Zobrazeno 1 - 10
of 398
pro vyhledávání: '"G, Kéri"'
Autor:
G Kéri, M Idei, Jenő Major, Mátyás G. Jakab, Jozsef Bocsi, Anna Tompa, Béla Szende, Rudolf Mihalik
Publikováno v:
Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 465:61-68
Somatostatin receptors are supposed to be important in the regulation of apoptosis. In this study, we measured apoptosis occurring spontaneously, or induced by the synthetic somatostatin analogue, the peptide TT-232. We examined isolated human periph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe2e6197e21af924a1d49c90e2158ac9
https://doi.org/10.1016/s1383-5718(99)00212-0
https://doi.org/10.1016/s1383-5718(99)00212-0
Autor:
F, Hollósy, M, Idei, G, Csorba, E, Szabó, G, Bökönyi, A, Seprödi, G, Mészáros, B, Szende, G, Kéri
Publikováno v:
Anticancer research. 21(5)
The apoptosis-inducing effect of the triterpene saponins, namely, ursolic acid and its natural derivative, methyl-ursolate beta-D-glucoside on A431 human epidermoid carcinoma cells was studied. The cells treated with 5-50 microg/ml of ursolic acid re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2bee18662aecb805646bf1e5f32f66b1
https://pubmed.ncbi.nlm.nih.gov/11848513
https://pubmed.ncbi.nlm.nih.gov/11848513
Publikováno v:
British journal of pharmacology. 134(7)
1. Somatostatin (6.11 nmol kg(-1) i.p.) inhibited neurogenic plasma extravasation evoked by 1% mustard oil and non-neurogenic oedema induced by 5% dextran in the rat skin. 2. Cyclic synthetic octapeptide (TT-248 and TT-250) and heptapeptide (TT-232)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::85adc971fcd68c5dc4f422c17f38e441
https://pubmed.ncbi.nlm.nih.gov/11724765
https://pubmed.ncbi.nlm.nih.gov/11724765
Autor:
T, Vántus, G, Kéri, Z, Krivickiene, M, Valius, A, Steták, S, Keppens, P, Csermely, P I, Bauer, G, Bökönyi, W, Declercq, P, Vandenabeele, W, Merlevede, J R, Vandenheede
Publikováno v:
Cellular signalling. 13(10)
TT-232 is a somatostatin analogue containing a five-residue ring structure. The present report describes TT-232-induced signalling events in A431 cells, where a 4-h preincubation with the peptide irreversibly induced a cell death program, which invol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bb8a67f0ebdb7fc61f9ed691c0e19652
https://pubmed.ncbi.nlm.nih.gov/11602182
https://pubmed.ncbi.nlm.nih.gov/11602182
Publikováno v:
European journal of biochemistry. 268(14)
The immunoreceptor tyrosine-based inhibitory motif (ITIM) of human type IIb Fcgamma receptor (FcgammaRIIb) is phosphorylated on its tyrosine upon co-clustering with the B cell receptor (BCR). The phosphorylated ITIM (p-ITIM) binds to the SH2 domains
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::79b8cf396abaf5d17e9a85b28126159f
https://pubmed.ncbi.nlm.nih.gov/11453982
https://pubmed.ncbi.nlm.nih.gov/11453982
Autor:
R E, Schwab, S, Froidevaux, S, Paku, M, Tejeda, B, Szende, A, Pap, C, Beglinger, A N, Eberle, G, Kéri
Publikováno v:
Anticancer research. 21(1A)
TT-232, a somatostatin analogue, induces apoptosis in various tumours. The aim of our study was to characterise its effect on human melanoma cells and tumours.Proliferation of seven melanoma cell lines was tested in vitro with the methylene blue test
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::919f1ae76c85d7bdfcf0220f988c8ca6
https://pubmed.ncbi.nlm.nih.gov/11299792
https://pubmed.ncbi.nlm.nih.gov/11299792
Publikováno v:
Journal of neural transmission (Vienna, Austria : 1996). 108(1)
The mode of cytoprotective action of the monoamine oxydase B inhibitor (-)-deprenyl was studied using A-2058 human melanoma cells in culture. Serum deprivation caused apoptosis of the cultured cells, which could be decreased by administration of 10(-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2ca88bcc779d7cdf004b982591996277
https://pubmed.ncbi.nlm.nih.gov/11261744
https://pubmed.ncbi.nlm.nih.gov/11261744
Autor:
M, Kunvári, C, Páska, M, László, L, Orfi, I, Kövesdi, D, Eros, G, Bökönyi, G, Kéri, I, Gyurján
Publikováno v:
Acta pharmaceutica Hungarica. 69(5)
Tyrosine kinase inhibition and tumor growth inhibition activity of verbascoside and homoplantaginin are described. Both molecules proved to be equally significant inhibitors of isolated EGF-R tyrosine kinases, nevertheless their in vitro antiprolifer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1438964bbd6f55f36e051c6b7295ab97
https://pubmed.ncbi.nlm.nih.gov/10652790
https://pubmed.ncbi.nlm.nih.gov/10652790
Autor:
L, Orfi, F, Wáczek, M, Szabó, I, Kövesdi, G, Mészáros, M, Idei, A, Horváth, F, Hollósy, M, Mák, Z, Szegedi, B, Szende, G, Kéri, B, Noszál
Publikováno v:
Acta pharmaceutica Hungarica. 69(3)
A parallel combinatorial library of over sixteen hundred compounds has been designed and synthesized for the development of new potential peptidomimetic protein tyrosine kinase (PTK) inhibitor leads that is aimed for intervening with the substrate bi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0bfaa065cc458f7508c318c5f4a2a350
https://pubmed.ncbi.nlm.nih.gov/10401154
https://pubmed.ncbi.nlm.nih.gov/10401154
Autor:
I, Mezô, J, Seprôdi, B, Vincze, I, Pályi, G, Kéri, Z, Vadász, G, Tóth, M, Kovács, M, Koppán, J E, Horváth, A, Kálnay, I, Teplán
Publikováno v:
Biomedical peptides, proteinsnucleic acids : structure, synthesisbiological activity. 2(2)
New chicken I GnRH agonists and antagonists have been synthesized and tested for their biological activities. The common feature of these analogs was that the molecules had a beta-L-aspartyl residue inserted in position 6. The agonist bound to the pi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d0a122f120953b5977266acb9db69df2
https://pubmed.ncbi.nlm.nih.gov/9346824
https://pubmed.ncbi.nlm.nih.gov/9346824