HbA2 levels in normal adults are influenced by two distinct genetic mechanisms
暂无分享,去创建一个
T. Spector | S. Thein | S. Menzel | C. Garner | Helen Rooks | H. Rooks
[1] 田原 康玄,et al. 生活習慣病とgenome-wide association study , 2015 .
[2] P. Moi,et al. KLF1 gene mutations cause borderline HbA(2). , 2011, Blood.
[3] Christian Gieger,et al. A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium , 2009, Nature Genetics.
[4] R. Nagel,et al. Disorders of Hemoglobin: Hemoglobins of the Embryo, Fetus, and Adult , 2009 .
[5] R. Hardison,et al. Disorders of Hemoglobin: The Normal Structure and Regulation of Human Globin Gene Clusters , 2009 .
[6] Gonçalo R. Abecasis,et al. Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of β-thalassemia , 2008, Proceedings of the National Academy of Sciences.
[7] F. Grosveld,et al. Beta-globin regulation and long-range interactions. , 2008, Advances in genetics.
[8] T. Spector,et al. The HBS1L-MYB intergenic region on chromosome 6q23.3 influences erythrocyte, platelet, and monocyte counts in humans. , 2007, Blood.
[9] Simon Heath,et al. A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15 , 2007, Nature Genetics.
[10] T. Spector,et al. Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults , 2007, Proceedings of the National Academy of Sciences.
[11] A. Jeffreys,et al. Allelic recombination and de novo deletions in sperm in the human beta-globin gene region. , 2006, Human molecular genetics.
[12] Jeffery L. Miller,et al. Fetal and adult hemoglobin production during adult erythropoiesis: coordinate expression correlates with cell proliferation. , 2002, Blood.
[13] T. Spector,et al. A candidate gene study of F cell levels in sibling pairs using a joint linkage and association analysis. , 1999 .
[14] T. Huisman,et al. Levels of Hb A2 in heterozygotes and homozygotes for beta-thalassemia mutations: influence of mutations in the CACCC and ATAAA motifs of the beta-globin gene promoter. , 1997, Acta haematologica.
[15] R. Kaufman,et al. Characterization of the DNase I hypersensitive site 3' of the human beta globin gene domain. , 1993, Blood.
[16] T. Huisman,et al. Observations on the levels of Hb A2 in patients with different beta-thalassemia mutations and a delta chain variant. , 1990, Blood.
[17] J. B. Clegg,et al. The thalassaemia syndromes , 1965 .