Mgr. Michaela Pešová
Research specialist - PhD student, Šárka Pospíšilová Research Group
Office: bldg. E35/215
Kamenice 753/5
625 00 Brno
Phone: | +420 549 49 7428 |
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E‑mail: |
social and academic networks: |
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Total number of publications: 25
2021
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Functional analysis of germlineETV6 W380Rmutation causing inherited thrombocytopenia and secondary acute lymphoblastic leukemia or essential thrombocythemia
Platelets, year: 2021, volume: 32, edition: 6, DOI
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Phosphorylation patterns of tumor suppressor P53 and their impact on the P53 pathway activity in chronic lymphocytic leukemia.
Year: 2021, type: Conference abstract
2020
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Functional testing of gene variants in inherited thrombocytopenias.
Year: 2020, type: Conference abstract
2019
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A novel germline mutation in GP1BA gene in family with hereditary macrothrombocytopenia
Year: 2019, type: Conference abstract
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A novel germline mutation of the SFTPA1 gene in familial interstitial pneumonia
HUMAN GENOME VARIATION, year: 2019, volume: 6, edition: MAR, DOI
2018
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A novel germline mutation in GP1BA gene N-terminal domain in monoallelic Bernard-Soulier syndrome
Platelets, year: 2018, volume: 29, edition: 8, DOI
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C-terminal RUNX1 mutation in familial platelet disorder with predisposition to myeloid malignancies
International journal of hematology, year: 2018, volume: 108, edition: 6, DOI
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Dědičné trombocytopenie
Transfuze a Hematologie Dnes, year: 2018, volume: 24, edition: 1
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Detekce patogenních variant u rodin s výskytem dědičného onemocnění metodou celoexomového sekvenování – kazuistiky
Year: 2018, type: Conference abstract
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Determination of causal variants in iherited thrombocytopenias
Year: 2018, type: Conference abstract