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Bohatá, Jana
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1

Identification of a dysfunctional exon-skipping splice vari..:

Toyoda, Yu ; Cho, Sung Kweon ; Tasic, Velibor...
Frontiers in Genetics.  13 (2023)  - p. , 2023
Link: https://doi.org/10.3389/..
 
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2

Functional Characterization of Rare Variants in OAT1/SLC22A..:

Vávra, Jiří ; Mančíková, Andrea ; Pavelcová, Kateřina...
Cells.  11 (2022)  7 - p. 1063 , 2022
Link: https://doi.org/10.3390/..
 
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3

Identification of Two Dysfunctional Variants in the ABCG2 U..:

Toyoda, Yu ; Pavelcová, Kateřina ; Bohatá, Jana...
International Journal of Molecular Sciences.  22 (2021)  4 - p. 1935 , 2021
Link: https://doi.org/10.3390/..
 
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4

Renal Hypouricemia 1: Rare Disorder as Common Disease in Ea..:

Stiburkova, Blanka ; Bohatá, Jana ; Pavelcová, Kateřina...
Biomedicines.  9 (2021)  11 - p. 1607 , 2021
Link: https://doi.org/10.3390/..
 
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5

Circulating microRNA alternations in primary hyperuricemia ..:

Bohatá, Jana ; Horváthová, Veronika ; Pavlíková, Markéta.
Arthritis Research & Therapy.  23 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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6

Evaluation of the Influence of Genetic Variants of SLC2A9 (..:

Pavelcova, Katerina ; Bohata, Jana ; Pavlikova, Marketa...
Journal of Clinical Medicine.  9 (2020)  8 - p. 2510 , 2020
Link: https://doi.org/10.3390/..
 
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7

Clinical and Functional Characterization of a Novel URAT1 D..:

Stiburkova, Blanka ; Bohata, Jana ; Minarikova, Iveta...
Applied Sciences.  9 (2019)  17 - p. 3479 , 2019
Link: https://doi.org/10.3390/..
 
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8

Interaction of the p.Q141K Variant of the ABCG2 Gene with C..:

Horváthová, Veronika ; Bohatá, Jana ; Pavlíková, Markéta...
Journal of Clinical Medicine.  8 (2019)  11 - p. 1965 , 2019
Link: https://doi.org/10.3390/..
 
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9

Functional Characterization of Clinically-Relevant Rare Var..:

Toyoda, Yu ; Mančíková, Andrea ; Krylov, Vladimír...
Cells.  8 (2019)  4 - p. 363 , 2019
Link: https://doi.org/10.3390/..
 
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10

Identification of a dysfunctional exon-skipping splice vari..:

Toyoda, Yu ; Cho, Sung Kweon ; Tasic, Velibor...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9887137/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
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11

Functional Characterization of Rare Variants in OAT1/SLC22A..:

Vávra, Jiří ; Mančíková, Andrea ; Pavelcová, Kateřina...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8997829/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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12

Molekulární patofyziologie primární hyperurikemie a dny ; M..:

Bohatá, Jana
http://hdl.handle.net/20.500.11956/171783.  , 2022
Link: https://hdl.handle.net/2..
 
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13

Identification of Two Dysfunctional Variants in the ABCG2 U..:

Toyoda, Yu ; Pavelcová, Kateřina ; Bohatá, Jana...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7920026/.  , 2021
Link: http://www.ncbi.nlm.nih...
 
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14

Renal Hypouricemia 1: Rare Disorder as Common Disease in Ea..:

Stiburkova, Blanka ; Bohatá, Jana ; Pavelcová, Kateřina...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8615432/.  , 2021
Link: http://www.ncbi.nlm.nih...
 
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15

Circulating microRNA alternations in primary hyperuricemia ..:

Bohatá, Jana ; Horváthová, Veronika ; Pavlíková, Markéta.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8272270/.  , 2021
Link: http://www.ncbi.nlm.nih...
 
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