subject area of
- A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression Academic Article
- A Comprehensive, Ethnically Diverse Library of Sickle Cell Disease-Specific Induced Pluripotent Stem Cells Academic Article
- A Mild Phenotype of Severe β+ Thalassemia in a 16-Month-Old Boy Academic Article
- A T-to-G Transversion at Nucleotide −567 Upstream of HBG2 in a GATA-1 Binding Motif Is Associated with Elevated Hemoglobin F Academic Article
- A candidate transacting modulator of fetal hemoglobin gene expression in the Arab-Indian haplotype of sickle cell anemia Academic Article
- A long noncoding RNA from the HBS1L-MYB intergenic region on chr6q23 regulates human fetal hemoglobin expression Academic Article
- A phase 2 study of HQK-1001, an oral fetal haemoglobin inducer, in β-thalassaemia intermedia Academic Article
- A phase 2 trial of HQK-1001 in HbE-β thalassemia demonstrates HbF induction and reduced anemia Academic Article
- A variant Sp1 (R218Q) transcription factor might enhance HbF expression in β0-thalassaemia homozygotes Academic Article
- BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia Academic Article
- BCL11A is a major HbF quantitative trait locus in three different populations with β-hemoglobinopathies Academic Article
- Clinical course and molecular characterization of a compound heterozygote for sickle hemoglobin and hemoglobin kenya Academic Article
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Clinical phenotypes of three children with sickle cell disease caused by
HbS /Sicilian (δβ)0‐thalassemia deletion Academic Article - Compound Heterozygosity for Hb S [β6(A3)Glu→Val] and Hb Kenya (Aγ81Leu-β86Ala) in a Ugandan Woman Academic Article
- Developmental changes in red cell creatine and free erythrocyte protoporphyrin in healthy premature infants during the first six months of life Academic Article
- Elimination of Transfusions Through Induction of Fetal Hemoglobin Synthesis in Cooley's Anemiaa Academic Article
- Embryonic Hemoglobins Are Expressed in Definitive Cells Academic Article
- Embryonic and fetal globins are expressed in adult erythroid progenitor cells and in erythroid cell cultures Academic Article
- Evaluation of a Dual Hemoglobin A2/A1c Quantitation Kit on the Bio-Rad Variant II Automated Hemoglobin Analyzer Academic Article
- Expression of embryonic zeta-globin and epsilon-globin chains in a 10- year-old girl with congenital anemia Academic Article
- Fanconi’s Anemia Effect or Sickle Cell Anemia Effect: That is the Question Academic Article
- Fetal globin gene inducers: novel agents and new potential Academic Article
- Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin Academic Article
- Fetal hemoglobin in sickle cell anemia Academic Article
- Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype Academic Article
- Fetal hemoglobin in sickle cell anemia: Molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans Academic Article
- Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans Academic Article
- Fetal hemoglobin in sickle cell anemia: a glass half full? Academic Article
- Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5′ olfactory receptor gene cluster Academic Article
- Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-β0thalassemia Academic Article
- Hb FM-Fort Ripley: Confirmation of autosormal dominant inheritance and diagnosis by PCR and direct nucleotide sequencing Academic Article
- Hb S/β°-Thalassemia due to the ˜1.4-kb deletion is associated with a relatively mild phenotype Academic Article
- Hemoglobin Bart's Disease in an Italian Boy Academic Article
- Hemoglobin H identification by high-performance liquid chromatography in confirmed hemoglobin H disease Academic Article
- Hemoglobin Kenya composed of α- and (Aγβ)-fusion-globin chains, associated with hereditary persistence of fetal hemoglobin Academic Article
- Hemoglobin abnormalities in neoplastic hematological disorders. Academic Article
- Hemoglobin shady grove: A novel fetal methemoglobin variant Academic Article
- Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease Academic Article
- High Hb A2β-Thalassemia Due to a 468 bp Deletion in a Patient with Hb S/β-Thalassemia Academic Article
- Homozygosity for a haplotype in theHBG2-OR51B4region is exclusive to Arab-Indian haplotype sickle cell anemia Academic Article
- Human embryonic zeta-globin chains in fetal and newborn blood Academic Article
- Inhibition of LSD1 by small molecule inhibitors stimulates fetal hemoglobin synthesis Academic Article
- Massive splenic infarction in an adolescent with hemoglobin S-HPFH Academic Article
- Molecular Characterization of a Novel 55.1 kbGγ(Aγδβ)0-thalassemia Deletion in Two Canadian Families Academic Article
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Pharmacologic induction of
PGC ‐1α stimulates fetal haemoglobin gene expression Academic Article - Predicting Intrauterine Transfusion Interval and Perinatal Outcomes in Alloimmunized Pregnancies: Time-to-Event Survival Analysis Academic Article
- Pregnancy outcomes in women with elevated levels of fetal hemoglobin Academic Article
- Proportion of fetal hemoglobin synthesis decreases during erythroid cell maturation. Academic Article
- Recurrent fetomaternal transfusion in two consecutive pregnancies Academic Article
- Sickle Cell Traits in Canada Academic Article
- Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign Academic Article
- The Patterns of Fetal Haemoglobin Production in Leukaemia Academic Article
- The association of HBG2, BCL11A, and HMIP polymorphisms with fetal hemoglobin and clinical phenotype in Iraqi Kurds with sickle cell disease Academic Article
- The clinical severity of hemoglobin S/Black (A γδβ)0 -thalassemia Academic Article
- The effects of hydroxycarbamide and magnesium on haemoglobin SC disease: results of the multi-centre CHAMPS trial Academic Article
- The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β0-thalassaemia homozygotes Academic Article
- The genetics of hemoglobin A2regulation in sickle cell anemia Academic Article
- Three New β-Globin Gene Promoter Mutations Identified Through Newborn Screening Academic Article
- Variation and heritability of Hb F and F-cells among β-thalassemia heterozygotes in Hong Kong Academic Article