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prof. MUDr. Ondřej Hrušák Ph.D.
Academic staff at Second Faculty of Medicine
161 publications
Publications
publication
Deficit of GATA-2 transcription factor: new immunodeficiency syndrome with broad phenotype. First patients diagnosed in the Czech Republic and review of the literature
2013 |
First Faculty of Medicine, Faculty of Physical Education and Sport, Faculty of Medicine in Pilsen, Second Faculty of Medicine
publication
Real-time quantitative PCR detection of WT1 gene expression in children with AML: prognostic significance, correlation with disease status and residual disease detection by flow cytometry
2002 |
First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
publication
Fast Reduction of TEL/AML1 Transcript Levels by RQ-PCR in 53 Paediatric TEL/AML1-Positive Patients. Comparison to Flow Cytometry MRD Detection
2001 |
Second Faculty of Medicine, Central Library of Charles University
publication
No Evidence for MLL/AF4 Expression in Normal Cord Blood Samples
1999 |
First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
publication
RT-PCR based detection of TEL/AML 1 fusion transcript in childhood B
1998 |
Second Faculty of Medicine, Central Library of Charles University
publication
FCM marker importance for MRD assessment in T-cell acute lymphoblastic leukemia: An AIEOP-BFM-ALL-FLOW study group report
2024 |
Second Faculty of Medicine
publication
CD371+ pediatric B-cell acute lymphoblastic leukemia: propensity to lineage switch and slow early response to treatment
2024 |
Second Faculty of Medicine
publication
B cell phenotype and serum levels of interferons, BAFF, and APRIL in multisystem inflammatory syndrome in children associated with COVID-19 (MIS-C)
2023 |
First Faculty of Medicine, Faculty of Medicine in Pilsen, Second Faculty of Medicine
publication
Improved survival and MRD remission with blinatumomab vs. chemotherapy in children with first high-risk relapse B-ALL
2023 |
Second Faculty of Medicine
publication
TLR8/TLR7 dysregulation due to a novel TLR8 mutation causes severe autoimmune hemolytic anemia and autoinflammation in identical twins
2022 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Mathematics and Physics
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