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Page 1
Translocation of outer membrane vesicles from enterohemorrhagic Escherichia coli O157 across the intestinal epithelial barrier.
Front Microbiol. 2023 May 25;14:1198945. doi: 10.3389/fmicb.2023.1198945. eCollection 2023.
Front Microbiol. 2023.
PMID: 37303786
Free PMC article.
Functional Characterization of Rare Variants in OAT1/SLC22A6 and OAT3/SLC22A8 Urate Transporters Identified in a Gout and Hyperuricemia Cohort.
Vávra J, Mančíková A, Pavelcová K, Hasíková L, Bohatá J, Stibůrková B.
Vávra J, et al. Among authors: mancikova a.
Cells. 2022 Mar 22;11(7):1063. doi: 10.3390/cells11071063.
Cells. 2022.
PMID: 35406626
Free PMC article.
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A homozygous deletion in the SLC19A1 gene as a cause of folate-dependent recurrent megaloblastic anemia.
Svaton M, Skvarova Kramarzova K, Kanderova V, Mancikova A, Smisek P, Jesina P, Krijt J, Stiburkova B, Dobrovolny R, Sokolova J, Bakardjieva-Mihaylova V, Vodickova E, Rackova M, Stuchly J, Kalina T, Stary J, Trka J, Fronkova E, Kozich V.
Svaton M, et al. Among authors: mancikova a.
Blood. 2020 Jun 25;135(26):2427-2431. doi: 10.1182/blood.2019003178.
Blood. 2020.
PMID: 32276275
Free PMC article.
No abstract available.
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Functional Characterization of Clinically-Relevant Rare Variants in ABCG2 Identified in a Gout and Hyperuricemia Cohort.
Toyoda Y, Mančíková A, Krylov V, Morimoto K, Pavelcová K, Bohatá J, Pavelka K, Pavlíková M, Suzuki H, Matsuo H, Takada T, Stiburkova B.
Toyoda Y, et al. Among authors: mancikova a.
Cells. 2019 Apr 18;8(4):363. doi: 10.3390/cells8040363.
Cells. 2019.
PMID: 31003562
Free PMC article.
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Examining the Association of Rare Allelic Variants in Urate Transporters SLC22A11, SLC22A13, and SLC17A1 with Hyperuricemia and Gout.
Vávra J, Pavelcová K, Mašínová J, Hasíková L, Bubeníková E, Urbanová A, Mančíková A, Stibůrková B.
Vávra J, et al. Among authors: mancikova a.
Dis Markers. 2024 Jan 6;2024:5930566. doi: 10.1155/2024/5930566. eCollection 2024.
Dis Markers. 2024.
PMID: 38222853
Free PMC article.
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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 on hyperuricemia and gout.
Hurba O, Mancikova A, Krylov V, Pavlikova M, Pavelka K, Stibůrková B.
Hurba O, et al. Among authors: mancikova a.
PLoS One. 2014 Sep 30;9(9):e107902. doi: 10.1371/journal.pone.0107902. eCollection 2014.
PLoS One. 2014.
PMID: 25268603
Free PMC article.
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Functional analysis of novel allelic variants in URAT1 and GLUT9 causing renal hypouricemia type 1 and 2.
Mancikova A, Krylov V, Hurba O, Sebesta I, Nakamura M, Ichida K, Stiburkova B.
Mancikova A, et al.
Clin Exp Nephrol. 2016 Aug;20(4):578-584. doi: 10.1007/s10157-015-1186-z. Epub 2015 Oct 24.
Clin Exp Nephrol. 2016.
PMID: 26500098
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