ThalassemiaGlobinsHemoglobinsalpha-GlobinsHematologic Diseasesalpha-ThalassemiaAnemia, Sickle CellHemoglobins, AbnormalHylobatesFetal HemoglobinHemoglobinopathiesbeta-ThalassemiaErythrocyte CountChromosomes, Human, Pair 16ReticulocytesGenesHemoglobin Abeta-GlobinsDNA Restriction EnzymesHemoglobin EBase SequenceTerminator Regions, GeneticHemoglobin A2Molecular Sequence DataHemoglobin, SickleDNAChelation TherapyLeukemia, Erythroblastic, AcuteHemoglobin CHeterozygoteNucleic Acid HybridizationHemoglobin HErythropoiesisgamma-GlobinsIron OverloadErythrocytesLocus Control RegionRNA, MessengerTranscription, Geneticalpha 1-AntitrypsinGenes, SwitchIron Chelating AgentsErythroid CellsMultigene FamilyErythroid Precursor CellsMutationChromosome DeletionDNA, RecombinantHemoglobin JOxyhemoglobinsPromoter Regions, GeneticGene Expression RegulationBlood TransfusionReceptors, Adrenergic, alphaCloning, MolecularHeminAmino Acid SequenceIronSickle Cell TraitBipolar DisorderAnemiaHemoglobin A, GlycosylatedHypoxia-Inducible Factor 1, alpha SubunitHemoglobinometryChromosome MappingErythroblastsHomozygoteDeferoxamineTruncated HemoglobinsErythrocytes, AbnormalGenetic LinkageMental DisordersPyridonesErythrocyte IndicesNF-E2 Transcription Factor, p45 SubunitMethemoglobinFerritinsNF-E2 Transcription FactorAnxiety DisordersOxygenMood DisordersRestriction MappingErythroid-Specific DNA-Binding Factorsalpha7 Nicotinic Acetylcholine ReceptorChromosomes, Artificial, YeastHemoglobin C DiseaseProtein BindingKineticsBinding SitesTranscription FactorsK562 CellsDeoxyribonuclease ICarboxyhemoglobinHemeSicilyMice, TransgenicPhenotypeIntegrin alpha3beta1Integrin alpha4Integrin alpha6