Transcription factor gene GATA2 : Association of leukemia and nonsynonymous to the synonymous substitution rate across five mammals
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference35 articles.
1. Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia;Hahn;Nat. Genet.,2011
2. Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency;Dickinson;Blood,2011
3. Gain-of-function mutation of GATA-2 in acute myeloid transformation of chronic myeloid leukemia;Zhang;Proc. Natl. Acad. Sci. U. S. A.,2008
4. GATA2 zinc finger 1 mutations associated with biallelic CEBPA mutations define a unique genetic entity of acute myeloid leukemia;Greif;Blood,2012
5. RNA codewords and protein synthesis, VII. On the general nature of the RNA code;Nirenberg;Proc. Natl. Acad. Sci. U. S. A.,1965
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