Maeda H - Search Results

1

Anti-ORAI1 antibody DS-2741a, a specific CRAC channel blocker, shows ideal therapeutic profiles for allergic disease via suppression of aberrant T-cell and mast cell activation.

Aki A, Tanaka K, Nagaoka N, Kimura T, Baba D, Onodera Y, Wada T, Maeda H, Nakanishi T, Agatsuma T, Komai T. Aki A, et al. Among authors: maeda h. FASEB Bioadv. 2020 Jul 8;2(8):478-488. doi: 10.1096/fba.2020-00008. eCollection 2020 Aug. FASEB Bioadv. 2020. PMID: 32821879 Free PMC article.

2

Medium-chain fatty acid-sensing receptor, GPR84, is a proinflammatory receptor.

Suzuki M, Takaishi S, Nagasaki M, Onozawa Y, Iino I, Maeda H, Komai T, Oda T. Suzuki M, et al. Among authors: maeda h. J Biol Chem. 2013 Apr 12;288(15):10684-91. doi: 10.1074/jbc.M112.420042. Epub 2013 Feb 28. J Biol Chem. 2013. PMID: 23449982 Free PMC article.

3

Formyl peptide receptor 1 and 2 dual agonist inhibits human neutrophil chemotaxis by the induction of chemoattractant receptor cross-desensitization.

Sogawa Y, Ohyama T, Maeda H, Hirahara K. Sogawa Y, et al. Among authors: maeda h. J Pharmacol Sci. 2011;115(1):63-8. doi: 10.1254/jphs.10194fp. Epub 2010 Dec 14. J Pharmacol Sci. 2011. PMID: 21173551 Free article.

4

Evaluation of the therapeutic index of a novel phosphodiesterase 4B-selective inhibitor over phosphodiesterase 4D in mice.

Suzuki O, Mizukami K, Etori M, Sogawa Y, Takagi N, Tsuchida H, Morimoto K, Goto T, Yoshino T, Mikkaichi T, Hirahara K, Nakamura S, Maeda H. Suzuki O, et al. Among authors: maeda h. J Pharmacol Sci. 2013;123(3):219-26. doi: 10.1254/jphs.13103fp. Epub 2013 Oct 22. J Pharmacol Sci. 2013. PMID: 24152964 Free article.

5

Design of 2'-O-methyl RNA and DNA double-stranded oligonucleotides: naturally-occurring nucleotide components with strong RNA interference gene expression inhibitory activity.

Koizumi M, Hirota Y, Nakayama M, Tamura M, Obuchi W, Kurimoto A, Tsuchida H, Maeda H. Koizumi M, et al. Among authors: maeda h. Nucleosides Nucleotides Nucleic Acids. 2020;39(1-3):292-309. doi: 10.1080/15257770.2019.1663384. Epub 2019 Sep 11. Nucleosides Nucleotides Nucleic Acids. 2020. PMID: 31509065

6

Discovery and pharmacological effects of a novel GPR142 antagonist.

Murakoshi M, Kuwabara H, Nagasaki M, Xiong YM, Reagan JD, Maeda H, Nara F. Murakoshi M, et al. Among authors: maeda h. J Recept Signal Transduct Res. 2017 Jun;37(3):290-296. doi: 10.1080/10799893.2016.1247861. Epub 2016 Nov 3. J Recept Signal Transduct Res. 2017. PMID: 27807998

7

ASB20123: A novel C-type natriuretic peptide derivative for treatment of growth failure and dwarfism.

Morozumi N, Yotsumoto T, Yamaki A, Yoshikiyo K, Yoshida S, Nakamura R, Jindo T, Furuya M, Maeda H, Minamitake Y, Kangawa K. Morozumi N, et al. Among authors: maeda h. PLoS One. 2019 Feb 22;14(2):e0212680. doi: 10.1371/journal.pone.0212680. eCollection 2019. PLoS One. 2019. PMID: 30794654 Free PMC article.

8

Safety assessment of a novel C-type natriuretic peptide derivative and the mechanism of bone- and cartilage-specific toxicity.

Yotsumoto T, Morozumi N, Nakamura R, Jindo T, Furuya M, Abe Y, Nishimura T, Maeda H, Ogasawara H, Minamitake Y, Kangawa K. Yotsumoto T, et al. Among authors: maeda h. PLoS One. 2019 Sep 11;14(9):e0218229. doi: 10.1371/journal.pone.0218229. eCollection 2019. PLoS One. 2019. PMID: 31509532 Free PMC article.

9

The pyrazolone originally reported to be a formyl peptide receptor (FPR) 2/ALX-selective agonist is instead an FPR1 and FPR2/ALX dual agonist.

Sogawa Y, Shimizugawa A, Ohyama T, Maeda H, Hirahara K. Sogawa Y, et al. Among authors: maeda h. J Pharmacol Sci. 2009 Nov;111(3):317-21. doi: 10.1254/jphs.09196sc. J Pharmacol Sci. 2009. PMID: 19926937 Free article.

10

C-type natriuretic peptide improves growth retardation in a mouse model of cardio-facio-cutaneous syndrome.

Inoue SI, Morozumi N, Yoshikiyo K, Maeda H, Aoki Y. Inoue SI, et al. Among authors: maeda h. Hum Mol Genet. 2019 Jan 1;28(1):74-83. doi: 10.1093/hmg/ddy333. Hum Mol Genet. 2019. PMID: 30239744

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