Translocation of outer membrane vesicles from enterohemorrhagic Escherichia coli O157 across the intestinal epithelial barrier von Krsek, Daniel, Yara, Daniel Alejandro, Hrbáčková, Hana, Daniel, Ondřej, Mančíková, Andrea, Schüller, Stephanie, Bielaszewska, Martina

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Functional Characterization of Clinically-Relevant Rare Variants in ABCG2 Identified in a Gout and Hyperuricemia Cohort von Toyoda, Yu, Mančíková, Andrea, Krylov, Vladimír, Morimoto, Keito, Pavelcová, Kateřina, Bohatá, Jana, Pavelka, Karel, Pavlíková, Markéta, Suzuki, Hiroshi, Matsuo, Hirotaka, Takada, Tappei, Stiburkova, Blanka

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Functional Characterization of Rare Variants in OAT1/ SLC22A6 and OAT3/ SLC22A8 Urate Transporters Identified in a Gout and Hyperuricemia Cohort von Vávra, Jiří, Mančíková, Andrea, Pavelcová, Kateřina, Hasíková, Lenka, Bohatá, Jana, Stibůrková, Blanka

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Examining the Association of Rare Allelic Variants in Urate Transporters SLC22A11, SLC22A13, and SLC17A1 with Hyperuricemia and Gout von Vávra, Jiří, Pavelcová, Kateřina, Mašínová, Jana, Hasíková, Lenka, Bubeníková, Eliška, Urbanová, Aneta, Mančíková, Andrea, Stibůrková, Blanka

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Complex analysis of urate transporters SLC2A9, SLC22A12 and functional characterization of non-synonymous allelic variants of GLUT9 in the Czech population: no evidence of effect o... von Hurba, Olha, Mancikova, Andrea, Krylov, Vladimir, Pavlikova, Marketa, Pavelka, Karel, Stibůrková, Blanka

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Functional analysis of novel allelic variants in URAT1 and GLUT9 causing renal hypouricemia type 1 and 2 von Mancikova, Andrea, Krylov, Vladimir, Hurba, Olha, Sebesta, Ivan, Nakamura, Makiko, Ichida, Kimiyoshi, Stiburkova, Blanka

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Clinical and Functional Characterization of a Novel URAT1 Dysfunctional Variant in a Pediatric Patient with Renal Hypouricemia von Stiburkova, Blanka, Bohata, Jana, Minarikova, Iveta, Mancikova, Andrea, Vavra, Jiri, Krylov, Vladimír, Doležel, Zdenek

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A homozygous deletion in the SLC19A1 gene as a cause of folate-dependent recurrent megaloblastic anemia von Svaton, Michael, Skvarova Kramarzova, Karolina, Kanderova, Veronika, Mancikova, Andrea, Smisek, Petr, Jesina, Pavel, Krijt, Jakub, Stiburkova, Blanka, Dobrovolny, Robert, Sokolova, Jitka, Bakardjieva-Mihaylova, Violeta, Vodickova, Elena, Rackova, Marketa, Stuchly, Jan, Kalina, Tomas, Stary, Jan, Trka, Jan, Fronkova, Eva, Kozich, Viktor

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Folate-Dependent Normocytic Anemia Caused By a Hypomorphic Mutation in SLC19A1 gene von Svaton, Michael, Skvarova Kramarzova, Karolina, Kanderova, Veronika, Smisek, Petr, Jesina, Pavel, Krijt, Jakub, Stiburkova, Blanka, Mancikova, Andrea, Dobrovolny, Robert, Bakardjieva-Mihaylova, Violeta, Vodickova, Elena, Stuchly, Jan, Kalina, Tomas, Stary, Jan, Trka, Jan, Fronkova, Eva, Kozich, Viktor

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SP013IDIOPATHIC RENAL HYPOURICEMIA: IDENTIFICATION AND CHARACTERIZATION OF SLC22A12 MUTATIONS IN SPANISH PATIENTS von Claverie-Martin, Felix, Stiburkova, Blanka, Nakamura, Makiko, Gonzalez-Acosta, Hilaria, Mancikova, Andrea, Trujillo-Suarez, Jorge, Krylov, Vladimir

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