Search Results - "Saez, M. E."

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    EDIL3 promotes epithelial–mesenchymal transition and paclitaxel resistance through its interaction with integrin αVβ3 in cancer cells by Gasca, J., Flores, M. L., Jiménez-Guerrero, R., Sáez, M. E., Barragán, I., Ruíz-Borrego, M., Tortolero, M., Romero, F., Sáez, C., Japón, M. A.

    Published in Cell death discovery (16-09-2020)
    “…Epithelial–mesenchymal transition (EMT) has recently been associated with tumor progression, metastasis, and chemotherapy resistance in several tumor types. We…”
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    Journal Article
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    Specific polymorphisms in the RET proto-oncogene are over-represented in patients with Hirschsprung disease and may represent loci modifying phenotypic expression by BORREGO, S, SAEZ, M. E, RUIZ, A, GIMM, O, LOPEZ-ALONSO, M, ANTINOLO, G, ENG, C

    Published in Journal of medical genetics (01-10-1999)
    “…Hirschsprung disease (HSCR) is a common genetic disorder presenting with functional intestinal obstruction secondary to enteric aganglionosis. HSCR can be…”
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    Journal Article
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    Whole-genome conditional two-locus analysis identifies novel candidate genes for late-onset Parkinson’s disease by González-Pérez, A., Gayán, J., Marín, J., Galán, J. J., Sáez, M. E., Real, L. M., Antúnez, C., Ruiz, A.

    Published in Neurogenetics (01-07-2009)
    “…Whole-genome epistasis analysis may add a new layer of knowledge to whole-genome association studies, permitting the identification of new candidate genes…”
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    Journal Article
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    RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung disease by Borrego, Salud, Ruiz, Agustín, Saez, María Eugenia, Gimm, Oliver, Gao, Xin, López-Alonso, Manuel, Hernández, Antonio, Wright, Fred A, Antiñolo, Guillermo, Eng, Charis

    Published in Journal of medical genetics (01-08-2000)
    “…BACKGROUND Hirschsprung disease (HSCR), which may be sporadic or familial, occurs in 1:5000 live births and presents with functional intestinal obstruction…”
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    Journal Article
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    GAB2 gene does not modify the risk of Alzheimer’s disease in Spanish APOE 4 carriers by Ramírez-Lorca, Reposo, Boada, M., Saez, M. E., Hernandez, I., Mauleon, A., Rosende-Roca, M., Martinez-Lage, P., Gutierrez, M., Real, L. M., Lopez-Arrieta, J., Gayan, J., Antunez, C., Gonzalez-Perez, A., Tarraga, L., Ruiz, A.

    Published in The Journal of nutrition, health & aging (01-03-2009)
    “…Objectives The genetic basis of Alzheimer’s disease (AD) is being analyzed in multiple whole genome association studies (WGAS). The GAB2 gene has been proposed…”
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    Journal Article Conference Proceeding
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    Specific haplotypes of the CALPAIN-5 gene are associated with polycystic ovary syndrome by González, A., Sáez, M.E., Aragón, M.J., Galán, J.J., Vettori, P., Molina, L., Rubio, C., Real, L.M., Ruiz, Agustín, Ramírez-Lorca, R.

    Published in Human reproduction (Oxford) (01-04-2006)
    “…BACKGROUND: Polycystic ovary syndrome (PCOS) is a common endocrine disorder in women of reproductive age. The aim of the present study was to investigate the…”
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    Journal Article
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    Common variants in Alzheimer's disease and risk stratification by polygenic risk scores by Moreno-Grau, Sonia, Grenier-Boley, Benjamin, Andrade, Victor, Duron, Emmanuelle, Küçükali, Fahri, Pasquier, Florence, Sanchez-Garcia, Florentino, Nicolas, Gaël, Selbæk, Geir, Chêne, Geneviève, Hampel, Harald, Bailly, Henri, Zetterberg, Henrik, Alvarez, Ignacio, Appollonio, Ildebrando, Rainero, Innocenzo, Rosas Allende, Irene, Diehl-Schmid, Janine, Van Dongen, Jasper, Bis, Joshua C., Popp, Julius, Deckert, Jürgen, Buerger, Katharina, Fließbach, Klaus, Kilander, Lena, Weinhold, Leonie, Tremolizzo, Lucio, Bellenguez, Céline, Löwenmark, Malin, Hulsman, Marc, Spallazzi, Marco, Quintela, Inés, Dalmasso, Maria Carolina, Martínez-Larrad, María Teresa, Yannakoulia, Mary, Wagner, Michael, Scamosci, Michela, Calero, Miguel, Banaj, Nerisa, Scarmeas, Nikolaos, Hanon, Oliver, Peters, Oliver, Skrobot, Olivia Anna, Dionigi Rossi, Paolo, Holmans, Peter A., Fischer, Peter, Yang, Qiong, Vandenberghe, Rik, Ghidoni, Roberta, Sorbi, Sandro, Helisalmi, Seppo, Cervera-Carles, Laura, Fostinelli, Silvia, Djurovic, Srdjan, Menéndez-González, Manuel, Deramecourt, Vincent, Frank-García, Ana, Kehoe, Patrick Gavin, Sánchez-Juan, Pascual, García-Alberca, Jose María, Real, Luis M., Marquié, Marta, Moreno, Fermin, Amouyel, Philippe, Schellenberg, Gerard D., Sánchez-Valle, Raquel, Serrano-Ríos, Manuel, Andreassen, Ole A, Posthuma, Danielle, Lambert, Jean-Charles, Baquero, Miquel, García-Madrona, Sebastián, García-González, Pablo, Valero, Sergi, Sotolongo-Grau, Oscar, Ullgren, Abbe, Naj, Adam C., Benaque, Alba, Pérez-Cordón, Alba, Benussi, Alberto, Rábano, Alberto, Padovani, Alessandro, Squassina, Alessio, de Mendonça, Alexandre, Meggy, Alun, Schneider, Anja, Corbatón-Anchuelo, Arturo, Borroni, Barbara, Nordestgaard, Børge G., Masullo, Carlo, Martínez Rodríguez, Carmen, Muñoz-Fernandez, Carmen, Dufouil, Carole, Van Broeckhoven, Christine, Holmes, Clive, Buiza-Rueda, Dolores, Aarsland, Dag, Galimberti, Daniela, Scarpini, Elio, Rodriguez-Rodriguez, Eloy

    Published in Nature communications (2021)
    “…© The Author(s) 2021. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing,…”
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    Journal Article
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    Genome Wide Meta-Analysis identifies common genetic signatures shared by heart function and Alzheimer’s disease by Sáez, M. E., González-Pérez, A., Hernández-Olasagarre, B., Beà, A., Moreno-Grau, S., de Rojas, I., Monté-Rubio, G., Orellana, A., Valero, S., Comella, J. X., Sanchís, D., Ruiz, A.

    Published in Scientific reports (13-11-2019)
    “…Echocardiography has become an indispensable tool for the study of heart performance, improving the monitoring of individuals with cardiac diseases. Diverse…”
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    Journal Article
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    High prevalence of the C634Y mutation in the RET proto-oncogene in MEN 2A families in Spain by Sánchez, Beatriz, Robledo, Mercedes, Biarnes, Josefina, Sáez, María-Eugenia, Volpini, Victor, Benítez, Javier, Navarro, Elena, Ruiz, Agustín, Antiñolo, Guillermo, Borrego, Salud

    Published in Journal of medical genetics (01-01-1999)
    “…The RET proto-oncogene encodes a receptor tyrosine kinase expressed in neural crest derived tissues. Germline mutations in the RET proto-oncogene are…”
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    Journal Article
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    DI-034 Drug usage evaluation of abiraterone in metastasic castration resistant prostate cancer: 4 Years of experience by Palomares, MV Villacañas, Fernández, EM Sáez, García, G Martín, Domínguez, E Fernández, Hernández, MV Calvo

    “…BackgroundAbiraterione is an expensive drug indicated for the treatment of metastasic castration resistant prostate cancer. In order to optimise its use,…”
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    Journal Article
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    Absence of allelic imbalance involving EMSY, CAPN5, and PAK1 genes in papillary thyroid carcinoma by Hidalgo, M., Saez, M. E., Martinez-Tello, F. J., Moron, F. J., Ferrero-Herrero, E., Labalde-Martinez, M., Rigopoulou, D., Ballestin-Carcavilla, C., Ruiz, A., Royo, J. L., Ramirez-Lorca, R.

    Published in Journal of endocrinological investigation (01-07-2008)
    “…Papillary thyroid cancer (PTC) accounts for 80% of all thyroid malignancies, and genetic alterations associated to its etiology remain largely unknown…”
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    Journal Article
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    Renal decline in patients with atrial fibrillation treated with rivaroxaban or warfarin: a population-based cohort study in the United Kingdom by Garcia Rodriguez, L A, Balabanova, Y, Saez, M E, Brobert, G, Gonzalez-Perez, A

    Published in European heart journal (12-10-2021)
    “…Abstract Background A recent observational study (1) has suggested that renal decline among patients with non-valvular atrial fibrillation (NVAF) could be…”
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    Journal Article
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    Molecular analysis of the ret and GDNF genes in a family with multiple endocrine neoplasia type 2A and Hirschsprung disease by BORREGO, S, ENG, C, SANCHEZ, B, SAEZ, M.-E, NAVARRO, E, ANTINOLO, G

    “…The clinical association between multiple endocrine neoplasia type 2 (MEN2) and Hirschsprung disease (HSCR) is infrequent. Germline mutations of the ret…”
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    Journal Article
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    Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores by de Rojas, Itziar, Tesi, Niccolo, Zettergren, Anna, Montrreal, Laura, Antonell, Anna, Bis, Joshua C., González-Perez, Antonio, Calero, Miguel, Blesa, Rafael, Sotolongo-Grau, Oscar, Benaque, Alba, Benussi, Alberto, de Mendonça, Alexandre, Arias Pastor, Alfonso, Espinosa, Ana, Sanabria, Ángela, DeStefano, Anita L., Schneider, Anja, Haapasalo, Annakaisa, Tybjærg-Hansen, Anne, Hartmann, Annette M., Spottke, Annika, Corbatón-Anchuelo, Arturo, Arosio, Beatrice, Nacmias, Benedetta, Kunkle, Brian W., Charbonnier, Camille, Martínez Rodríguez, Carmen, Reynolds, Chandra A., Fenoglio, Chiara, Van Broeckhoven, Christine, Clark, Christopher, Buiza-Rueda, Dolores, Alcolea, Daniel, Grünblatt, Edna, Dardiotis, Efthimios, Conti, Elisa, Boerwinkle, Eric, Ferri, Evelyn, Pasquier, Florence, Mangialasche, Francesca, Hadjigeorgiou, Georgios, Spalletta, Gianfranco, Soininen, Hilkka, Rainero, Innocenzo, Hort, Jakub, Kornhuber, Johannes, Pineda, Juan A., Fortea, Juan, Popp, Julius, Buerger, Katharina, Molina-Porcel, Laura, Wang, Li-San, Farotti, Lucia, Tsolaki, Magda, Rosende-Roca, Maitée, Hulsman, Marc, Spallazzi, Marco, Bernal Sánchez-Arjona, María, Dalmasso, Maria Carolina, Fernández-Fuertes, Marta, Herrmann, Martin J., Vyhnalek, Martin, Yannakoulia, Mary, Schmid, Matthias, Armstrong, Nicola J., Skrobot, Olivia Anna, Quenez, Olivier, Bossù, Paola, Caffarra, Paolo, Dionigi Rossi, Paolo, Sakka, Paraskevi, Riederer, Peter, Kalaria, Rajesh N., Mayeux, Richard, Vandenberghe, Rik, Sorbi, Sandro, Hägg, Sara, Engelborghs, Sebastiaan, Helisalmi, Seppo, Kern, Silke, Boschi, Silvia, Fostinelli, Silvia, Gil, Silvia, Ciccone, Simona, Djurovic, Srdjan, Riedel-Heller, Steffi, Kuulasmaa, Teemu, del Ser, Teodoro, Ngandu, Tiia, García-Alberca, Jose María, Lleó, Alberto, Real, Luis M., Mir, Pablo, Scheltens, Philip, Holstege, Henne, Amouyel, Philippe, Blennow, Kaj, Andreassen, Ole A., Posthuma, Danielle

    Published in Nature communications (09-02-2023)
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    4CPS-264 Population pharmacokinetic model of etanercept in rheumatic disease: prognostic factors and dose recommendations by Sanchez-Hernandez, JG, Pérez-Blanco, JS, Beunza-Sola, M, Rebollo-Diaz, N, Saez-Fernandez, EM, Laso-Lucas, E, Rodriguez-Cajaraville, L, Calvo, MV

    “…BackgroundEtanercept is an approved monoclonal antibody for the treatment of rheumatic disease (RD). Individual clinical response to etanercept can be…”
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    Journal Article
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    4CPS-157 Vedolizumab: early experience and medium-term outcomes in inflammatory bowel disease by Nieto, L Pedraza, Caballero, R Fernández, Sánchez-Hernández, JG, Rebollo, N, Pérez, MC Piñero, González, D García, Fernández, EM Sáez, López, MJ Otero

    “…BackgroundVedolizumab is a monoclonal antibody approved for the treatment of moderate to severe inflammatory bowel disease (IBD) for those patients who have…”
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    Journal Article
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    New insights into the genetic etiology of Alzheimer’s disease and related dementias by Holmans, Peter A., de Rojas, Itziar, Bis, Joshua C., Alarcón-Martín, Emilio, Alcolea, Daniel, Alegret, Montserrat, Alvarez, Ignacio, Álvarez, Victoria, Antúnez, Carmen, Arosio, Beatrice, Athanasiu, Lavinia, Banaj, Nerisa, Below, Jennifer E., Benussi, Luisa, Bossù, Paola, Burholt, Vanessa, Calero, Miguel, Cervera-Carles, Laura, Chen, Hung-Hsin, Custodero, Carlo, de Paiva Lopes, Katia, DeStefano, Anita, Dichgans, Martin, Diehl-Schmid, Janine, Duron, Emmanuelle, Dufouil, Carole, Espinosa, Ana, Nielsen, Sune Fallgaard, Fenoglio, Chiara, Ferrari, Raffaele, Fox, Nick C., Frank-García, Ana, Galimberti, Daniela, Grande, Giulia, Green, Emma, Grünblatt, Edna, Grunin, Michelle, Gudnason, Vilmundur, Hampel, Harald, Hausner, Lucrezia, Hulsman, Marc, Kivipelto, Miia, Kornhuber, Johannes, Kuzma, Amanda B., Launer, Lenore, Ma, Yiyi, Maier, Wolfgang, Montes, Angel Martín, Masullo, Carlo, Mendoza, Silvia, Moebus, Susanne, Morgan, Kevin, Muchnik, Carolina, Mukherjee, Shubhabrata, Nacmias, Benedetta, Ngandu, Tiia, Nicolas, Gael, Nordestgaard, Børge G., Ortega, Gemma, Paolo, Caffarra, Papenberg, Goran, Peloso, Gina, Pérez-Cordón, Alba, Pérez-Tur, Jordi, Pineda, Juan A., Pisanu, Claudia, Polak, Thomas, Quintela, Inés, Rábano, Alberto, Reinders, Marcel J. T., Riedel-Heller, Steffi, Rubino, Elisa, Rujescu, Dan, Sanabria, Ángela, Sánchez-Valle, Raquel, Satizabal, Claudia L., Scarpini, Elio, Scheltens, Philip, Schmid, Matthias, Schneider, Anja, Serrano, Manuel, Solomon, Alina, Song, Yeunjoo, Spalletta, Gianfranco, Squassina, Alessio, Stordal, Eystein, Tartan, Juan Pablo, Tárraga, Lluís, Thomas, Tegos, Tosto, Giuseppe, Wallon, David, Wang, Li-San, Weinhold, Leonie, Wiltfang, Jens, Zare, Habil, Farrer, Lindsay A., Psaty, Bruce M., Williams, Julie, Frikke-Schmidt, Ruth, Deleuze, Jean-François

    Published in Nature genetics (2022)
    “…Characterization of the genetic landscape of Alzheimer’s disease (AD) and related dementias (ADD) provides a unique opportunity for a better understanding of…”
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    Journal Article
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