Loh HH - Search Results

1

Morphine drives internal ribosome entry site-mediated hnRNP K translation in neurons through opioid receptor-dependent signaling.

Lee PT, Chao PK, Ou LC, Chuang JY, Lin YC, Chen SC, Chang HF, Law PY, Loh HH, Chao YS, Su TP, Yeh SH. Lee PT, et al. Among authors: loh hh. Nucleic Acids Res. 2014 Dec 1;42(21):13012-25. doi: 10.1093/nar/gku1016. Epub 2014 Oct 31. Nucleic Acids Res. 2014. PMID: 25361975 Free PMC article.

2

Translational repression of mouse mu opioid receptor expression via leaky scanning.

Song KY, Hwang CK, Kim CS, Choi HS, Law PY, Wei LN, Loh HH. Song KY, et al. Among authors: loh hh. Nucleic Acids Res. 2007;35(5):1501-13. doi: 10.1093/nar/gkm034. Epub 2007 Feb 6. Nucleic Acids Res. 2007. PMID: 17284463 Free PMC article.

3

Nuclear factor kappaB signaling in opioid functions and receptor gene expression.

Chen YL, Law PY, Loh HH. Chen YL, et al. Among authors: loh hh. J Neuroimmune Pharmacol. 2006 Sep;1(3):270-9. doi: 10.1007/s11481-006-9028-0. Epub 2006 Jul 8. J Neuroimmune Pharmacol. 2006. PMID: 18040804 Free PMC article. Review.

4

Search for the "ideal analgesic" in pain treatment by engineering the mu-opioid receptor.

Tao PL, Law PY, Loh HH. Tao PL, et al. Among authors: loh hh. IUBMB Life. 2010 Feb;62(2):103-11. doi: 10.1002/iub.292. IUBMB Life. 2010. PMID: 20039371 Free PMC article. Review.

5

Discovery, structure-activity relationship studies, and anti-nociceptive effects of 1-phenyl-3,6,6-trimethyl-1,5,6,7-tetrahydro-4H-indazol-4-one as novel opioid receptor agonists.

Cheng MF, Ou LC, Chen SC, Chang WT, Law PY, Loh HH, Chao YS, Shih C, Yeh SH, Ueng SH. Cheng MF, et al. Among authors: loh hh. Bioorg Med Chem. 2014 Sep 1;22(17):4694-703. doi: 10.1016/j.bmc.2014.07.012. Epub 2014 Jul 16. Bioorg Med Chem. 2014. PMID: 25087049

6

Post-Transcriptional Regulation of the Human Mu-Opioid Receptor (MOR) by Morphine-Induced RNA Binding Proteins hnRNP K and PCBP1.

Song KY, Choi HS, Law PY, Wei LN, Loh HH. Song KY, et al. Among authors: loh hh. J Cell Physiol. 2017 Mar;232(3):576-584. doi: 10.1002/jcp.25455. Epub 2016 Jun 24. J Cell Physiol. 2017. PMID: 27292014 Free PMC article.

7

Discovery, structure-activity relationship studies, and anti-nociceptive effects of N-(1,2,3,4-tetrahydro-1-isoquinolinylmethyl)benzamides as novel opioid receptor agonists.

Chen SR, Ke YY, Yeh TK, Lin SY, Ou LC, Chen SC, Chang WT, Chang HF, Wu ZH, Hsieh CC, Law PY, Loh HH, Shih C, Lai YK, Yeh SH, Ueng SH. Chen SR, et al. Among authors: loh hh. Eur J Med Chem. 2017 Jan 27;126:202-217. doi: 10.1016/j.ejmech.2016.09.003. Epub 2016 Sep 20. Eur J Med Chem. 2017. PMID: 27776274

8

The in vivo antinociceptive and μ-opioid receptor activating effects of the combination of N-phenyl-2',4'-dimethyl-4,5'-bi-1,3-thiazol-2-amines and naloxone.

Lin SY, Kuo YH, Tien YW, Ke YY, Chang WT, Chang HF, Ou LC, Law PY, Xi JH, Tao PL, Loh HH, Chao YS, Shih C, Chen CT, Yeh SH, Ueng SH. Lin SY, et al. Among authors: loh hh. Eur J Med Chem. 2019 Apr 1;167:312-323. doi: 10.1016/j.ejmech.2019.01.063. Epub 2019 Feb 2. Eur J Med Chem. 2019. PMID: 30776693

9

Convallatoxin enhance the ligand-induced mu-opioid receptor endocytosis and attenuate morphine antinociceptive tolerance in mice.

Chao PK, Chang HF, Ou LC, Chuang JY, Lee PT, Chang WT, Chen SC, Ueng SH, Hsu JT, Tao PL, Law PY, Loh HH, Yeh SH. Chao PK, et al. Among authors: loh hh. Sci Rep. 2019 Feb 20;9(1):2405. doi: 10.1038/s41598-019-39555-x. Sci Rep. 2019. PMID: 30787373 Free PMC article.

10

BPR1M97, a dual mu opioid receptor/nociceptin-orphanin FQ peptide receptor agonist, produces potent antinociceptive effects with safer properties than morphine.

Chao PK, Chang HF, Chang WT, Yeh TK, Ou LC, Chuang JY, Tsu-An Hsu J, Tao PL, Loh HH, Shih C, Ueng SH, Yeh SH. Chao PK, et al. Among authors: loh hh. Neuropharmacology. 2020 Apr;166:107678. doi: 10.1016/j.neuropharm.2019.107678. Epub 2019 Jul 3. Neuropharmacology. 2020. PMID: 31278929

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