Diverse mechanisms of leukemogenesis associated with PAX5 germline mutation
Author:
Funder
Associazione Italiana per la Ricerca sul Cancro
EU-COST ActionCA16223 “LEukaemiaGENe Discovery by data sharing, mining, and collaboration”
Publisher
Springer Science and Business Media LLC
Link
https://www.nature.com/articles/s41375-024-02399-0.pdf
Reference15 articles.
1. Wagener R, Elitzur S, Brozou T, Kubaczkova V, Bibi S, Hof J, et al. Functional damaging germline variants in ETV6, IKZF1, PAX5 and RUNX1 predisposing to B-cell precursor acute lymphoblastic leukemia. Eur J Med Genet. 2023;66:104725.
2. Mullighan CG, Goorha S, Radtke I, Miller CB, Coustan-Smith E, Dalton JD, et al. Genome-wide analysis of genetic alterations in acute lymphoblastic leukemia. Nature. 2007;446:758–64.
3. Stasevich I, Inglott S, Austin N, Bown N, Hall G, Harrison CJ, et al. PAX5 alterations in genetically unclassified childhood precursor B-cell acute lymphoblastic leukemia. Br J Haematol. 2015;171:263–72.
4. Shah S, Schrader KA, Waanders E, Timms AE, Vijai J, Miething C, et al. A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia. Nat Genet. 2013;45:1226–31.
5. Auer F, Ruschendorf F, Gombert M, Husemann P, Ginzel S, Izraeli S, et al. Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G>A. Leukemia. 2014;28:1136–8.
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