Characterization of ketolactia in dairy cows during early lactation von Kowalski, Z.M., Sabatowicz, M., Barć, J., Jagusiak, W., Młocek, W., Van Saun, R.J., Dechow, C.D.

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Canola meal or soybean meal as protein source and the effect of microencapsulated sodium butyrate supplementation in calf starter mixture. II. Development of the gastrointestinal t... von Burakowska, K., Penner, G.B., Flaga, J., Przybyło, M., Barć, J., Wojciechowska-Puchałka, J., Wojtysiak, D., Kowalski, Z.M., Górka, P.

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Roles of leptin and resistin in metabolism, reproduction, and leptin resistance von Zieba, D.A., Biernat, W., Barć, J.

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Effect of supplemental sodium butyrate on gastrointestinal tract measurements in sheep von Górka, P, Śliwiński, B, Flaga, J, Barć, J, Olszewski, J, Godlewski, M M, Zabielski, R, Kowalski, Z M

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641 Effect of supplemental sodium butyrate on gastrointestinal tract measurements in sheep von Górka, P., Śliwiński, B., Flaga, J., Barć, J., Olszewski, J., Godlewski, M. M., Zabielski, R., Kowalski, Z. M.

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Effect of supplemental sodium butyrate on the activity of carbohydrate-digesting enzymes in the reticulo-ruminal digesta and brush border enzymes in sheep von Górka, P, Śliwiński, B, Miltko, R, Flaga, J, Barć, J, Godlewski, M M, Zabielski, R, Kowalski, Z M

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642 Effect of supplemental sodium butyrate on the activity of carbohydrate-digesting enzymes in the reticulo-ruminal digesta and brush border enzymes in sheep von Górka, P., Śliwiński, B., Miltko, R., Flaga, J., Barć, J., Godlewski, M. M., Zabielski, R., Kowalski, Z. M.

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HEY2 , A NOVEL SUSCEPTIBILITY GENE FOR BRUGADA SYNDROME, CONTROLS DEPOLARIZATION AND REPOLARIZATION GRADIENTS IN THE RVOT AND ACROSS THE VENTRICULAR WALL von Podliesna, S, Verkerk, A.O, Wolswinkel, R, Beekman, L, Barc, J, Gessler, M, Christoffels, V.M, Wilde, A.A, Remme, C.A, Bezzina, C.R

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Genome-Wide Association Analysis Identifies 3 Common Variants Predisposing to Brugada Syndrome, a Rare Disease with High Risk of Sudden Cardiac Death von Barc, J, Bezzina, C, Mizusawa, Y, Remme, C, Gourraud, J, Verkerk, A, Schwartz, P, Guicheney, P, Antzelevitch, C, Schulze-Bahr, E, Behr, E, Tfelt-Hanson, J, Kaab, S, Watanabe, H, Horie, M, Makita, N, Shimizu, W, Roden, D, Christoffels, V, Gessler, M, Wilde, A, Probst, V, Schott, J, Dina, C, Redon, R

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Role of common variants and new genes associated with arrhythmogenic cardiomyopathy von Barc, J, Ruffier, L, Simonet, F, Baron, E, Forest, V, Roux-Buisson, N, Crotti, L, Chevalier, P, Sommariva, E, Villard, E, Moore-Morris, T, Schott, J J, Gandjbakhch, E, Probst, V

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Modeling familial sinus node dysfunction with a large intergenic deletion between PITX2 and ANK2 using iPS cell-derived sinoatrial nodal-like cardiomyocytes von Aizawa, T, Makiyama, T, Murata, H, Takaki, T, Baudic, M, Gao, J, Imamura, T, Ohno, S, Yoshida, Y, Shimizu, W, Makita, N, Barc, J, Schott, J J, Horie, M, Kimura, T

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Population-specific and cross-ancestry genome-wide association study identifies shared genetic architecture and 6 new risk loci including CAMK2D associated for Brugada syndrome von Makita, N, Ishikawa, T, Masuda, T, Hachiya, T, Dina, C, Simonet, F, Tank, M W T, Wilde, A A, Redon, R, Bezzina, C R, Tanaka, T, Barc, J, Okada, Y, Schott, J J

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Syndromic cardiac disorder is associated with a non-coding deletion that induces a 3D chromatin remodeling and PITX2 expression dysregulation von Baudic, M, Murata, H, Bosada, F M, Souto Melo, U, Aizawa, T, Guedon, A, Lindenbaum, P, Gourraud, J B, Makita, N, Mundlos, S, Christoffels, V M, Makiyama, T, Probst, V, Schott, J J, Barc, J

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SURFBAT: a surrogate family-based association test building on large imputation reference panels von Herzig, A F, Rubinacci, S, Marenne, G, Perdry, H, Deleuze, J-F, Dina, C, Barc, J, Redon, R, Delaneau, O, Génin, E

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GENECHOC study: genetic markers of arrhythmic risk in heart failure von Anys, S, Rigade, S, Baron, E, Lecointe, S, Guyomarch, B, Klug, D, Babuty, D, Mansourati, J, Bordachar, P, Mabo, P, Thollet, A, Dina, C, Schott, J.J, Barc, J, Probst, V

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Genome-wide association study identifies 18 new susceptibility variants loci associated with Brugada Syndrome von Barc, J, Trados, R, Glinge, C, Simonet, F, Chiang, D, Jouni, M, Jurgens, S, The Brugada Syndrome Genetic Consortium, B.R.S, Tanck, M, Dina, C, Probst, V, Wilde, A, Redon, R, Schott, J.J, Bezzina, C

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Molecular mechanism of a new cardiac syndrome associated with a regulatory element deletion of chromosome 4q25 von Baudic, M, Murata, H, Le Scouarnec, S, Foucal, A, Lindenbaum, P, Ishikawa, T, Si-Tayeb, K, Gaborit, N, Makita, N, Makiyama, T, Shimizu, W, Vieyres, C, Probst, V, Schott, J.J, Barc, J

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98Risk stratification of arrhythmia and death in ARVC von Gourraud, J.B., Morio, F., Amara, N., Sacher, F., Mabo, P., Babuty, D., Mansourati, J., Pasquie, J.L., Maury, P., Jesel, L., Guyomarch, B., Kyndt, F., Barc, J., Thollet, A., Probst, V.

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Non-coding deletion induces 3D chromatin remodelling and PITX2 expression dysregulation associated with a syndromic cardiac disorder von Baudic, M., Murata, H., Bosada, F., Souto Melo, U., Aizawa, T., Guedon, A., Lindenbaum, P., Gourraud, J.-B., Makita, N., Mundlos, S., Christoffels, V.M., Makiyama, T., Probst, V., Schott, J.-J., Barc, J.

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G022 Loss-of-function mutation of the cardiac CAV1.2 channel in the short QT syndrome von Amarouch, M, Barc, J, Béziau, D, Kyndt, F, Le Marec, H, Babuty, D, Probst, V, Schott, J.-J, Baro, I

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