Sickle cell disease at 100 years

Science

Volumn 329, Issue 5989, 2010, Pages 291-292

  Orkin, Stuart H ^a   Higgs, Douglas R ^b  

^a BOSTON CHILDREN S HOSPITAL   (United States)

^b JOHN RADCLIFFE HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA GLOBIN; BETA GLOBIN; HEMOGLOBIN F; HYDROXYUREA; METHEMOGLOBIN; BCL11A PROTEIN, HUMAN; CARRIER PROTEIN; GAMMA GLOBIN; GUANINE NUCLEOTIDE BINDING PROTEIN; HEMOGLOBIN S; NUCLEAR PROTEIN;

CYTOLOGY; HEMOGLOBIN; TEMPORAL ANALYSIS;

AMINO ACID SUBSTITUTION; BLOOD TRANSFUSION; CLINICAL FEATURE; FLUID THERAPY; GENE EXPRESSION; GENE THERAPY; GENETIC ASSOCIATION; HUMAN; PLURIPOTENT STEM CELL; PRIORITY JOURNAL; REVIEW; SICKLE CELL; ARTICLE; BIOSYNTHESIS; BLOOD; CHEMISTRY; GENE EXPRESSION REGULATION; GENETICS; MULTIGENE FAMILY; MUTATION; ONCOGENE MYB; SICKLE CELL ANEMIA;

ANEMIA, SICKLE CELL; BETA-GLOBINS; CARRIER PROTEINS; FETAL HEMOGLOBIN; GAMMA-GLOBINS; GENE EXPRESSION REGULATION; GENES, MYB; GTP-BINDING PROTEINS; HEMOGLOBIN, SICKLE; HUMANS; MULTIGENE FAMILY; MUTATION; NUCLEAR PROTEINS;

EID: 77954809883     PISSN: 00368075     EISSN: 10959203     Source Type: Journal    
DOI: 10.1126/science.1194035     Document Type: Review

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