Sophie Gandrille - Dissemin

Papers authored by Sophie Gandrille

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2000 Olivier Morbœuf, Delphine Borgel, Martine Aiach, Tahar Kaabache, Sophie Gandrille

, Pascale Gaussem

Expression and Characterization of Recombinant Protein S with the Ser 460 Pro Mutation

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1999 Véronique Le Cam-Duchez, Veronique Le Cam-Duchez, Sophie Gandrille

, David Trégouët, Martine Alhenc-Gelas, Joseph Emmerich, Jean-Noël Fiessinger, Jeanne-Yvonne Borg, Martine Aiach

Influence of three potential genetic risk factors for thrombosis in 43 families carrying the factor V Arg 506 to Gln mutation

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Martine Aiach, Viviane Nicaud, Martine Alhenc Gelas, Sophie Gandrille

, Emmanuel Arnaud, Jean Amiral, Louis Guize, Jean-Noël Fiessinger, Joseph Emmerich

Complex Association of Protein C Gene Promoter Polymorphism With Circulating Protein C Levels and Thrombotic Risk

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Léna Le Flem, Véronique Picard, Joseph Emmerich, Sophie Gandrille

, Jean-Noël Fiessinger, Martine Aiach, Martine Alhenc Gelas

Mutations in Promoter Region of Thrombomodulin and Venous Thromboembolic Disease

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1996 D. Borgel, J. Duchemin, M. Alhencgelas, C. Matheron, M. Aiach, S. Gandrille

, The, Proteinsdeficiencies

Molecular basis for protein S hereditary deficiency: Genetic defects observed in 118 patients with type I and type IIa deficiencies1

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1995 Judith S. Greengard, Xiao Xu, Sophie Gandrille

, John H. Griffin

Alternative PCR method for diagnosis of mutation causing activated protein C resistant Gln506-factor V

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1994 Martine Alhenc-Gelas, Sophie Gandrille

, Marie-Laurence Aubry, Joseph Emmerich, Jean-Noel Fiessinger, Martine Aiach

Unexplained thrombosis and factor V Leiden mutation

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Saloua Najjam, Gilliane Chadeuf, Sophie Gandrille

, Martine Aiach

Arg-129 plays a specific role in the confirmation of antithrombin and in the enhancement of factor Xa inhibition by the pentasaccharode sequence of heparin

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S. Gandrille

, M. Goossens, M. Aiach

Scanning method to establish the molecular basis of protein C deficiencies

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1992 S. Gandrille

, M. Vidaud, M. Aiach, M. Alhenc-Gelas, A. M. Fischer, M. Gouault-Heilman, P. Toulon, J. N. Fiessinger, M. Goossens

Two novel mutations responsible for hereditary type I protein C deficiency: Characterization by denaturing gradient gel electrophoresis

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1991 S. Gandrille

, D. Vidaud, J. Emmerich, E. Clauser, P. Sié, J. N. Fiessinger, M. Alhenc-Gelas, P. Priollett, M. Aiach

Molecular basis for hereditary antithrombin III quantitative deficiencies: a stop codon in exon IIIa and a frameshift in exon VI

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S. Gandrille

, M. Alach

Polymorphism in the protein C gene detected by denaturing gradient gel electrophoresis

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1990 P. Toulon, S. Gandrille

, J. F. Vitoux, J. N. Fiessinger, Y. Sultan, M. Aiach

High total and free protein S in patients with acute deep vein thrombosis

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1988 S. Gandrille

, P. Priollet, L. Capron, M. Roncato, J. N. Fiessinger, M. Aiach

Association of inherited dysfibrinogenaemia and protein C deficiency in two unrelated families

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Papers authored by Sophie Gandrille