The JAK2 46/1 haplotype: a marker of inappropriate myelomonocytic response to cytokine stimulation, leading to increased risk of inflammation, myeloid neoplasm, and impaired defense against infection?
نویسندگان
چکیده
haematologica | 2011; 96(11) 1575 are partially controlled by an X-linked gene located at Xp22.2. Blood. 1992;80(3):816-24. 17. Garner C, Silver N, Best S, Menzel S, Martin C, Spector TD, et al. Quantitative trait locus on chromosome 8q influences the switch from fetal to adult hemoglobin. Blood. 2004;104(7):2184-6. 18. Menzel S, Thein SL. Genetic architecture of hemoglobin F control. Curr Opin Hematol. 2009;16(3):179-86. 19. Badens C, Joly P, Agouti I, Thuret I, Gonnet K, Fattoum S, et al. Variants in genetic modifiers of {beta}-thalassemia can help to predict the major or intermedia type of the disease. Haematologica. 2011 Jul 26. [Epub ahead of print] 20. Farrell JJ, Sherva RM, Chen Z-Y, Luo H-Y, Chu BF, Ha SY, et al. A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression. Blood. 2011;117(18):4935-45.
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ورودعنوان ژورنال:
- Haematologica
دوره 96 11 شماره
صفحات -
تاریخ انتشار 2011