Andras Z. Ronai, Ph.D.

Affiliations: 
2004 Semmelweis Egyetem, Hungary 
Area:
Pharmacology, Psychobiology Psychology
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"Andras Ronai"
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Kalman Magyar grad student 2004 Semmelweis Egyetem
 (Natural opioid peptides, synthetic analogs, peptidases: Pharmacological analysis and drug design.)
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Publications

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Király K, Lambeir AM, Szalai J, et al. (2011) The dipeptidyl peptidase IV (CD26, EC 3.4.14.5) inhibitor vildagliptin is a potent antihyperalgesic in rats by promoting endomorphin-2 generation in the spinal cord. European Journal of Pharmacology. 650: 195-9
Szentirmay A, Király K, Puskár Z, et al. (2011) The antihyperalgesic and acute antinociceptive effects of intrathecally injected DAMGO, endomorphin 2 and the endomorphin 2 biosynthesis inducers ILE-PRO-ILE and vildagliptin in rats Pharmacological Reports. 63: 242-242
Király K, Kozsurek M, Puskár Z, et al. (2011) The possible role of endomorphin 2 biosynthesis and CART peptide in the nociceptive information processing in rat spinal dorsal horn: pharmacology and immunohistochemistry Pharmacological Reports. 63: 241
Király K, Szalay B, Szalai J, et al. (2009) Intrathecally injected Ile-Pro-Ile, an inhibitor of membrane ectoenzyme dipeptidyl peptidase IV, is antihyperalgesic in rats by switching the enzyme from hydrolase to synthase functional mode to generate endomorphin 2. European Journal of Pharmacology. 620: 21-6
Rónai AZ, Király K, Szebeni A, et al. (2009) Immunoreactive endomorphin 2 is generated extracellularly in rat isolated L4,5 dorsal root ganglia by DPP-IV. Regulatory Peptides. 157: 1-2
Szemenyei E, Barna I, Mergl Z, et al. (2008) Detection of a novel immunoreactive endomorphin 2-like peptide in rat brain extracts. Regulatory Peptides. 148: 54-61
Kató E, Lipták L, Shujaa N, et al. (2008) alpha2B-adrenoceptor agonist ST-91 antagonizes beta2-adrenoceptor-mediated relaxation in rat mesenteric artery rings. European Journal of Pharmacology. 580: 361-5
Rónai AZ, Szemenyei E, Kató E, et al. (2006) Endomorphin synthesis in rat brain from intracerebroventricularly injected [3H]-Tyr-Pro: a possible biosynthetic route for endomorphins. Regulatory Peptides. 134: 54-60
Rónai AZ, Al-Khrasani M, Benyhe S, et al. (2006) Partial and full agonism in endomorphin derivatives: comparison by null and operational model. Peptides. 27: 1507-13
Ligeti M, Gündüz O, Magyar A, et al. (2005) Synthesis and biological studies of nociceptin derivatives containing the DTPA chelating group for further labeling with therapeutic radionuclides. Peptides. 26: 1159-66
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