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A mutation in the SAA1 promoter causes hereditary amyloid A amyloidosis.
Sikora J, Kmochová T, Mušálková D, Pohludka M, Přikryl P, Hartmannová H, Hodaňová K, Trešlová H, Nosková L, Mrázová L, Stránecký V, Lunová M, Jirsa M, Honsová E, Dasari S, McPhail ED, Leung N, Živná M, Bleyer AJ, Rychlík I, Ryšavá R, Kmoch S. Sikora J, et al. Among authors: prikryl p. Kidney Int. 2022 Feb;101(2):349-359. doi: 10.1016/j.kint.2021.09.007. Epub 2021 Sep 21. Kidney Int. 2022. PMID: 34560138
Iron Overload Causes Alterations of E-Cadherin in the Liver.
Fujikura Y, Krijt J, Povýšil C, Mělková Z, Přikryl P, Vokurka M, Nečas E. Fujikura Y, et al. Among authors: prikryl p. Folia Biol (Praha). 2016;62(3):95-102. Folia Biol (Praha). 2016. PMID: 27516188 Free article.
Effect of Erythropoietin on the Expression of Murine Transferrin Receptor 2.
Berezovsky B, Báječný M, Frýdlová J, Gurieva I, Rogalsky DW, Přikryl P, Pospíšil V, Nečas E, Vokurka M, Krijt J. Berezovsky B, et al. Among authors: prikryl p. Int J Mol Sci. 2021 Jul 30;22(15):8209. doi: 10.3390/ijms22158209. Int J Mol Sci. 2021. PMID: 34360974 Free PMC article.
Study of urinary proteomes in Anderson-Fabry disease.
Vojtová L, Zima T, Tesař V, Michalová J, Přikryl P, Dostálová G, Linhart A. Vojtová L, et al. Among authors: prikryl p. Ren Fail. 2010;32(10):1202-9. doi: 10.3109/0886022X.2010.516859. Ren Fail. 2010. PMID: 20954982
82 results