Kateřina Pavelcová (Katerina Pavelcova)

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 8

Top Topics

Cancer Stem Cells

Metabolic Syndrome

Top Venues

Journal of clinical medicine

Arthritis research & therapy

International journal of molecular sciences

This page only lists publications with an associated author ORCID identifier.

Publications

Jiří Vávra, Kateřina Pavelcová, Jana Mašínová, Lenka Hasikova, Eliška Bubeníková, Aneta Urbanová, Andrea Mančíková, Blanka Stibůrková
Examining the Association of Rare Allelic Variants in Urate Transporters SLC22A11 , SLC22A13 , and SLC17A1 with Hyperuricemia and Gout. Disease markers 2024 (2024)
Jiří Vávra, Kateřina Pavelcová, Jana Mašínová, Lenka Hasikova, Eliška Bubeníková, Aneta Urbanová, Andrea Mančíková, Blanka Stibůrková
Examining the Association of Rare Allelic Variants in Urate Transporters SLC22A11 , SLC22A13 , and SLC17A1 with Hyperuricemia and Gout. Disease markers 2024 (2024)
Jiří Vávra, Kateřina Pavelcová, Jana Mašínová, Lenka Hasikova, Eliška Bubeníková, Aneta Urbanová, Andrea Mančíková, Blanka Stibůrková
Examining the Association of Rare Allelic Variants in Urate Transporters SLC22A11 , SLC22A13 , and SLC17A1 with Hyperuricemia and Gout. Disease markers 2024 (2024)
Aleš Kvasnička, David Friedecký, Radana Brumarová, Markéta Pavlíková, Kateřina Pavelcová, Jana Mašínová, Lenka Hasikova, Jakub Závada, Karel Pavelka, Pavel Ješina, Blanka Stibůrková
Alterations in lipidome profiles distinguish early-onset hyperuricemia, gout, and the effect of urate-lowering treatment. Arthritis research & therapy 25 (1) (2023)
Jiří Vávra, Andrea Mančíková, Kateřina Pavelcová, Lenka Hasikova, Jana Mašínová, Blanka Stibůrková
Functional Characterization of Rare Variants in OAT1/ SLC22A6 and OAT3/ SLC22A8 Urate Transporters Identified in a Gout and Hyperuricemia Cohort. Cells 11 (7) (2022)
Yu Toyoda, Kateřina Pavelcová, Jana Mašínová, Pavel Ješina, Yu Kubota, Hiroshi Suzuki, Tappei Takada, Blanka Stibůrková
Identification of Two Dysfunctional Variants in the ABCG2 Urate Transporter Associated with Pediatric-Onset of Familial Hyperuricemia and Early-Onset Gout. International journal of molecular sciences 22 (4) (2021)
Blanka Stibůrková, Jana Mašínová, Kateřina Pavelcová, Velibor Tasic, Dijana Plaseska-Karanfilska, Sung-Kweon Cho, Ludmila Potočnaková, Jana Šaligová
Renal Hypouricemia 1: Rare Disorder as Common Disease in Eastern Slovakia Roma Population. Biomedicines 9 (11) (2021)
Kateřina Pavelcová, Jana Mašínová, Marketa Pavlikova, Eliska Bubenikova, Karel Pavelka, Blanka Stiburkova
Evaluation of the Influence of Genetic Variants of SLC2A9 (GLUT9) and SLC22A12 (URAT1) on the Development of Hyperuricemia and Gout. Journal of clinical medicine 9 (8) (2020)