1-10 of 10
C Mazurier
Close
Sort by
Journal Articles

Stro-1 Positive and Stro-1 − Negtive Human Mesenchymal Stem Cells Express Different Levels of Immunosuppression.

Dominique Thierry 9, Y. Z. Zhang 1, A. Chapel 2, M. Benshidoum 3, C. Mazurier 4, S. Bouchet 5, A. Nashef 6, M. C. Lopez 7, N. C. Gorin 8, L. Fouillard 9
Journal: Blood
Blood (2004) 104 (11): 4964.
https://doi.org/10.1182/blood.V104.11.4964.4964
Published: 2004
Journal Articles

A Novel Mutation in the D3 Domain of von Willebrand Factor Markedly Decreases Its Ability to Bind Factor VIII and Affects Its Multimerization

S. Jorieux, C. Gaucher, J. Goudemand, C. Mazurier
Journal: Blood
Blood (1998) 92 (12): 4663–4670.
https://doi.org/10.1182/blood.V92.12.4663
Published: 1998
Journal Articles

A Patient With Type 2N von Willebrand Disease Is Heterozygous for a New Mutation: Gly22Glu. Demonstration of a Defective Expression of the Second Allele by the Use of Monoclonal Antibodies

J. Gu, S. Jorieux, J.M. Lavergne, C. Ruan, C. Mazurier, D. Meyer
Journal: Blood
Blood (1997) 89 (9): 3263–3269.
https://doi.org/10.1182/blood.V89.9.3263
Published: 1997
Journal Articles

Identification of two mutations (Arg611Cys and Arg611His) in the A1 loop of von Willebrand factor (vWF) responsible for type 2 von Willebrand disease with decreased platelet-dependent function of vWF [see comments]

L Hilbert, C Gaucher, C Mazurier
Journal: Blood
Blood (1995) 86 (3): 1010–1018.
https://doi.org/10.1182/blood.V86.3.1010.1010
Published: 1995
Journal Articles

Characterization of von Willebrand factor gene defects in two unrelated patients with type IIC von Willebrand disease

C Gaucher, J Dieval, C Mazurier
Journal: Blood
Blood (1994) 84 (4): 1024–1030.
https://doi.org/10.1182/blood.V84.4.1024.1024
Published: 1994
Journal Articles

Leu 697-->Val mutation in mature von Willebrand factor is responsible for type IIB von Willebrand disease

L Hilbert, C Gaucher, C de Romeuf, MH Horellou, T Vink, C Mazurier
Journal: Blood
Blood (1994) 83 (6): 1542–1550.
https://doi.org/10.1182/blood.V83.6.1542.1542
Published: 1994
Journal Articles

The mutation Arg (53)----Trp causes von Willebrand disease Normandy by abolishing binding to factor VIII. Studies with recombinant von Willebrand factor

S Jorieux, EA Tuley, C Gaucher, C Mazurier, JE Sadler
Journal: Blood
Blood (1992) 79 (3): 563–567.
https://doi.org/10.1182/blood.V79.3.563.563
Published: 1992
Journal Articles

The "Normandy" variant of von Willebrand disease: characterization of a point mutation in the von Willebrand factor gene

C Gaucher, S Jorieux, B Mercier, D Oufkir, C Mazurier
Journal: Blood
Blood (1991) 77 (9): 1937–1941.
https://doi.org/10.1182/blood.V77.9.1937.1937
Published: 1991
Journal Articles

A new von Willebrand factor (vWF) defect in a patient with factor VIII (FVIII) deficiency but with normal levels and multimeric patterns of both plasma and platelet vWF. Characterization of abnormal vWF/FVIII interaction

C Mazurier, J Dieval, S Jorieux, J Delobel, M Goudemand
Journal: Blood
Blood (1990) 75 (1): 20–26.
https://doi.org/10.1182/blood.V75.1.20.20
Published: 1990
Journal Articles

Adhesive properties of the carbohydrate-modified von Willebrand factor (CHO-vWF)

AB Federici, C De Romeuf, PG De Groot, B Samor, R Lombardi, P D'Alessio, C Mazurier, PM Mannucci, JJ Sixma
Journal: Blood
Blood (1988) 71 (4): 947–952.
https://doi.org/10.1182/blood.V71.4.947.947
Published: 1988