A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome von Neyroud, Nathalie, Leibovici, Michel, Tesson, Frédérique, Donger, Claire, Denjoy, Isabelle, Gary, Françoise, Guicheney, Pascale, Coumel, Philippe, Petit, Christine, Barhanin, Jacques, Fauré, Sabine, Schwartz, Ketty

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A CRISPR/Cas9 zebrafish lamin A/C mutant model of muscular laminopathy von Nicolas, Hannah A., Hua, Khang, Quigley, Hailey, Ivare, Joshua, Tesson, Frédérique, Akimenko, Marie‐Andrée

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Mutations in the laminin α2-chain gene ( LAMA2 ) cause merosin-deficient congenital muscular dystrophy von Cruaud, Corinne, Tesson, Frédérique, Topaloglu, Haluk, Tomé, Fernando M.S, Weissenbach, Jean, Zhang, Xu, Tryggvason, Karl, Fardeau, Michel, Guicheney, Pascale, Helbling-Leclerc, Anne, Schwartz, Ketty

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ACSL5 genotype influence on fatty acid metabolism: a cellular, tissue, and whole-body study von Rajkumar, Abishankari, Liaghati, Awa, Chan, Jessica, Lamothe, Gilles, Dent, Robert, Doucet, Éric, Rabasa-Lhoret, Rémi, Prud'homme, Denis, Harper, Mary-Ellen, Tesson, Frédérique

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Lamin A/C mutants disturb sumo1 localization and sumoylation in vitro and in vivo von Boudreau, Émilie, Labib, Sarah, Bertrand, Anne T, Decostre, Valérie, Bolongo, Pierrette M, Sylvius, Nicolas, Bonne, Gisèle, Tesson, Frédérique

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Decreased Mitochondrial Proton Leak and Reduced Expression of Uncoupling Protein 3 in Skeletal Muscle of Obese Diet-Resistant Women von HARPER, Mary-Ellen, DENT, Robert, MONEMDJOU, Shadi, BEZAIRE, Véronic, VAN WYCK, Lloyd, WELLS, George, GUL NIHAN KAVASLAR, GAUTHIER, Andre, TESSON, Frédérique, MCPHERSON, Ruth

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Cellular and Animal Models of Striated Muscle Laminopathies von Nicolas, Hannah A, Akimenko, Marie-Andrée, Tesson, Frédérique

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Lamin A/C and cardiac diseases von Sylvius, Nicolas, Tesson, Frédérique

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Somatic Mutations in the Connexin 40 Gene (GJA5) in Atrial Fibrillation von Gollob, Michael H, Jones, Douglas L, Krahn, Andrew D, Danis, Lynne, Gong, Xiang-Qun, Shao, Qing, Liu, Xiaoqin, Veinot, John P, Tang, Anthony S.L, Stewart, Alexandre F.R, Tesson, Frederique, Klein, George J, Yee, Raymond, Skanes, Allan C, Guiraudon, Gerard M, Ebihara, Lisa, Bai, Donglin

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Lamin A/C mutations in dilated cardiomyopathy von Tesson, Frédérique, Saj, Michal, Uvaize, Musfira Mohamed, Nicolas, Hannah, Płoski, Rafał, Bilińska, Zofia

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Localization of I2-imidazoline binding sites on monoamine oxidases von Tesson, F, Limon-Boulez, I, Urban, P, Puype, M, Vandekerckhove, J, Coupry, I, Pompon, D, Parini, A

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Protein Kinase C Alpha Cellular Distribution, Activity, and Proximity with Lamin A/C in Striated Muscle Laminopathies von Nicolas, Hannah A, Bertrand, Anne T, Labib, Sarah, Mohamed-Uvaize, Musfira, Bolongo, Pierrette M, Wu, Wen Yu, Bilińska, Zofia T, Bonne, Gisèle, Akimenko, Marie-Andrée, Tesson, Frédérique

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Characterization of a Unique Genetic Variant in the β1-adrenoceptor Gene and Evaluation of its Role in Idiopathic Dilated Cardiomyopathy von Tesson, Frédérique, Charron, Philippe, Peuchmaurd, Mireille, Nicaud, Viviane, Cambien, François, Tiret, Laurence, Poirier, Odette, Desnos, Michel, Jullières, Yves, Amouyel, Philippe, Roizès, Gérard, Dorent, Richard, Schwartz, Ketty, Komajda, Michel

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The TaqIA RFLP is associated with attenuated intervention-induced body weight loss and increased carbohydrate intake in post-menopausal obese women von Cameron, Jameason D, Riou, Marie-Ève, Tesson, Frédérique, Goldfield, Gary S, Rabasa-Lhoret, Rémi, Brochu, Martin, Doucet, Éric

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Acyl-CoA synthetase long-chain 5 genotype is associated with body composition changes in response to lifestyle interventions in postmenopausal women with overweight and obesity: a... von Rajkumar, Abishankari, Lamothe, Gilles, Bolongo, Pierrette, Harper, Mary-Ellen, Adamo, Kristi, Doucet, Éric, Rabasa-Lhoret, Remi, Prud'homme, Denis, Tesson, Frédérique

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Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption von Gupta, Pallavi, Bilinska, Zofia T., Sylvius, Nicolas, Boudreau, Emilie, Veinot, John P., Labib, Sarah, Bolongo, Pierrette M., Hamza, Akil, Jackson, Tracy, Ploski, Rafal, Walski, Michal, Grzybowski, Jacek, Walczak, Ewa, Religa, Grzegorz, Fidzianska, Anna, Tesson, Frédérique

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Can Circulating Cardiac Biomarkers Be Helpful in the Assessment of LMNA Mutation Carriers? von Chmielewski, Przemyslaw, Michalak, Ewa, Kowalik, Ilona, Franaszczyk, Maria, Sobieszczanska-Malek, Malgorzata, Truszkowska, Grazyna, Stepien-Wojno, Malgorzata, Biernacka, Elzbieta Katarzyna, Foss-Nieradko, Bogna, Lewandowski, Michal, Oreziak, Artur, Bilinska, Maria, Kusmierczyk, Mariusz, Tesson, Frédérique, Grzybowski, Jacek, Zielinski, Tomasz, Ploski, Rafal, Bilinska, Zofia T

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Still Building on Candidate-Gene Strategy in Hypertension? von Tesson, Frédérique, Leenen, Frans H.H

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Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult population von CHARRON, P, DUBOURG, O, BOUHOUR, J.-B, SCHWARTZ, K, KOMAJDA, M, DESNOS, M, ISNARD, R, HAGEGE, A, MILLAIRE, A, CARRIER, L, BONNE, G, TESSON, F, RICHARD, P

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Peroxisome Proliferator-activated Receptor γ 2 and Acyl-CoA Synthetase 5 Polymorphisms Influence Diet Response von Adamo, Kristi B, Dent, Robert, Langefeld, Carl D, Cox, Miranda, Williams, Kathryn, Carrick, Kevin M, Stuart, Joan S, Sundseth, Scott S, Harper, Mary-Ellen, McPherson, Ruth, Tesson, Frédérique

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