Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Maria Szilagyi"'
Autor:
Cyril Benoît, Ana-Maria Szilagyi
Publikováno v:
Journal of Legislative Studies
Journal of Legislative Studies, Taylor & Francis (Routledge): SSH Titles, 2021, pp.Online. ⟨10.1080/13572334.2021.1986281⟩
Journal of Legislative Studies,-Online (2021-10)
Journal of Legislative Studies, Taylor & Francis (Routledge): SSH Titles, 2021, pp.Online. ⟨10.1080/13572334.2021.1986281⟩
Journal of Legislative Studies,-Online (2021-10)
Independent regulatory agency has become the standard institutional choice in Western Europe. Little is known, however, about the involvement of legislators in their design and in their monitoring. In this paper, we analyse ex-ante and ex-post legisl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dcabe0cbdb4c50b5aa97610f56b648f
https://hal.archives-ouvertes.fr/hal-03370739
https://hal.archives-ouvertes.fr/hal-03370739
Publikováno v:
Bioelectromagnetics. 23:271-277
The hypothesis investigated is that exposure of a mammalian cell to high peak power pulsed RF, at the frequency of 8.2 GHz, can result in the activation of an important eukaryotic transcriptional regulator, nuclear factor kappa B (NF-κB). This DNA-b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c12010b7391eab81bf4532808d2336a
https://doi.org/10.1002/bem.10018
https://doi.org/10.1002/bem.10018
Autor:
Maria Szilagyi
Publikováno v:
Patty's Toxicology
Aliphatic carboxylic acids include a very wide range of chemicals that perform a diverse range of industrial functions. Many occur naturally and serve an important function in nutrition, and others are intermediates in normal biochemical processes. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec64e668f5b21aacc3af3a8077140871
https://doi.org/10.1002/0471435139.tox070.pub2
https://doi.org/10.1002/0471435139.tox070.pub2
Autor:
Maria Szilagyi, Wai-Man Lau
Publikováno v:
Pharmacology. 47:223-229
Tacrine (THA) selectively modulates binding of M1 ligands in an allosteric fashion causing positive cooperativity. The binding affinity of THA to M1 and M2 cholinoceptors is similar. It is therefore proposed that the allosteric selectivity of THA is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56053afb7aace1cc60269210a99a1d34
https://doi.org/10.1159/000139101
https://doi.org/10.1159/000139101
Publikováno v:
General pharmacology. 24(3)
1. Crude and purified synaptosomes were prepared from the cerebral cortex of the rat or the guinea pig and used to study the uptake and release of [3H]GABA and [3H]glutamate. 2. Baclofen at 10(-5) M inhibited stimulated release of [3H]GABA from crude
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29c31f12843d96cdfafb8a42ba241b6e
https://pubmed.ncbi.nlm.nih.gov/8103493
https://pubmed.ncbi.nlm.nih.gov/8103493
Autor:
Wai-Man Lau, Maria Szilagyi
Publikováno v:
General pharmacology. 23(6)
1. Glycopyrrolate, a synthetic quaternary ammonium compound had biphasic effects on the contraction of guinea-pig atrium. At concentrations between 0.4 and 20 microM, glycopyrrolate induced a small but consistent increase in the contraction force. 2.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21c12c05aefa6fd87a9ef5b1620d3781
https://pubmed.ncbi.nlm.nih.gov/1283139
https://pubmed.ncbi.nlm.nih.gov/1283139
Publikováno v:
BMC Genomics
BMC Genomics, Vol 10, Iss 1, p 202 (2009)
BMC Genomics, Vol 10, Iss 1, p 202 (2009)
Background The wide use of organophosphorus (OP) pesticides makes them an important public health concern. Persistent effects of exposure and the mechanism of neuronal degeneration are continuing issues in OP toxicology. To elucidate early steps in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5ae2ac0f4c45cd710c10033b8ea89e9
https://doi.org/10.1186/1471-2164-10-202
https://doi.org/10.1186/1471-2164-10-202
Publikováno v:
Journal of applied toxicology : JAT. 11(6)
8-Cyclopentyl-1,3-[3H] dipropylxanthine [( 3H]CPX) is a potent radioligand that specifically binds to the A1 adenosine receptors. Its high specificity makes it a suitable ligand for the characterization of A1 adenosine receptors in tissues with low r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::feea0eb79eac51997b4a58f1e0ef9217
https://pubmed.ncbi.nlm.nih.gov/1761798
https://pubmed.ncbi.nlm.nih.gov/1761798
Publikováno v:
European Journal of Pharmacology. 154:59-65
The centrally acting anticholinesterase drug tacrine has been shown to block K + channels in guinea pig left atrium. It competitively blocks the negative inotropic effects of adenosine, 2-chloroadenosine and carbachol. K a values obtained from dose r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a7633ff01daf4feb40f824affd1a168
https://doi.org/10.1016/0014-2999(88)90363-9
https://doi.org/10.1016/0014-2999(88)90363-9
Publikováno v:
Neuroscience letters. 94(1-2)
The organophosphorus compounds, sarin, tabun and soman are known to be potent inhibitors of cholinesterase. It was claimed that these agents also interact at neurotransmitter receptor sites. We were unable to detect any interaction at the acetylcholi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f90b8343106cd9dccb960562111b42de
https://pubmed.ncbi.nlm.nih.gov/3241661
https://pubmed.ncbi.nlm.nih.gov/3241661