Chromosome 12p deletions in TEL-AML1 childhood acute lymphoblastic leukemia are associated with retrotransposon elements and occur postnatally

TEL-AML1 (ETV6-RUNX1) is the most common translocation in the childhood leukemias, and is a prenatal mutation in most children. This translocation has been detected at a high rate among newborns (∼1%); therefore the rate-limiting event for leukemia appears to be secondary mutations. A frequent such...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Glavni autori: Wiemels, Joseph L., Hofmann, Jerry, Kang, Michelle, Selzer, Rebecca, Green, Roland, Zhou, Mi, Zhong, Sheng, Zhang, Luoping, Smith, Martyn T., Marsit, Carmen, Loh, Mignon, Buffler, Patricia, Yeh, Ru-Fang
Format: Artigo
Jezik:Inglês
Izdano: 2008
Teme:
Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2597307/
https://ncbi.nlm.nih.gov/pubmed/19047175
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1158/0008-5472.CAN-08-2139
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!

Similar Items