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Acute myeloid leukemia with del(9q) is characterized by frequent mutations of NPM1, DNMT3A, WT1 and low expression of TLE4.
- Published in:
- Genes, Chromosomes & Cancer, 2017, v. 56, n. 1, p. 75, doi. 10.1002/gcc.22418
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- Article
ZBTB7A mutations in acute myeloid leukaemia with t(8;21) translocation.
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- Nature Communications, 2016, v. 7, n. 6, p. 11733, doi. 10.1038/ncomms11733
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- Article
Monitoring minimal residual disease in acute myeloid leukaemia with NPM1 mutations by quantitative PCR: clonal evolution is a limiting factor.
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- British Journal of Haematology, 2009, v. 144, n. 4, p. 517, doi. 10.1111/j.1365-2141.2008.07488.x
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- Article
Rapid and sensitive screening for CEBPA mutations in acute myeloid leukaemia.
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- British Journal of Haematology, 2008, v. 143, n. 2, p. 230, doi. 10.1111/j.1365-2141.2008.07328.x
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- Article
The NPM1 Mutation Type Has No Impact on Survival in Cytogenetically Normal AML.
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- PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0109759
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- Article
The new and recurrent FLT3 juxtamembrane deletion mutation shows a dominant negative effect on the wild-type FLT3 receptor.
- Published in:
- Scientific Reports, 2016, p. 28032, doi. 10.1038/srep28032
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- Article