Whole transcriptome sequencing of a paediatric case ofde novoacute myeloid leukaemia with del(5q) revealsRUNX1-USP42andPRDM16-SKIfusion transcripts-Reference-Cited by-同舟云学术

Whole transcriptome sequencing of a paediatric case ofde novoacute myeloid leukaemia with del(5q) revealsRUNX1-USP42andPRDM16-SKIfusion transcripts

Published:2014-03-27 Issue:3 Volume:166 Page:449-452
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Masetti Riccardo¹,Togni Marco¹,Astolfi Annalisa²,Pigazzi Martina³,Indio Valentina²,Rivalta Beatrice¹,Manara Elena³,Rutella Sergio⁴,Basso Giuseppe³,Pession Andrea¹,Locatelli Franco⁵

Affiliation:

1. Paediatric Oncology and Haematology “Lalla Seràgnoli”; University of Bologna; Bologna Italy

2. Giorgio Prodi Cancer Research Centre; University of Bologna; Bologna Italy

3. Department of Paediatric Haematology; University of Padova; Padova Italy

4. Department of Haematology; Catholic University Medical School; Roma Italy

5. Department of Paediatric Haematology-Oncology; IRCCS Ospedale Bambino Gesù; University of Pavia; Rome Italy

Funder

Fondazione Umberto Veronesi

Fondazione Istituto di Ricerca Pediatrica-Città della Speranza Padova

AIRC

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.12855/fullpdf

Reference10 articles.

1. PRDM16 (1p36) translocations define a distinct entity of myeloid malignancies with poor prognosis but may also occur in lymphoid malignancies;Duhoux;British journal of haematology,2012

2. Molecular characterisation of a recurrent, semi-cryptic RUNX1 translocation t(7;21) in myelodysplastic syndrome and acute myeloid leukaemia;Foster;British journal of haematology,2010

3. Chromosomal aberrations and fusion genes in myeloid malignancies;Gianfelici;Expert review of hematology,2012

4. Microhomologies and topoisomerase II consensus sequences identified near the breakpoint junctions of the recurrent t(7;21)(p22;q22) translocation in acute myeloid leukemia;Giguère;Genes, chromosomes & cancer,2011

5. 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;Jeandidier;Cancer genetics,2012

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