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1 bond of big endothelin-3 producing bioactive endothelin-3.
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
8 ptor, endothelin receptor-B, and its ligand, endothelin-3, are required for the development of both m
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
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
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
21 endothelin receptor-B (Ednrb) and its ligand endothelin-3 (Edn3) affect the development of two neural
25 spectively, by the endogenous neuropeptides, endothelin-3 (ET-3) and atrial natriuretic peptide (ANP)
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
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.
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
40 crest-derived cells were exposed in vitro to endothelin-3, IRL 1620 (an endothelin B agonist), and/or
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
47 up to 3-fold) by three known glial mitogens, endothelin-3, platelet-derived growth factor, or phorbol
51 mpetitive inhibition of 125I-endothelin 1 by endothelin 3 was significant for a two-site binding mode
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