Ablation of DNA-methyltransferase 3A in skeletal muscle does not affect energy metabolism or exercise capacity von Small, Lewin, Ingerslev, Lars R., Manitta, Eleonora, Laker, Rhianna C., Hansen, Ann N., Deeney, Brendan, Carrie, Alain, Couvert, Philippe, Barres, Romain

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Insights into medical students' perceptions of work culture during the COVID-19 pandemic: a mixed method study von Mouchabac, Stephane, Adrien, Vladimir, Diot, Thomas, Renaud, Marie-Christine, Carrié, Alain, Bourla, Alexis, Ferreri, Florian

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Familial hypercholesterolemia: experience from France von Rabès, Jean-Pierre, Béliard, Sophie, Carrié, Alain

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Lessons from the impact of COVID-19 on medical educational continuity and practices von Vatier, Camille, Carrie, Alain, Renaud, Marie-Christine, Simon-Tillaux, Noemie, Hertig, Alexandre, Jeru, Isabelle

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Clinical Expression of Familial Hypercholesterolemia in Patients from France and French Canada Carrying Identical-by-Descent Pathogenic LDLR Gene Variants: A Proof-of-Concept Study von Larouche, Miriam, Bluteau, Olivier, Carrié, Alain, Lauzière, Alex, Khoury, Etienne, Brisson, Diane, Gaudet, Daniel, Gallo, Antonio

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Robust validation of methylation levels association at CPT1A locus with lipid plasma levels von Gagnon, France, Aïssi, Dylan, Carrié, Alain, Morange, Pierre-Emmanuel, Trégouët, David-Alexandre

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IL1 receptor accessory protein like, a protein involved in X-linked mental retardation, interacts with Neuronal Calcium Sensor-1 and regulates exocytosis von Bahi, Nadia, Friocourt, Gaelle, Carrié, Alain, Graham, Margaret E., Weiss, Jamie L., Chafey, Philippe, Fauchereau, Fabien, Burgoyne, Robert D., Chelly, Jamel

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LDL-apheresis depletes apoE-HDL and pre-β1-HDL in familial hypercholesterolemia: relevance to atheroprotection von Orsoni, Alexina, Saheb, Samir, Levels, Johannes H.M., Dallinga-Thie, Geesje, Atassi, Marielle, Bittar, Randa, Robillard, Paul, Bruckert, Eric, Kontush, Anatol, Carrié, Alain, Chapman, M. John

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Evaluation of a semi-automatic isoelectric focusing method for apolipoprotein E phenotyping von Bittar, Randa, Carrié, Alain, Nouadje, Georges, Cherfils, Corinne, Fesel-Fouquier, Valérie, Barbot-Trystram, Laurence, Giral, Philippe, Bonnefont-Rousselot, Dominique

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Robust validation of methylation levels association at CPT1A locus with lipid plasma levels1 von Gagnon, France, Aïssi, Dylan, Carrié, Alain, Morange, Pierre-Emmanuel, Trégouët, David-Alexandre

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The Clinical Genome Resource (ClinGen) Familial Hypercholesterolemia Variant Curation Expert Panel consensus guidelines for LDLR variant classification von Chora, Joana R., Iacocca, Michael A., Tichý, Lukáš, Wand, Hannah, Kurtz, C. Lisa, Zimmermann, Heather, Leon, Annette, Williams, Maggie, Humphries, Steve E., Hooper, Amanda J., Trinder, Mark, Brunham, Liam R., Costa Pereira, Alexandre, Jannes, Cinthia E., Chen, Margaret, Chonis, Jessica, Wang, Jian, Kim, Serra, Johnston, Tami, Soucek, Premysl, Kramarek, Michal, Leigh, Sarah E., Carrié, Alain, Sijbrands, Eric J., Hegele, Robert A., Freiberger, Tomáš, Knowles, Joshua W., Bourbon, Mafalda

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MECP2 mutations account for most cases of typical forms of Rett syndrome von Bienvenu, T, Carrié, A, de Roux, N, Vinet, M C, Jonveaux, P, Couvert, P, Villard, L, Arzimanoglou, A, Beldjord, C, Fontes, M, Tardieu, M, Chelly, J

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APOE Molecular Spectrum in a French Cohort with Primary Dyslipidemia von Abou Khalil, Yara, Marmontel, Oriane, Ferrières, Jean, Paillard, François, Yelnik, Cécile, Carreau, Valérie, Charrière, Sybil, Bruckert, Eric, Gallo, Antonio, Giral, Philippe, Philippi, Anne, Bluteau, Olivier, Boileau, Catherine, Abifadel, Marianne, Di-Filippo, Mathilde, Carrié, Alain, Rabès, Jean-Pierre, Varret, Mathilde

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LDL apheresis as an alternate method for plasma LPS purification in healthy volunteers and dyslipidemic and septic patients von Dargent, Auguste, Pais de Barros, Jean-Paul, Saheb, Samir, Bittar, Randa, Le Goff, Wilfried, Carrié, Alain, Gautier, Thomas, Fournel, Isabelle, Rerole, Anne Laure, Choubley, Hélène, Masson, David, Lagrost, Laurent, Quenot, Jean-Pierre

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Effect of the LDL receptor mutation type on incident major adverse cardiovascular events in familial hypercholesterolaemia von Paquette, Martine, Carrié, Alain, Bernard, Sophie, Cariou, Bertrand, Hegele, Robert A, Genest, Jacques, Trinder, Mark, Brunham, Liam R, Béliard, Sophie, Baass, Alexis

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The singular French PCSK9-p.Ser127Arg gain-of-function variant: A significant player in cholesterol levels from a 775-year-old common ancestor von Azar, Yara, Ludwig, Thomas E., Le Bon, Hugo, Strøm, Thea Bismo, Bluteau, Olivier, Di-Filippo, Mathilde, Carrié, Alain, Chtioui, Hedi, Béliard, Sophie, Marmontel, Oriane, Fonteille, Annie, Gebhart, Maite, Peretti, Noël, Moulin, Philippe, Ferrières, Jean, Pradignac, Alain, Farnier, Michel, Gallo, Antonio, Yelnik, Cécile, Blom, Dirk, Génin, Emmanuelle, Bogsrud, Martin Prøven, Leren, Trond P., Boileau, Catherine, Abifadel, Marianne, Rabès, Jean-Pierre, Varret, Mathilde

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Parental origin of de novo MECP2 mutations in Rett syndrome von Girard, M, Couvert, P, Carrié, A, Tardieu, M, Chelly, J, Beldjord, C, Bienvenu, T

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Maternal Inheritance of Familial Hypercholesterolemia Gene Mutation Predisposes to Coronary Atherosclerosis as Assessed by Calcium Score in Adulthood von Mourre, Florian, Giorgi, Roch, Gallo, Antonio, Boccara, Franck, Bruckert, Eric, Carrié, Alain, Hankard, Regis, Inamo, Jocelyn, Laboureau, Sandrine, Moulin, Philippe, Valéro, René, Béliard, Sophie

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Intronic mutations outside of Alu-repeat-rich domains of the LDL receptor gene are a cause of familial hypercholesterolemia von AMSELLEM, Sabine, BRIFFAUT, Dorothée, DE GENNES, Jean Luc, BRUKERT, Eric, BENLIAN, Pascale, CARRIE, Alain, RABES, Jean Pierre, GIRARDET, Jean Philippe, FREDENRICH, Alexandre, MOULIN, Philippe, KREMPF, Michel, REZNIK, Yves, VIALETTES, Bernard

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Lipoprotein-apheresis in familial hypercholesterolemia: Long-term patient compliance in a French cohort von Beliard, Sophie, Gallo, Antonio, Duchêne, Emilie, Carrié, Alain, Bittar, Randa, Chapman, M. John, Bruckert, Eric, Saheb, Samir

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