CareLit · DOI-Nachweis · Klinische Pädiatrie
Identification and characterization of FoxP1 as a candidate tumor suppressor gene in neuroblastoma
DOI 10.1055/s-0031-1277076
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Nachweis in CareLit
Autor:innenS Ackermann, B Hero, V Ehemann, H Kocak, A Oberthuer, B Brors, F Westermann, Y Kahlert, M Odenthal, F Berthold, M Fischer
ZeitschriftKlinische Pädiatrie
Ausgabe05/2011
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
To identify genes differenzially expressed between favourable and unfavourable neuroblastomas (NB), microarray profiles of 476 NB specimens were generated. High expression of FOXP1 (forkhead box P1) was found in favourable NBs. FOXP1 maps to a tumour suppressor locus frequently deleted aggressive NB (3p14) and belongs to a family of winged-helix transcription factors that are involved in processes of cell proliferat…
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Zitierempfehlung
S Ackermann, B Hero, V Ehemann, H Kocak, A Oberthuer, B Brors, F Westermann, Y Kahlert, M Odenthal, F Berthold, M Fischer (2011) Identification and characterization of FoxP1 as a candidate tumor suppressor gene in neuroblastoma. Klinische Pädiatrie (05). https://doi.org/10.1055/s-0031-1277076
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