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GATA2
Publication
Class
Person
Publication
Programmes
publication
Synonymous GATA2 mutations result in selective loss of mutated RNA and are common in patients with GATA2 deficiency
2020 |
Second Faculty of Medicine
publication
MonoMAC syndrome with GATA2 novel mutation: A case report
2022 |
Faculty of Medicine in Hradec Králové
publication
Association of Unbalanced Translocation der(1;7) with Germline GATA2 Mutations
2021 |
Second Faculty of Medicine, First Faculty of Medicine
publication
Germ-line GATA2 p.THR354MET mutation in familial myelodysplastic syndrome with acquired monosomy 7 and ASXL1 mutation demonstrating rapid onset and poor survival
2012 |
Second Faculty of Medicine
publication
High GATA2 expression is a poor prognostic marker in pediatric acute myeloid leukemia
2012 |
Second Faculty of Medicine
publication
Hematopoietic stem cell transplantation in children and adolescents with GATA2-related myelodysplastic syndrome
2021 |
Second Faculty of Medicine
publication
Adolescent onset of localized papillomatosis, lymphedema, and multiple Beta-papillomavirus infection: epidermal nevus, segmental lymphedema praecox, or verrucosis? A case report and case series of epidermal nevi
2014 |
Faculty of Medicine in Pilsen
publication
Novel treatment options for anaemia in patients with chronic kidney disease
+1
2018 |
First Faculty of Medicine
publication
Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents
2016 |
Second Faculty of Medicine
publication
Loss of B cells and their precursors is the most constant feature of GATA-2 deficiency in childhood myelodysplastic syndrome
2016 |
Second Faculty of Medicine, Faculty of Medicine in Pilsen, First Faculty of Medicine, Faculty of Physical Education and Sport, Faculty of Medicine in Hradec Králové
publication
Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS): comparison with multiple myeloma
2019 |
Faculty of Medicine in Pilsen, First Faculty of Medicine
publication
Diffuse parenchymal lung disease as first clinical manifestation of GATA-2 deficiency in childhood
2015 |
Second Faculty of Medicine, Third Faculty of Medicine
publication
Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes
2021 |
Second Faculty of Medicine
publication
PATZ1 fusions define a novel molecularly distinct neuroepithelial tumor entity with a broad histological spectrum
2021 |
Second Faculty of Medicine