Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Julie Stichova"'
Autor:
Julie Stichova, Peter Slanina, Zita Chovancova, Jan Baros, Marek Litzman, Jiri Litzman, Marcela Vlkova
Publikováno v:
Frontiers in Allergy, Vol 5 (2024)
BackgroundPrevious research showed that the intracellular complement system, with CD46 as its central molecule, regulates the Th1 response associated with IFN-γ production and transition to a type 1 regulatory response (Tr1) characterized by IL-10 p
Externí odkaz:
https://doaj.org/article/a939423bc67b4332b988b74dd813a23a
Autor:
Tereza Grymova, Marcela Vlkova, Premysl Soucek, Roman Hakl, Jana Nechvatalova, Peter Slanina, Julie Stichova, Jiri Litzman, Tomas Freiberger
Publikováno v:
Mediators of Inflammation, Vol 2019 (2019)
Neutrophils impact on processes preceding the formation of bradykinin, a major swelling mediator in hereditary angioedema (HAE), yet their potential role in HAE pathogenesis has not been sufficiently studied. We assessed the relative mRNA expression
Externí odkaz:
https://doaj.org/article/a2a35a4c26974bf78115c9d22cf318de
Autor:
Lukas Moos, Julie Stichova, Peter Slanina, Isabelle Bekeredjian-Ding, Marcela Vlková, Olga Ticha
Publikováno v:
European journal of immunology, 51(5):1195-1205
Tumor Necrosis Factor Receptor 2 (TNFR2) expression is increasingly being linked to tolerogenic immune reactions and cells with suppressor function including a subset of T-regulatory cells. B-regulatory cells play an important role in control of T-ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc8bc26fec0b2eaa810239ccbdfe811b
https://doi.org/10.1002/eji.202048988
https://doi.org/10.1002/eji.202048988
Autor:
Jiri Litzman, Peter Slanina, Julie Stichova, Roman Hakl, Jana Nechvatalova, Tereza Grymova, Tomáš Freiberger, Premysl Soucek, Marcela Vlková
Publikováno v:
Mediators of Inflammation, Vol 2019 (2019)
Mediators of Inflammation
Mediators of Inflammation
Neutrophils impact on processes preceding the formation of bradykinin, a major swelling mediator in hereditary angioedema (HAE), yet their potential role in HAE pathogenesis has not been sufficiently studied. We assessed the relative mRNA expression
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::231a7ad71aa830bdcb0904c8b4878f0d
https://doaj.org/article/a2a35a4c26974bf78115c9d22cf318de
https://doaj.org/article/a2a35a4c26974bf78115c9d22cf318de
Autor:
Lucie Ballonová, Přemysl Souček, Peter Slanina, Kamila Réblová, Ondřej Zapletal, Marcela Vlková, Roman Hakl, Viktor Bíly, Hana Grombiříková, Eliška Svobodová, Petra Kulíšková, Julie Štíchová, Marta Sobotková, Radana Zachová, Jana Hanzlíková, Martina Vachová, Pavlína Králíčková, Irena Krčmová, Miloš Jeseňák, Tomáš Freiberger
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Hereditary angioedema (HAE) is a rare genetic disorder with variable expressivity even in carriers of the same underlying genetic defect, suggesting other genetic and epigenetic factors participate in modifying HAE severity. Recent knowledge indicate
Externí odkaz:
https://doaj.org/article/1d1b0d48084f450184f9a098e21c6523