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Sophie Gandrille

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Sophie Gandrille; Sarah Abbes; Anne-Marie Fischer; Isabelle Galy-Fauroux; Emeline Levionnois; Régis Peffault de Latour; Anna Petropoulou; Paula Rodriguez-Otero; Gérard Socié; Laurence Zemori; Dominique Helley
Endothelial colony-forming cells from patients with paroxysmal nocturnal haemoglobinuria are not PIGA mutated.
A D Mumford; Stuart J Mundell; S Nisar; F Zinzindohoue; Christilla Bachelot-Loza; L Darnige; A-M Fischer; Sophie Gandrille; Pascale Gaussem; M L Jones
Platelet dysfunction associated with the novel Trp29Cys thromboxane A₂ receptor variant.
Béatrice Saposnik; Maud Simansour; Alain Stepanian; Gabriel Baron; Dominique de Prost; Laurent Mandelbrot; Edith Peynaud-Debayle; Sophie Gandrille
Elevated soluble endothelial cell protein C receptor (sEPCR) levels in women with preeclampsia: a marker of endothelial activation/damage?

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All Publications

2013: Sophie Gandrille; Sarah Abbes; Anne-Marie Fischer; Isabelle Galy-Fauroux; Emeline Levionnois; Régis Peffault de Latour; Anna Petropoulou; Paula Rodriguez-Otero; Gérard Socié; Laurence Zemori; Dominique Helley
Endothelial colony-forming cells from patients with paroxysmal nocturnal haemoglobinuria are not PIGA mutated.
British journal of haematology 2013;161(1):144-7.
2013: A D Mumford; Stuart J Mundell; S Nisar; F Zinzindohoue; Christilla Bachelot-Loza; L Darnige; A-M Fischer; Sophie Gandrille; Pascale Gaussem; M L Jones
Platelet dysfunction associated with the novel Trp29Cys thromboxane A₂ receptor variant.
Journal of thrombosis and haemostasis : JTH 2013;11(3):547-54.
2012: Béatrice Saposnik; Maud Simansour; Alain Stepanian; Gabriel Baron; Dominique de Prost; Laurent Mandelbrot; Edith Peynaud-Debayle; Sophie Gandrille
Elevated soluble endothelial cell protein C receptor (sEPCR) levels in women with preeclampsia: a marker of endothelial activation/damage?
Thrombosis research 2012;129(2):152-7.
2010: David M Smadja; Pascale Gaussem; Laetitia Mauge; Romaric Lacroix; Sophie Gandrille; Véronique Remones; Séverine Peyrard; Florence Sabatier; Damien Bonnet; Marilyne Lévy
Comparison of endothelial biomarkers according to reversibility of pulmonary hypertension secondary to congenital heart disease.
Pediatric cardiology 2010;31(5):657-62.
2010: Marcello Baroni; Giulia Pavani; Diego Marescotti; Tahar Kaabache; Delphine Borgel; Sophie Gandrille; Giovanna Marchetti; Cristina Legnani; Armando D'Angelo; Mirko Pinotti; francesco bernardi
Membrane binding and anticoagulant properties of protein S natural variants.
Thrombosis research 2010;125(2):e33-9.
2009: Pascale Gaussem; Brian Y Ishida; Pierre Fontana; Clive R Pullinger; John P Khane; Martine Aiach; Christilla Bachelot-Loza; Sophie Gandrille
No influence of the VAMP8 rs1010 single nucleotide polymorphism on platelet functions in vitro.
Journal of cellular and molecular medicine 2009;13(3):601-3.
2008: Mary J Heeb; Sophie Gandrille; J A Fernandez; John H Griffin; P F Fedullo
Late onset thrombosis in a case of severe protein S deficiency due to compound heterozygosity for PROS1 mutations.
Journal of thrombosis and haemostasis : JTH 2008;6(7):1235-7.
2008: Sophie Gandrille
Endothelial cell protein C receptor and the risk of venous thrombosis.
Haematologica 2008;93(6):812-6.
2008: Beatrice Saposnik; Elodie Lesteven; Anna Lokajczyk; Charles T Esmon; Martine Aiach; Sophie Gandrille
Alternative mRNA is favored by the A3 haplotype of the EPCR gene PROCR and generates a novel soluble form of EPCR in plasma.
Blood 2008;111(7):3442-51.
2007: Delphine Borgel; Caroline Bornstain; Pieter H Reitsma; Nicolas Lerolle; Sophie Gandrille; Fouad Dali-Ali; Charles T Esmon; Jean-Yves Fagon; Martine Aiach; Jean-Luc Diehl
A comparative study of the protein C pathway in septic and nonseptic patients with organ failure.
American journal of respiratory and critical care medicine 2007;176(9):878-85.
2007: Martine Alhenc-Gelas; Fabrice Juin; Emmanuelle de Raucourt; Sophie Gandrille; Delphine Borgel; Martine Aiach
Influence of PROS1 gene mutations affecting protein S amino-acid 275 on plasma free protein S measurement.
Thrombosis and haemostasis 2007;97(4):678-80.
2006: Martine Aiach; Martine Alhenc-Gelas; Delphine Borgel; Joseph Emmerich; Sophie Gandrille; Véronique Picard
[Coagulation factor mutations and thrombosis].
Médecine sciences : M/S 2006;22(11):985-9.
2006: Pierre Fontana; Sophie Gandrille; Véronique Remones; Annabelle Dupont; Jean-Luc Reny; Martine Aiach; Pascale Gaussem
Identification of functional polymorphisms of the thromboxane A2 receptor gene in healthy volunteers.
Thrombosis and haemostasis 2006;96(3):356-60.
2006: F Saller; Tahar Kaabache; Martine Aiach; Sophie Gandrille; Delphine Borgel
The protein S thrombin-sensitive region modulates phospholipid binding and the gamma-carboxyglutamic acid-rich (Gla) domain conformation in a non-specific manner.
Journal of thrombosis and haemostasis : JTH 2006;4(3):704-6.
2006: M Baroni; G Mazzola; Tahar Kaabache; Delphine Borgel; Sophie Gandrille; S Vigano' D'Angelo; Giovanna Marchetti; Maria Grazia di Iasio; Mirko Pinotti; A D'Angelo; francesco bernardi
Molecular bases of type II protein S deficiency: the I203-D204 deletion in the EGF4 domain alters GLA domain function.
Journal of thrombosis and haemostasis : JTH 2006;4(1):186-91.
2005: François Saller; Bruno Villoutreix; Aymeric Amelot; Tahar Kaabache; Bernard F Le Bonniec; Martine Aiach; Sophie Gandrille; Delphine Borgel
The gamma-carboxyglutamic acid domain of anticoagulant protein S is involved in activated protein C cofactor activity, independently of phospholipid binding.
Blood 2005;105(1):122-30.
2004: Beatrice Saposnik; Jean-Luc Reny; Pascale Gaussem; Joseph Emmerich; Martine Aiach; Sophie Gandrille
A haplotype of the EPCR gene is associated with increased plasma levels of sEPCR and is a candidate risk factor for thrombosis.
Blood 2004;103(4):1311-8.
2003: Sophie Gandrille; Véronique Remones; Martine Aiach
[Validation of a diagnostic kit for factor V Leiden mutation].
Annales de biologie clinique 2003;61(6):723-7.
2003: Pierre Fontana; Annabelle Dupont; Sophie Gandrille; Christilla Bachelot-Loza; Jean-Luc Reny; Martine Aiach; Pascale Gaussem
Adenosine diphosphate-induced platelet aggregation is associated with P2Y12 gene sequence variations in healthy subjects.
Circulation 2003;108(8):989-95.
2003: Delphine Borgel; Jean-Luc Reny; David Fischelis; Sophie Gandrille; Joseph Emmerich; Jean-Noël Fiessinger; Martine Aiach
Cleaved protein S (PS), total PS, free PS, and activated protein C cofactor activity as risk factors for venous thromboembolism.
Clinical chemistry 2003;49(4):575-80.
2003: Béatrice Saposnik; Delphine Borgel; Martine Aiach; Sophie Gandrille
Functional properties of the sex-hormone-binding globulin (SHBG)-like domain of the anticoagulant protein S.
European journal of biochemistry / FEBS 2003;270(3):545-55.
2001: Delphine Borgel; Pascale Gaussem; C Garbay; Christilla Bachelot-Loza; Tahar Kaabache; Wang-Qing Liu; Brigitte Brohard-Bohn; Bernard F Le Bonniec; Martine Aiach; Sophie Gandrille
Implication of protein S thrombin-sensitive region with membrane binding via conformational changes in the gamma-carboxyglutamic acid-rich domain.
The Biochemical journal 2001;360(Pt 2):499-506.
2001: Bruno Villoutreix; Björn Dahlbäck; Delphine Borgel; Sophie Gandrille; Y A Muller
Three-dimensional model of the SHBG-like region of anticoagulant protein S: new structure-function insights.
Proteins 2001;43(2):203-16.
2000: Sophie Gandrille; Delphine Borgel; Núria Sala; Yolanda Espinosa-Parrilla; Rachel E Simmonds; S Rezende; B Lind; C Mannhalter; I Pabinger; Pieter H Reitsma; C Formstone; D N Cooper; H Saito; K Suzuki; francesco bernardi; Martine Aiach
Protein S deficiency: a database of mutations--summary of the first update.
Thrombosis and haemostasis 2000;84(5):918.
2000: O Morboeuf; Delphine Borgel; Pascale Gaussem; A Vincenot; J L Pittet; Martine Aiach; Sophie Gandrille
Characterization of cleaved plasma protein S with a monoclonal antibody-based assay.
Thrombosis and haemostasis 2000;84(4):604-10.
2000: O Morboeuf; Delphine Borgel; Martine Aiach; Tahar Kaabache; Sophie Gandrille; Pascale Gaussem
Expression and characterization of recombinant protein S with the Ser 460 Pro mutation.
Thrombosis research 2000;100(1):81-8.
2000: Martine Alhenc-Gelas; Sophie Gandrille; Marie-Laurence Aubry; Martine Aiach
Thirty-three novel mutations in the protein C gene. French INSERM network on molecular abnormalities responsible for protein C and protein S.
Thrombosis and haemostasis 2000;83(1):86-92.
1999: Véronique Le Cam-Duchez; Sophie Gandrille; D Trégouët; Martine Alhenc-Gelas; J Emmerich; Jean-Noël Fiessinger; Jeanne-Yvonne Borg; M Aiach
Influence of three potential genetic risk factors for thrombosis in 43 families carrying the factor V Arg 506 to Gln mutation.
British journal of haematology 1999;106(4):889-97.
1999: Martine Aiach; V Nicaud; Martine Alhenc-Gelas; Sophie Gandrille; E Arnaud; J Amiral; L Guize; Jean-Noël Fiessinger; Joseph Emmerich
Complex association of protein C gene promoter polymorphism with circulating protein C levels and thrombotic risk.
Arteriosclerosis, thrombosis, and vascular biology 1999;19(6):1573-6.
1999: L 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.
Arteriosclerosis, thrombosis, and vascular biology 1999;19(4):1098-104.
1999: Martine Alhenc-Gelas; V Nicaud; Sophie Gandrille; van dreden patrick; J Amiral; Marie-Laurence Aubry; Jean-Noël Fiessinger; Joseph Emmerich; Martine Aiach
The factor V gene A4070G mutation and the risk of venous thrombosis.
Thrombosis and haemostasis 1999;81(2):193-7.
1998: Sabri KEMAHLI; Martine Alhenc-Gelas; Sophie Gandrille; M Aiach; Nejat Akar; Sükrü Cin
Homozygous protein C deficiency with a double variant His 202 to Tyr and Ala 346 to Thr.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 1998;9(4):351-4.
1998: O Morboeuf; Martine Aiach; Sophie Gandrille
Lack of sequence variations in the C4b-BP beta-chain in patients with type III protein S deficiency bearing the Ser 460 to Pro mutation: description of two new intragenic isomorphisms in the C4b-BP beta-chain gene (C4BPB).
British journal of haematology 1998;101(1):10-5.
1998: D Brunet; MC Barthet; Pierre Morange; Marie-Christine Alessi; Delphine Borgel; Sophie Gandrille; Marie-Françoise Aillaud; Irène Juhan-Vague
Protein S deficiency: different biological phenotypes according to the assays used.
Thrombosis and haemostasis 1998;79(2):446-7.
1997: Martine Aiach; Delphine Borgel; Pascale Gaussem; Joseph Emmerich; Martine Alhenc-Gelas; Sophie Gandrille
Protein C and protein S deficiencies.
Seminars in hematology 1997;34(3):205-16.
1997: Delphine Borgel; Sophie Gandrille; Martine Aiach
Protein S deficiency.
Thrombosis and haemostasis 1997;78(1):351-6.
1997: Sophie Gandrille; Delphine Borgel; H Ireland; David A Lane; Rachel E Simmonds; Pieter H Reitsma; C Mannhalter; I Pabinger; H Saito; K Suzuki; C Formstone; D N Cooper; Y Espinosa; Núria Sala; francesco bernardi; Martine Aiach
Protein S deficiency: a database of mutations. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.
Thrombosis and haemostasis 1997;77(6):1201-14.
1996: Martine Aiach; Sophie Gandrille
Molecular basis for protein C hereditary deficiency.
Haemostasis 1996;26 Suppl 4():9-19.
1996: Delphine Borgel; J Duchemin; Martine Alhenc-Gelas; C Matheron; Martine Aiach; Sophie Gandrille
Molecular basis for protein S hereditary deficiency: genetic defects observed in 118 patients with type I and type IIa deficiencies. The French Network on Molecular Abnormalities Responsible for Protein C and Protein S Deficiencies.
The Journal of laboratory and clinical medicine 1996;128(2):218-27.
1996: Delphine Borgel; Brigitte Jude; Martine Aiach; Sophie Gandrille
First case of sporadic protein S deficiency due to a novel candidate mutation, Ala 484-->Pro, in the protein S active gene (PROS1).
Thrombosis and haemostasis 1996;75(6):883-6.
1996: J Duchemin; Jeanne-Yvonne Borg; Delphine Borgel; Marc Vasse; H Lévèque; Martine Aiach; Sophie Gandrille
Five novel mutations of the protein S active gene (PROS 1) in 8 Norman families.
Thrombosis and haemostasis 1996;75(3):437-44.
1995: J S Greengard; X Xu; Sophie Gandrille; John H Griffin
Alternative PCR method for diagnosis of mutation causing activated protein C resistant Gln506-factor V.
Thrombosis research 1995;80(5):441-3.
1995: J Duchemin; Sophie Gandrille; Delphine Borgel; P Feurgard; Martine Alhenc-Gelas; C Matheron; M Dreyfus; E Dupuy; Irène Juhan-Vague; Martine Aiach
The Ser 460 to Pro substitution of the protein S alpha (PROS1) gene is a frequent mutation associated with free protein S (type IIa) deficiency.
Blood 1995;86(9):3436-43.
1995: Martine Aiach; Sophie Gandrille; J Emmerich
A review of mutations causing deficiencies of antithrombin, protein C and protein S.
Thrombosis and haemostasis 1995;74(1):81-9.
1995: Sophie Gandrille; J S Greengard; Martine Alhenc-Gelas; I Juhan-Vague; J F Abgrall; Brigitte Jude; John H Griffin; Martine Aiach
Incidence of activated protein C resistance caused by the ARG 506 GLN mutation in factor V in 113 unrelated symptomatic protein C-deficient patients. The French Network on the behalf of INSERM.
Blood 1995;86(1):219-24.
1995: Sophie Gandrille; Martine Alhenc-Gelas; Martine Aiach
A rapid screening method for the factor V Arg506-->Gln mutation.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 1995;6(3):245-8.
1995: P H Reitsma; F Bernardi; R G Doig; Sophie Gandrille; J S Greengard; H Ireland; M Krawczak; B Lind; G L Long; swibertus rudolfus poort
Protein C deficiency: a database of mutations, 1995 update. On behalf of the Subcommittee on Plasma Coagulation Inhibitors of the Scientific and Standardization Committee of the ISTH.
Thrombosis and haemostasis 1995;73(5):876-89.
1995: J Emmerich; Martine Alhenc-Gelas; Sophie Gandrille; C Guichet; J N Fiessinger; Martine Aiach
Mechanism of protein C deficiency in a patient with arginine 358 alpha 1-antitrypsin (Pittsburgh mutation): role in the maintenance of hemostatic balance.
The Journal of laboratory and clinical medicine 1995;125(4):531-9.
1995: Martine Alhenc-Gelas; J Emmerich; Sophie Gandrille; M L Aubry; N Benaily; J N Fiessinger; M Aiach
Protein C infusion in a patient with inherited protein C deficiency caused by two missense mutations: Arg 178 to Gln and Arg-1 to His.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 1995;6(1):35-41.
1995: Sophie Gandrille; Delphine Borgel; V Eschwege-Gufflet; Marie-Françoise Aillaud; M Dreyfus; C Matheron; Pascale Gaussem; J F Abgrall; Brigitte Jude; P Sie
Identification of 15 different candidate causal point mutations and three polymorphisms in 19 patients with protein S deficiency using a scanning method for the analysis of the protein S active gene.
Blood 1995;85(1):130-8.
1994: Michèle Gouault-Heilmann; P Quetin; M Dreyfus; Sophie Gandrille; J Emmerich; Catherine Leroy-Matheron; M Guesnu
Massive thrombosis of venous cerebral sinuses in a 2-year-old boy with a combined inherited deficiency of antithrombin III and protein C.
Thrombosis and haemostasis 1994;72(5):782-3.
1994: Sophie Gandrille; Brigitte Jude; Martine Alhenc-Gelas; J Emmerich; Martine Aiach
First de novo mutations in the protein C gene of two patients with type I deficiency: a missense mutation and a splice site deletion.
Blood 1994;84(8):2566-70.
1994: J Emmerich; Martine Alhenc-Gelas; Sophie Gandrille; J N Fiessinger; M Aiach
[A new cause of familial thrombophilia: resistance to the effect of activated protein C].
Presse médicale (Paris, France : 1983) 1994;23(28):1285-7.
1994: M Alhenc-Gelos; Sophie Gandrille; M L Aubry; J Emmerich; J N Flessinger; M Aiach
Unexplained thrombosis and factor V Leiden mutation.
Lancet 1994;344(8921):555-6.
1994: Delphine Borgel; Sophie Gandrille; Michèle Gouault-Heilmann; Martine Aiach
First frameshift mutation in the active protein S gene associated with a quantitative hereditary deficiency.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 1994;5(4):593-600.
1994: Pascale Gaussem; Sophie Gandrille; J Duchemin; J Emmerich; Martine Alhenc-Gelas; Marie-Françoise Aillaud; Martine Aiach
Influence of six mutations of the protein C gene on the Gla domain conformation and calcium affinity.
Thrombosis and haemostasis 1994;71(6):748-54.
1994: S Najjam; G Chadeuf; Sophie Gandrille; Martine Aiach
Arg-129 plays a specific role in the conformation of antithrombin and in the enhancement of factor Xa inhibition by the pentasaccharide sequence of heparin.
Biochimica et biophysica acta 1994;1225(2):135-43.
1994: Sophie Gandrille; M Goossens; Martine Aiach
Scanning method to establish the molecular basis of protein C deficiencies.
Human mutation 1994;4(1):20-30.
1993: Sophie Gandrille; Brigitte Jude; Martine Alhenc-Gelas; A Millaire; Martine Aiach
Compound heterozygosity in a family with protein C deficiency illustrating the complexity of the underlying molecular mechanism.
Thrombosis and haemostasis 1993;70(5):747-52.
1993: Sophie Gandrille; Martine Alhenc-Gelas; Pascale Gaussem; Marie-Françoise Aillaud; E Dupuy; I Juhan-Vague; Martine Aiach
Five novel mutations located in exons III and IX of the protein C gene in patients presenting with defective protein C anticoagulant activity.
Blood 1993;82(1):159-68.
1993: J Emmerich; Martine Alhenc-Gelas; Sophie Gandrille; C Laurian; L Capron; M Aiach; J N Fiessinger
[Protein C deficiency: cause or coincidence in arterial vascular accidents].
Presse médicale (Paris, France : 1983) 1993;22(17):830.
1993: P H Reitsma; swibertus rudolfus poort; F Bernardi; Sophie Gandrille; G L Long; N Sala; David N Cooper
Protein C deficiency: a database of mutations. For the Protein C & S Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.
Thrombosis and haemostasis 1993;69(1):77-84.
1992: Pierre Toulon; Sophie Gandrille; P Remy; G Chadeuf; M H Jouvin; Martine Aiach
Significance of high levels of heparin cofactor II in the plasma and urine of adult patients with nephrotic syndrome.
Nephron 1992;60(2):176-80.
1992: M Aiach; Sophie Gandrille; J Emmerich; Martine Alhenc-Gelas; J N Fiessinger
Molecular abnormalities responsible for thrombosis. Genetic aspects.
Nouvelle revue française d'hématologie 1992;34(4):279-85.
1992: Sophie Gandrille; M Vidaud; Martine Aiach; Martine Alhenc-Gelas; A M Fischer; M Gouault-Heilman; Pierre Toulon; J N Fiessinger; Michel Goossens
Two novel mutations responsible for hereditary type I protein C deficiency: characterization by denaturing gradient gel electrophoresis.
Human mutation 1992;1(6):491-500.
1991: Sophie Gandrille; D Vidaud; J Emmerich; Eric Clauser; P Sié; J N Fiessinger; Martine Alhenc-Gelas; P Priollet; Martine Aiach
Molecular basis for hereditary antithrombin III quantitative deficiencies: a stop codon in exon IIIa and a frameshift in exon VI.
British journal of haematology 1991;78(3):414-20.
1991: Eric Clauser; Sophie Gandrille; D Vidaud; P Molho Sabatier; J n Fiessinger; Martine Aiach
Genetic diagnosis of qualitative and quantitative antithrombin III deficiencies.
Nouvelle revue française d'hématologie 1991;33(2):141-3.
1990: Sophie Gandrille; Martine Aiach; D A Lane; D Vidaud; P Molho-Sabatier; R Caso; P de Moerloose; J N Fiessinger; Eric Clauser
Important role of arginine 129 in heparin-binding site of antithrombin III. Identification of a novel mutation arginine 129 to glutamine.
The Journal of biological chemistry 1990;265(31):18997-9001.
1990: Pierre Toulon; Sophie Gandrille; J F Vitoux; J N Fiessinger; Y Sultan; Martine Aiach
High total and free protein S in patients with acute deep vein thrombosis.
Thrombosis research 1990;59(1):213-7.
1990: A Mossaz; Sophie Gandrille; J F Vitoux; N Abdoucheli-Baudot; M Aiach; J N Fiessinger
[The value of D-dimer assays in the emergency diagnosis of venous thrombosis].
Presse médicale (Paris, France : 1983) 1990;19(22):1055.
1990: Pascale Gaussem; Sophie Gandrille; P Molho-Sabatier; L Capron; J N Fiessinger; Martine Aiach
A plasma clot lysis assay based on the release of fibrin degradation products: application to the diagnosis of hypofibrinolytic states.
Thrombosis and haemostasis 1990;63(1):76-81.
1988: Sophie Gandrille; M H Jouvin; Pierre Toulon; P Remy; J N Fiessinger; M Roncato; N Moatti; Martine Aiach
A study of fibrinogen and fibrinolysis in 10 adults with nephrotic syndrome.
Thrombosis and haemostasis 1988;59(3):445-50.
1988: Sophie Gandrille; P Priollet; L Capron; M Roncato; J N Fiessinger; M Aiach
Association of inherited dysfibrinogenaemia and protein C deficiency in two unrelated families.
British journal of haematology 1988;68(3):329-37.