BRCA1 negatively regulates formation of autophagic vacuoles in MCF-7 breast cancer cells by Esteve, Juan M., Armengod, María Eugenia, Knecht, Erwin

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The GTPase Activity and C-terminal Cysteine of the Escherichia coli MnmE Protein Are Essential for Its tRNA Modifying Function by Yim, Lucía, Martínez-Vicente, Marta, Villarroya, Magdalena, Aguado, Carmen, Knecht, Erwin, Armengod, María-Eugenia

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A single point mutation in the low-density lipoprotein receptor switches the degradation of its mature protein from the proteasome to the lysosome by Martín de Llano, José Javier, Fuertes, Graciela, Andreu, Enrique José, Puig, Oscar, Chaves, F. Javier, Soutar, Anne K., Armengod, María-Eugenia, Knecht, Erwin

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Analysis of BRCA1 and BRCA2 genes in Spanish breast/ovarian cancer patients: A high proportion of mutations unique to Spain and evidence of founder effects by Díez, Orland, Osorio, Ana, Durán, Mercedes, Martinez-Ferrandis, José Ignacio, Hoya, Miguel de la, Salazar, Raquel, Vega, Ana, Campos, Berta, Rodríguez-López, Raquel, Velasco, Eladio, Chaves, Javier, Díaz-Rubio, Eduardo, Jesús Cruz, Juan, Torres, María, Esteban, Eva, Cervantes, Andrés, Alonso, Carmen, San Román, Juan Manuel, González-Sarmiento, Rogelio, Miner, Cristina, Carracedo, Angel, Eugenia Armengod, María, Caldés, Trinidad, Benítez, Javier, Baiget, Montserrat

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Structural insights into the GTPase domain of Escherichia coli MnmE protein by Monleón, Daniel, Martínez-Vicente, Marta, Esteve, Vicent, Yim, Lucia, Prado, Silvia, Armengod, Maria-Eugenia, Celda, Bernardo

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Haplotype analysis of the BRCA2 9254delATCAT recurrent mutation in breast/ovarian cancer families from Spain by Campos, Berta, Díez, Orland, Odefrey, Fabrice, Domènech, Montserrat, Moncoutier, Virginie, Martínez-Ferrandis, José Ignacio, Osorio, Ana, Balmaña, Judith, Barroso, Alicia, Armengod, María Eugenia, Benítez, Javier, Alonso, Carmen, Stoppa-Lyonnet, Dominique, Goldgar, David, Baiget, Montserrat

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Influence of the I/D Polymorphism of the Angiotensin-Converting Enzyme Gene on the Outcome of Microalbuminuria in Essential Hypertension by Redon, Josep, Chaves, Felipe Javier, Liao, Youlian, Pascual, Jose Maria, Rovira, Eduardo, Armengod, Maria Eugenia, Cooper, Richard S

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Haplotype analysis of the BRCA2 9254delATCAT recurrent mutation in breast/ovarian cancer families from Spain: MUTATIONS IN BRIEF by Campos, Berta, Díez, Orland, Odefrey, Fabrice, Domènech, Montserrat, Moncoutier, Virginie, Martínez-Ferrandis, José Ignacio, Osorio, Ana, Balmaña, Judith, Barroso, Alicia, Armengod, María Eugenia, Benítez, Javier, Alonso, Carmen, Stoppa-Lyonnet, Dominique, Goldgar, David, Baiget, Montserrat

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Analysis of BRCA1 and BRCA2 genes in Spanish breast/ovarian cancer patients: A high proportion of mutations unique to Spain and evidence of founder effects: BRCA1 AND BRCA2 MUTATIO... by Díez, Orland, Osorio, Ana, Durán, Mercedes, Martinez-Ferrandis, José Ignacio, Hoya, Miguel de la, Salazar, Raquel, Vega, Ana, Campos, Berta, Rodríguez-López, Raquel, Velasco, Eladio, Chaves, Javier, Díaz-Rubio, Eduardo, Jesús Cruz, Juan, Torres, María, Esteban, Eva, Cervantes, Andrés, Alonso, Carmen, San Román, Juan Manuel, González-Sarmiento, Rogelio, Miner, Cristina, Carracedo, Angel, Eugenia Armengod, María, Caldés, Trinidad, Benítez, Javier, Baiget, Montserrat

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Angiotensin II AT1 receptor gene polymorphism and microalbuminuria in essential hypertension by Chaves, Felipe Javier, Pascual, Jose Maria, Rovira, Eduardo, Armengod, Maria Eugenia, Redon, Josep

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Molecular Analysis of the recF Gene of Escherichia coli by Blanar, Michael A., Sandler, Steven J., Armengod, Maria-Eugenia, Ream, Lloyd W., Clark, Alvin J.

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Enzymology of tRNA modification in the bacterial MnmEG pathway by Armengod, M.-Eugenia, Moukadiri, Ismaïl, Prado, Silvia, Ruiz-Partida, Rafael, Benítez-Páez, Alfonso, Villarroya, Magda, Lomas, Rodrigo, Garzón, María J., Martínez-Zamora, Ana, Meseguer, Salvador, Navarro-González, Carmen

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Identification of copy‐number variants in patients with overgrowth disorders by Miranda‐Alcaraz, Lucía, Silván, Cristina, Arias, Pedro, Pozo‐Román, Jesús, Arroyo, Ignacio, Galán, Enrique, Blanquer, Aleixandre, Garcı'a‐Alix, Alfredo, Santana, Alfredo, Alonso, Almudena, Gar‐cía, Ana Patiño, Bredani, Analía, Villavicencio, Andrea, Acosta, Angelina, González, Anna María Cueto, Baldellón, Antonio, Meneses, Antonio González, Gener, Blanca, Groisman, Boris, Perando‐nes, Claudia, Olivas, Cristina, Armenta, Daniel, Elorza, Dolores, Zamora, Elena, Zambrano, Elisa, Steichen, Elisabeth, Cruz, Enrique Caro, Gómez, Enrique Galán, Román, Enriqueta, Goldschmidt, Ernesto, Marfil, Esteban, Antolín, Eugenia, Ramos, Feliciano, Grondona, Fermina López, Martínez, Francisco, Uzielli, Giovannucci, Mercado, Graciela, Cassinelli, Hamilton, Arroyo, Ignacio, Pascual, Ignacio Pascual, Rio, Ignacio Vázquez, Bueno, Inés, Sánchez, Isabel Lorda, Campistol, Jaume, Arcas, Javier, Planells, Javier García, Liria, María José Jiménez, Almeida, José Carlos Cabral, Labarta, José Ignacio, Fuster, José Luis, Gutiérrez, Juan Carlos López, López Siguero, Juan P., Lara, Julián, Arranz, Leonor, Soriano, Leandro, De Alba, Liliana, Mar‐torell, Loreto, Jurado, Luis Pérez, Lozano, M. Ferrer, Merillas, M. Jesús Alija, Pérez, María Asunción García, Segovia, Mabel, Martínez, Margarita, Tabernero, Margarita, Ramos, María Antonia, Ballesta, Maria, Guardia, M. Nieves Martínez, Artigas, Mercedes, Villanueva, Mercedes, Campo, Miguel, Rosello, Mónica, Kantaputra, Nik, Matos, Pablo Prieto, Casano, Paula, Mallada, Paula Lalaguna, Olivares, Pe‐dro, Delgado, Raquel Perez, Bernardi, Priscila, León, Rafael Camino, Villaverde, Raquel Sáez, Gracia, Ricardo, Scott, Richard, Valdez, Rita, Arteaga, Rosa, Cazorla, Rosario, Iglesias, Rosario Marín, Bronberg, Rubén, Barreiro, Santiago Conde, Kapoor, Seema, Lopez, Trinidad García, Vendrell, Teresa, Tirado, Pilar, Huertos, Alicia Ureta, Lotersztein, Vanesa, Martín, Selma Vázquez, Seidel, Verónica, Albiach, Vicente, Soler, Virgina, Cosentino, Viviana, Lapunzina, Pablo

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Genetic and phenotypic findings in 34 novel Spanish patients with DDX3X neurodevelopmental disorder by Parra, Alejandro, Pascual, Patricia, Cazalla, Mario, Arias, Pedro, Gallego-Zazo, Natalia, San-Martín, Esteban A, Silván, Cristina, Santos-Simarro, Fernando, Nevado, Julián, Tenorio-Castano, Jair, Lapunzina, Pablo

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Further delineation of neuropsychiatric findings in Tatton-Brown-Rahman syndrome due to disease-causing variants in DNMT3A: seven new patients by Tenorio, Jair, Alarcón, Pablo, Arias, Pedro, Dapía, Irene, García-Miñaur, Sixto, Palomares Bralo, María, Campistol, Jaume, Climent, Salvador, Valenzuela, Irene, Ramos, Sergio, Monseny, Antonio Martínez, Grondona, Fermina López, Botet, Javier, Serrano, Mercedes, Solís, Mario, Santos-Simarro, Fernando, Álvarez, Sara, Teixidó-Tura, Gisela, Fernández Jaén, Alberto, Gordo, Gema, Bardón Rivera, María Belén, Nevado, Julián, Hernández, Alicia, Cigudosa, Juan C, Ruiz-Pérez, Víctor L, Tizzano, Eduardo F, Lapunzina, Pablo

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