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Corinne Vasseur

Observed names: C Vasseur, C. Vasseur, C. Vasseur-Godbillon, Corinne Vasseur-Godbillon, Corinne Vasseur-godbillon, Corinne Vasseur‐Godbillon, VASSEUR C, Vasseur, Corinne
Observed institutions: Université Paris-Sud, Inserm, Collège de France, Université Paris-Est Créteil, Laboratory of Excellence GR-Ex, Assistance Publique – Hôpitaux de Paris, Institut Mondor de Recherche Biomédicale, Bicêtre Hospital, Université Paris Diderot, University of Naples Federico II
ORCID: 0000-0002-4422-7069
Observed ORCID: 0000-0002-4422-7069
OpenAlex ID: A5085819910
Human erythrocyte band 3 polymorphism (band 3 Memphis): characterization of the structural modification (Lys 56----Glu) by protein chemistry methods
1991 · D Yannoukakos, C Vasseur, et al. · Blood · 80
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Unstable Alpha Hemoglobin Stabilizing Protein as a Cause of Thalassemia: Proof of Concept.
2009 · Serge Pissard, Corinne Vasseur, et al. · Blood · 67
Phosphorylation sites in human erythrocyte band 3 protein
1991 · Drakoulis Yannoukakos, Corinne Vasseur, et al. · Biochimica et Biophysica Acta (BBA) - Biomembranes · 59
High-yield expression in Escherichia coli of soluble human α-hemoglobin complexed with its molecular chaperone
2006 · Corinne Vasseur-Godbillon, Djemel Hamdane, et al. · Protein Engineering Design and Selection · 45
Three regions of erythrocyte band 3 protein are phosphorylated on tyrosines: characterization of the phosphorylation sites by solid phase sequencing combined with capillary electrophoresis
1991 · Drakoulis Yannoukakos, Helmut E. Meyer, et al. · Biochimica et Biophysica Acta (BBA) - Biomembranes · 42
Impaired binding of AHSP to α chain variants: Hb Groene Hart illustrates a mechanism leading to unstable hemoglobins with α thalassemic like syndrome
2006 · Corinne Vasseur-Godbillon, Michael C. Marden, et al. · Blood Cells Molecules and Diseases · 39
Transfer of Human α- to β-Hemoglobin via Its Chaperone Protein
2004 · Véronique Baudin-Creuza, Corinne Vasseur-Godbillon, et al. · Journal of Biological Chemistry · 36
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Unstable alpha‐chain hemoglobin variants with factitious beta‐thalassemia biosynthetic ratio: Hb questembert (α131[H14] Ser→Pro) and Hb Caen (α132[H15] Val→Gly)
1993 · H. Wajcman, C. Vasseur, et al. · American Journal of Hematology · 34
Hemoglobin Thionville. An alpha-chain variant with a substitution of a glutamate for valine at NA-1 and having an acetylated methionine NH2 terminus.
1992 · C Vasseur, Y Blouquit, et al. · Journal of Biological Chemistry · 31
Inhibition of membrane erythrocyte (Ca2+ +Mg2+)-ATPase by hemin
1988 · L. Leclerc, C. Vasseur, et al. · Biochimica et Biophysica Acta (BBA) - Biomembranes · 27
Structure of the EF corner favors deamidation of asparaginyl residues in hemoglobin: the example of Hb La Roche-sur-Yon [β81 (EF5) Leu → His]
1992 · H. Wajcman, J. Kister, et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 26
Hemoglobin redondo [β 92(F8) His → Asn]: An unstable hemoglobin variant associated with heme loss which occurs in two forms
1991 · H. Wajcman, C. Vasseur, et al. · American Journal of Hematology · 26
Role of α-Globin H Helix in the Building of Tetrameric Human Hemoglobin: Interaction with α-Hemoglobin Stabilizing Protein (AHSP) and Heme Molecule
2014 · Elisa Domingues-Hamdi, Corinne Vasseur, et al. · PLoS ONE · 25
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α-Hemoglobin Stabilizing Protein (AHSP), a Kinetic Scheme of the Action of a Human Mutant, AHSPV56G
2010 · Thomas Brillet, Véronique Baudin-Creuza, et al. · Journal of Biological Chemistry · 25
Reversible Hexacoordination of α-Hemoglobin-stabilizing Protein (AHSP)/α-Hemoglobin Versus Pressure
2006 · Djemel Hamdane, Corinne Vasseur-Godbillon, et al. · Journal of Biological Chemistry · 25
The α-hemoglobin stabilizing protein and expression of unstable α-Hb variants
2009 · Corinne Vasseur, Elisa Domingues-Hamdi, et al. · Clinical Biochemistry · 23
Two new human hemoglobin variants caused by unusual mutational events: Hb Zaïre contains a five residue repetition within the α-chain and Hb Duino has two residues substituted in the β-chain
1992 · H. Wajcman, Y. Blouquit, et al. · Human Genetics · 21
Octamers and nanoparticles as hemoglobin based blood substitutes
2008 · Véronique Baudin-Creuza, Cédric Chauvierre, et al. · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · 18
Evaluation of the free α‐hemoglobin pool in red blood cells: A new test providing a scale of β‐thalassemia severity
2010 · Corinne Vasseur, Serge Pissard, et al. · American Journal of Hematology · 17
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Recombinant hemoglobin βG83C‐F41Y
2005 · Corinne Vasseur‐Godbillon, Sarata C. Sahu, et al. · FEBS Journal · 16
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Evidence for the presence of tropomyosin in the cytoskeletons of ADP‐ and thrombin‐stimulated blood platelets
1984 · D.B. Pho, C. Vasseur, et al. · FEBS Letters · 14
Dynamics of α-Hb chain binding to its chaperone AHSP depends on heme coordination and redox state
2013 · Laurent Kiger, Corinne Vasseur, et al. · Biochimica et Biophysica Acta (BBA) - General Subjects · 13
Cleavage by protease from Straphylococcus aureus V8: an improvement in the sequence analysis of human hemoglobin variants
1991 · C. Vasseur, F. Galacteros, et al. · Journal of Biochemical and Biophysical Methods · 13
Rôle du chaperon moléculaire de l’alpha-hémoglobine dans la formation de l’hémoglobine et l’expression clinique de certaines hémoglobinopathies
2015 · C. Vasseur, V. Baudin-Creuza · Transfusion Clinique et Biologique · 11
Hereditary spherocytosis (HS) due to loss of anion exchange transporter.
1992 · A Iolascon, E Miraglia del Giudice, et al. · PubMed · 11
Works count: 54
Citation count: 841
H-index: 18
I10-index: 27
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