Bohatá J - Search Results

1

Identification of Two Dysfunctional Variants in the ABCG2 Urate Transporter Associated with Pediatric-Onset of Familial Hyperuricemia and Early-Onset Gout.

Toyoda Y, Pavelcová K, Bohatá J, Ješina P, Kubota Y, Suzuki H, Takada T, Stiburkova B. Toyoda Y, et al. Among authors: bohata j. Int J Mol Sci. 2021 Feb 16;22(4):1935. doi: 10.3390/ijms22041935. Int J Mol Sci. 2021. PMID: 33669292 Free PMC article.

2

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: bohata j. Cells. 2019 Apr 18;8(4):363. doi: 10.3390/cells8040363. Cells. 2019. PMID: 31003562 Free PMC article.

3

Interaction of the p.Q141K Variant of the ABCG2 Gene with Clinical Data and Cytokine Levels in Primary Hyperuricemia and Gout.

Horváthová V, Bohatá J, Pavlíková M, Pavelcová K, Pavelka K, Šenolt L, Stibůrková B. Horváthová V, et al. Among authors: bohata j. J Clin Med. 2019 Nov 14;8(11):1965. doi: 10.3390/jcm8111965. J Clin Med. 2019. PMID: 31739430 Free PMC article.

4

Evaluation of the Influence of Genetic Variants of SLC2A9 (GLUT9) and SLC22A12 (URAT1) on the Development of Hyperuricemia and Gout.

Pavelcova K, Bohata J, Pavlikova M, Bubenikova E, Pavelka K, Stiburkova B. Pavelcova K, et al. Among authors: bohata j. J Clin Med. 2020 Aug 4;9(8):2510. doi: 10.3390/jcm9082510. J Clin Med. 2020. PMID: 32759716 Free PMC article.

5

Circulating microRNA alternations in primary hyperuricemia and gout.

Bohatá J, Horváthová V, Pavlíková M, Stibůrková B. Bohatá J, et al. Arthritis Res Ther. 2021 Jul 10;23(1):186. doi: 10.1186/s13075-021-02569-w. Arthritis Res Ther. 2021. PMID: 34246297 Free PMC article.

6

Renal Hypouricemia 1: Rare Disorder as Common Disease in Eastern Slovakia Roma Population.

Stiburkova B, Bohatá J, Pavelcová K, Tasic V, Plaseska-Karanfilska D, Cho SK, Potočnaková L, Šaligová J. Stiburkova B, et al. Among authors: bohata j. Biomedicines. 2021 Nov 3;9(11):1607. doi: 10.3390/biomedicines9111607. Biomedicines. 2021. PMID: 34829836 Free PMC article.

7

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: bohata j. Cells. 2022 Mar 22;11(7):1063. doi: 10.3390/cells11071063. Cells. 2022. PMID: 35406626 Free PMC article.

8

Identification of a dysfunctional exon-skipping splice variant in GLUT9/SLC2A9 causal for renal hypouricemia type 2.

Toyoda Y, Cho SK, Tasic V, Pavelcová K, Bohatá J, Suzuki H, David VA, Yoon J, Pallaiova A, Šaligová J, Nousome D, Cachau R, Winkler CA, Takada T, Stibůrková B. Toyoda Y, et al. Among authors: bohata j. Front Genet. 2023 Jan 17;13:1048330. doi: 10.3389/fgene.2022.1048330. eCollection 2022. Front Genet. 2023. PMID: 36733941 Free PMC article.

9

Fine specificity of anti-Le(X) monoclonal antibody TEC-01.

Bohata J, Smíd F, Dráber P. Bohata J, et al. Folia Biol (Praha). 1998;44(1):27-31. Folia Biol (Praha). 1998. PMID: 10730872

10

Lex glycosphingolipids-mediated cell aggregation.

Boubelík M, Floryk D, Bohata J, Dráberová L, Macák J, Smíd F, Dráber P. Boubelík M, et al. Among authors: bohata j. Glycobiology. 1998 Feb;8(2):139-46. doi: 10.1093/glycob/8.2.139. Glycobiology. 1998. PMID: 9451023

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

22 results

Search Page

Filters