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PAX5-KIAA1549L: a novel fusion gene in a case of pediatric B-cell precursor acute lymphoblastic leukemia

Overview of attention for article published in Molecular Cytogenetics, July 2015
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Title
PAX5-KIAA1549L: a novel fusion gene in a case of pediatric B-cell precursor acute lymphoblastic leukemia
Published in
Molecular Cytogenetics, July 2015
DOI 10.1186/s13039-015-0138-3
Pubmed ID
Authors

Stefanie Anderl, Margit König, Andishe Attarbaschi, Sabine Strehl

Abstract

In B-cell precursor acute lymphoblastic leukemia (BCP-ALL) PAX5, a transcription factor pivotal for B-cell commitment and maintenance, is frequently affected by genetic alterations. In 2-3 % of the cases PAX5 rearrangements result in the expression of oncogenic fusion genes. The encoded chimeric proteins consist of the N-terminal PAX5 DNA-binding paired domain, which is fused to the C-terminal domains of a remarkable heterogeneous group of partner proteins. Employing fluorescence in situ hybridization and molecular methods PAX5-KIAA1549L was identified as novel fusion gene in a case of pediatric BCP-ALL. Our report underlines the high diversity of PAX5 fusion partners in BCP-ALL and we describe the second involvement of KIAA1549L in a genetic rearrangement in acute leukemia.

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Mendeley readers

The data shown below were compiled from readership statistics for 7 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 7 100%

Demographic breakdown

Readers by professional status Count As %
Student > Doctoral Student 2 29%
Researcher 1 14%
Student > Postgraduate 1 14%
Other 1 14%
Unknown 2 29%
Readers by discipline Count As %
Medicine and Dentistry 3 43%
Biochemistry, Genetics and Molecular Biology 1 14%
Unknown 3 43%