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Recurrent CDC25C mutations drive malignant transformation in FPD/AML

Akihide Yoshimi, Takashi Toya, Masahito Kawazu, Toshihide Ueno, Ayato Tsukamoto, Hiromitsu Iizuka, Masahiro Nakagawa, Yasuhito Nannya, Shunya Arai, Hironori Harada,

Nature Communications · 2014 · 82 citations · 26 references

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26

Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia

Woo‐Joo Song, Melanie G. Sullivan, Robert D. Legare et al. · Nature Genetics · 1999 · 1.1K citations

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Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome

Amy P. Hsu, Elizabeth P. Sampaio, Javed Khan et al. · Blood · 2011 · 636 citations

, , +12

Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia

Christopher N Hahn, Chan‐Eng Chong, Catherine Carmichael et al. · Nature Genetics · 2011 · 601 citations · Full text

, , +16

Nuclear localization of Cdc25 is regulated by DNA damage and a 14-3-3 protein

Antonia Lopez‐Girona, Beth Furnari, Odile Mondesert et al. · Nature · 1999 · 581 citations

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Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)

Pia Østergaard, Michael A. Simpson, Fiona Connell et al. · Nature Genetics · 2011 · 503 citations

, , +10