target the host
23 ffects of FTY720 on immune function and that sphingosine-1-phosphate lyase may be a potential target
26 ial role, mechanisms affecting expression of sphingosine-1-phosphate lyase remain poorly understood.
29 phingosine signaling pathways, we identified sphingosine-1-phosphate lyase (S1PL) as a drug target fo
30 iant, we describe the novel interaction with sphingosine 1-phosphate lyase (SGPL1)-a key enzyme for t
33 ctions between FTY720, FTY720-phosphate, and sphingosine-1-phosphate lyase, the enzyme responsible fo
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