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Transcriptional silencing of fetal hemoglobin by BCL11A.
Sankaran VG, Xu J, Orkin SH. Sankaran VG, et al. Among authors: orkin sh. Ann N Y Acad Sci. 2010 Aug;1202:64-8. doi: 10.1111/j.1749-6632.2010.05574.x. Ann N Y Acad Sci. 2010. PMID: 20712774
Saudi Arabian sickle cell anemia. A molecular approach.
Miller BA, Salameh M, Ahmed M, Olivieri N, Huisman TH, Orkin SH, Nathan DG. Miller BA, et al. Among authors: orkin sh. Ann N Y Acad Sci. 1989;565:143-51. doi: 10.1111/j.1749-6632.1989.tb24161.x. Ann N Y Acad Sci. 1989. PMID: 2476059 No abstract available.
Transcriptional control of erythropoiesis.
Andrews NC, Orkin SH. Andrews NC, et al. Among authors: orkin sh. Curr Opin Hematol. 1994 Mar;1(2):119-24. Curr Opin Hematol. 1994. PMID: 9371270 Review.
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.
Uda M, Galanello R, Sanna S, Lettre G, Sankaran VG, Chen W, Usala G, Busonero F, Maschio A, Albai G, Piras MG, Sestu N, Lai S, Dei M, Mulas A, Crisponi L, Naitza S, Asunis I, Deiana M, Nagaraja R, Perseu L, Satta S, Cipollina MD, Sollaino C, Moi P, Hirschhorn JN, Orkin SH, Abecasis GR, Schlessinger D, Cao A. Uda M, et al. Among authors: orkin sh. Proc Natl Acad Sci U S A. 2008 Feb 5;105(5):1620-5. doi: 10.1073/pnas.0711566105. Epub 2008 Feb 1. Proc Natl Acad Sci U S A. 2008. PMID: 18245381 Free PMC article.
652 results