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1 ining the vasodilator/clearance functions of endothelin-B receptors.
2                                    Selective endothelin B receptor activation may prove to be a novel
3       Second, the possible dilator effect of endothelin-B receptor activation was tested by the admin
4                                              Endothelin B receptor agonist, IRL-1620, has been shown
5  to a cysteine sulfenic acid modification in endothelin B receptor and consequently decreased endothe
6          These responses are mediated by the endothelin-B receptor and are sustained over a 40 h time
7 transcripts encoding fibronectin, integrins, endothelin B receptor, angiopoietin 2, and delta-like li
8 BR-4628 against IR was lost when a selective endothelin B receptor antagonist was coadministered.
9 nthase inhibitor, NG-nitro-L-arginine or the endothelin B receptor antagonist, BQ-788.
10      All effects of IRL-1620 were blocked by endothelin B receptor antagonist, BQ788.
11  and NMDA-induced behaviours while BQ788, an endothelin B receptor antagonist, did not.
12    We have earlier shown that stimulation of endothelin B receptors by IRL-1620 provides significant
13 ult of autocrine ET-1 release and subsequent endothelin B receptor-dependent NO production, and sugge
14 s in this model, suggesting that blockade of endothelin-B receptors did not yield any additional prot
15      These include mice with deficiencies of endothelin B receptor (Ednrb(s-l); refs 1,2) endothelin
16 we have cloned three previously unrecognized endothelin B receptor (EDNRB) transcripts from a human m
17 ntified in the RET receptor tyrosine kinase, endothelin-B receptor (EDNRB) and its physiological liga
18 schsprung disease, carries a deletion in the endothelin-B receptor (EDNRB) gene that abrogates expres
19 ald locus on mouse chromosome 14 encodes the endothelin-B receptor (EDNRB), a G protein-coupled, seve
20                        Overexpression of the endothelin B receptor (ET(B)R) was associated with the a
21 , the endothelin A receptor (ET(A)R) and the endothelin B receptor (ET(B)R).
22                              The role of the endothelin-B receptor (ET(B)) in vascular homeostasis is
23 thelial nitric oxide synthase (eNOS) via the endothelin-B receptor (ET(B)), suggesting that this sign
24 reased expression of endothelin-1 (ET-1) and endothelin-B receptor (ET-BR) from human pulmonary micro
25                  Endothelin-1 binding to the endothelin B receptor (ETB), a member of the superfamily
26  developmental phenotype seen in ET-3-/- and endothelin B receptor (ETB)-/- mice.
27 lular loop (IL2 or IL3, respectively) of the endothelin B receptor (ETB).
28                 It was hypothesized that the endothelin B receptor (ETBR) and/or the extracellular Ca
29  levels and immunoreactivity of ET-1 and the endothelin B receptor (ETBR) were increased in preeclamp
30  data suggest that the cytosolic tail of the endothelin B receptor is involved in calcium mobilizatio
31                                              Endothelin-B receptors on the pulmonary artery cause vas
32                    The functional effects of endothelin-B receptors on tone are lost after lipopolysa
33 ing IRL-1620 demonstrated an upregulation of endothelin B receptor only in the infarcted hemisphere 7
34 ng through the c-Ret tyrosine kinase and the endothelin B receptor pathways is known to be critical f
35 -1, and determined the vasomotor role of the endothelin-B receptors that are known to be located on r
36 e specific contributions of endothelin-A and endothelin-B receptors to the changes in renal function
37                                           An endothelin B receptor truncated at the C-terminal tail w
38     In the present study, stimulation of the endothelin B receptor was found to activate three distin
39                  The cytoplasmic tail of the endothelin B receptor was found to be required for activ
40              In addition, immunostaining for endothelin-B receptors was present in sections of unoper

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