Search Results - "Ransdorfova, S"

P445: CRYPTIC TRANSLOCATION T(5;11)(Q35;P15) RESULTING IN NUP98::NSD1 GENE FUSION IN ADULTS WITH DE NOVO ACUTE MYELOID LEUKEMIA (AML) by Ransdorfova, S., Markova, J., Valerianova, M., Brezinova, J., Onderkova, M., Mendlikova, I., Lizcova, L., Pavlistova, L., Svobodova, K., Izakova, S., Jonasova, A., Salek, C., Racil, Z., Zemanova, Z.

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Cytogenetic Clonal Evolution in Myelodysplastic Syndromes (MDS) with Isolated Del(5Q) by Zemanova, Z, Michalova, K, Brezinova, J, Svobodova, K, Lhotska, H, Sarova, I, Lizcova, L, Izakova, S, Ransdorfova, S, Pavlistova, L, Berkova, A, Skipalova, K, Belickova, M, Siskova, M, Neuwirtova, R, Cermak, J, Stopka, T, Jonasova, A

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170 MECHANISM OF FORMATION OF COMPLEX CHROMOSOMAL ABERRATIONS IN PATIENTS WITH MYELODYSPLASTIC SYNDROMES (MDS): CLONAL EVOLUTION OR CHROMOTHRIPSIS? by Zemanova, Z, Michalova, K, Brezinova, J, Lhotska, H, Svobodova, K, Sarova, I, Lizcova, L, Izakova, S, Ransdorfova, S, Krejcik, Z, Belickova, M, Siskova, M, Jonasova, A, Neuwirtova, R, Cermak, J

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Topic: AS04-MDS Biology and Pathogenesis/AS04d-Somatic mutations by Zemanova, Z., Brezinova, J., Svobodova, K., Lhotska, H., Aghova, T., Vidlakova, D., Izakova, S., Lizcova, L., Ransdorfova, S., Mendlikova, I., Pavlistova, L., Belickova, M., Vesela, J., Siskova, M., Neuwirtova, R., Cermak, J., Stopka, T., Jonasova, A.

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P22 - Topic: AS04-MDS Biology and Pathogenesis/AS04d-Somatic mutations: THE DEL(5Q) SIZE IN MDS IS CORRELATED TO KARYOTYPE COMPLEXITY AND FREQUENCY OF TP53 MUTATIONS by Zemanova, Z., Brezinova, J., Svobodova, K., Lhotska, H., Aghova, T., Vidlakova, D., Izakova, S., Lizcova, L., Ransdorfova, S., Mendlikova, I., Pavlistova, L., Belickova, M., Vesela, J., Siskova, M., Neuwirtova, R., Cermak, J., Stopka, T., Jonasova, A.

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PB1710 ACUTE MYELOID LEUKEMIA WITH A RARE CRYPTIC T(8;16)(P11;P13) TRANSLOCATION AND MYST3/CREBBP FUSION by Brezinova, J., Ransdorfova, S., Valerianova, M., Onderkova, M., Izakova, S., Zemanova, Z., Markova, J., Vitek, A.

“…Background: The translocation t(8;16)(p11;p13) is a very rare cytogenetic finding in pediatric and adult de novo and therapy‐related acute myeloid leukemia…”
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90 - Cytogenetic Clonal Evolution in Myelodysplastic Syndromes (MDS) with Isolated Del(5Q) by Zemanova, Z., Michalova, K., Brezinova, J., Svobodova, K., Lhotska, H., Sarova, I., Lizcova, L., Izakova, S., Ransdorfova, S., Pavlistova, L., Berkova, A., Skipalova, K., Belickova, M., Siskova, M., Neuwirtova, R., Cermak, J., Stopka, T., Jonasova, A.

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PB2076 MOLECULAR CYTOGENETIC ANALYSIS OF CHROMOSOME 7 ABERRATIONS IN MYELOID DISEASES by Ransdorfova, S., Onderkova, M., Brezinova, J., Sarova, I., Valerianova, M., Svobodova, K., Lhotska, H., Pavlistova, L., Lizcova, L., Michalova, K., Zemanova, Z., Jonasova, A., Stopka, T., Cermak, J.

“…Background: Complete or partial loss of chromosome 7 is a recurrent chromosomal aberration frequently found in myeloid disorders such as myelodysplastic…”
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PS1330 VARIABILITY IN THE EXTENT OF DEL(5Q) AND ITS CLINICAL IMPLICATION IN MYELODYSPLASTIC SYNDROMES (MDS) by Zemanova, Z., Brezinova, J., Michalova, K., Svobodova, K., Lhotska, H., Vesela, D., Izakova, S., Sarova, I., Lizcova, L., Ransdorfova, S., Pavlistova, L., Belickova, M., Vesela, J., Siskova, M., Neuwirtova, R., Cermak, J., Stopka, T., Jonasova, A.

“…Background: The interstitial deletion of the long arm of chromosome 5—del(5q)—is the most common cytogenetic abnormality in MDS occurring either as a sole…”
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Cytogenetic analyses in 81 patients with brain gliomas: correlation with clinical outcome and morphological data by Kramar, F, Zemanova, Z, Michalova, K, Babicka, L, Ransdorfova, S, Hrabal, P, Kozler, P

“…Specific gene mutations, loss of heterozygosity, deletions and/or amplifications of entire chromosomal regions and gene silencing have been described in…”
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Prognostic value of structural chromosomal rearrangements and small cell clones with high hyperdiploidy in children with acute lymphoblastic leukemia by Zemanova, Zuzana, Michalova, Kyra, Sindelarova, Lenka, Smisek, Petr, Brezinova, Jana, Ransdorfova, Sarka, Vavra, Vladimir, Dohnalova, Alena, Stary, Jan

“…In this study, 107 children with acute lymphoblastic leukemia (ALL) were analysed for the presence of hyperdiploidy by cytogenetics and interphase fluorescence…”
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Molecular cytogenetic stratification of recurrent oligodendrogliomas: utility of interphase fluorescence in situ hybridization (I-FISH) by Zemanová, Z, Kramar, F, Babická, L, Ransdorfová, S, Melichercíková, J, Hrabal, P, Kozler, P, Michalová, K

“…In oligodendroglial brain tumours, losses of chromosomal material of the short arm of chromosome 1 and long arm of chromosome 19 have been shown to predict…”
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Prognostic relevance of the FAB morphological criteria in chronic lymphocytic leukemia: correlations with IgVH gene mutational status and other prognostic markers by Schwarz, J, Mikulenková, D, Cermáková, M, Polanská, V, Michalová, K, Marinov, I, Campr, V, Ransdorfová, S, Marková, J, Pavlistová, L, Brezinová, J, Sajdová, J, Sponerová, D, Volková, Z, Benesová, K, Cermák, J, Vítek, A, Cetkovský, P

“…Morphological examination is the routine first step in the diagnosis of hematological malignancies, including chronic lymphocytic leukemia (CLL). Atypical cell…”
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Molecular cytogenetic analysis of chromosomal aberrations in cells of low grade gliomas and its contribution for tumour classification by Lhotská, H, Zemanová, Z, Kramář, F, Lizcová, L, Svobodová, K, Ransdorfová, S, Bystřická, D, Krejčík, Z, Hrabal, P, Dohnalová, A, Kaiser, M, Michalová, K

“…Low-grade gliomas represent a heterogeneous group of primary brain malignancies. The current diagnostics of these tumors rely strongly on histological…”
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Incidence of chromosomal anomalies detected with FISH and their clinical correlations in B-chronic lymphocytic leukemia by Šindelářová, Lenka, Michalová, Kyra, Zemanová, Zuzana, Ransdorfová, Šárka, Březinová, Jana, Peková, Soňa, Schwarz, Jiří, Karban, Josef, Cmunt, Eduard

“…B-chronic lymphocytic leukemia (B-CLL) is the most common adult leukemia. Molecular genetic characterization of B-CLL has made significant progress and typical…”
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Prognostic significance of del(20q) in patients with hematological malignancies by Brezinova, Jana, Zemanova, Zuzana, Ransdorfova, Sarka, Sindelarova, Lenka, Siskova, Magda, Neuwirtova, Radana, Cermak, Jaroslav, Michalova, Kyra

“…Deletions of the long arm of chromosome 20 represent a common chromosomal abnormality associated with myeloid malignancies, in particular with…”
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