S Bajusz
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Explore the profile of S Bajusz including associated specialties, affiliations and a list of published articles.
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87
Citations
309
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Recent Articles
1.
Bojnik E, Magyar A, Toth G, Bajusz S, Borsodi A, Benyhe S
Neuroscience
. 2008 Nov;
158(2):867-74.
PMID: 18977279
Leu- and Met-enkephalin were the first endogenous opioid peptides identified in different mammalian species including the human. Comparative biochemical and bioinformatic evidence indicates that enkephalins are not limited to mammals....
2.
Bajusz S
Acta Pharm Hung
. 2002 Jan;
71(1):13-24.
PMID: 11769093
Research on synthetic peptides at the Institute for Drug Research (IDR) is exemplified by an overview of the projects that resulted in significant results. The first synthesis of oxytocin, a...
3.
Bajusz S
Pharmazie
. 2001 Nov;
56 Suppl 1:S4-11.
PMID: 11686090
Research on synthetic peptides at the Institute for Drug Research (IDR) is exemplified by an overview of the projects that resulted in significant results.
4.
Bajusz S, FAUSZT I, Nemeth K, Barabas E, Juhasz A, Patthy M, et al.
Biopolymers
. 1999 Jun;
51(1):109-18.
PMID: 10380358
Interleukin-1 beta (IL-1 beta)-converting enzyme (ICE, caspase-1) processes the IL-1 beta precursor to mature inflammatory cytokine IL-1 beta. ICE has been identified as a unique cysteine protease, which cleaves Asp-X...
5.
Bajusz S, FAUSZT I, Nemeth K, Barabas E, Juhasz A, Patthy M
Bioorg Med Chem Lett
. 1999 Jan;
8(12):1477-82.
PMID: 9873373
Inhibition of interleukin-1 beta converting enzyme (ICE), apopain, papain, thrombin and trypsin with substrate like peptidyl L- and D-alpha-aldehydes and their L-beta-homo-aldehyde analogues was investigated. The L-beta-homo-aspartals appear to be...
6.
Bajusz S, Barabas E, FAUSZT I, Feher A, Horvath G, Juhasz A, et al.
Semin Thromb Hemost
. 1996 Jan;
22(3):243-6.
PMID: 8836008
D-alpha-Hydroxyacyl-prolyl-arginals, a new type of analogues of D-Phe-Pro-Arg-H (R1), have been prepared and evaluated. Unlike R1, whose terminal group is NH2, the new analogues with a terminal OH group are...
7.
Nemeth K, Patthy M, FAUSZT I, SZELL E, Szekely J, Bajusz S
Int J Immunopharmacol
. 1995 Dec;
17(12):985-93.
PMID: 8964658
Tripeptide and pentapeptide aldehydes as substrate-base inhibitors of cysteine proteases were designed in our laboratory for the inhibition of interleukin-1 beta converting enzyme (ICE), a recently described cysteine protease responsible...
8.
Bajusz S, Barabas E, FAUSZT I, Feher A, Horvath G, Juhasz A, et al.
Bioorg Med Chem
. 1995 Aug;
3(8):1079-89.
PMID: 7582981
D-alpha-Hydroxyacyl-prolyl-arginals have been designed and synthesized as orally active stable analogs of D-Phe-Pro-Arg-H, the active site-directed peptidyl thrombin inhibitor prototype. Many of the new analogs possess high in vitro anticoagulant...
9.
Orosz G, Ronai A, Bajusz S, Medzihradszky K
Biochem Biophys Res Commun
. 1994 Aug;
202(3):1285-90.
PMID: 8060305
Opioid receptor antagonist properties of the mu opioid receptor selective peptide, BOC-Tyr-Lys-Lys-Trp-Trp-NH2 and its systematically modified analogues were determined in guinea pig ileum, mouse vas deferens and rabbit vas deferens...
10.
Bacher P, Walenga J, Iqbal O, Bajusz S, BREDDIN K, Fareed J
Thromb Res
. 1993 Aug;
71(4):251-63.
PMID: 8236155
The pharmacologic activities of two thrombin inhibitors (D-MePhe-Pro-Arg-H, recombinant-hirudin) were compared in two animal models. The antithrombotic effect was investigated in vivo in rabbits using a modified Wessler stasis thrombosis...