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Page 1
Microsatellite instability in hematological malignancies.
Krsková-Honzátková L, Cermák J, Sajdová J, Starý J, Sedlácek P, Sieglová Z. Krsková-Honzátková L, et al. Among authors: cermak j. Leuk Lymphoma. 2002 Oct;43(10):1979-86. doi: 10.1080/1042819021000015835. Leuk Lymphoma. 2002. PMID: 12481896
Dynamics of telomere erosion and its association with genome instability in myelodysplastic syndromes (MDS) and acute myelogenous leukemia arising from MDS: a marker of disease prognosis?
Sieglová Z, Zilovcová S, Cermák J, Ríhová H, Brezinová D, Dvoráková R, Marková M, Maaloufová J, Sajdová J, Brezinová J, Zemanová Z, Michalová K. Sieglová Z, et al. Among authors: cermak j. Leuk Res. 2004 Oct;28(10):1013-21. doi: 10.1016/j.leukres.2003.11.020. Leuk Res. 2004. PMID: 15289012
The presence of clonal cell subpopulations in peripheral blood and bone marrow of patients with refractory cytopenia with multilineage dysplasia but not in patients with refractory anemia may reflect a multistep pathogenesis of myelodysplasia.
Cermák J, Belicková M, Krejcová H, Michalová K, Zilovcová S, Zemanová Z, Brezinová J, Sieglová Z. Cermák J, et al. Leuk Res. 2005 Apr;29(4):371-9. doi: 10.1016/j.leukres.2004.08.008. Epub 2004 Dec 22. Leuk Res. 2005. PMID: 15725470
Prognostic significance of del(20q) in patients with hematological malignancies.
Brezinová J, Zemanová Z, Ransdorfová S, Sindelárová L, Sisková M, Neuwirtová R, Cermák J, Michalová K. Brezinová J, et al. Among authors: cermak j. Cancer Genet Cytogenet. 2005 Jul 15;160(2):188-92. doi: 10.1016/j.cancergencyto.2004.12.019. Cancer Genet Cytogenet. 2005. PMID: 15993278
Deletion of the long arm but not the 5q31 region of chromosome 5 in myeloid malignancies.
Brezinova J, Zemanova Z, Bystricka D, Sarova I, Lizcova L, Malinova E, Izakova S, Sajdova J, Sponerova D, Jonasova A, Cermak J, Michalova K. Brezinova J, et al. Among authors: cermak j. Leuk Res. 2012 Mar;36(3):e43-5. doi: 10.1016/j.leukres.2011.11.007. Epub 2011 Dec 6. Leuk Res. 2012. PMID: 22153775 No abstract available.
Copy number neutral loss of heterozygosity at 17p and homozygous mutations of TP53 are associated with complex chromosomal aberrations in patients newly diagnosed with myelodysplastic syndromes.
Svobodova K, Zemanova Z, Lhotska H, Novakova M, Podskalska L, Belickova M, Brezinova J, Sarova I, Izakova S, Lizcova L, Berkova A, Siskova M, Jonasova A, Cermak J, Michalova K. Svobodova K, et al. Among authors: cermak j. Leuk Res. 2016 Mar;42:7-12. doi: 10.1016/j.leukres.2016.01.009. Epub 2016 Jan 24. Leuk Res. 2016. PMID: 26851439
360 results