Genetic modifiers in hemoglobinopathies

Current Molecular Medicine

Volumn 8, Issue 7, 2008, Pages 600-608

  Rund, Deborah ^a   Fucharoen, Suthat ^b  

^a HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

^b MAHIDOL UNIVERSITY   (Thailand)

Author keywords

Globin; HbE; HbF; Phenotype genotype; Sickle cell; Thalassemia; Transcription factors

Indexed keywords

ALPHA GLOBIN; ALPHA HEMOGLOBIN STABILIZING PROTEIN; BETA GLOBIN; BILIRUBIN; BISPHOSPHONIC ACID DERIVATIVE; GAMMA GLOBIN; GLOBIN; HEMOGLOBIN; HEMOGLOBIN E; HEMOGLOBIN F; HYDROXYUREA; PLASMA PROTEIN; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ALPHA THALASSEMIA; BETA THALASSEMIA; BILIRUBIN METABOLISM; BLOOD TRANSFUSION; BONE DISEASE; BONE NECROSIS; CHOLELITHIASIS; CLINICAL FEATURE; DISEASE SEVERITY; GALLSTONE; GENE EXPRESSION; GENETIC COUNSELING; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; GENETIC VARIABILITY; GENOME ANALYSIS; GENOTYPE PHENOTYPE CORRELATION; GLOBIN SYNTHESIS; HAPLOTYPE; HEART FAILURE; HEMOGLOBIN BLOOD LEVEL; HEMOGLOBIN SYNTHESIS; HEMOGLOBINOPATHY; HUMAN; IRON OVERLOAD; LEG ULCER; MOLECULAR BIOLOGY; MUTATIONAL ANALYSIS; NONHUMAN; OSTEOPENIA; OSTEOPOROSIS; PATHOPHYSIOLOGY; PRENATAL DIAGNOSIS; PRIAPISM; QUANTITATIVE TRAIT LOCUS MAPPING; REVIEW; SICKLE CELL ANEMIA; SINGLE NUCLEOTIDE POLYMORPHISM; STROKE; GENETICS;

ALPHA-THALASSEMIA; ANEMIA, SICKLE CELL; BETA-THALASSEMIA; HEMOGLOBINOPATHIES; HUMANS;

EID: 59249088084     PISSN: 15665240     EISSN: None     Source Type: Journal    
DOI: 10.2174/156652408786241410     Document Type: Review

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