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Chromothripsis in Chronic Lymphocytic Leukemia: A Driving Force of Genome Instability
Chromothripsis in Chronic Lymphocytic Leukemia: A Driving Force of Genome Instability
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Chromothripsis in Chronic Lymphocytic Leukemia: A Driving Force of Genome Instability

Zavacka, Kristyna ; Plevova, Karla

Frontiers in oncology, 2021-11, Vol.11, p.771664-771664 [Periódico revisado por pares]

Switzerland: Frontiers Media S.A

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2
Towards error-free profiling of immune repertoires
Towards error-free profiling of immune repertoires
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Towards error-free profiling of immune repertoires

Shugay, Mikhail ; Britanova, Olga V ; Merzlyak, Ekaterina M ; Turchaninova, Maria A ; Mamedov, Ilgar Z ; Tuganbaev, Timur R ; Bolotin, Dmitriy A ; Staroverov, Dmitry B ; Putintseva, Ekaterina V ; Plevova, Karla ; Linnemann, Carsten ; Shagin, Dmitriy ; Pospisilova, Sarka ; Lukyanov, Sergey ; Schumacher, Ton N ; Chudakov, Dmitriy M

Nature methods, 2014-06, Vol.11 (6), p.653-655 [Periódico revisado por pares]

United States: Nature Publishing Group

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3
Identification of Clinically Relevant Subgroups of Chronic Lymphocytic Leukemia Through Discovery of Abnormal Molecular Pathways
Identification of Clinically Relevant Subgroups of Chronic Lymphocytic Leukemia Through Discovery of Abnormal Molecular Pathways
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Identification of Clinically Relevant Subgroups of Chronic Lymphocytic Leukemia Through Discovery of Abnormal Molecular Pathways

Taus, Petr ; Pospisilova, Sarka ; Plevova, Karla

Frontiers in genetics, 2021-06, Vol.12, p.627964-627964 [Periódico revisado por pares]

Frontiers Media S.A

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4
The importance of complex karyotype in prognostication and treatment of chronic lymphocytic leukemia (CLL): a comprehensive review of the literature
The importance of complex karyotype in prognostication and treatment of chronic lymphocytic leukemia (CLL): a comprehensive review of the literature
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The importance of complex karyotype in prognostication and treatment of chronic lymphocytic leukemia (CLL): a comprehensive review of the literature

Jarošová, Marie ; Plevová, Karla ; Kotašková, Jana ; Doubek, Michael ; Pospíšilová, Šárka

Leukemia & lymphoma, 2019-08, Vol.60 (10), p.2348-2355 [Periódico revisado por pares]

United States: Taylor & Francis

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5
Cerebral organoids derived from patients with Alzheimer’s disease with PSEN1/2 mutations have defective tissue patterning and altered development
Cerebral organoids derived from patients with Alzheimer’s disease with PSEN1/2 mutations have defective tissue patterning and altered development
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Cerebral organoids derived from patients with Alzheimer’s disease with PSEN1/2 mutations have defective tissue patterning and altered development

Vanova, Tereza ; Sedmik, Jiri ; Raska, Jan ; Amruz Cerna, Katerina ; Taus, Petr ; Pospisilova, Veronika ; Nezvedova, Marketa ; Fedorova, Veronika ; Kadakova, Sona ; Klimova, Hana ; Capandova, Michaela ; Orviska, Petra ; Fojtik, Petr ; Bartova, Simona ; Plevova, Karla ; Spacil, Zdenek ; Hribkova, Hana ; Bohaciakova, Dasa

Cell reports (Cambridge), 2023-11, Vol.42 (11), p.113310-113310, Article 113310 [Periódico revisado por pares]

United States: Elsevier Inc

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6
Telomere dynamics in adult hematological malignancies
Telomere dynamics in adult hematological malignancies
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Telomere dynamics in adult hematological malignancies

Olbertova, Helena ; Plevova, Karla ; Stranska, Kamila ; Pospisilova, Sarka

Biomedical papers of the Medical Faculty of the University Palacký, Olomouc, Czechoslovakia, 2019-02, Vol.163 (1), p.1-7 [Periódico revisado por pares]

Czech Republic: Palacký University Olomouc, Faculty of Medicine and Dentistry

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7
Memory B-cell like chronic lymphocytic leukaemia is associated with specific methylation profile of WNT5A promoter and undetectable expression of WNT5A gene
Memory B-cell like chronic lymphocytic leukaemia is associated with specific methylation profile of WNT5A promoter and undetectable expression of WNT5A gene
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Memory B-cell like chronic lymphocytic leukaemia is associated with specific methylation profile of WNT5A promoter and undetectable expression of WNT5A gene

Poppova, Lucie ; Pavlova, Sarka ; Gonzalez, Beatriz ; Kotaskova, Jana ; Plevova, Karla ; Dumbovic, Gabrijela ; Janovska, Pavlina ; Bystry, Vojtech ; Panovska, Anna ; Bezdekova, Lucie ; Maslejova, Stanislava ; Brychtova, Yvona ; Doubek, Michael ; Krzyzankova, Marcela ; Borsky, Marek ; Mayer, Jiri ; Bryja, Vitezslav ; Alonso, Sergio ; Pospisilova, Sarka

Epigenetics, 2022-12, Vol.17 (12), p.1628-1635 [Periódico revisado por pares]

United States: Taylor & Francis

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8
Evolution of TP53 abnormalities during CLL disease course is associated with telomere length changes
Evolution of TP53 abnormalities during CLL disease course is associated with telomere length changes
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Evolution of TP53 abnormalities during CLL disease course is associated with telomere length changes

Olbertova, Helena ; Plevova, Karla ; Pavlova, Sarka ; Malcikova, Jitka ; Kotaskova, Jana ; Stranska, Kamila ; Spunarova, Michaela ; Trbusek, Martin ; Navrkalova, Veronika ; Dvorackova, Barbara ; Tom, Nikola ; Pal, Karol ; Jarosova, Marie ; Brychtova, Yvona ; Panovska, Anna ; Doubek, Michael ; Pospisilova, Sarka

BMC cancer, 2022-02, Vol.22 (1), p.137-137, Article 137 [Periódico revisado por pares]

England: BioMed Central Ltd

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9
Distinct p53 phosphorylation patterns in chronic lymphocytic leukemia patients are reflected in the activation of circumjacent pathways upon DNA damage
Distinct p53 phosphorylation patterns in chronic lymphocytic leukemia patients are reflected in the activation of circumjacent pathways upon DNA damage
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Distinct p53 phosphorylation patterns in chronic lymphocytic leukemia patients are reflected in the activation of circumjacent pathways upon DNA damage

Mancikova, Veronika ; Pesova, Michaela ; Pavlova, Sarka ; Helma, Robert ; Zavacka, Kristyna ; Hejret, Vaclav ; Taus, Petr ; Hynst, Jakub ; Plevova, Karla ; Malcikova, Jitka ; Pospisilova, Sarka

Molecular oncology, 2023-01, Vol.17 (1), p.82-97 [Periódico revisado por pares]

United States: John Wiley & Sons, Inc

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10
C-terminal RUNX1 mutation in familial platelet disorder with predisposition to myeloid malignancies
C-terminal RUNX1 mutation in familial platelet disorder with predisposition to myeloid malignancies
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C-terminal RUNX1 mutation in familial platelet disorder with predisposition to myeloid malignancies

Staňo Kozubík, Kateřina ; Radová, Lenka ; Pešová, Michaela ; Réblová, Kamila ; Trizuljak, Jakub ; Plevová, Karla ; Fiamoli, Veronika ; Gumulec, Jaromír ; Urbánková, Helena ; Szotkowski, Tomáš ; Mayer, Jiří ; Pospíšilová, Šárka ; Doubek, Michael

International journal of hematology, 2018-12, Vol.108 (6), p.652-657 [Periódico revisado por pares]

Tokyo: Springer Japan

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