The α-hemoglobin stabilizing protein and expression of unstable α-Hb variants

Clinical Biochemistry

Volumn 42, Issue 18, 2009, Pages 1818-1823

  Vasseur, Corinne ^a   Domingues Hamdi, Elisa ^a   Brillet, Thomas ^a   Marden, Michael C ^a   Baudin Creuza, Véronique ^a  

^a INSERM   (France)

Author keywords

1 1 interface; Alpha thalassemia; Human hemoglobin; Molecular chaperone AHSP; Protein precipitation; Unstable variants Hb

Indexed keywords

ARGININE; CYSTEINE; GLUTATHIONE TRANSFERASE; HEMOGLOBIN A; HEMOGLOBIN VARIANT; LEUCINE; PROLINE; SERINE; TYROSINE;

ALPHA HELIX; ALPHA THALASSEMIA; ARTICLE; CONTROLLED STUDY; ERYTHROCYTE MEMBRANE; GENE MUTATION; HUMAN; HUMAN CELL; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN MODIFICATION; PROTEIN STABILITY; PROTEIN SYNTHESIS;

BLOOD PROTEINS; ELECTROPHORESIS, POLYACRYLAMIDE GEL; HEMOGLOBINS; HUMANS; MOLECULAR CHAPERONES; MUTANT PROTEINS; PEPTIDE FRAGMENTS; PROTEIN STABILITY; PROTEIN STRUCTURE, SECONDARY; RECOMBINANT FUSION PROTEINS; SOLUBILITY;

EID: 70449416679     PISSN: 00099120     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.clinbiochem.2009.05.011     Document Type: Article

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