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Chromosome 21 gain is dispensable for transient myeloproliferative disorder driven by a novel GATA1 mutation.

作者信息

Lukes Julius, Danek Petr, Alejo-Valle Oriol, Potuckova Eliska, Gahura Ondrej, Heckl Dirk, Starkova Julia, Stary Jan, Mejstrikova Ester, Alberich-Jorda Meritxell, Zuna Jan, Trka Jan, Klusmann Jan-Henning, Zaliova Marketa

机构信息

CLIP-Childhood Leukaemia Investigation Prague, Prague, Czech Republic.

Department of Paediatric Haematology and Oncology, Second Faculty of Medicine, Charles University, Prague, Czech Republic.

出版信息

Leukemia. 2020 Sep;34(9):2503-2508. doi: 10.1038/s41375-020-0769-1. Epub 2020 Feb 24.

DOI:10.1038/s41375-020-0769-1
PMID:32094462
Abstract
摘要

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Chromosome 21 gain is dispensable for transient myeloproliferative disorder driven by a novel GATA1 mutation.对于由新型GATA1突变驱动的短暂性骨髓增殖性疾病而言,21号染色体增加并非必需。
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[Abnormal hematopoiesis in Down syndrome].[唐氏综合征中的异常造血]
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引用本文的文献

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Leukemogenesis in infants and young children with trisomy 21.21 三体综合征婴儿和幼儿的白血病发生。
Hematology Am Soc Hematol Educ Program. 2022 Dec 9;2022(1):1-8. doi: 10.1182/hematology.2022000395.
2
Pediatric Germline Predisposition to Myeloid Neoplasms.儿童髓系肿瘤的胚系易感性
Curr Hematol Malig Rep. 2022 Dec;17(6):266-274. doi: 10.1007/s11899-022-00681-5. Epub 2022 Sep 19.
3
Clinical and biological aspects of myeloid leukemia in Down syndrome.唐氏综合征相关髓系白血病的临床和生物学特征。
Leukemia. 2021 Dec;35(12):3352-3360. doi: 10.1038/s41375-021-01414-y. Epub 2021 Sep 13.
4
Molecular Mechanisms of the Genetic Predisposition to Acute Megakaryoblastic Leukemia in Infants With Down Syndrome.唐氏综合征婴儿急性巨核细胞白血病遗传易感性的分子机制
Front Oncol. 2021 Mar 11;11:636633. doi: 10.3389/fonc.2021.636633. eCollection 2021.