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RUNX1
Publication
Class
Person
Publication
Programmes
publication
RUNX1 regulates the CD34 gene in haematopoietic stem cells by mediating interactions with a distal regulatory element
2011 |
Central Library of Charles University
publication
The role of TEL and AML1 genes in the pathogenesis of hematologic malignancies
2001 |
Second Faculty of Medicine
publication
RUNX1 mutations contribute to the progression of MDS due to disruption of antitumor cellular defense: a study on patients with lower-risk MDS
2022 |
First Faculty of Medicine, Faculty of Science
publication
Transmembrane adaptor protein WBP1L regulates CXCR4 signalling and murine haematopoiesis
2020 |
Second Faculty of Medicine, First Faculty of Medicine, Faculty of Science, Faculty of Physical Education and Sport, Central Library of Charles University
publication
Transmembrane adaptor protein WBP1L regulates CXCR4 signalling and murine haematopoiesis
2020 |
Central Library of Charles University
publication
Transcriptional and epigenetic regulation in the development of myeloid cells: normal and diseased myelopoiesis
2014 |
First Faculty of Medicine
publication
Frequency and clinical implications of additional chromosomal aberrations in ETV6/RUNX1 positive childhood ALL
Publication without faculty affiliation
publication
Hypoplastic form of myelodysplastic neoplasm
2023 |
Faculty of Physical Education and Sport, Faculty of Medicine in Pilsen
publication
Somatické mutace u myelodysplastického syndromu a jejich klinické využití
2016 |
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
Prognostic significance of mutation profile at diagnosis and mutation persistence during disease remission in adult acute myeloid leukaemia patients
2019 |
Publication without faculty affiliation
publication
Common variability in oestrogen-related genes and pancreatic ductal adenocarcinoma risk in women
2022 |
First Faculty of Medicine, Faculty of Medicine in Pilsen, Third Faculty of Medicine
publication
The KMT2A recombinome of acute leukemias in 2023
2023 |
Second Faculty of Medicine
publication
TEL deletion analysis supports a novel view of relapse in childhood acute lymphoblastic leukemia
2004 |
Second Faculty of Medicine
publication
Spontaneous remission and loss of monosomy 7: a window of opportunity for young children with SAMD9L syndrome
2024 |
Second Faculty of Medicine
publication
Characteristics and outcome of patients with acute myeloid leukaemia and t(8;16)(p11;p13): results from an International Collaborative Study
2021 |
Faculty of Medicine in Hradec Králové
publication
Hematopoietic stem cells of lower-risk MDS patients with rapid progression show quiescent-like cell state similar to that of higher-risk MDS cells
Publication without faculty affiliation
publication
Genomic landscape of B-other acute lymphoblastic leukemia in an adult retrospective cohort with a focus on BCR-ABL1-like subtype
2021 |
First 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
Aging-Related Gene Expression Signatures Define Likelihood of Disease Progression in Patients with Lower-Risk Myelodysplastic Syndromes
Publication without faculty affiliation