The -158 site 5' to the G g gene and G g expression, Blood, vol.66, pp.1463-1468, 1985. ,
DNA sequence variation associated with elevated G g globin production, Blood, vol.66, pp.783-790, 1985. ,
Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2, Blood, vol.80, pp.816-840, 1992. ,
Quantitative trait locus on chromosome 8q influences the switch from fetal to adult hemoglobin, Blood, vol.104, issue.7, pp.2184-2190, 2004. ,
DOI : 10.1182/blood-2004-02-0527
Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults, Proceedings of the National Academy of Sciences, vol.104, issue.27, pp.11046-51, 2007. ,
DOI : 10.1073/pnas.0611393104
A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15, Nature Genetics, vol.434, issue.10, pp.1197-1206, 2007. ,
DOI : 10.1038/ng2108
BCL11A is a major HbF quantitative trait locus in three different populations with ??-hemoglobinopathies, Blood Cells, Molecules, and Diseases, vol.41, issue.3, pp.255-263, 2008. ,
DOI : 10.1016/j.bcmd.2008.06.007
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of ??-thalassemia, Proceedings of the National Academy of Sciences, vol.105, issue.5, pp.1620-1625, 2008. ,
DOI : 10.1073/pnas.0711566105
DNA sequence variation in a negative control region 5' to the b-globin gene correlates with the phenotypic expression of the bS mutation, Blood, vol.79, pp.787-92, 1992. ,
DNA polymorphisms at the BCL11A, HBS1L-MYB, and ??-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease, Proceedings of the National Academy of Sciences, vol.105, issue.33, pp.11869-74, 2008. ,
DOI : 10.1073/pnas.0804799105
Human Fetal Hemoglobin Expression Is Regulated by the Developmental Stage-Specific Repressor BCL11A, Science, vol.322, issue.5909, pp.1839-1881, 2008. ,
DOI : 10.1126/science.1165409
Functional studies of BCL11A : characterization of the conserved BCL11A-XL splice variant and its interaction with BCL6 in nuclear paraspeckles of germinal center B cells, Molecular Cancer, vol.5, issue.1, pp.18-33, 2006. ,
DOI : 10.1186/1476-4598-5-18
BCL11B functionally associates with the NuRD complex in T lymphocytes to repress targeted promoter, Oncogene, vol.983, issue.45, pp.6753-64, 2005. ,
DOI : 10.1101/GAD.13.18.2388
A Lentiviral RNAi Library for Human and Mouse Genes Applied to an Arrayed Viral High-Content Screen, Cell, vol.124, issue.6, pp.1283-98, 2006. ,
DOI : 10.1016/j.cell.2006.01.040
Asymptomatic and mild b-thalassemia in homozygotes and compound heterozygotes for the IVS2+1G>A mutation : role of the bglobin gene haplotype, Haematologica, vol.88, pp.1099-105, 2003. ,