1 - 25 of 47 results for author:"Aiach M." in Literature citations
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| Detection and characterisation of large SERPINC1 deletions in type I inherited antithrombin deficiency. Picard V., Chen J.M., Tardy B., Aillaud M.F., Boiteux-Vergnes C., Dreyfus M., Emmerich J., Lavenu-Bombled C., Nowak-Gottl U., Trillot N. et al. Hum. Genet. 127:45-53(2010) · Mapped (10) |
| No influence of the VAMP8 rs1010 single nucleotide polymorphism on platelet functions in vitro. Gaussem P., Ishida B.Y., Fontana P., Pullinger C.R., Khane J.P., Aiach M., Bachelot-Loza C., Gandrille S. J. Cell. Mol. Med. 13:601-603(2009) · Mapped (1) |
| Plasma Gas6 levels and coronary artery disease. Borgel D., Durand E., Clauser S., Bachelot-Loza C., Peyrard S., Remones V., Aiach M., Lafont A. Thromb. Haemost. 101:215-216(2009) · Mapped (3) |
| Bone morphogenetic proteins 2 and 4 are selectively expressed by late outgrowth endothelial progenitor cells and promote neoangiogenesis. Smadja D.M., Bieche I., Silvestre J.S., Germain S., Cornet A., Laurendeau I., Duong-Van-Huyen J.P., Emmerich J., Vidaud M., Aiach M. et al. Arterioscler. Thromb. Vasc. Biol. 28:2137-2143(2008) · Mapped (5) |
| Interleukin 8 is differently expressed and modulated by PAR-1 activation in early and late endothelial progenitor cells. Smadja D.M., Bieche I., Susen S., Mauge L., Laurendeau I., d'Audigier C., Grelac F., Emmerich J., Aiach M., Gaussem P. J. Cell. Mol. Med. 13:2534-2546(2009) · Mapped (8) |
| Thrombomodulin gene polymorphisms in brain infarction and mortality after stroke. Olivot J.M., Labreuche J., De Broucker T., Poirier O., Cambien F., Aiach M., Amarenco P., Amarenco P. J. Neurol. 255:514-519(2008) · Mapped (2) |
| Alternative mRNA is favored by the A3 haplotype of the EPCR gene PROCR and generates a novel soluble form of EPCR in plasma. Saposnik B., Lesteven E., Lokajczyk A., Esmon C.T., Aiach M., Gandrille S. Blood 111:3442-3451(2008) · Mapped (1) |
| Increased VEGFR2 expression during human late endothelial progenitor cells expansion enhances in vitro angiogenesis with up-regulation of integrin alpha(6). Smadja D.M., Bieche I., Helley D., Laurendeau I., Simonin G., Muller L., Aiach M., Gaussem P. J. Cell. Mol. Med. 11:1149-1161(2007) · Mapped (6) |
| Purinergic receptor P2Y, G-protein coupled, 12 gene variants and risk of incident ischemic stroke, myocardial infarction, and venous thromboembolism. Zee R.Y., Michaud S.E., Diehl K.A., Chasman D.I., Emmerich J., Gaussem P., Aiach M., Ridker P.M. Atherosclerosis 197:694-699(2008) · Mapped (4) |
| Influence of PROS1 gene mutations affecting protein S amino-acid 275 on plasma free protein S measurement. Alhenc Gelas M., Juin F., de Raucourt E., Gandrille S., Borgel D., Aiach M. Thromb. Haemost. 97:678-680(2007) · Mapped (28) |
| Identification of functional polymorphisms of the thromboxane A2 receptor gene in healthy volunteers. Fontana P., Gandrille S., Remones V., Dupont A., Reny J.L., Aiach M., Gaussem P. Thromb. Haemost. 96:356-360(2006) · Mapped (4) |
| The angiopoietin pathway is modulated by PAR-1 activation on human endothelial progenitor cells. Smadja D.M., Laurendeau I., Avignon C., Vidaud M., Aiach M., Gaussem P. J. Thromb. Haemost. 4:2051-2058(2006) · Mapped (12) |
| Cytochrome P450 2C19 loss-of-function polymorphism is a major determinant of clopidogrel responsiveness in healthy subjects. Hulot J.S., Bura A., Villard E., Azizi M., Remones V., Goyenvalle C., Aiach M., Lechat P., Gaussem P. Blood 108:2244-2247(2006) · Mapped (22) |
| Molecular bases of antithrombin deficiency: twenty-two novel mutations in the antithrombin gene. Picard V., Nowak-Gottl U., Biron-Andreani C., Fouassier M., Frere C., Goualt-Heilman M., de Maistre E., Regina S., Rugeri L., Ternisien C. et al. Hum. Mutat. 27:600-600(2006) · Mapped (10) |
| Elevated growth-arrest-specific protein 6 plasma levels in patients with severe sepsis. Borgel D., Clauser S., Bornstain C., Bieche I., Bissery A., Remones V., Fagon J.Y., Aiach M., Diehl J.L. Crit. Care Med. 34:219-222(2006) · Mapped (2) |
| PAR-1 activation on human late endothelial progenitor cells enhances angiogenesis in vitro with upregulation of the SDF-1/CXCR4 system. Smadja D.M., Bieche I., Uzan G., Bompais H., Muller L., Boisson-Vidal C., Vidaud M., Aiach M., Gaussem P. Arterioscler. Thromb. Vasc. Biol. 25:2321-2327(2005) · Mapped (7) |
| Conformational Asn187Asp/Lys antithrombin variants and thrombosis. Clinical and biological features in 13 new heterozygotes. Picard V., Bauters A., Khairy M., Ochat N., Jude B., Aiach M., Alhenc-Gelas M. Thromb. Haemost. 93:57-62(2005) · Mapped (10) |
| The gamma-carboxyglutamic acid domain of anticoagulant protein S is involved in activated protein C cofactor activity, independently of phospholipid binding. Saller F., Villoutreix B.O., Amelot A., Kaabache T., Le Bonniec B.F., Aiach M., Gandrille S., Borgel D. Blood 105:122-130(2005) · Mapped (20) |
| The factor II G20210A gene polymorphism, but not factor V Arg506Gln, is associated with peripheral arterial disease: results of a case-control study. Reny J.L., Alhenc-Gelas M., Fontana P., Bissery A., Julia P.L., Fiessinger J.N., Aiach M., Emmerich J. J. Thromb. Haemost. 2:1334-1340(2004) · Mapped (21) |
| The TF-603A/G gene promoter polymorphism and circulating monocyte tissue factor gene expression in healthy volunteers. Reny J.L., Laurendeau I., Fontana P., Bieche I., Dupont A., Remones V., Emmerich J., Vidaud M., Aiach M., Gaussem P. Thromb. Haemost. 91:248-254(2004) · Mapped (5) |
| Validation of a diagnostic kit for factor V Leiden mutation. Gandrille S., Remones V., Aiach M. Ann. Biol. Clin. (Paris) 61:723-727(2003) · Mapped (13) |
| P2Y12 H2 haplotype is associated with peripheral arterial disease: a case-control study. Fontana P., Gaussem P., Aiach M., Fiessinger J.N., Emmerich J., Reny J.L. Circulation 108:2971-2973(2003) · Mapped (5) |
| A haplotype of the EPCR gene is associated with increased plasma levels of sEPCR and is a candidate risk factor for thrombosis. Saposnik B., Reny J.L., Gaussem P., Emmerich J., Aiach M., Gandrille S. Blood 103:1311-1318(2004) · Mapped (1) |
| Adenosine diphosphate-induced platelet aggregation is associated with P2Y12 gene sequence variations in healthy subjects. Fontana P., Dupont A., Gandrille S., Bachelot-Loza C., Reny J.L., Aiach M., Gaussem P. Circulation 108:989-995(2003) · Mapped (4) |
| Factor V Leiden mutation in Sneddon syndrome. Besnier R., Frances C., Ankri A., Aiach M., Piette J.C. Lupus 12:406-408(2003) · Mapped (13) |