检索结果 - Bayès, Mónica

Design and evaluation of a panel of single-nucleotide polymorphisms in microRNA genomic regions for association studies in human disease 由 Muiños-Gimeno, Margarita, Montfort, Magda, Bayés, Mònica, Estivill, Xavier, Espinosa-Parrilla, Yolanda

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Mutational Mechanisms of Williams-Beuren Syndrome Deletions 由 Bayés, Mònica, Magano, Luis F., Rivera, Núria, Flores, Raquel, A. Pérez Jurado, Luis

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Low Exchangeability of Selenocysteine, the 21st Amino Acid, in Vertebrate Proteins 由 Castellano, Sergi, Andrés, Aida M., Bosch, Elena, Bayes, Mònica, Guigó, Roderic, Clark, Andrew G.

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Characterization of alternatively spliced products and tissue-specific isoforms of USP28 and USP25 由 Valero, Rebeca, Bayés, Mònica, Francisca Sánchez-Font, M, González-Angulo, Olga, Gonzàlez-Duarte, Roser, Marfany, Gemma

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Copy number variation at the 7q11.23 segmental duplications is a susceptibility factor for the Williams-Beuren syndrome deletion 由 Cuscó, Ivon, Corominas, Roser, Bayés, Mònica, Flores, Raquel, Rivera-Brugués, Núria, Campuzano, Victoria, Pérez-Jurado, Luis A.

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The Fungus Candida albicans Tolerates Ambiguity at Multiple Codons 由 Simões, João, Bezerra, Ana R., Moura, Gabriela R., Araújo, Hugo, Gut, Ivo, Bayes, Mónica, Santos, Manuel A. S.

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Hemizygosity at the NCF1 Gene in Patients with Williams-Beuren Syndrome Decreases Their Risk of Hypertension 由 Del Campo, Miguel, Antonell, Anna, Magano, Luis F., Muñoz, Francisco J., Flores, Raquel, Bayés, Mònica, Pérez Jurado, Luis A.

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Association between the NMDA glutamate receptor GRIN2B gene and obsessive–compulsive disorder 由 Alonso, Pino, Gratacós, Mónica, Segalàs, Cinto, Escaramís, Georgia, Real, Eva, Bayés, Mónica, Labad, Javier, López-Solà, Clara, Estivill, Xavier, Menchón, José M.

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Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes 由 Torrico, Bàrbara, Shaw, Alex D., Mosca, Roberto, Vivó-Luque, Norma, Hervás, Amaia, Fernàndez-Castillo, Noèlia, Aloy, Patrick, Bayés, Mònica, Fullerton, Janice M., Cormand, Bru, Toma, Claudio

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Colorectal Adenomas Contain Multiple Somatic Mutations That Do Not Coincide with Synchronous Adenocarcinoma Specimens 由 Vaqué, José P., Martínez, Nerea, Varela, Ignacio, Fernández, Fidel, Mayorga, Marta, Derdak, Sophia, Beltrán, Sergi, Moreno, Thaidy, Almaraz, Carmen, De las Heras, Gonzalo, Bayés, Mónica, Gut, Ivo, Crespo, Javier, Piris, Miguel A.

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Correction: Colorectal Adenomas Contain Multiple Somatic Mutations That Do Not Coincide with Synchronous Adenocarcinoma Specimens 由 Vaqué, José P., Martínez, Nerea, Varela, Ignacio, Fernández, Fidel, Mayorga, Marta, Derdak, Sophia, Beltrán, Sergi, Moreno, Thaidy, Almaraz, Carmen, De las Heras, Gonzalo, Bayés, Mónica, Gut, Ivo, Crespo, Javier, Piris, Miguel A.

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Adaptive Mistranslation Accelerates the Evolution of Fluconazole Resistance and Induces Major Genomic and Gene Expression Alterations in Candida albicans 由 Weil, Tobias, Santamaría, Rodrigo, Lee, Wanseon, Rung, Johan, Tocci, Noemi, Abbey, Darren, Bezerra, Ana R., Carreto, Laura, Moura, Gabriela R., Bayés, Mónica, Gut, Ivo G., Csikasz-Nagy, Attila, Cavalieri, Duccio, Berman, Judith, Santos, Manuel A. S.

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Reversion of a fungal genetic code alteration links proteome instability with genomic and phenotypic diversification 由 Bezerra, Ana R., Simões, João, Lee, Wanseon, Rung, Johan, Weil, Tobias, Gut, Ivo G., Gut, Marta, Bayés, Mónica, Rizzetto, Lisa, Cavalieri, Duccio, Giovannini, Gloria, Bozza, Silvia, Romani, Luigina, Kapushesky, Misha, Moura, Gabriela R., Santos, Manuel A. S.

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Spinal Muscular Atrophy Associated with Progressive Myoclonic Epilepsy Is Caused by Mutations in ASAH1 由 Zhou, Jie, Tawk, Marcel, Tiziano, Francesco Danilo, Veillet, Julien, Bayes, Monica, Nolent, Flora, Garcia, Virginie, Servidei, Serenella, Bertini, Enrico, Castro-Giner, Francesc, Renda, Yavuz, Carpentier, Stéphane, Andrieu-Abadie, Nathalie, Gut, Ivo, Levade, Thierry, Topaloglu, Haluk, Melki, Judith

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Microarray and deep sequencing cross-platform analysis of the mirRNome and isomiR variation in response to epidermal growth factor 由 Llorens, Franc, Hummel, Manuela, Pantano, Lorena, Pastor, Xavier, Vivancos, Ana, Castillo, Ester, Mattlin, Heidi, Ferrer, Anna, Ingham, Matthew, Noguera, Marc, Kofler, Robert, Dohm, Juliane C, Pluvinet, Raquel, Bayés, Mònica, Himmelbauer, Heinz, del Rio, José Antonio, Martí, Eulàlia, Sumoy, Lauro

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Differential Association of Circadian Genes with Mood Disorders: CRY1 and NPAS2 are Associated with Unipolar Major Depression and CLOCK and VIP with Bipolar Disorder 由 Soria, Virginia, Martínez-Amorós, Èrika, Escaramís, Geòrgia, Valero, Joaquín, Pérez-Egea, Rosario, García, Cecilia, Gutiérrez-Zotes, Alfonso, Puigdemont, Dolors, Bayés, Mònica, Crespo, José M, Martorell, Lourdes, Vilella, Elisabet, Labad, Antonio, Vallejo, Julio, Pérez, Víctor, Menchón, José M, Estivill, Xavier, Gratacòs, Mònica, Urretavizcaya, Mikel

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Multiple platform assessment of the EGF dependent transcriptome by microarray and deep tag sequencing analysis 由 Llorens, Franc, Hummel, Manuela, Pastor, Xavier, Ferrer, Anna, Pluvinet, Raquel, Vivancos, Ana, Castillo, Ester, Iraola, Susana, Mosquera, Ana M, González, Eva, Lozano, Juanjo, Ingham, Matthew, Dohm, Juliane C, Noguera, Marc, Kofler, Robert, del Río, Jose Antonio, Bayés, Mònica, Himmelbauer, Heinz, Sumoy, Lauro

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Recurrent inactivation of STAG2 in bladder cancer is not associated with aneuploidy 由 Balbás-Martínez, Cristina, Sagrera, Ana, Carrillo-de-Santa-Pau, Enrique, Earl, Julie, Márquez, Mirari, Vazquez, Miguel, Lapi, Eleonora, Castro-Giner, Francesc, Beltran, Sergi, Bayés, Mònica, Carrato, Alfredo, Cigudosa, Juan C., Domínguez, Orlando, Gut, Marta, Herranz, Jesús, Juanpere, Núria, Kogevinas, Manolis, Langa, Xavier, López-Knowles, Elena, Lorente, José A., Lloreta, Josep, Pisano, David G., Richart, Laia, Rico, Daniel, Salgado, Rocío N., Tardón, Adonina, Chanock, Stephen, Heath, Simon, Valencia, Alfonso, Losada, Ana, Gut, Ivo, Malats, Núria, Real, Francisco X.

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Case–Control Genome-Wide Association Study of Persistent Attention-Deficit Hyperactivity Disorder Identifies FBXO33 as a Novel Susceptibility Gene for the Disorder 由 Sánchez-Mora, Cristina, Ramos-Quiroga, Josep A, Bosch, Rosa, Corrales, Montse, Garcia-Martínez, Iris, Nogueira, Mariana, Pagerols, Mireia, Palomar, Gloria, Richarte, Vanesa, Vidal, Raquel, Arias-Vasquez, Alejandro, Bustamante, Mariona, Forns, Joan, Gross-Lesch, Silke, Guxens, Monica, Hinney, Anke, Hoogman, Martine, Jacob, Christian, Jacobsen, Kaya K, Kan, Cornelis C, Kiemeney, Lambertus, Kittel-Schneider, Sarah, Klein, Marieke, Onnink, Marten, Rivero, Olga, Zayats, Tetyana, Buitelaar, Jan, Faraone, Stephen V, Franke, Barbara, Haavik, Jan, Johansson, Stefan, Lesch, Klaus-Peter, Reif, Andreas, Sunyer, Jordi, Bayés, Mònica, Casas, Miguel, Cormand, Bru, Ribasés, Marta

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Multicenter Analysis of the SLC6A3/DAT1 VNTR Haplotype in Persistent ADHD Suggests Differential Involvement of the Gene in Childhood and Persistent ADHD 由 Franke, Barbara, Vasquez, Alejandro Arias, Johansson, Stefan, Hoogman, Martine, Romanos, Jasmin, Boreatti-Hümmer, Andrea, Heine, Monika, Jacob, Christian P, Lesch, Klaus-Peter, Casas, Miguel, Ribasés, Marta, Bosch, Rosa, Sánchez-Mora, Cristina, Gómez-Barros, Núria, Fernàndez-Castillo, Noèlia, Bayés, Mònica, Halmøy, Anne, Halleland, Helene, Landaas, Elisabeth T, Fasmer, Ole B, Knappskog, Per M, Heister, Angelien J G A M, Kiemeney, Lambertus A, Kooij, J J Sandra, Boonstra, A Marije, Kan, Cees C, Asherson, Philip, Faraone, Stephen V, Buitelaar, Jan K, Haavik, Jan, Cormand, Bru, Ramos-Quiroga, Josep Antoni, Reif, Andreas

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