Merle phenotypes in dogs - SILV SINE insertions from Mc to Mh
Langevin, Mary, Synkova, Helena, Jancuskova, Tereza, Pekova, Sona
Published in PloS one (20.09.2018)
Published in PloS one (20.09.2018)
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Comprehensive Analyses of White-Handed Gibbon Chromosomes Enables Access to 92 Evolutionary Conserved Breakpoints Compared to the Human Genome
Weise, Anja, Kosyakova, Nadezda, Voigt, Martin, Aust, Nadine, Mrasek, Kristin, Löhmer, Sharon, Rubtsov, Nikolai, Karamysheva, Tatyana V., Trifonov, Vladimir A., Hardekopf, David, Jančušková, Tereza, Pekova, Sona, Wilhelm, Kathleen, Liehr, Thomas, Fan, Xiaobo
Published in Cytogenetic and genome research (01.01.2015)
Published in Cytogenetic and genome research (01.01.2015)
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Parental origin of deletions and duplications - about the necessity to check for cryptic inversions
Liehr, Thomas, Schreyer, Isolde, Kuechler, Alma, Manolakos, Emmanouil, Singer, Sylke, Dufke, Andreas, Wilhelm, Kathleen, Jančušková, Tereza, Čmejla, Radek, Othman, Moneeb A K, Al-Rikabi, Ahmed H, Mrasek, Kristin, Ziegler, Monika, Kankel, Stefanie, Kreskowski, Katharina, Weise, Anja
Published in Molecular cytogenetics (09.03.2018)
Published in Molecular cytogenetics (09.03.2018)
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Heterogeneous aetiology and clinical presentation of cardiac involvement in hypereosinophilic syndrome: A case series
Kotrč, Martin, Kubánek, Miloš, Malíková, Pavlína, Kautznerová, Dana, Maalouf, Jacqueline, Jančušková, Tereza, Lupínek, Petr, Vrbská, Jana, Melenovský, Vojtěch, Kautzner, Josef
Published in Cor et vasa (English ed.) (01.06.2018)
Published in Cor et vasa (English ed.) (01.06.2018)
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Candidatus Neoehrlichia mikurensis infection identified in 2 hematooncologic patients: benefit of molecular techniques for rare pathogen detection
Pekova, Sona, Vydra, Jan, Kabickova, Hana, Frankova, Sona, Haugvicova, Renata, Mazal, Oldrich, Cmejla, Radek, Hardekopf, David W, Jancuskova, Tereza, Kozak, Tomas
Published in Diagnostic microbiology and infectious disease (01.03.2011)
Published in Diagnostic microbiology and infectious disease (01.03.2011)
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Mantle cell lymphoma‐variant Richter syndrome: Detailed molecular‐cytogenetic and backtracking analysis reveals slow evolution of a pre‐MCL clone in parallel with CLL over several years
Klener, Pavel, Fronkova, Eva, Berkova, Adela, Jaksa, Radek, Lhotska, Halka, Forsterova, Kristina, Soukup, Jan, Kulvait, Vojtech, Vargova, Jarmila, Fiser, Karel, Prukova, Dana, Alam, Mahmudul, Calvin Lenyeletse Maswabi, Bokang, Michalova, Kyra, Zemanova, Zuzana, Jancuskova, Tereza, Pekova, Sona, Trneny, Marek
Published in International journal of cancer (15.11.2016)
Published in International journal of cancer (15.11.2016)
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Long term follow-up in a patient with a de novo microdeletion of 14q11.2 involving CHD8
Drabova, Jana, Seemanova, Eva, Hancarova, Miroslava, Pourova, Radka, Horacek, Martin, Jancuskova, Tereza, Pekova, Sona, Novotna, Drahuse, Sedlacek, Zdenek
Published in American journal of medical genetics. Part A (01.04.2015)
Published in American journal of medical genetics. Part A (01.04.2015)
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A method to identify new molecular markers for assessing minimal residual disease in acute leukemia patients
Jancuskova, Tereza, Plachy, Radek, Stika, Jiri, Zemankova, Lucie, Hardekopf, David W, Liehr, Thomas, Kosyakova, Nadezda, Cmejla, Radek, Zejskova, Lenka, Kozak, Tomas, Zak, Pavel, Zavrelova, Alzbeta, Havlikova, Pavlina, Karas, Michal, Junge, Annelore, Ramel, Christian, Pekova, Sona
Published in Leukemia research (01.10.2013)
Published in Leukemia research (01.10.2013)
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Five-Color Multiplex Real-Time PCR Technology to Detect Over 75 Recurrent Chromosomal Abnormalities in Acute Myeloid Leukemia; Benefits for Minimal Residual Disease Detection
Plachy, Radek, Zejskova, Lenka, Cmejla, Radek, Hardekopf, David Warren, Jancuskova, Tereza, Krutilkova, Lucie, Karas, Michal, Koza, Vladimir, Vydra, Jan, Zak, Pavel, Smolej, Lukas, Pekova, Sona
Published in Blood (18.11.2011)
Published in Blood (18.11.2011)
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A comprehensive study of TP53 mutations in chronic lymphocytic leukemia: Analysis of 1287 diagnostic and 1148 follow-up CLL samples
Pekova, Sona, Mazal, Oldrich, Cmejla, Radek, Hardekopf, David W, Plachy, Radek, Zejskova, Lenka, Haugvicova, Renata, Jancuskova, Tereza, Karas, Michal, Koza, Vladimir, Smolej, Lukas, Bezdickova, Ludmila, Kozak, Tomas
Published in Leukemia research (01.07.2011)
Published in Leukemia research (01.07.2011)
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Identification of Novel Molecular Markers for the Follow-up of Minimal Residual Disease in Hematooncological Disorders
Hardekopf, David Warren, Jancuskova, Tereza, Jarosova, Marie, Krutilkova, Lucie, Plachy, Radek, Zejskova, Lenka, Cmejla, Radek, Vydra, Jan, Kozak, Tomas, Karas, Michal, Koza, Vladimir, Zavrelova, Alzbeta, Zak, Pavel, Smolej, Lukas, Pekova, Sona
Published in Blood (18.11.2011)
Published in Blood (18.11.2011)
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Journal Article
Molecular characterization of the rare translocation t(3;10)(q26;q21) in an acute myeloid leukemia patient
Jancuskova, Tereza, Plachy, Radek, Zemankova, Lucie, Hardekopf, David Warren, Stika, Jiri, Zejskova, Lenka, Praulich, Inka, Kreuzer, Karl-Anton, Rothe, Achim, Othman, Moneeb Ak, Kosyakova, Nadezda, Pekova, Sona
Published in Molecular cytogenetics (15.07.2014)
Published in Molecular cytogenetics (15.07.2014)
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Quantification of extracellular DNA using hypermethylated RASSF1A, SRY, and GLO sequences--evaluation of diagnostic possibilities for predicting placental insufficiency
Hromadnikova, Ilona, Zejskova, Lenka, Kotlabova, Katerina, Jancuskova, Tereza, Doucha, Jindrich, Dlouha, Klara, Krofta, Ladislav, Jirasek, Jan E, Vlk, Radovan
Published in DNA and cell biology (01.06.2010)
Published in DNA and cell biology (01.06.2010)
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Journal Article
Molecular characterization of the rare translocation t(3;10)(q26;q21) in an acute myeloid leukemia patient
Jancuskova, Tereza, Plachy, Radek, Zemankova, Lucie, Hardekopf, David Warren, Stika, Jiri, Zejskova, Lenka, Praulich, Inka, Kreuzer, Karl-Anton, Rothe, Achim, Othman, Moneeb Ak, Kosyakova, Nadezda, Pekova, Sona
Published in Molecular cytogenetics (01.01.2014)
Published in Molecular cytogenetics (01.01.2014)
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