Artériopathie et hétérogénéité artérielle von Gouëffic, Y., Davaine, J.-M., Merlini, T., Rimbert, A., Hérisson, F., Heymann, M.-F., Heymann, D., Steenman, M., Lambert, G.

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Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour von Steenman, Marja J. C, Rainier, Shirley, Dobry, Craig J, Grundy, Paul, Horon, Isabelle L, Feinberg, Andrew P

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Transcriptomal analysis of failing and nonfailing human hearts von Steenman, M, Chen, Y.-W, Le Cunff, M, Lamirault, G, Varro, A, Hoffman, E, Leger, J. J

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Global/temporal gene expression in diaphragm and hindlimb muscles of dystrophin-deficient (mdx) mice von Rouger, Karl, Le Cunff, Martine, Steenman, Marja, Potier, Marie-Claude, Gibelin, Nathalie, Dechesne, Claude A, Leger, Jean J

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Arterial heterogeneity von Gouëffic, Y, Davaine, J-M, Merlini, T, Rimbert, A, Hérisson, F, Heymann, M-F, Heymann, D, Steenman, M, Lambert, G

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Human atrial ion channel and transporter subunit gene-expression remodeling associated with valvular heart disease and atrial fibrillation von GABORIT, Nathalie, STEENMAN, Marja, ESCANDE, Denis, NATTEL, Stanley, DEMOLOMBE, Sophie, LAMIRAULT, Guillaume, LE MEUR, Nolwenn, LE BOUTER, Sabrina, LANDE, Gilles, LEGER, Jean, CHARPENTIER, Flavien, CHRIST, Torsten, DOBREV, Dobromir

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Multiple Genetic Loci within 11p15 Defined by Beckwith-Wiedemann Syndrome Rearrangement Breakpoints and Subchromosomal Transferable Fragments von Hoovers, J M, Kalikin, L M, Johnson, L A, Alders, M, Redeker, B, Law, D J, Bliek, J, Steenman, M, Benedict, M, Wiegant, J, Lengauer, C, Taillon-Miller, P, Schlessinger, D, Edwards, M C, Elledge, S J, Ivens, A, Westerveld, A, Little, P, Mannens, M, Feinberg, A P

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Mouse model of SCN5A-linked hereditary lenègre's disease : Age-related conduction slowing and myocardial fibrosis von ROYER, Anne, VAN VEEN, Toon A. B, RICHER, Christine, ESCOUBET, Brigitte, JARRY-GUICHARD, Thérèse, COLLEDGE, William H, GROS, Daniel, DE BAKKER, Jacques M. T, GRACE, Andrew A, ESCANDE, Denis, CHARPENTIER, Flavien, LE BOUTER, Sabrina, MARIONNEAU, Céline, GRIOL-CHARHBILI, Violaine, LEONI, Anne-Laure, STEENMAN, Marja, VAN RIJEN, Harold V. M, DEMOLOMBE, Sophie, GODDARD, Catharine A

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Comparative genomic hybridization analysis of hepatoblastomas: additional evidence for a genetic link with Wilms tumor and rhabdomyosarcoma von Steenman, M., Tomlinson, G., Westerveld, A., Mannens, M.

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L009 Changes in cardiac transcriptome induced by altered corticosteroid receptor signaling in the heart von Latouche, C, Sainte-marie, Y, Steenman, M, Léger, J, Fejes-toth, A, Farman, N, Jaisser, F

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Shared gene expression profile between aging and diseased hearts in man von Steenman, M., Stefani, M., Thebaud, N., Szüts, V., Varro, A., Dos Remedios, C., Houlgatte, R.

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Gene expression profile associated with chronic atrial fibrillation and underlying valvular heart disease in man von Lamirault, Guillaume, Gaborit, Nathalie, Le Meur, Nolwenn, Chevalier, Catherine, Lande, Gilles, Demolombe, Sophie, Escande, Denis, Nattel, Stanley, Léger, Jean J., Steenman, Marja

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Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia von Mannens, M, Hoovers, J M, Redeker, E, Verjaal, M, Feinberg, A P, Little, P, Boavida, M, Coad, N, Steenman, M, Bliek, J

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Delineation and physical separation of novel translocation breakpoints on chromosome 1p in two genetically closely associated childhood tumors von Steenman, M.J.C., Zijlstra, N., Kruitbosch, D.L., Wiesmeijer, C., Larizza, L., Voûte, P.A., Westerveld, A., Mannens, M.M.A.M.

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Identification of signalling pathways potentially involved in the development of heart failure with preserved ejection fraction von Dhot, J., Steenman, M., Prat, V., Ferron, M., Persello, A., Erraud, A., Rozec, B., Lauzier, B., Gauthier, C.

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Identification of metabolic targets and signalling pathways involved in the pathophysiology of heart failure with preserved ejection fraction von Dhot, J., Prat, V., Ferron, M., Erraud, A., Aillerie, V., Erfanian, M., Tesse, A., Rozec, B., Steenman, M., Gauthier, C., Lauzier, B.

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Genetics of Beckwith-Wiedemann syndrome-associated tumors: Common genetic pathways von Steenman, Marja, Westerveld, Andries, Mannens, Marcel

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Distinct molecular portraits of human failing hearts identified by dedicated cDNA microarrays von Steenman, Marja, Lamirault, Guillaume, Le Meur, Nolwenn, Le Cunff, Martine, Escande, Denis, Léger, Jean J.

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A dynamic, web-accessible resource to process raw microarray scan data into consolidated gene expression values: importance of replication von Le Meur, Nolwenn, Lamirault, Guillaume, Bihouée, Audrey, Steenman, Marja, Bédrine-Ferran, Hélène, Teusan, Raluca, Ramstein, Gérard, Léger, Jean J.

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Gene expression profiling in human cardiovascular disease von Steenman, Marja, Lamirault, Guillaume, Le Meur, Nolwenn, Léger, Jean J.

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