A human antibody directed to the factor VIII C1 domain inhibits factor VIII cofactor activity and binding to von Willebrand factor von JACQUEMIN, M, BENHIDA, A, GILLES, J.-G, VERMYLEN, J, SAINT-REMY, J.-M, PEERLINCK, K, DESQUEPER, B, ELST, L. V, LAVEND'HOMME, R, D'OIRON, R, SCHWAAB, R, BAKKUS, M, THIELEMANS, K

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Deletion of alanine 2201 in the FVIII C2 domain results in mild hemophilia A by impairing FVIII binding to VWF and phospholipids and destroys a major FVIII antigenic determinant in... von d’Oiron, Roseline, Lavergne, Jean-Maurice, Lavend’homme, Renaud, Benhida, Abdellah, Bordet, Jean-Claude, Negrier, Claude, Peerlinck, Kathelijne, Vermylen, Jos, Saint-Remy, Jean-Marie, Jacquemin, Marc

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Mechanism and Kinetics of Factor VIII Inactivation: Study With an IgG4 Monoclonal Antibody Derived From a Hemophilia A Patient With Inhibitor von Jacquemin, Marc G., Desqueper, Benoı̂t G., Benhida, Abdellah, Vander Elst, Luc, Hoylaerts, Marc F., Bakkus, Marleen, Thielemans, Kris, Arnout, Jef, Peerlinck, Kathelijne, Gilles, Jean Guy G., Vermylen, Jos, Saint-Remy, Jean-Marie R.

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Peptide decoys selected by phage display block in vitro and in vivo activity of a human anti-FVIII inhibitor von Villard, Sylvie, Lacroix-Desmazes, Sébastien, Kieber-Emmons, Thomas, Piquer, Dominique, Grailly, Sabrina, Benhida, Abdellah, Kaveri, Srini V., Saint-Remy, Jean-Marie, Granier, Claude

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Mechanism and Kinetics of Factor VIII Inactivation: Study With an IgG4 Monoclonal Antibody Derived From a Hemophilia A Patient With Inhibitor von Jacquemin, Marc G., Desqueper, Benoı̂t G., Benhida, Abdellah, Vander Elst, Luc, Hoylaerts, Marc F., Bakkus, Marleen, Thielemans, Kris, Arnout, Jef, Peerlinck, Kathelijne, Gilles, Jean Guy G., Vermylen, Jos, Saint-Remy, Jean-Marie R.

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A novel cause of mild/moderate hemophilia A: mutations scattered in the factor VIII C1 domain reduce factor VIII binding to von Willebrand factor von Jacquemin, Marc, Lavend'homme, Renaud, Benhida, Abdellah, Vanzieleghem, Beatrijs, d'Oiron, Roseline, Lavergne, Jean-Maurice, Brackmann, Hans H., Schwaab, Rainer, VandenDriessche, Thierry, Chuah, Marinee K. L., Hoylaerts, Marc, Gilles, Jean Guy G., Peerlinck, Kathelijne, Vermylen, Jos, Saint-Remy, Jean-Marie R.

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Thymic neurohypophysial-related peptides and T cell selection von Geenen, Vincent, Cormann-Goffin, Nadine, Martens, Henri, Vandersmissen, Eric, Robert, Françoise, Benhida, Abdellah, Legros, Jean-Jacques, Martial, Joseph, Franchimont, Paul

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Rupture of T Cell Tolerance to Self Factor VIII in Mild/Moderate Hemophilia A von Jacquemin, Marc G., Lavend'homme, Renaud, Abdellah, Benhida, Peerlinck, Kathelijne, Vermylen, Jos, Deneys, Véronique, Saint-Remy, Jean-Marie, Hermans, Cédric

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Deletion of alanine 2201 in the FVIII C2 domain results in mild hemophilia A by impairing FVIII binding to VWF and phospholipids and destroys a major FVIII antigenic determinant in... von d'Oiron, Roseline, Lavergne, Jean-Maurice, Lavend'homme, Renaud, Benhida, Abdellah, Bordet, Jean-Claude, Negrier, Claude, Peerlinck, Kathelijne, Vermylen, Jozef, Saint-Remy, Jean-Marie, Jacquemin, Marc

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Epitope specificity of anti-FVIII antibodies during immune tolerance therapy with factor VIII preparation containing von Willebrand factor von Kallas, Ade, Pooga, Margus, Benhida, Abdellah, Jacquemin, Marc, Saint-Remy, Jean-Marie

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A novel cause of mild/moderate hemophilia A: mutations scattered in the factor VIII C1 domain reduce factor VIII binding to von Willebrand factor von Jacquemin, Marc, Lavend'homme, R, Benhida, Abdellah, Vanzieleghem, Beatrijs, d'Oiron, R, Lavergne, J.M, Brackmann, H.H, Schwaab, R, Vandendriessche, Thierry, Chuah, Marinee, Hoylaerts, Marc, Gilles, J.G, Peerlinck, Kathelijne, Vermylen, Jozef, Saint-Remy, Jean-Marie

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A human antibody directed to the factor VIII C1 domain inhibits factor VIII cofactor activity and binding to von Willebrand factor von Jacquemin, Marc, Benhida, Abdellah, Peerlinck, Kathelijne, Desqueper, Benoı̂t, Vander Elst, Luc, Lavend'homme, Renaud, d'Oiron, Roseline, Schwaab, Rainer, Bakkus, Marleen, Thielemans, Kris, Gilles, Jean-Guy, Vermylen, Jos, Saint-Remy, Jean-Marie

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A novel cause of mild/moderate hemophilia A : mutations scattered in the factor VIII C1 domain reduce factor VIII binding to von Willebrand factor von JACQUEMIN, M, LAVEND'HOMME, R, HOYLAERTS, M, GILLES, J. G. G, PEERLINCK, K, VERMYLEN, J, SAINT-REMY, J.-M. R, BENHIDA, A, VANZIELEGHEM, B, D'OIRON, R, LAVERGNE, J.-M, BRACKMANN, H. H, SCHWAAB, R, VANDENDRIESSCHE, T, CHUAH, M. K. L

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Cryptocrine Signaling in the Thymus Network von GEENEN, VINCENT, CORMANN, NADINE, VANDERSMISSEN, ERIC, MARTENS, HENRI, BENHIDA, ABDELLAH, MARTIAL, JOSEPH, FRANCHIMONT, PAUL

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Cryptocrine signaling in the thymus network. Implications for central T-cell tolerance of neuroendocrine functions von Geenen, V, Cormann-Goffin, N, Vandersmissen, E, Martens, H, Benhida, A, Martial, J, Franchimont, P

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The Dual Role of Thymic Neurohypophysial-Related Self Peptides in T Cell Selection von GEENEN, VINCENT, MARTENS, HENRI, ROBERT, FRANÇOISE, BENHIDA, ABDELLAH, CORMANN-GOFFIN, NADINE, LEGROS, JEAN-JACQUES, MARTIAL, JOSEPH, FRANCHIMONT, PAUL

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The dual role of thymic neurohypophysial-related self peptides in T cell selection. Physiological and pharmacological implications von Geenen, V, Martens, H, Robert, F, Benhida, A, Cormann-Goffin, N, Legros, J J, Martial, J, Franchimont, P

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