Role of α-Globin H Helix in the Building of Tetrameric Human Hemoglobin: Interaction with α-Hemoglobin Stabilizing Protein (AHSP) and Heme Molecule

Dynamics of α-Hb chain binding to its chaperone AHSP depends on heme coordination and redox state

(2013) Laurent Kiger et al.   BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS

Insights into Hemoglobin Assembly throughin VivoMutagenesis of α-Hemoglobin Stabilizing Protein

(2012) Eugene Khandros et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

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

(2009) Corinne Vasseur et al.   CLINICAL BIOCHEMISTRY

Enhancing stability and expression of recombinant human hemoglobin in E. coli: Progress in the development of a recombinant HBOC source

(2008) Philip E. Graves et al.   BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS

Chaperoning erythropoiesis

(2008) M. J. Weiss et al.   BLOOD

Hb Foggia or  117(GH5)Phe -> Ser : a new  2 globin allele affecting the  Hb-AHSP interaction

(2008) G. Lacerra et al.   HAEMATOLOGICA

Unstable and Thalassemic α Chain Hemoglobin Variants: A Cause of Hb H Disease and Thalassemia Intermedia

(2008) Henri Wajcman et al.   HEMOGLOBIN