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Homozygous EXOSC3 mutation c.92G→C, p.G31A is a founder mutation causing severe pontocerebellar hypoplasia type 1 among the Czech Roma.
Schwabova J, Brozkova DS, Petrak B, Mojzisova M, Pavlickova K, Haberlova J, Mrazkova L, Hedvicakova P, Hornofova L, Kaluzova M, Fencl F, Krutova M, Zamecnik J, Seeman P. Schwabova J, et al. Among authors: mrazkova l. J Neurogenet. 2013 Dec;27(4):163-9. doi: 10.3109/01677063.2013.814651. Epub 2013 Jul 25. J Neurogenet. 2013. PMID: 23883322
[Pseudotumors of the central nervous system].
Zámečník J, Mrázková L. Zámečník J, et al. Among authors: mrazkova l. Cesk Patol. 2012 Oct;48(4):184-9. Cesk Patol. 2012. PMID: 23121027 Review. Czech.
The final walk with preptin.
Mrázková L, Lubos M, Voldřich J, Kužmová E, Zrubecká D, Gwozdiaková P, Buděšínský M, Asai S, Marek A, Pícha J, Tencerová M, Ferenčáková M, Barrera GA, Kaminský J, Jiráček J, Žáková L. Mrázková L, et al. PLoS One. 2024 Sep 12;19(9):e0309726. doi: 10.1371/journal.pone.0309726. eCollection 2024. PLoS One. 2024. PMID: 39264940 Free PMC article.
Non-glycosylated IGF2 prohormones are more mitogenic than native IGF2.
Potalitsyn P, Mrázková L, Selicharová I, Tencerová M, Ferenčáková M, Chrudinová M, Turnovská T, Brzozowski AM, Marek A, Kaminský J, Jiráček J, Žáková L. Potalitsyn P, et al. Among authors: mrazkova l. Commun Biol. 2023 Aug 19;6(1):863. doi: 10.1038/s42003-023-05239-6. Commun Biol. 2023. PMID: 37598269 Free PMC article.
Functional stapled fragments of human preptin of minimised length.
Lubos M, Mrázková L, Gwozdiaková P, Pícha J, Buděšínský M, Jiráček J, Kaminský J, Žáková L. Lubos M, et al. Among authors: mrazkova l. Org Biomol Chem. 2022 Mar 23;20(12):2446-2454. doi: 10.1039/d1ob02193a. Org Biomol Chem. 2022. PMID: 35253830