Colonization by non-pathogenic bacteria alters mRNA expression of cytochromes P450 in originally germ-free mice von Jourová, L., Anzenbacher, P., Lišková, B., Matušková, Z., Hermanová, P., Hudcovic, T., Kozáková, H., Hrnčířová, L., Anzenbacherová, E.

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Presence or absence of microbiome modulates the response of mice organism to administered drug nabumetone von Jourová, L, Lišková, B, Lněničková, K, Zemanová, N, Anzenbacher, P, Hermanová, P, Hudcovic, T, Kozáková, H, Anzenbacherová, E

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The analysis of the regional self-governing units forests in selected European countries von Liskova, B., Bilavsko 55, Bystrice pod Hostynem (Czech Republic)

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Phage therapy combined with Gum Karaya injectable hydrogels for treatment of methicillin-resistant Staphylococcus aureus deep wound infection in a porcine model von Vacek, L., Polaštík Kleknerová, D., Lipový, B., Holoubek, J., Matysková, D., Černá, E., Brtníková, J., Jeklová, E., Kobzová, Š., Janda, L., Lišková, L., Diabelko, D., Botka, T., Pantůček, R., Růžička, F., Vojtová, L.

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Review of SRD5A3 Disease-Causing Sequence Variants and Ocular Findings in Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation, and a Detailed New Case von Kousal, B, Honzík, T, Hansíková, H, Ondrušková, N, Čechová, A, Tesařová, M, Stránecký, V, Meliška, M, Michaelides, M, Lišková, P

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Molecular genetic cause of achromatopsia in two patients of Czech origin von Hlavatá, L, Ďuďáková, Ľ, Moravíková, J, Zobanová, A, Kousal, B, Lišková, P

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Clinical Tests Testing New Therapies for Stargardt Disease von Kousal, B, Ďuďáková, Ľ, Hlavatá, L, Lišková, P

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Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics von Khan, Mubeen, Cornelis, Stéphanie S., Pozo-Valero, Marta Del, Whelan, Laura, Runhart, Esmee H., Mishra, Ketan, Bults, Femke, AlSwaiti, Yahya, AlTalbishi, Alaa, De Baere, Elfride, Banfi, Sandro, Banin, Eyal, Bauwens, Miriam, Ben-Yosef, Tamar, Boon, Camiel J. F., van den Born, L. Ingeborgh, Defoort, Sabine, Devos, Aurore, Dockery, Adrian, Dudakova, Lubica, Fakin, Ana, Farrar, G. Jane, Sallum, Juliana Maria Ferraz, Fujinami, Kaoru, Gilissen, Christian, Glavač, Damjan, Gorin, Michael B., Greenberg, Jacquie, Hayashi, Takaaki, Hettinga, Ymkje M., Hoischen, Alexander, Hoyng, Carel B., Hufendiek, Karsten, Jägle, Herbert, Kamakari, Smaragda, Karali, Marianthi, Kellner, Ulrich, Klaver, Caroline C. W., Kousal, Bohdan, Lamey, Tina M., MacDonald, Ian M., Matynia, Anna, McLaren, Terri L., Mena, Marcela D., Meunier, Isabelle, Miller, Rianne, Newman, Hadas, Ntozini, Buhle, Oldak, Monika, Pieterse, Marc, Podhajcer, Osvaldo L., Puech, Bernard, Ramesar, Raj, Rüther, Klaus, Salameh, Manar, Salles, Mariana Vallim, Sharon, Dror, Simonelli, Francesca, Spital, Georg, Steehouwer, Marloes, Szaflik, Jacek P., Thompson, Jennifer A., Thuillier, Caroline, Tracewska, Anna M., van Zweeden, Martine, Vincent, Andrea L., Zanlonghi, Xavier, Liskova, Petra, Stöhr, Heidi, Roach, John N. De, Ayuso, Carmen, Roberts, Lisa, Weber, Bernhard H. F., Dhaenens, Claire‐Marie, Cremers, Frans P. M.

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Gene Therapy for Inherited RETINAL AND OPTIC NERVE Disorders: Current Knowledge von Ďuďáková, Ľ, Kousal, B, Kolářová, H, Hlavatá, L, Lišková, P

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Porcine model of a complicated skin and soft tissue infection caused by  Pseudomonas aeruginosa von Lipovy, Bretislav, Vacek, Lukas, Kleknerova, Dominika Polastik, Jeklova, Edita, Liskova, Lenka, Holoubek, Jakub, Matyskova, Dominika, Ruzicka, Filip

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Siponimod versus placebo in secondary progressive multiple sclerosis (EXPAND): a double-blind, randomised, phase 3 study von Kappos, Ludwig, Fox, Robert J, Wallström, Erik, Akman-Demir, Gulsen, Allen, Alison B, Applebee, Angela M, Balci, Belgin Petek, Barnett, Michael, Bass, Ann, Bejinariu, Mihaela, Bernitsas, Evanthia, Bhan, Virender, Boehringer, Matthias, Bracknies, Vera, Brescia Morra, Vincenzo, Brozman, Miroslav, Calkwood, Jonathan C, Cascione, Mark, Castelnovo, Giovani, Cooper, Joanna A, Corboy, John, Coyle, Patricia K, Craner, Matthew, Cunha, Luis, da Silva, Ana Martins, Deri, Norma H, Edan, Gilles, Elias, Stanton, Estruch, Bonaventura Casanova, Faiss, Juergen, Fedyanin, Alexander S, Fermont, Jiske, Fernandez, Oscar Fernandez, Ferrer, Francisco Coret, Ford, Corey, Gehring, Klaus, Gobbi, Claudio, Grandmaison, Francois, Grimaldi, Luigi Maria Edoardo, Haas, Judith, Harmjanz, Arndt, Herbert, Joseph, Hofmann, Werner E, Huang, Dehui, Huang, DeRen, Hupperts, Raymond, Karussis, Dimitrios, Khabirov, Farit A, Kister, Ilya, Krastev, Georgi, Lassek, Christoph, Laureys, Guy, Lee, Liesly, Li, Hongzeng, Linnebank, Michael, Maeurer, Mathias, Marfia, Girolama Alessandra, Meca-Lallana, Jose, Mihetiu, Ioan Gheorghe, Miller, Aaron E, Montoya, Lilina, Nakatsuji, Yuji, Nicholas, Richard, Nikfekr, Esmaeil, Odinak, Miroslav M, Olsson, Tomas, van Oosten, B W, Oreja-Guevara, Celia, Oschmann, Patrick, Pachner, Andrew, Panczel, Gyula, Pandolfo, Massimo, Pelletier, Jean, Piedrabuena, Raul, Rastenyte, Daiva, Rey, Roberto, Rozsa, Csilla, Rusek, Stanislaw, Saida, Takahiko, Salgado, Antonio Vasco, Sanders, Kalina, Schwab, Matthias, Scott, James, Shafer, Stuart, Shotekov, Penko, Siever, Arno, Sigel, Karl-Otto, Simu, Mihaela, Stangel, Martin, Stourac, Pavel, Tavernarakis, Antonios, Terzi, Murat, Ticmeanu, Marina, Tiel-Wilck, Klaus, Turcani, Peter, Valikovics, Attila, Weiss, Sara, Vermersch, Patrick, Yamamura, Takashi, Zacharias, Alan

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Preimplantation genetic diagnosis and monogenic inherited eye diseases von Hlavatá, L, Ďuďáková, Ľ, Trková, M, Soldátová, I, Skalická, P, Kousal, B, Lišková, P

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Targeted sequencing and in vitro splice assays shed light on ABCA4-associated retinopathies missing heritability von Corradi, Zelia, Khan, Mubeen, Hitti-Malin, Rebekkah, Mishra, Ketan, Whelan, Laura, Cornelis, Stéphanie S., Hoyng, Carel B., Kämpjärvi, Kati, Klaver, Caroline C.W., Liskova, Petra, Stöhr, Heidi, Weber, Bernhard H.F., Banfi, Sandro, Farrar, G. Jane, Sharon, Dror, Zernant, Jana, Allikmets, Rando, Dhaenens, Claire-Marie, Cremers, Frans P.M.

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Epidemiology, practice of ventilation and outcome for patients at increased risk of postoperative pulmonary complications: LAS VEGAS - an observational study in 29 countries von Hemmes, Sabrine N. T., Neto, Ary Serpa, Binnekade, Jan M., Canet, Jaume, Hedenstierna, Göran, Jaber, Samir, Hiesmayr, Michael, Hollmann, Markus W., Mills, Gary H., Melo, Marcos F. Vidal, Pearse, Rupert, Putensen, Christian, Schmid, Werner, Severgnini, Paolo, Wrigge, Hermann, de Abreu, Marcelo Gama, Pelosi, Paolo, Schultz, Marcus J.

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Genetic causes of deaf‐blindness in sixteen Czech families von Kousal, B., Dudakova, L., Bujakowska, K., Liskova, P.

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Patient management – genetic testing and practical considerations von Liskova, P., Kolarova, H., Kousal, B., Honzik, T.

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B33 Non-neural Mitochondrial Impairment In Huntington’s Disease Patients And Minipigs Transgenic For The N-terminal Part Of Human Mutated Huntingtin von Hansíková, H, Rodinová, M, Spáčilová, J, Kratochvílová, H, Sládková, J, Marková, M, Mačáková, M, Bohuslavová, B, Ellederová, Z, Juhasová, J, Lišková, I, Klempir, J, Roth, J, Motlik, J, Zeman, J

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Molecular genetic basis of Usher syndrome in the Czech population von Liskova, P., Kousal, B., Bujakowska, K., Dudakova, L.

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Representation of Women Among Individuals With Mild Variants in ABCA4-Associated Retinopathy: A Meta-Analysis von Cornelis, Stéphanie S, IntHout, Joanna, Runhart, Esmee H, Grunewald, Olivier, Lin, Siying, Corradi, Zelia, Khan, Mubeen, Hitti-Malin, Rebekkah J, Whelan, Laura, Farrar, G Jane, Sharon, Dror, van den Born, L Ingeborgh, Arno, Gavin, Simcoe, Mark, Michaelides, Michel, Webster, Andrew R, Roosing, Susanne, Mahroo, Omar A, Dhaenens, Claire-Marie, Cremers, Frans P M

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Cognitive sequelae of methanol poisoning involve executive dysfunction and memory impairment in cross-sectional and long-term perspective von Bezdicek, O, Michalec, J, Vaneckova, M, Klempir, J, Liskova, I, Seidl, Z, Janikova, B, Miovsky, M, Hubacek, J, Diblik, P, Kuthan, P, Pilin, A, Kurcova, I, Fenclova, Z, Petrik, V, Navratil, T, Pelclova, D, Zakharov, S, Ruzicka, E

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