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Germline pathogenic variants in transcription factors predisposing to pediatric acute myeloid leukemia: results from the French ELAM02 trial.

作者信息

Fenwarth Laurène, Duployez Nicolas, Marceau-Renaut Alice, Chahla Wadih Abou, Ducassou Stéphane, Gandemer Virginie, Pasquet Marlène, Leblanc Thierry, Schneider Pascale, Domenech Carine, Saultier Paul, Leverger Guy, Lapillonne Hélène, Preudhomme Claude, Petit Arnaud

机构信息

Laboratory of Hematology, CHU Lille, INSERM UMR-S 1277 - 9020 CNRS, Lille

Pediatric Hematology Department, CHU Lille, Lille

出版信息

Haematologica. 2021 Mar 1;106(3):908-912. doi: 10.3324/haematol.2020.248872.

DOI:10.3324/haematol.2020.248872
PMID:32554555
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7928013/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cc8/7928013/3b4e3ba6fc4c/106908.fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cc8/7928013/cd0b023aedd0/106908.fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cc8/7928013/3b4e3ba6fc4c/106908.fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cc8/7928013/cd0b023aedd0/106908.fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cc8/7928013/3b4e3ba6fc4c/106908.fig2.jpg

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本文引用的文献

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2
Molecular Profiling Defines Distinct Prognostic Subgroups in Childhood AML: A Report From the French ELAM02 Study Group.分子谱分析确定儿童急性髓系白血病的不同预后亚组：来自法国ELAM02研究组的报告
Hemasphere. 2018 Feb 21;2(1):e31. doi: 10.1097/HS9.0000000000000031. eCollection 2018 Jan-Feb.
3
ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants.
Front Oncol. 2023 Jan 30;13:1084736. doi: 10.3389/fonc.2023.1084736. eCollection 2023.
4
Somatic genetic alterations predict hematological progression in GATA2 deficiency.体细胞基因突变可预测 GATA2 缺陷所致血液学进展。
Haematologica. 2023 Jun 1;108(6):1515-1529. doi: 10.3324/haematol.2022.282250.
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Genetics of Myelodysplastic Syndromes.骨髓增生异常综合征的遗传学
Cancers (Basel). 2021 Jul 6;13(14):3380. doi: 10.3390/cancers13143380.
ClinGen 髓系恶性肿瘤变异体校正专家组关于胚系 RUNX1 变异体的建议。
Blood Adv. 2019 Oct 22;3(20):2962-2979. doi: 10.1182/bloodadvances.2019000644.
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