Functional characterization, localization, and inhibitor sensitivity of the TPR-FGFR1 fusion in 8p11 myeloproliferative syndrome

Myeloid and lymphoid neoplasms with fibroblast growth factor receptor 1 (FGFR1) abnormalities, also known as 8p11 myeloproliferative syndrome (EMS), represent rare and aggressive disorders, associated with chromosomal aberrations that lead to the fusion of FGFR1 to different partner genes. We report...

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Veröffentlicht in:Genes chromosomes & cancer 2016-01, Vol.55 (1), p.60-68
Hauptverfasser: Malli, Theodora, Buxhofer-Ausch, Veronika, Rammer, Melanie, Erdel, Martin, Kranewitter, Wolfgang, Rumpold, Holger, Marschon, Renate, Deutschbauer, Sabine, Simonitsch-Klupp, Ingrid, Valent, Peter, Muellner-Ammer, Kirsten, Sebesta, Christian, Birkner, Thomas, Webersinke, Gerald
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Sprache:eng
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