Works matching DE "RUNX protein genetics"
Results: 6
CSF3R Mutations are frequently associated with abnormalities of RUNX1, CBFB, CEBPA, and NPM1 genes in acute myeloid leukemia.
- Published in:
- 2018
- By:
- Publication type:
- journal article
RUNX2: A Master Bone Growth Regulator That May Be Involved in the DNA Damage Response.
- Published in:
- DNA & Cell Biology, 2015, v. 34, n. 5, p. 305, doi. 10.1089/dna.2014.2688
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- Publication type:
- Article
Loss of expression rather than cytoplasmic mislocalization of RUNX3 predicts worse outcome in non-small cell lung cancer.
- Published in:
- Oncology Letters, 2018, v. 15, n. 4, p. 5043, doi. 10.3892/ol.2018.7993
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- Publication type:
- Article
The effects of biodegradable poly(lactic‐co‐glycolic acid)‐based microspheres loaded with quercetin on stemness, viability and osteogenic differentiation potential of stem cell spheroids.
- Published in:
- Journal of Periodontal Research, 2018, v. 53, n. 5, p. 801, doi. 10.1111/jre.12569
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- Publication type:
- Article
A novel prospective isolation of murine fetal liver progenitors to study in utero hematopoietic defects.
- Published in:
- PLoS Genetics, 2018, v. 14, n. 1, p. 1, doi. 10.1371/journal.pgen.1007127
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- Publication type:
- Article
FGFR1 rearranged hematological neoplasms - molecularly defined and clinically heterogeneous.
- Published in:
- Leukemia & Lymphoma, 2018, v. 59, n. 7, p. 1520, doi. 10.1080/10428194.2018.1429607
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- Publication type:
- Article