Tóth G - Search Results

1

Endomorphin synthesis in rat brain from intracerebroventricularly injected [3H]-Tyr-Pro: a possible biosynthetic route for endomorphins.

Rónai AZ, Szemenyei E, Kató E, Kocsis L, Orosz G, Al-Khrasani M, Tóth G. Rónai AZ, et al. Among authors: toth g. Regul Pept. 2006 Mar 15;134(1):54-60. doi: 10.1016/j.regpep.2005.12.004. Epub 2006 Feb 7. Regul Pept. 2006. PMID: 16464510

2

Partial and full agonism in endomorphin derivatives: comparison by null and operational model.

Rónai AZ, Al-Khrasani M, Benyhe S, Lengyel I, Kocsis L, Orosz G, Tóth G, Kató E, Tóthfalusi L. Rónai AZ, et al. Among authors: toth g. Peptides. 2006 Jun;27(6):1507-13. doi: 10.1016/j.peptides.2005.12.003. Epub 2006 Jan 18. Peptides. 2006. PMID: 16413634

3

Detection of a novel immunoreactive endomorphin 2-like peptide in rat brain extracts.

Szemenyei E, Barna I, Mergl Z, Keresztes A, Darula Z, Kató E, Tóth G, Rónai AZ. Szemenyei E, et al. Among authors: toth g. Regul Pept. 2008 Jun 5;148(1-3):54-61. doi: 10.1016/j.regpep.2008.03.001. Epub 2008 Mar 18. Regul Pept. 2008. PMID: 18440655

4

Immunoreactive endomorphin 2 is generated extracellularly in rat isolated L4,5 dorsal root ganglia by DPP-IV.

Rónai AZ, Király K, Szebeni A, Szemenyei E, Prohászka Z, Darula Z, Tóth G, Till I, Szalay B, Kató E, Barna I. Rónai AZ, et al. Among authors: toth g. Regul Pept. 2009 Oct 9;157(1-3):1-2. doi: 10.1016/j.regpep.2009.06.006. Epub 2009 Jun 21. Regul Pept. 2009. PMID: 19540879

5

Nociceptin antagonism: probing the receptor by N-acetyl oligopeptides.

Kocsis L, Orosz G, Magyar A, Al-Khrasani M, Kató E, Rónai AZ, Bes B, Meunier JC, Gündüz O, Tóth G, Borsodi A, Benyhe S. Kocsis L, et al. Among authors: toth g. Regul Pept. 2004 Nov 15;122(3):199-207. doi: 10.1016/j.regpep.2004.06.019. Regul Pept. 2004. PMID: 15491792

6

Synthesis and biological studies of nociceptin derivatives containing the DTPA chelating group for further labeling with therapeutic radionuclides.

Ligeti M, Gündüz O, Magyar A, Kató E, Rónai AZ, Vita C, Varga I, Hudecz F, Tóth G, Borsodi A, Benyhe S. Ligeti M, et al. Among authors: toth g. Peptides. 2005 Jul;26(7):1159-66. doi: 10.1016/j.peptides.2005.01.018. Epub 2005 Mar 2. Peptides. 2005. PMID: 15949634

7

Structure-activity study on the Phe side chain arrangement of endomorphins using conformationally constrained analogues.

Tömböly C, Kövér KE, Péter A, Tourwé D, Biyashev D, Benyhe S, Borsodi A, Al-Khrasani M, Rónai AZ, Tóth G. Tömböly C, et al. Among authors: toth g. J Med Chem. 2004 Jan 29;47(3):735-43. doi: 10.1021/jm0310028. J Med Chem. 2004. PMID: 14736254

8

Side chain modifications change the binding and agonist properties of endomorphin 2.

Lengyel I, Orosz G, Biyashev D, Kocsis L, Al-Khrasani M, Rónai A, Tömböly C, Fürst Z, Tóth G, Borsodi A. Lengyel I, et al. Among authors: toth g. Biochem Biophys Res Commun. 2002 Jan 11;290(1):153-61. doi: 10.1006/bbrc.2001.6136. Biochem Biophys Res Commun. 2002. PMID: 11779147

9

Diprotin A, an inhibitor of dipeptidyl aminopeptidase IV(EC 3.4.14.5) produces naloxone-reversible analgesia in rats.

Rónai AZ, Timár J, Makó E, Erdö F, Gyarmati Z, Tóth G, Orosz G, Fürst S, Székely JI. Rónai AZ, et al. Among authors: toth g. Life Sci. 1999;64(2):145-52. doi: 10.1016/s0024-3205(98)00544-x. Life Sci. 1999. PMID: 10069492

10

Opioid antagonist properties of the highly delta-receptor-selective BOC-Tyr-Pro-Gly-Phe-Leu-Thr (OtBu) peptide and of its Phe1 and Mel1 analogues.

Rónai AZ, Magyar A, Orosz G, Borsodi A, Benyhe S, Tóth G, Makó E, Kátay E, Babka E, Medzihradszky K. Rónai AZ, et al. Among authors: toth g. Arch Int Pharmacodyn Ther. 1995 Nov-Dec;330(3):361-9. Arch Int Pharmacodyn Ther. 1995. PMID: 8836454

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