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1 bond of big endothelin-3 producing bioactive endothelin-3.
2 potent bioactive peptide, by cleavage of big endothelin-3, a larger intermediate precursor.
3  protein is a zinc endopeptidase that yields endothelin-3, a potent bioactive peptide, by cleavage of
4 roblast growth factor, stem cell factor, and endothelin-3, along with exposure to UVB can transform n
5                                              Endothelin-3 also does not increase the number of enteri
6 -crest-derived cell cultures was promoted by endothelin-3 and inhibited by BQ 788.
7                             Endothelin-1 and endothelin-3 are principally produced by vascular endoth
8 ptor, endothelin receptor-B, and its ligand, endothelin-3, are required for the development of both m
9 er of neuronal development, was inhibited by endothelin-3, but promoted by BQ 788.
10 , expressed in K562 and HEK293 cells, had no endothelin-3-converting activity, in contrast to the com
11 frican heritage than in Caucasians also have endothelin-3-converting enzyme activity and that the rec
12 y of zinc endopeptidases and functions as an endothelin-3-converting enzyme.
13  neural crest cells is reduced in the gut of endothelin 3-deficient embryos.
14 explants of the terminal bowel of E12 ls/ls (endothelin-3-deficient) mice, but could be induced to do
15 d the mutant cells never responded to Mgf or endothelin 3, did not express Dct, and never showed pigm
16 endothelin B receptor (Ednrb(s-l); refs 1,2) endothelin 3 (Edn3(ls): refs 1,3) the tyrosine kinase re
17                                              Endothelin 3 (Edn3) encodes a ligand important to develo
18 in white mutants a transcriptional defect in endothelin 3 (edn3), encoding a peptide factor that prom
19 d by molecules such as the signaling protein endothelin 3 (EDN3), its receptor (the endothelin recept
20 ceptor (EDNRB) and its physiological ligand, endothelin 3 (EDN3).
21 endothelin receptor-B (Ednrb) and its ligand endothelin-3 (Edn3) affect the development of two neural
22                              We suggest that endothelin-3/endothelin B normally prevents the prematur
23                    To analyze the effects of endothelin-3/endothelin B on the differentiation of ente
24                                      Loss of Endothelin-3/Endothelin receptor B (EDNRB) signaling lea
25 spectively, by the endogenous neuropeptides, endothelin-3 (ET-3) and atrial natriuretic peptide (ANP)
26                                 In addition, endothelin-3 (ET-3) and N-succinyl-[Glu9, Ala11, 15]-ET-
27 rol mutant protein, specifically cleaved big endothelin-3 (ET-3) at Trp(21)-Ile(22), yielding ET-3, a
28 eptides which render endothelin-1 (ET-1) and endothelin-3 (ET-3) relatively unreactive and resistant
29                      Endothelin-1 (ET-1) and endothelin-3 (ET-3) were injected via a double-injection
30  and distribution of endothelin-1 (ET-1) and endothelin-3 (ET-3) were studied in the retinas of diabe
31 sly shown that the endogenous neuropeptides, endothelin-3 (ET-3), and atrial natriuretic peptide (ANP
32 otein-coupled growth factor receptor ligand, endothelin-3 (ET-3), regulate astrocyte proliferation at
33 oenvironment is critical in this process and endothelin-3 (ET3) is known to have an essential role.
34                                              Endothelin-3 failed to stimulate the incorporation of [3
35         Our findings indicate that SOX10 and endothelin 3 have a crucial role in the maintenance of m
36  regulator SOX10 and the signalling molecule endothelin 3 have important roles in the development of
37 ient) mice, but could be induced to do so by endothelin-3 if a source of neural precursors was presen
38                                              Endothelin-3 inhibited neuronal development, an effect t
39                     We also demonstrate that endothelin 3 inhibits reversibly the commitment and diff
40 crest-derived cells were exposed in vitro to endothelin-3, IRL 1620 (an endothelin B agonist), and/or
41         The dependence of ENS progenitors on endothelin 3 is more pronounced at the migratory front o
42 , provided that the melanocyte growth factor endothelin-3 is present, a small number of MITF/beta-Gal
43     In combination with stem cell factor and endothelin 3, LIF induced formation of disorganized stru
44 is associated with relatively high levels of endothelin 3 mRNA.
45            Addition of the Kit ligand Mgf or endothelin 3 or a combination of these factors all rapid
46 erminal colon is aganglionic in mice lacking endothelin-3 or its receptor, endothelin B.
47 up to 3-fold) by three known glial mitogens, endothelin-3, platelet-derived growth factor, or phorbol
48            C-ANP also strongly inhibited the endothelin-3-, platelet-derived growth factor-, and phor
49 tially cleaves a Trp(21)-Ile(22) bond of big endothelin-3 producing bioactive endothelin-3.
50      The magnitude of contractions caused by endothelin 3 was reduced further when infection was pres
51 mpetitive inhibition of 125I-endothelin 1 by endothelin 3 was significant for a two-site binding mode
52 of crest-derived cells, and did so even when endothelin-3 was absent and BQ 788 was present.
53          In contrast, contractions caused by endothelin 3 were reduced in bronchi from rejecting allo
54                                              Endothelin 3 (which stimulates endothelin A and B recept

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