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The DNMT3A R882H mutation does not cause dominant negative effects in purified mixed DNMT3A/R882H complexes
The DNA methyltransferase DNMT3A R882H mutation is observed in 25% of all AML patients. DNMT3A is active as tetramer and the R882H mutation is located in one of the subunit/subunit interfaces. Previous work has reported that formation of mixed wildtype/R882H complexes leads to a strong loss of catal...
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| Publicado no: | Sci Rep |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group UK
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6125428/ https://ncbi.nlm.nih.gov/pubmed/30185810 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-018-31635-8 |
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