Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis by Schormair, Barbara, Zhao, Chen, Bell, Steven, Tilch, Erik, Salminen, Aaro V, Pütz, Benno, Dauvilliers, Yves, Stefani, Ambra, Högl, Birgit, Poewe, Werner, Kemlink, David, Sonka, Karel, Bachmann, Cornelius G, Paulus, Walter, Trenkwalder, Claudia, Oertel, Wolfgang H, Hornyak, Magdolna, Teder-Laving, Maris, Metspalu, Andres, Hadjigeorgiou, Georgios M, Polo, Olli, Fietze, Ingo, Ross, Owen A, Wszolek, Zbigniew, Butterworth, Adam S, Soranzo, Nicole, Ouwehand, Willem H, Roberts, David J, Danesh, John, Allen, Richard P, Earley, Christopher J, Ondo, William G, Xiong, Lan, Montplaisir, Jacques, Gan-Or, Ziv, Perola, Markus, Vodicka, Pavel, Dina, Christian, Franke, Andre, Tittmann, Lukas, Stewart, Alexandre F R, Shah, Svati H, Gieger, Christian, Peters, Annette, Rouleau, Guy A, Berger, Klaus, Oexle, Konrad, Di Angelantonio, Emanuele, Hinds, David A, Müller-Myhsok, Bertram, Winkelmann, Juliane, Balkau, B, Ducimetière, P, Eschwège, E, Rancière, F, Alhenc-Gelas, F, Gallois, Y, Girault, A, Fumeron, F, Marre, M, Roussel, R, Bonnet, F, Bonnefond, A, Cauchi, S, Froguel, P, Cogneau, J, Born, C, Caces, E, Cailleau, M, Lantieri, O, Moreau, JG, Rakotozafy, F, Tichet, J, Vol, S, Agee, Michelle, Alipanahi, Babak, Auton, Adam, Bell, Robert K, Bryc, Katarzyna, Elson, Sarah L, Fontanillas, Pierre, Furlotte, Nicholas A, Hinds, David A, Hromatka, Bethann S, Huber, Karen E, Kleinman, Aaron, Litterman, Nadia K, McIntyre, Matthew H, Mountain, Joanna L, Northover, Carrie AM, Pitts, Steven J, Sathirapongsasuti, J Fah, Sazonova, Olga V, Shelton, Janie F, Shringarpure, Suyash, Tian, Chao, Tung, Joyce Y, Vacic, Vladimir, Wilson, Catherine H

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Differences in the properties and enzymatic specificities of the two active sites of angiotensin I-converting enzyme (kininase II). Studies with bradykinin and other natural peptid... by Jaspard, E, Wei, L, Alhenc-Gelas, F

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CARDIOPROTECTION AND KALLIKREIN-KININ SYSTEM IN ACUTE MYOCARDIAL ISCHAEMIA IN MICE by Messadi-Laribi, E, Griol-Charhbili, V, Gaies, E, Vincent, MP, Heudes, D, Meneton, P, Alhenc-Gelas, F, Richer, C

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The two homologous domains of human angiotensin I-converting enzyme are both catalytically active by Wei, L, Alhenc-Gelas, F, Corvol, P, Clauser, E

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Tissue kallikrein is required for the cardioprotective effect of Cyclosporin A in myocardial ischemia in the mouse by Youcef, G., Belaidi, E., Waeckel, L., Fazal, L., Clemessy, M., Vincent, M.P., Zadigue, G., Richer, C., Alhenc-Gelas, F., Ovize, M., Pizard, A.

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Two Putative Active Centers in Human Angiotensin I-Converting Enzyme Revealed by Molecular Cloning by Soubrier, Florent, Alhenc-Gelas, François, Hubert, Christine, Allegrini, Jacqueline, John, Marie, Tregear, Geoffrey, Corvol, Pierre

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Blood microbiota dysbiosis is associated with the onset of cardiovascular events in a large general population: the D.E.S.I.R. study by Amar, Jacques, Lange, Céline, Payros, Gaëlle, Garret, Celine, Chabo, Chantal, Lantieri, Olivier, Courtney, Michael, Marre, Michel, Charles, Marie Aline, Balkau, Beverley, Burcelin, Rémy

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Role of tissue kallikrein in the cardioprotective effects of ischemic and pharmacological preconditioning in myocardial ischemia by Griol-Charhbili, V, Messadi-Laribi, E, Bascands, J. L, Heudes, D, Meneton, P, Giudicelli, J. F, Alhenc-Gelas, F, Richer, C

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Tissue kallikrein-deficient mice display a defect in renal tubular calcium absorption by PICARD, Nicolas, VAN ABEL, Monique, ALHENC-GELAS, Francois, HOUILLIER, Pascal, CAMPONE, Christelle, SEILER, Michelle, BLOCH-FAURE, May, HOENDEROP, Joost G. J, LOFFING, Johannes, MENETON, Pierre, BINDELS, René J. M, PAILLARD, Michel

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An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels by RIGAT, B, HUBERT, C, ALHENC-GELAS, F, CAMBIEN, F, CORVOL, P, SOUBRIER, F

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Angiotensin I-converting enzyme in human circulating mononuclear cells : genetic polymorphism of expression in T-lymphocytes by COSTEROUSSE, O, ALLEGRINI, J, LOPEZ, M, ALHENC-GELAS, F

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Contribution of genetic polymorphism in the renin-angiotensin system to the development of renal complications in insulin-dependent diabetes: Genetique de la Nephropathie Diabetiqu... by Marre, M, Jeunemaitre, X, Gallois, Y, Rodier, M, Chatellier, G, Sert, C, Dusselier, L, Kahal, Z, Chaillous, L, Halimi, S, Muller, A, Sackmann, H, Bauduceau, B, Bled, F, Passa, P, Alhenc-Gelas, F

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Angiotensin-I-converting enzyme insertion/deletion polymorphism and high urinary albumin concentration in French Type 2 diabetes patients by Hadjadj, S., Gallois, Y., Alhenc-Gelas, F., Chatellier, G., Marre, M.

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Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes by Albrechtsen, A., Grarup, N., Li, Y., Sparsø, T., Cao, H., Jiang, T., Kim, S. Y., Korneliussen, T., Li, Q., Nie, C., Wu, R., Morris, A. P., Ladenvall, C., Cauchi, S., Stančáková, A., Andersen, G., Astrup, A., Banasik, K., Bennett, A. J., Bolund, L., Charpentier, G., Chen, Y., Dekker, J. M., Doney, A. S. F., Dorkhan, M., Forsen, T., Frayling, T. M., Gui, Y., Hallmans, G., Hattersley, A. T., He, K., Hitman, G. A., Holmkvist, J., Huang, S., Jiang, H., Jin, X., Justesen, J. M., Kristiansen, K., Kuusisto, J., Lajer, M., Lantieri, O., Li, W., Liao, Q., Liu, X., Ma, T., Ma, X., Marre, M., Mokrosiński, J., Morris, A. D., Mu, B., Nielsen, A. A., Nijpels, G., Nilsson, P., Palmer, C. N. A., Rayner, N. W., Renström, F., Ribel-Madsen, R., Robertson, N., Rolandsson, O., Rossing, P., Schwartz, T. W., Slagboom, P. E., Sterner, M., Tang, M., Tarnow, L., Tuomi, T., van’t Riet, E., van Leeuwen, N., Varga, T. V., Vestmar, M. A., Walker, M., Wang, B., Wang, Y., Wu, H., Xi, F., Yengo, L., Yu, C., Zhang, J., Zhang, Q., Zhang, W., Zheng, H., Zhou, Y., Altshuler, D., ‘t Hart, L. M., Franks, P. W., Balkau, B., Froguel, P., McCarthy, M. I., Laakso, M., Groop, L., Christensen, C., Brandslund, I., Lauritzen, T., Witte, D. R., Linneberg, A., Jørgensen, T., Hansen, T., Wang, J., Nielsen, R., Pedersen, O.

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Fine-scale human genetic structure in Western France by Karakachoff, Matilde, Duforet-Frebourg, Nicolas, Simonet, Floriane, Le Scouarnec, Solena, Pellen, Nadine, Lecointe, Simon, Charpentier, Eric, Gros, Françoise, Cauchi, Stéphane, Froguel, Philippe, Copin, Nane, Le Tourneau, Thierry, Probst, Vincent, Le Marec, Hervé, Molinaro, Sabrina, Balkau, Beverley, Redon, Richard, Schott, Jean-Jacques, Blum, Michael Gb, Dina, Christian

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Murine models of myocardial and limb ischemia: Diagnostic end-points and relevance to clinical problems by Madeddu, P., Emanueli, C., Spillmann, F., Meloni, M., Bouby, N., Richer, C., Alhenc-Gelas, F., Van Weel, V., Eefting, D., Quax, P.H.A., Hu, Y., Xu, Q., Hemdahl, A.L., van Golde, J., Huijberts, M., de Lussanet, Q., Boudier, H. Struijker, Couffinhal, T., Duplaa, C., Chimenti, S., Staszewsky, L., Latini, R., Baumans, V., Levy, B.I.

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CO-19: Effets neuroprotecteurs de l'activation des récepteurs B1 des kinines chez la souris diabétique soumise à une ischémie cérébrale by Desposito, D, Zadigue, G, Taveau, C, Adam, C, Bouby, N, Alhenc-Gelas, F, Roussel, R

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The two homologous domains of human angiotensin I-converting enzyme interact differently with competitive inhibitors by WEI, L, CLAUSER, E, ALHENC-GELAS, F, CORVOL, P

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Plasma level and gene polymorphism of angiotensin-converting enzyme in relation to myocardial infarction by CAMBIEN, F, COSTEROUSSE, O, RAKOTOVAO, R, DUCIMETIERE, P, SOUBRIER, F, ALHENC-GELAS, F, TIRET, L, POIRIER, O, LECERF, L, GONZALES, M. F, EVANS, A, ARVEILER, D, CAMBOU, J. P, LUC, G

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PO1 Système Kallicréine-Kinine et cicatrisation cutanée chez la souris diabétique by Desposito, D, Chollet, C, Taveau, C, Roussel, R, Alhenc-Gelas, F, Bouby, N, Waeckel, L

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