The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesity von Maillard, A M, Ruef, A, Pizzagalli, F, Migliavacca, E, Hippolyte, L, Adaszewski, S, Dukart, J, Ferrari, C, Conus, P, Männik, K, Zazhytska, M, Siffredi, V, Maeder, P, Kutalik, Z, Kherif, F, Hadjikhani, N, Beckmann, J S, Reymond, A, Draganski, B, Jacquemont, S

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The Wnt receptor FZD1 mediates chemoresistance in neuroblastoma through activation of the Wnt β-catenin pathway von Flahaut, M, Meier, R, Coulon, A, Nardou, K A, Niggli, F K, Martinet, D, Beckmann, J S, Joseph, J-M, Mühlethaler-Mottet, A, Gross, N

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FoldIndex©: a simple tool to predict whether a given protein sequence is intrinsically unfolded von Prilusky, Jaime, Felder, Clifford E., Zeev-Ben-Mordehai, Tzviya, Rydberg, Edwin H., Man, Orna, Beckmann, Jacques S., Silman, Israel, Sussman, Joel L.

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Molecular adaptations of neuromuscular disease-associated proteins in response to eccentric exercise in human skeletal muscle von Féasson, L., Stockholm, D., Freyssenet, D., Richard, I., Duguez, S., Beckmann, J. S., Denis, C.

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Penetrance of marked cognitive impairment in older male carriers of the FMR1 gene premutation von Sévin, M, Kutalik, Z, Bergman, S, Vercelletto, M, Renou, P, Lamy, E, Vingerhoets, F J, Di Virgilio, G, Boisseau, P, Bezieau, S, Pasquier, L, Rival, J-M, Beckmann, J S, Damier, P, Jacquemont, S

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c-Jun N-terminal kinase JNK participates in cytokine- and isolation stress-induced rat pancreatic islet apoptosis von Abdelli, S, Abderrahmani, A, Hering, B. J, Beckmann, J. S, Bonny, C

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JNK3 is abundant in insulin-secreting cells and protects against cytokine-induced apoptosis von Abdelli, S, Puyal, J, Bielmann, C, Buchillier, V, Abderrahmani, A, Clarke, P. G. H, Beckmann, J. S, Bonny, C

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Secondary calpain3 deficiency in 2q-linked muscular dystrophy titin is the candidate gene von HARAVUORI, H, VIHOLA, A, BECKMANN, J. S, UDD, B, STRAUB, V, AURANEN, M, RICHARD, I, MARCHAND, S, VOIT, T, LABEIT, S, SOMER, H, PELTONEN, L

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Genetic characterization of CHO production host DG44 and derivative recombinant cell lines von Derouazi, M., Martinet, D., Besuchet Schmutz, N., Flaction, R., Wicht, M., Bertschinger, M., Hacker, D.L., Beckmann, J.S., Wurm, F.M.

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Dysferlin is a Plasma Membrane Protein and is Expressed Early in Human Development von Anderson, Louise V. B., Davison, Keith, Moss, Jennifer A., Young, Carol, Cullen, Michael J., Walsh, John, Johnson, Margaret A., Bashir, Rumaisa, Britton, Stephen, Keers, Sharon, Argov, Zohar, Mahjneh, Ibrahim, Fougerousse, Françoise, Beckmann, Jacques S., Bushby, Kate M. D.

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Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy von AOKI, M, LIU, J, BELEY, C, MCKENNA-YASEK, D, ARAHATA, K, BOHLEGA, S, CUPLER, E, ILLA, I, MAJNEH, I, BAROHN, R. J, URTIZBEREA, J. A, FARDEAU, M, RICHARD, I, AMATO, A, ANGELINI, C, BUSHBY, K, BECKMANN, J. S, BROWN, R. H, BASHIR, R, BRITTON, S, KEERS, S. M, OELTJEN, J, BROWN, H. E. V, MARCHAND, S, BOURG, N

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Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome von Grateau, Gilles, Beckmann, Jacques S, Drenth, Joost P.H, van de Velde-Visser, Saskia D, van der Meer, Jos W.M, Delpech & contributing members of the International Hyper-IgD Study Group, Marc, de Jong, Jan G.N, Cuisset, Laurence, Vasseur, Christian

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Series of Exon-Skipping Events in the Elastic Spring Region of Titin as the Structural Basis for Myofibrillar Elastic Diversity von Freiburg, Alexandra, Trombitas, Karoly, Hell, Wolfgang, Cazorla, Olivier, Fougerousse, Francoise, Centner, Thomas, Kolmerer, Bernhard, Witt, Christian, Beckmann, Jaques S, Gregorio, Carol C, Granzier, Henk, Labeit, Siegfried

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A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B von Bushby, Kate, Bashir, Rumaisa, Britton, Stephen, Strachan, Tom, Keers, Sharon, Vafiadaki, Elizabeth, Lako, Majlinda, Richard, Isabelle, Marchand, Sylvie, Bourg, Nathalie, Argov, Zohar, Sadeh, Menachem, Mahjneh, Ibrahim, Marconi, Giampiero, Passos-Bueno, Maria Rita, Moreira, Eloisa de S, Zatz, Mayana, Beckmann, Jacques S

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Confirmation of the origin of NISCH syndrome von Feldmeyer, L., Huber, M., Fellmann, F., Beckmann, J.S., Frenk, E., Hohl, D.

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Dynamic Molecular Combing: Stretching the Whole Human Genome for High-Resolution Studies von Michalet, Xavier, Ekong, Rosemary, Fougerousse, Françoise, Rousseaux, Sophie, Schurra, Catherine, Hornigold, Nick, van Slegtenhorst, Marjon, Wolfe, Jonathan, Povey, Sue, Beckmann, Jacques S., Bensimon, Aaron

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Stable Expression of Calpain 3 from a Muscle Transgene in vivo: Immature Muscle in Transgenic Mice Suggests a Role for Calpain 3 in Muscle Maturation von Spencer, M. J., Guyon, J. R., Sorimachi, H., Potts, A., Richard, I., Herasse, M., Chamberlain, J., Dalkilic, I., Kunkel, L. M., Beckmann, J. S.

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New quality measure for SNP array based CNV detection von Macé, A, Tuke, M A, Beckmann, J S, Lin, L, Jacquemont, S, Weedon, M N, Reymond, A, Kutalik, Z

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Autosomal dominant lateral temporal epilepsy: Clinical and genetic study of a large basque pedigree linked to chromosome 10q von Poza, J. J., Sáenz, A., Martínez-Gil, A., Cheron, N., Cobo, A. M., Urtasun, M., Martí-Massó, J. F., Grid, D., Beckmann, J. S., Prud'Homme, J. F., López De Munain, A.

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Circadian regulation of islet genes involved in insulin production and secretion von Allaman-Pillet, N., Roduit, R., Oberson, A., Abdelli, S., Ruiz, J., Beckmann, J.S., Schorderet, D.F., Bonny, C.

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