Fetal Hemoglobin Concept

subject area of

• A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression  Journal Articles
• A Comprehensive, Ethnically Diverse Library of Sickle Cell Disease-Specific Induced Pluripotent Stem Cells  Journal Articles
• A Mild Phenotype of Severe β+ Thalassemia in a 16-Month-Old Boy  Journal Articles
• A T-to-G Transversion at Nucleotide −567 Upstream of HBG2 in a GATA-1 Binding Motif Is Associated with Elevated Hemoglobin F  Journal Articles
• A candidate transacting modulator of fetal hemoglobin gene expression in the Arab—Indian haplotype of sickle cell anemia  Journal Articles
• A long noncoding RNA from the HBS1L-MYB intergenic region on chr6q23 regulates human fetal hemoglobin expression  Journal Articles
• A phase 2 study of HQK‐1001, an oral fetal haemoglobin inducer, in β‐thalassaemia intermedia  Journal Articles
• A phase 2 trial of HQK-1001 in HbE-β thalassemia demonstrates HbF induction and reduced anemia  Journal Articles
• A variant Sp1 (R218Q) transcription factor might enhance HbF expression in β⁰‐thalassaemia homozygotes  Journal Articles
• BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia  Journal Articles
• BCL11A is a major HbF quantitative trait locus in three different populations with β-hemoglobinopathies  Journal Articles
• Clinical course and molecular characterization of a compound heterozygote for sickle hemoglobin and hemoglobin kenya  Journal Articles
• Clinical phenotypes of three children with sickle cell disease caused by HbS/Sicilian (δβ)⁰‐thalassemia deletion  Journal Articles
• Compound Heterozygosity for Hb S [β6(A3)Glu→Val] and Hb Kenya (^Aγ81Leu-β86Ala) in a Ugandan Woman  Journal Articles
• Developmental changes in red cell creatine and free erythrocyte protoporphyrin in healthy premature infants during the first six months of life  Journal Articles
• Elimination of Transfusions Through Induction of Fetal Hemoglobin Synthesis in Cooley's Anemia^a  Journal Articles
• Embryonic Hemoglobins Are Expressed in Definitive Cells  Journal Articles
• Embryonic and fetal globins are expressed in adult erythroid progenitor cells and in erythroid cell cultures  Journal Articles
• Evaluation of a Dual Hemoglobin A2/A1c Quantitation Kit on the Bio-Rad Variant II Automated Hemoglobin Analyzer  Journal Articles
• Expression of embryonic zeta-globin and epsilon-globin chains in a 10- year-old girl with congenital anemia  Journal Articles
• Fanconi’s Anemia Effect or Sickle Cell Anemia Effect: That is the Question  Journal Articles
• Fetal globin gene inducers: novel agents and new potential  Journal Articles
• Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin  Journal Articles
• Fetal hemoglobin in sickle cell anemia  Journal Articles
• Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype  Journal Articles
• Fetal hemoglobin in sickle cell anemia: Molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans  Journal Articles
• Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans  Journal Articles
• Fetal hemoglobin in sickle cell anemia: a glass half full?  Journal Articles
• Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5′ olfactory receptor gene cluster  Journal Articles
• Genetic studies of fetal hemoglobin in the Arab‐Indian haplotype sickle cell‐β⁰ thalassemia  Journal Articles
• Hb FM-Fort Ripley: Confirmation of autosormal dominant inheritance and diagnosis by PCR and direct nucleotide sequencing  Journal Articles
• Hb S/β°‐Thalassemia due to the ˜1.4‐kb deletion is associated with a relatively mild phenotype  Journal Articles
• Hemoglobin Bart's Disease in an Italian Boy  Journal Articles
• Hemoglobin H identification by high‐performance liquid chromatography in confirmed hemoglobin H disease  Journal Articles
• Hemoglobin Kenya composed of α‐ and (^Aγβ)‐fusion‐globin chains, associated with hereditary persistence of fetal hemoglobin  Journal Articles
• Hemoglobin abnormalities in neoplastic hematological disorders.  Journal Articles
• Hemoglobin shady grove: A novel fetal methemoglobin variant  Journal Articles
• Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease  Journal Articles
• High Hb A₂β-Thalassemia Due to a 468 bp Deletion in a Patient with Hb S/β-Thalassemia  Journal Articles
• Homozygosity for a haplotype in the HBG2‐OR51B4 region is exclusive to Arab‐Indian haplotype sickle cell anemia  Journal Articles
• Human embryonic zeta-globin chains in fetal and newborn blood  Journal Articles
• Inhibition of LSD1 by small molecule inhibitors stimulates fetal hemoglobin synthesis  Journal Articles
• Massive splenic infarction in an adolescent with hemoglobin S‐HPFH  Journal Articles
• Molecular Characterization of a Novel 55.1 kb^Gγ(^Aγδβ)⁰-thalassemia Deletion in Two Canadian Families  Journal Articles
• Pharmacologic induction of PGC‐1α stimulates fetal haemoglobin gene expression  Journal Articles
• Predicting Intrauterine Transfusion Interval and Perinatal Outcomes in Alloimmunized Pregnancies: Time-to-Event Survival Analysis  Journal Articles
• Pregnancy outcomes in women with elevated levels of fetal hemoglobin  Journal Articles
• Proportion of fetal hemoglobin synthesis decreases during erythroid cell maturation.  Journal Articles
• Recurrent fetomaternal transfusion in two consecutive pregnancies  Journal Articles
• Sickle Cell Traits in Canada  Journal Articles
• Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab‐Indian haplotype is not benign  Journal Articles
• The Patterns of Fetal Haemoglobin Production in Leukaemia  Journal Articles
• The association of HBG2, BCL11A, and HMIP polymorphisms with fetal hemoglobin and clinical phenotype in Iraqi Kurds with sickle cell disease  Journal Articles
• The clinical severity of hemoglobin S/Black (^Aγδβ)⁰‐thalassemia  Journal Articles
• The effects of hydroxycarbamide and magnesium on haemoglobin SC disease: results of the multi‐centre CHAMPS trial  Journal Articles
• The genetic basis of asymptomatic codon 8 frame‐shift (HBB:c25_26delAA) β⁰‐thalassaemia homozygotes  Journal Articles
• The genetics of hemoglobin A₂ regulation in sickle cell anemia  Journal Articles
• Three New β-Globin Gene Promoter Mutations Identified Through Newborn Screening  Journal Articles
• Variation and heritability of Hb F and F‐cells among β‐thalassemia heterozygotes in Hong Kong  Journal Articles