1. Zagaria A, Anelli L, Coccaro N, et al. 5'RUNX1-3'USP42 chimeric gene in acute myeloid leukemia can occur through an insertion mechanism rather than translocation and may be mediated by genomic segmental duplications. Mol Cytogenet. 2014; 7:66. PMID:
25298786.
Article
2. Masetti R, Togni M, Astolfi A, et al. Whole transcriptome sequencing of a paediatric case of de novo acute myeloid leukaemia with del(5q) reveals RUNX1-USP42 and PRDM16-SKI fusion transcripts. Br J Haematol. 2014; 166:449–452. PMID:
24673627.
3. Ji J, Loo E, Pullarkat S, Yang L, Tirado CA. Acute myeloid leukemia with t(7;21)(p22;q22) and 5q deletion: a case report and literature review. Exp Hematol Oncol. 2014; 3:8. PMID:
24646765.
Article
4. Panagopoulos I, Gorunova L, Brandal P, Garnes M, Tierens A, Heim S. Myeloid leukemia with t(7;21)(p22;q22) and 5q deletion. Oncol Rep. 2013; 30:1549–1552. PMID:
23877199.
Article
5. Jeandidier E, Gervais C, Radford-Weiss I, et al. A cytogenetic study of 397 consecutive acute myeloid leukemia cases identified three with a t(7;21) associated with 5q abnormalities and exhibiting similar clinical and biological features, suggesting a new, rare acute myeloid leukemia entity. Cancer Genet. 2012; 205:365–372. PMID:
22867997.
Article
6. Giguère A, Hébert J. Microhomologies and topoisomerase II consensus sequences identified near the breakpoint junctions of the recurrent t(7;21)(p22;q22) translocation in acute myeloid leukemia. Genes Chromosomes Cancer. 2011; 50:228–238. PMID:
21319259.
Article
7. Foster N, Paulsson K, Sales M, et al. Molecular characterisation of a recurrent, semi-cryptic RUNX1 translocation t(7;21) in myelodysplastic syndrome and acute myeloid leukaemia. Br J Haematol. 2010; 148:938–943. PMID:
20064152.
8. Chessells JM, Harrison CJ, Kempski H, et al. Clinical features, cytogenetics and outcome in acute lymphoblastic and myeloid leukaemia of infancy: report from the MRC Childhood Leukaemia working party. Leukemia. 2002; 16:776–784. PMID:
11986937.
Article
9. Park KU, Lee DS, Lee HS, Kim CJ, Cho HI. Granulocytic sarcoma in MLL-positive infant acute myelogenous leukemia: fluorescence in situ hybridization study of childhood acute myelogenous leukemia for detecting MLL rearrangement. Am J Pathol. 2001; 159:2011–2016. PMID:
11733351.
10. Preiss BS, Kerndrup GB, Pedersen RK, Hasle H, Pallisgaard N. Lymphoma-Leukemia Study Group of the Region of Southern Denmark. Contribution of multiparameter genetic analysis to the detection of genetic alterations in hematologic neoplasia. An evaluation of combining G-band analysis, spectral karyotyping, and multiplex reverse-transcription polymerase chain reaction (multiplex RT-PCR). Cancer Genet Cytogenet. 2006; 165:1–8. PMID:
16490591.
Article
11. Paulsson K, Békássy AN, Olofsson T, Mitelman F, Johansson B, Panagopoulos I. A novel and cytogenetically cryptic t(7;21) (p22;q22) in acute myeloid leukemia results in fusion of RUNX1 with the ubiquitin-specific protease gene USP42. Leukemia. 2006; 20:224–229. PMID:
16357831.
12. Kim YK, Kim YS, Yoo KJ, et al. The expression of Usp42 during embryogenesis and spermatogenesis in mouse. Gene Expr Patterns. 2007; 7:143–148. PMID:
16904385.
Article
13. Hock AK, Vigneron AM, Carter S, Ludwig RL, Vousden KH. Regulation of p53 stability and function by the deubiquitinating enzyme USP42. EMBO J. 2011; 30:4921–4930. PMID:
22085928.
Article