Breath concentration of acetic acid vapour is elevated in patients with cystic fibrosis by Smith, David, Sovová, Kristýna, Dryahina, Kseniya, Doušová, Tereza, D evínek, Pavel, Špan l, Patrik

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Do linear logistic model analyses of volatile biomarkers in exhaled breath of cystic fibrosis patients reliably indicate Pseudomonas aeruginosa infection? by Špan l, Patrik, Sovová, Kristýna, Dryahina, Kseniya, Doušová, Tereza, D evínek, Pavel, Smith, David

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TMEM16A in Cystic Fibrosis: Activating or Inhibiting? by Kunzelmann, Karl, Ousingsawat, Jiraporn, Cabrita, Inês, Doušová, Tereza, Bähr, Andrea, Janda, Melanie, Schreiber, Rainer, Benedetto, Roberta

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Mutant CFTR Drives TWIST1 mediated epithelial–mesenchymal transition by Quaresma, Margarida C., Pankonien, Ines, Clarke, Luka A., Sousa, Luís S., Silva, Iris A. L., Railean, Violeta, Doušová, Tereza, Fuxe, Jonas, Amaral, Margarida D.

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Mucus Release and Airway Constriction by TMEM16A May Worsen Pathology in Inflammatory Lung Disease by Centeio, Raquel, Ousingsawat, Jiraporn, Cabrita, Inês, Schreiber, Rainer, Talbi, Khaoula, Benedetto, Roberta, Doušová, Tereza, Verbeken, Eric K., De Boeck, Kris, Cohen, Isaac, Kunzelmann, Karl

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Pulmonary tularaemia in a female adolescent with inflammatory bowel disease receiving infliximab: Do not miss the diagnosis by Schwarzová, Veronika, Schwarz, Jan, Mitrová, Katarina, Dřevínek, Pavel, Kreslová, Marcela, Sýkora, Josef, Doušová, Tereza

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Ivacaftor pharmacokinetics and lymphatic transport after enteral administration in rats by Pozniak, Jiří, Ryšánek, Pavel, Smrčka, David, Kozlík, Petr, Křížek, Tomáš, Šmardová, Jaroslava, Nováková, Anežka, Das, Debanjan, Bobek, Daniel, Arora, Mahak, Hofmann, Jiří, Doušová, Tereza, Šíma, Martin, Slanař, Ondřej

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Assessment of Distinct Electrophysiological Parameters in Rectal Biopsies for the Choice of the Best Diagnosis/Prognosis Biomarkers for Cystic Fibrosis by Silva, Iris A L, Duarte, Aires, Marson, Fernando A L, Centeio, Raquel, Doušová, Tereza, Kunzelmann, Karl, Amaral, Margarida D

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Gene expression profile of intestinal organoids from people with cystic fibrosis upon exposure to elexacaftor/tezacaftor/ivacaftor by Cinek, Ondrej, Furstova, Eva, Novotna, Stepanka, Hubackova, Klara, Dousova, Tereza, Borek-Dohalska, Lucie, Drevinek, Pavel

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Organoids as a personalized medicine tool for ultra-rare mutations in cystic fibrosis: The case of S955P and 1717-2A>G by Silva, Iris A.L., Doušová, Tereza, Ramalho, Sofia, Centeio, Raquel, Clarke, Luka A., Railean, Violeta, Botelho, Hugo M., Holubová, Andrea, Valášková, Iveta, Yeh, Jiunn-Tyng, Hwang, Tzyh-Chang, Farinha, Carlos M., Kunzelmann, Karl, Amaral, Margarida D.

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Response to elexacaftor/tezacaftor/ivacaftor in intestinal organoids derived from people with cystic fibrosis by Furstova, Eva, Dousova, Tereza, Beranek, Jakub, Libik, Malgorzata, Fila, Libor, Modrak, Martin, Cinek, Ondrej, Macek, Milan, Drevinek, Pavel

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Acetic acid is elevated in the exhaled breath of cystic fibrosis patients by Španěl, Patrik, Sovová, Kristýna, Dryahina, Kseniya, Doušová, Tereza, Dřevínek, Pavel, Smith, David

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