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Oncogenic Gata1 causes stage-specific megakaryocyte differentiation delay
The megakaryocyte/erythroid transient myeloproliferative disorder (TMD) in newborns with Down syndrome (DS) occurs when Nterminal truncating mutations of the hemopoietic transcription factor GATA1, that produce GATA1short protein (GATA1s), are acquired early in development. Prior work has shown that...
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| 出版年: | Haematologica |
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| 主要な著者: | , , , , , , , , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Fondazione Ferrata Storti
2020
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| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8018159/ https://ncbi.nlm.nih.gov/pubmed/32527952 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2019.244541 |
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