effect of mycotoxin deoxynivalenol (DON) on the oxidative stress markers in rainbow trout (Oncorhynchus mykiss, Walbaum 1792) von Šišperová, E, Modrá, H, Ziková, A, Kloas, W, Blahová, J, Matejová, I, Živná, D, Svobodová, Z

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Effects of the pharmaceutical contaminants ibuprofen, diclofenac, and carbamazepine alone, and in combination, on oxidative stress parameters in early life stages of tench (Tinca t... von Stancova, V., Plhalova, L., Blahova, J., Zivna, D., Bartoskova, M., Siroka, Z., Marsalek, P., Svobodova, Z.

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NeemAzal T/S - toxicity to early-life stages of common carp (Cyprinus carpio L.) von Chromcova, L., Blahova, J., Zivna, D., Plhalova, L., Casuscelli, F., Tocco, di, Divisova, L., Prokes, M., Faggio, C., Tichy, F., Svobodova, Z.

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Application of mtDNA markers for European huchen (Hucho hucho Linnaeus, 1758) management in Poland von Kucinski, M., Fopp-Bayat, D., Zivna, D., Liszewski, T., Svinger, V., Lebeda, I.

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Oxidative stress responses in early life stages of common carp (Cyprinus carpio) after subchronic exposure to NeeMazal T/S (azadirachtin 10 g/L) von di Tocco, F Casuscelli, Blahova, J, Plhalova, L, Zivna, D, Sevcikova, M, Chromcova, L, Divisova, L, Faggio, C, Svobodova, Z

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A mutation in the SAA1 promoter causes hereditary amyloid A amyloidosis von Sikora, Jakub, Kmochová, Tereza, Mušálková, Dita, Pohludka, Michal, Přikryl, Petr, Hartmannová, Hana, Hodaňová, Kateřina, Trešlová, Helena, Nosková, Lenka, Mrázová, Lenka, Stránecký, Viktor, Lunová, Mariia, Jirsa, Milan, Honsová, Eva, Dasari, Surendra, McPhail, Ellen D., Leung, Nelson, Živná, Martina, Bleyer, Anthony J., Rychlík, Ivan, Ryšavá, Romana, Kmoch, Stanislav

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Acadian variant of Fanconi syndrome is caused by mitochondrial respiratory chain complex I deficiency due to a non-coding mutation in complex I assembly factor NDUFAF6 von Hartmannová, Hana, Piherová, Lenka, Tauchmannová, Kateřina, Kidd, Kendrah, Acott, Philip D, Crocker, John F S, Oussedik, Youcef, Mallet, Marcel, Hodaňová, Kateřina, Stránecký, Viktor, Přistoupilová, Anna, Barešová, Veronika, Jedličková, Ivana, Živná, Martina, Sovová, Jana, Hůlková, Helena, Robins, Vicki, Vrbacký, Marek, Pecina, Petr, Kaplanová, Vilma, Houštěk, Josef, Mráček, Tomáš, Thibeault, Yves, Bleyer, Anthony J, Kmoch, Stanislav

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Autosomal dominant tubulointerstitial kidney disease (ADTKD) in Ireland von Cormican, S., Connaughton, D. M., Kennedy, C., Murray, S., Živná, M., Kmoch, S., Fennelly, N. K., O'Kelly, P., Benson, K. A., Conlon, E. T., Cavalleri, G., Foley, C., Doyle, B., Dorman, A., Little, M. A., Lavin, P., Kidd, K., Bleyer, A. J., Conlon, P. J.

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Autosomal dominant tubulointerstitial kidney disease-UMOD is the most frequent non polycystic genetic kidney disease von Gast, Christine, Marinaki, Anthony, Arenas-Hernandez, Monica, Campbell, Sara, Seaby, Eleanor G, Pengelly, Reuben J, Gale, Daniel P, Connor, Thomas M, Bunyan, David J, Hodaňová, Kateřina, Živná, Martina, Kmoch, Stanislav, Ennis, Sarah, Venkat-Raman, G

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Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney disease due to mutations in UMOD and MUC1 von Olinger, E, Hofmann, P, Kidd, K, Dufour, I, Belge, H, Schaeffer, C, Kipp, A, Bonny, O, Deltas, C, Demoulin, N, Fehr, T, Fuster, D G, Gale, D P, Goffin, E, Hodanova, K, Huynh-Do, Uyen, Kistler, Andreas, Morelle, J, Papagregoriou, G, Pirson, Y, Sandford, R, Sayer, J A, Torra, R, Venzin, C, Venzin, R, Vogt, B, Živná, M, Greka, A, Dahan, K, Rampoldi, L, Devuyst, Olivier

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Autosomal dominant ApoA4 mutations present as tubulointerstitial kidney disease with medullary amyloidosis von Kmochová, Tereza, Kidd, Kendrah O., Orr, Andrew, Hnízda, Aleš, Hartmannová, Hana, Hodaňová, Kateřina, Vyleťal, Petr, Naušová, Karolína, Brinsa, Vítězslav, Trešlová, Helena, Sovová, Jana, Barešová, Veronika, Svojšová, Klára, Vrbacká, Alena, Stránecký, Viktor, Robins, Victoria C., Taylor, Abbigail, Martin, Lauren, Rivas-Chavez, Ana, Payne, Riley, Bleyer, Heidi A., Williams, Adrienne, Rennke, Helmut G., Weins, Astrid, Short, Patrick J., Agrawal, Varun, Storsley, Leroy J., Waikar, Sushrut S., McPhail, Ellen D., Dasari, Surendra, Leung, Nelson, Hewlett, Tom, Yorke, Jake, Gaston, Daniel, Geldenhuys, Laurette, Samuels, Mark, Levine, Adam P., West, Michael, Hůlková, Helena, Pompach, Petr, Novák, Petr, Weinberg, Richard B., Bedard, Karen, Živná, Martina, Sikora, Jakub, Bleyer, Anthony J., Kmoch, Stanislav

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The utility of a genetic kidney disease clinic employing a broad range of genomic testing platforms: experience of the Irish Kidney Gene Project von Elhassan, Elhussein A. E., Murray, Susan L., Connaughton, Dervla M., Kennedy, Claire, Cormican, Sarah, Cowhig, Cliona, Stapleton, Caragh, Little, Mark A., Kidd, Kendrah, Bleyer, Anthony J., Živná, Martina, Kmoch, Stanislav, Fennelly, Neil K., Doyle, Brendan, Dorman, Anthony, Griffin, Matthew D., Casserly, Liam, Harris, Peter C., Hildebrandt, Friedhelm, Cavalleri, Gianpiero L., Benson, Katherine A., Conlon, Peter J.

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Clinical manifestations and molecular aspects of phosphoribosylpyrophosphate synthetase superactivity in females von Zikánová, Marie, Wahezi, Dawn, Hay, Arielle, Stibůrková, Blanka, Pitts, Charles, Mušálková, Dita, Škopová, Václava, Barešová, Veronika, Součková, Olga, Hodaňová, Kateřina, Živná, Martina, Stránecký, Viktor, Hartmannová, Hana, Hnízda, Ales, Bleyer, Anthony J, Kmoch, Stanislav

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Plasma Mucin-1 (CA15-3) Levels in Autosomal Dominant Tubulointerstitial Kidney Disease due to MUC1 Mutations von Vylet’al, Petr, Kidd, Kendrah, Ainsworth, Hannah C., Springer, Drahomíra, Vrbacká, Alena, Přistoupilová, Anna, Hughey, Rebecca P., Alper, Seth L., Lennon, Niall, Harrison, Steven, Harden, Maegan, Robins, Victoria, Taylor, Abbigail, Martin, Lauren, Howard, Katrice, Bitar, Ibrahim, Langefeld, Carl D., Barešová, Veronika, Hartmannová, Hana, Hodaňová, Kateřina, Zima, Tomáš, Živná, Martina, Kmoch, Stanislav, Bleyer, Anthony J.

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Mild hypothermia attenuates changes in respiratory system mechanics and modifies cytokine concentration in bronchoalveolar lavage fluid during low lung volume ventilation von Dostál, P, Šenkeřík, M, Pařízková, R, Bareš, D, Živný, P, Živná, H, Černý, V

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ApoA4 Mutations Cause Autosomal Dominant Tubulointerstitial Kidney Disease with Medullary Amyloidosis: TH-OR61 von Bleyer, Anthony J., Kmochova, Tereza, Zivna, Martina, Kidd, Kendrah O., Agrawal, Varun, West, Michael L., Orr, Andrew, Leung, Nelson, Weins, Astrid, Rennke, Helmut G., Levine, Adam P., Mcphail, Ellen D., Dasari, Surendra, Sikora, Jakub, Kmoch, Stanislav

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A Prospective Observational Study of Patients with Autosomal Dominant Tubulointerstitial Kidney Disease (ADTKD): PO1308 von Kidd, Kendrah O., Williams, Adrienne H., Robins, Victoria C., Taylor, Abbigail, Martin, Lauren, Kim, Alice, Zivna, Martina, Langefeld, Carl D., Kmoch, Stanislav, Bleyer, Anthony J.

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Maternal health and pregnancy outcomes in autosomal dominant tubulointerstitial kidney disease von Bleyer, Anthony J, Kidd, Kendrah O, Williams, Adrienne H, Johnson, Emily, Robins, Victoria, Martin, Lauren, Taylor, Abbigail, Kim, Alice, Bowline, Isai, Connaughton, Dervla M, Langefeld, Carl D, Zivna, Martina, Kmoch, Stanislav

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Maternal Health in Autosomal Dominant Tubulointerstitial Kidney Disease: PO2239 von Bowline, Isai G., Bleyer, Anthony J., Kidd, Kendrah O., Williams, Adrienne H., Connaughton, Dervla M., Robins, Victoria C., Taylor, Abbigail, Martin, Lauren, Kim, Alice, Langefeld, Carl D., Zivna, Martina, Kmoch, Stanislav

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T Cell Responses to an HLA-B07-Restricted Epitope on the Dengue NS3 Protein Correlate with Disease Severity von Zivna, Iva, Green, Sharone, Vaughn, David W, Kalayanarooj, Siripen, Stephens, Henry A. F, Chandanayingyong, Dasnayanee, Nisalak, Ananda, Ennis, Francis A, Rothman, Alan L

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