Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ignác Óvári"'
Autor:
Ignac Ovari, Gabor Viczjan, Tamas Erdei, Barbara Takacs, Vera Tarjanyi, Judit Zsuga, Miklos Szucs, Zoltan Szilvassy, Bela Juhasz, Rudolf Gesztelyi
Publikováno v:
Frontiers in Pharmacology, Vol 15 (2024)
The receptorial responsiveness method (RRM) enables the estimation of a change in concentration of an (even degradable) agonist, near its receptor, via curve fitting to (at least) two concentration-effect (E/c) curves of a stable agonist. One curve s
Externí odkaz:
https://doaj.org/article/972b6fd40489411ea1af45c47d01b30c
Autor:
Ignác Óvári, Viktória Szilágyi, Gábor Viczján, Nóra Lampé, Miklós Bege, Anikó Borbás, Pál Herczeg, Béla Juhász, Rudolf Gesztelyi, Tamás Erdei
Publikováno v:
Egészségügyi Innovációs Szemle. 1
A hipoxantin-triciklánó egy a DE GYTK Gyógyszerészi Kémia Tanszéken szintetizált adenozin analóg, melyben az adenint hipoxantin, a ribózt pedig egy kondenzált triciklikus molekularész helyettesíti. Munkánk során a hipoxantin-triciklán
Publikováno v:
Clinical child psychology and psychiatry. 27(1)
Spectrum of childhood symptoms caused by SARS-CoV-2 (severe acute respiratory syndrome-2) infection is widening. In contrast to adulthood, where psychiatric disorders caused by SARS-CoV-2 infection are widely known, recognition of such cases in child
Autor:
Gabor Viczjan, Anna Szilagyi, Barbara Takacs, Ignac Ovari, Reka Szekeres, Vera Tarjanyi, Tamas Erdei, Vanda Teleki, Judit Zsuga, Zoltan Szilvassy, Bela Juhasz, Balazs Varga, Rudolf Gesztelyi
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
Cannabidiol (CBD), the most extensively studied non-intoxicating phytocannabinoid, has been attracting a lot of interest worldwide owing to its numerous beneficial effects. The aim of this study was to explore the effect that CBD exerts on the adenos
Externí odkaz:
https://doaj.org/article/bcba8b436b4d4d11859545dfaf32956f
Autor:
Gabor Viczjan, Tamas Erdei, Ignac Ovari, Nora Lampe, Reka Szekeres, Mariann Bombicz, Barbara Takacs, Anna Szilagyi, Judit Zsuga, Zoltan Szilvassy, Bela Juhasz, Rudolf Gesztelyi
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 18, p 9831 (2021)
In previous studies using isolated, paced guinea pig left atria, we observed that FSCPX, known as a selective A1 adenosine receptor antagonist, paradoxically increased the direct negative inotropic response to A1 adenosine receptor agonists (determin
Externí odkaz:
https://doaj.org/article/f14ed653a36e41fe834c268f95691c8f