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Publikační činnost

Autoři Název Periodikum
Stejskal D, Vaclavik J, Smekal A, Svobodova G, Richterova R, Svestak M. Omentin-1 levels in patients with premature coronary artery disease, metabolic syndrome and healthy controls. Short communication. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2016 Apr 20. doi: 10.5507/bp.2016.019. [Epub ahead of print]
Kurfurstova D, Bartkova J, Vrtel R, Mickova A, Burdova A, Majera D, Mistrik M, Kral M, Santer FR, Bouchal J, Bartek J. DNA damage signalling barrier, oxidative stress and treatment-relevant DNA repair factor alterations during progression of human prostate cancer. Mol Oncol. 2016 Mar 3. pii: S1574-7891(16)00037-5. [Epub ahead of print]
Soumarova R, Boday A, Krhutova V, Janotova A, Dvorakova M, Jaluvkova E, Stursa M, Perkova H.  Prognostic and predictive molecular biological markers in prostate cancer - significance of expression of genes PCA3 and TMPRSS2 Neoplasma. 2015;62(1):114-8, ISSN 0028-2685 (print), ISSN 1338-4317 
Kucerova R, Bienova M, Kral M, Bouchal J, Trtkova KS, Burdova A, Student V, Kolar Z. Androgenetic alopecia and polymorphism of the androgen receptor gene (SNP rs6152) in patients with benign prostate hyperplasia or prostate cancer. J Eur Acad Dermatol Venereol. 2015 Jan;29(1):91-6. 
Kolar Z, Burdova A, Jamaspishvili T, Bouchal J, Kucerova R, Bienova M, Kral M, Student V. Relation of ETS transcription factor family member ERG, androgen receptor and topoisomerase 2β expression to TMPRSS2-ERG fusion status in prostate cancer. Neoplasma. 2014;61(1):9-16.
Boday A., Tavandzis S., Krhutova V., Horka K., Dvorakova H., Vanickova P., Ryskova J., Janeckova A., Nemecek M., Kaspercik I. Genetic and epigenetic changes and their effect on prognosis and prediction of colorectal cancer Asia-Pacific J. of Clin. Oncology, 2014, 10, Suppl. S8, 173, ISSN: 1743-7563
Burdova A, Bouchal J, Tavandzis S, Zdenek K TMPRSS2-ERG gene fusion in prostate cancer Biomedical Papers-Olomouc 2014; 158(4):502-510
Sípek A Jr, Grodecká L, Baxová A, Cibulková P, Dvořáková M, Mazurová S, Magner M, Zeman J, Honzík T, Freiberger T. Novel FBN1 gene mutation and maternal germinal mosaicism as the cause of neonatal form of Marfan syndrome. Am J Med Genet A. 2014 Jun;164A(6):1559-64.