Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Klára Németh"'
Autor:
Oncodermatology, András L. Kovács, Klára Németh, Éva Lábodi, Rolland Gyulai, Dorottya Kövesdi
Publikováno v:
Bőrgyógyászati és Venerológiai Szemle. 96:92-96
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::934fbedb88390197b40bdb0e451a4ff6
https://doi.org/10.7188/bvsz.2020.96.2.5
https://doi.org/10.7188/bvsz.2020.96.2.5
Publikováno v:
European journal of dermatology : EJD. 31(3)
Currently, there is a general lack of consensus regarding optimal strategy and imaging during follow-up for patients suffering from melanoma. Our aim was to analyse the utility of various imaging procedures, in particular CT scans, during the follow-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b818b678fa1eb0b9d85f6e6785daddba
https://pubmed.ncbi.nlm.nih.gov/34309521
https://pubmed.ncbi.nlm.nih.gov/34309521
Publikováno v:
Biochemical and Biophysical Research Communications. 346:45-50
The MDR1 transporter mediated efflux of different xenobiotics out of the cells serves as the most important mechanisms of the multidrug resistance in cancer cells, thus inhibition of the MDR1 transporter may increase the efficiency of anticancer drug
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78a0dc4e1dde5fd22157c21b12c7c472
https://doi.org/10.1016/j.bbrc.2006.05.058
https://doi.org/10.1016/j.bbrc.2006.05.058
Autor:
József I. Székely, Nicholas Bodor, Ágnes Pataki, Klára Németh, Katalin Horvath, Szilveszter Toth, István Kurucz, Viola Csillik-Perczel, Zoltán Lóránt Nagy, Cecília Haskáné Salamon, Katalin Török
Publikováno v:
Journal of Pharmacology and Experimental Therapeutics. 307:83-92
In the present study, the pharmacological effects of etiprednol dicloacetate (BNP-166; ethyl-17alpha-dichloroacetoxy-11beta-hydroxyandrosta-1,4-diene-3-one-17beta-carboxylate), a new soft steroid, intended to use for the treatment of asthma, were inv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::382132d3d5d9be4089f16432a2a5eb26
https://doi.org/10.1124/jpet.103.053652
https://doi.org/10.1124/jpet.103.053652
Autor:
Attila Juhasz, Miklós Patthy, Klára Németh, Irén Fauszt, Pal I. Bauer, Sandor Bajusz, Eva Barabas
Publikováno v:
Biopolymers. 51:109-118
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 bonds, shows resistance to E-64
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc74f6bf39e428a548affbaa691593ff
https://doi.org/10.1002/(sici)1097-0282(1999)51:1<109::aid-bip12>3.0.co
https://doi.org/10.1002/(sici)1097-0282(1999)51:1<109::aid-bip12>3.0.co
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 8:1477-1482
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 sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78f8b8c7055e990b03baedffaefc4f45
https://doi.org/10.1016/s0960-894x(98)00244-3
https://doi.org/10.1016/s0960-894x(98)00244-3
Publikováno v:
International Journal of Immunopharmacology. 19:215-225
The effect of several interleukin-1β converting enzyme (ICE) inhibitors on apoptosis was examined. The ICE inhibitors tested were peptide aldehydes such as ethyloxycarbonyl-Ala-Tyr-Val-Ala-Asp-aldehyde (Etoco-AYVAD-CHO), acetyl-Tyr-Val-Ala-Asp-aldeh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f6a1b328235b4d939a83beef0358277
https://doi.org/10.1016/s0192-0561(97)00026-x
https://doi.org/10.1016/s0192-0561(97)00026-x
Publikováno v:
Journal of Neurochemistry. 56:1897-1904
A monoclonal antibody (mAb), KA8, that interacts with the k-opioid receptor binding site was generated. BALB/ c female mice were immunized with a partially purified k-opioid receptor preparation from frog brain. Spleen cells were hybridized with SP2/
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1bd0efa10b78bee68a1d1cc357dd75ce
https://doi.org/10.1111/j.1471-4159.1991.tb03446.x
https://doi.org/10.1111/j.1471-4159.1991.tb03446.x
Publikováno v:
Peptides for the New Millennium ISBN: 0792364457
Diastereomeric pairs of peptide aldehydes (1-5) and amides (6-7) as well as the all-L substrates (S1-S4) were prepared by conventional synthesis in solution. The -isomers are known from the literature (e.g. 1 and S1 [2], 2 [3], and 5 [4]) or derived
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa6fe685600cd378be9434d4c02da328
https://doi.org/10.1007/0-306-46881-6_167
https://doi.org/10.1007/0-306-46881-6_167
Autor:
Klára Németh, István Kurucz
Publikováno v:
Biochemical pharmacology. 69(6)
Effect of unfractionated heparin (UFH), described as a cell-impermeant IP3 receptor antagonist, was studied on the capacitive Ca 2+ entry in non-permeabilized, intact cells, measuring the intracellular Ca 2+ levels using fluorescence microplate techn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2cf0d54c179eb051514bc4d42dfe947
https://pubmed.ncbi.nlm.nih.gov/15748704
https://pubmed.ncbi.nlm.nih.gov/15748704