CareLit · DOI-Nachweis · Klinische Pädiatrie
Genome-wide associations of genetic variation with minimal residual disease in ETV6-RUNX1-positive childhood acute lymphoblastic leukemia
DOI 10.1055/s-0031-1277065
Bibliografische Angaben
Nachweis in CareLit
Autor:innenT Bartram, E Ellinghaus, R Panzer-Grümayer, G Cario, A Teigler-Schlegel, A Nebel, B Meissner, P Breithaupt, A Schrauder, P Nürnberg, M Zimmermann, S Schreiber, M Schrappe, A Franke, M Stanulla
ZeitschriftKlinische Pädiatrie
Ausgabe05/2011
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Aim: To assess the association of host genetic variation and early response to treatment as measured by minimal residual disease (MRD) in ETV6-RUNX1 fusion gene-positive childhood acute lymphoblastic leukemia (ALL) treated on protocol ALL-BFM 2000. Methods: Genome-wide association analysis of 355,750 SNPs was performed in 311 patients demonstrating clearance of leukemic blasts from the bone marrow beyond measureable…
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Zitierempfehlung
T Bartram, E Ellinghaus, R Panzer-Grümayer, G Cario, A Teigler-Schlegel, A Nebel, B Meissner, P Breithaupt, A Schrauder, P Nürnberg, M Zimmermann, S Schreiber, M Schrappe, A Franke, M Stanulla (2011) Genome-wide associations of genetic variation with minimal residual disease in ETV6-RUNX1-positive childhood acute lymphoblastic leukemia. Klinische Pädiatrie (05). https://doi.org/10.1055/s-0031-1277065
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