Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Tereza Doušová"'
Autor:
Jiří Pozniak, Pavel Ryšánek, David Smrčka, Petr Kozlík, Tomáš Křížek, Jaroslava Šmardová, Anežka Nováková, Debanjan Das, Daniel Bobek, Mahak Arora, Jiří Hofmann, Tereza Doušová, Martin Šíma, Ondřej Slanař
Publikováno v:
Frontiers in Pharmacology, Vol 15 (2024)
Background: Ivacaftor is a modern drug used in the treatment of cystic fibrosis. It is highly lipophilic and exhibits a strong positive food effect. These characteristics can be potentially connected to a pronounced lymphatic transport after oral adm
Externí odkaz:
https://doaj.org/article/a97021bba87c4ffb97563ac5f4adf948
Autor:
Iris A. L. Silva, Aires Duarte, Fernando A. L. Marson, Raquel Centeio, Tereza Doušová, Karl Kunzelmann, Margarida D. Amaral
Publikováno v:
Frontiers in Physiology, Vol 11 (2020)
Most cases of Cystic Fibrosis (CF) are diagnosed early in life. However, people with atypical CF forms pose diagnosis dilemmas, requiring laboratory support for diagnosis confirmation/exclusion. Ex vivo analysis of fresh rectal biopsies by Ussing cha
Externí odkaz:
https://doaj.org/article/815f2523473f48c48693bc41f9c09bba
Autor:
Raquel Centeio, Jiraporn Ousingsawat, Inês Cabrita, Rainer Schreiber, Khaoula Talbi, Roberta Benedetto, Tereza Doušová, Eric K. Verbeken, Kris De Boeck, Isaac Cohen, Karl Kunzelmann
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 15, p 7852 (2021)
Activation of the Ca2+ activated Cl− channel TMEM16A is proposed as a treatment in inflammatory airway disease. It is assumed that activation of TMEM16A will induce electrolyte secretion, and thus reduce airway mucus plugging and improve mucociliar
Externí odkaz:
https://doaj.org/article/7df563b8230b4606afa44c639172b86c
Autor:
Karl Kunzelmann, Jiraporn Ousingsawat, Inês Cabrita, Tereza Doušová, Andrea Bähr, Melanie Janda, Rainer Schreiber, Roberta Benedetto
Publikováno v:
Frontiers in Pharmacology, Vol 10 (2019)
The inflammatory airway disease cystic fibrosis (CF) is characterized by airway obstruction due to mucus hypersecretion, airway plugging, and bronchoconstriction. The cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel is dysf
Externí odkaz:
https://doaj.org/article/3f433d166663496689b1f4725e6e86dc
Autor:
Tereza, Doušová (AUTHOR)
Publikováno v:
Czecho-Slovak Pediatrics / Česko-Slovenská Pediatrie. 2023, Vol. 78 Issue 5, p254-257. 4p.
Autor:
Jana Haberlová, Petra Hedvičáková, Petra Fuchsová, Markéta Jílková, Lucie Holubová, Tereza Doušová
Publikováno v:
Neurologie pro praxi. 23:9-13
Publikováno v:
Intervenční a akutní kardiologie. 20:228-232
Autor:
Veronika Schwarzová, Jan Schwarz, Katarina Mitrová, Pavel Dřevínek, Marcela Kreslová, Josef Sýkora, Tereza Doušová
Publikováno v:
Pediatric pulmonologyREFERENCES.
We report the first described case of pulmonary tularaemia in the pediatric patient receiving infliximab for ulcerative colitis. We highlight the importance of considering Francisella tularensis in diagnostically challenging cases of persistent respi
Autor:
Tereza Doušová, Martin Modrak, Milan Macek, Pavel Drevinek, E. Furstova, M. Libik, Libor Fila, Jakub Beranek, Ondrej Cinek
Publikováno v:
Journal of Cystic Fibrosis. 21:243-245
Superior efficacy of elexacaftor/tezacaftor/ivacaftor (ELX/TEZ/IVA) over tezacaftor/ivacaftor (TEZ/IVA) in people with cystic fibrosis (CF) and Phe508del/Phe508del genotype was shown in clinical trials. We utilized intestinal organoid approach to com
Autor:
Lucie, Hrdličková, Gražina, Kleinová Kokešová, Lenka, Nováková, Denisa, Makešová, Tereza, Doušová, Markéta, Taberyová, Daniela, Snítilová
Publikováno v:
Czecho-Slovak Pediatrics / Česko-Slovenská Pediatrie; 2023, Vol. 78 Issue 1, p44-47, 4p