## Abstract The 8p11 myeloproliferative syndrome (EMS) is a chronic myeloproliferative disorder molecularly characterized by fusion of various 5β² partner genes to the 3β² part of the fibroblast growth factor receptor 1 (__FGFR1__) gene at 8p, resulting in constitutive activation of the tyrosine kina
siRNA-mediated transcriptional gene silencing: the potential mechanism and a possible role in the histone code
β Scribed by K. V. Morris
- Publisher
- Springer
- Year
- 2005
- Tongue
- English
- Weight
- 340 KB
- Volume
- 62
- Category
- Article
- ISSN
- 1420-682X
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