Contribution of β-globin cluster polymorphisms to raise fetal hemoglobin levels in normal adults.

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Effect of Cis Acting Potential Regulators in the β Globin Gene Cluster on the Production of HbF in Thalassemia Patients.Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients.

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Contribution of β-globin cluster polymorphisms to raise fetal hemoglobin levels in normal adults.

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2011 nî lūn-bûn

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2011年の論文

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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Contribution of β-globin clust ...... lobin levels in normal adults.

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Contribution of β-globin clust ...... lobin levels in normal adults.

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Contribution of β-globin clust ...... lobin levels in normal adults.

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Contribution of β-globin clust ...... lobin levels in normal adults.

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Contribution of β-globin clust ...... lobin levels in normal adults.

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Contribution of β-globin clust ...... lobin levels in normal adults.

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Contribution of β-globin clust ...... lobin levels in normal adults.

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Amina Bibi

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Faida Ouali

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Fekria Ouennich

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Hajer Siala

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Latifa Jouini

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Slaheddine Fattoum

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Sondess Hadj Fredj

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Taieb Messaoud

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P2860

Increased gamma-globin expression in a nondeletion HPFH mediated by an erythroid-specific DNA-binding factor

Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin

Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia

Cis- and trans-acting elements involved in the regulation of the erythroid promoter of the human porphobilinogen deaminase gene

Rapid identification by denaturing gradient gel electrophoresis of mutations in the gamma-globin gene promoters in non-deletion type HPFH.

A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.

A common protein binds to two silencers 5' to the human beta-globin gene.

Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults.

DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease.

Genetic modifiers of the beta-haemoglobinopathies.

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s11033-011-1253-9

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4619-4625

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10.1007/S11033-011-1253-9

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2011-09-27T00:00:00Z

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21947948

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Contribution of β-globin cluster polymorphisms to raise fetal hemoglobin levels in normal adults.

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P2860

P2860

Contribution of β-globin cluster polymorphisms to raise fetal hemoglobin levels in normal adults.

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