| Literature DB >> 23403250 |
Motohiro Kato1, Naoko Yasui, Masafumi Seki, Hiroshi Kishimoto, Aiko Sato-Otsubo, Daisuke Hasegawa, Nobutaka Kiyokawa, Ryoji Hanada, Seishi Ogawa, Atsushi Manabe, Junko Takita, Katsuyoshi Koh.
Abstract
A small fraction of cases of juvenile myelomonocytic leukemia (JMML) develop massive disease activation. Through genomic analysis of JMML, which developed in an individual with mosaicism for oncogenic KRAS mutation with rapid progression, we identified acquired uniparental disomy at 12p. We demonstrated that duplication of oncogenic KRAS is associated with rapid JMML progression.Entities:
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Year: 2013 PMID: 23403250 DOI: 10.1016/j.jpeds.2013.01.003
Source DB: PubMed Journal: J Pediatr ISSN: 0022-3476 Impact factor: 4.406