E-LIB Suche - Ergebnisse für: Stiburkova, Blanka

1

Interleukin-37: associations of plasma levels and genetic v..:

Andres Cerezo, Lucie ; Navrátilová, Adéla ; Hulejová, Hana...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10583385/. , 2023

Link: http://www.ncbi.nlm.nih...

2

Alterations in lipidome profiles distinguish early-onset hy..:

Kvasnička, Aleš ; Friedecký, David ; Brumarová, Radana...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693150/. , 2023

Link: http://www.ncbi.nlm.nih...

3

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...

4

Human ultrarare genetic disorders of sulfur metabolism demo..:

Kožich, Viktor ; Schwahn, Bernd ; Sokolová, Jitka...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.redox.2022.102517. , 2022

Link: https://hal.inrae.fr/hal..

5

Human ultrarare genetic disorders of sulfur metabolism demo..:

Kožich, Viktor ; Schwahn, Bernd ; Sokolová, Jitka...
https://discovery.ucl.ac.uk/id/eprint/10158121/1/1-s2.0-S2213231722002890-main.pdf. , 2022

Link: https://discovery.ucl.ac..

6

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...

7

Human ultrarare genetic disorders of sulfur metabolism demo..:

Kožich, Viktor ; Schwahn, Bernd ; Sokolová, Jitka...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.redox.2022.102517. , 2022

Link: https://hal.inrae.fr/hal..

8

Analysis of Purine Metabolism to Elucidate the Pathogenesis..:

Miyamoto, Daisuke ; Sato, Nana ; Nagata, Koji...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9312704/. , 2022

Link: http://www.ncbi.nlm.nih...

9

Human ultrarare genetic disorders of sulfur metabolism demo..:

Kožich, Viktor ; Schwahn, Bernd C ; Sokolová, Jitka...
Redox Biology. -58 (2022), p.1-13. -Redox Biol. - 2213-2317. , 2022

Link: https://hdl.handle.net/2..

10

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...

11

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...

12

Subtype-specific gout susceptibility loci and enrichment of..:

Nakayama, Akiyoshi ; Nakatochi, Masahiro ; Kawamura, Yusuke...
http://repo.lib.tokushima-u.ac.jp/files/public/11/115836/2021031810544035118/annrheumdis_79_5_657.pdf. , 2021

Link: http://repo.lib.tokushim..

13

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...

14

Subtype-specific gout susceptibility loci and enrichment of..:

Nakayama, Akiyoshi ; Nakatochi, Masahiro ; Kawamura, Yusuke...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7213308/. , 2020

Link: http://www.ncbi.nlm.nih...

15

Genome-wide association study revealed novel loci which agg..:

Kawamura, Yusuke ; Nakaoka, Hirofumi ; Nakayama, Akiyoshi...
http://repo.lib.tokushima-u.ac.jp/files/public/11/114985/20200722115433633266/annrheumdis_78_10_1430.pdf. , 2020

Link: http://repo.lib.tokushim..