Targeted Exome Sequencing of Krebs Cycle Genes Reveals Candidate Cancer-Predisposing Mutations in Pheochromocytomas and Paragangliomas von Remacha, Laura, Comino-Méndez, Iñaki, Richter, Susan, Contreras, Laura, Currás-Freixes, María, Pita, Guillermo, Letón, Rocío, Galarreta, Antonio, Torres-Pérez, Rafael, Honrado, Emiliano, Jiménez, Scherezade, Maestre, Lorena, Moran, Sebastian, Esteller, Manel, Satrústegui, Jorgina, Eisenhofer, Graeme, Robledo, Mercedes, Cascón, Alberto

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Molecular characterization of chromophobe renal cell carcinoma reveals mTOR pathway alterations in patients with poor outcome von Roldan-Romero, Juan María, Santos, María, Lanillos, Javier, Caleiras, Eduardo, Anguera, Georgia, Maroto, Pablo, García-Donas, Jesús, de Velasco, Guillermo, Martinez-Montes, Ángel Mario, Calsina, Bruna, Monteagudo, María, Letón, Rocío, Leandro-García, Luis Javier, Montero-Conde, Cristina, Cascón, Alberto, Robledo, Mercedes, Rodriguez-Antona, Cristina

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Germline mutations in FH confer predisposition to malignant pheochromocytomas and paragangliomas von Castro-Vega, Luis Jaime, Buffet, Alexandre, De Cubas, Aguirre A, Cascón, Alberto, Menara, Mélanie, Khalifa, Emmanuel, Amar, Laurence, Azriel, Sharona, Bourdeau, Isabelle, Chabre, Olivier, Currás-Freixes, Maria, Franco-Vidal, Valérie, Guillaud-Bataille, Marine, Simian, Christophe, Morin, Aurélie, Letón, Rocío, Gómez-Graña, Alvaro, Pollard, Patrick J, Rustin, Pierre, Robledo, Mercedes, Favier, Judith, Gimenez-Roqueplo, Anne-Paule

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Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma von Comino-Méndez, Iñaki, Gracia-Aznárez, Francisco J, Schiavi, Francesca, Landa, Iñigo, Leandro-García, Luis J, Letón, Rocío, Honrado, Emiliano, Ramos-Medina, Rocío, Caronia, Daniela, Pita, Guillermo, Gómez-Graña, Álvaro, de Cubas, Aguirre A, Inglada-Pérez, Lucía, Maliszewska, Agnieszka, Taschin, Elisa, Bobisse, Sara, Pica, Giuseppe, Loli, Paola, Hernández-Lavado, Rafael, Díaz, José A, Gómez-Morales, Mercedes, González-Neira, Anna, Roncador, Giovanna, Rodríguez-Antona, Cristina, Benítez, Javier, Mannelli, Massimo, Opocher, Giuseppe, Robledo, Mercedes, Cascón, Alberto

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Tumoral EPAS1 (HIF2A) mutations explain sporadic pheochromocytoma and paraganglioma in the absence of erythrocytosis von Comino-Méndez, Iñaki, de Cubas, Aguirre A, Bernal, Carmen, Álvarez-Escolá, Cristina, Sánchez-Malo, Carolina, Ramírez-Tortosa, César L, Pedrinaci, Susana, Rapizzi, Elena, Ercolino, Tonino, Bernini, Giampaolo, Bacca, Alessandra, Letón, Rocío, Pita, Guillermoó, Alonso, María R, Leandro-García, Luis J, Gómez-Graña, Alvaro, Inglada-Pérez, Lucía, Mancikova, Veronika, Rodríguez-Antona, Cristina, Mannelli, Massimo, Robledo, Mercedes, Cascón, Alberto

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Research Resource: Transcriptional Profiling Reveals Different Pseudohypoxic Signatures in SDHB and VHL-Related Pheochromocytomas von López-Jiménez, Elena, Gómez-López, Gonzalo, Leandro-García, L. Javier, Muñoz, Iván, Schiavi, Francesca, Montero-Conde, Cristina, de Cubas, Aguirre A, Ramires, Ricardo, Landa, Iñigo, Leskelä, Susanna, Maliszewska, Agnieszka, Inglada-Pérez, Lucía, de la Vega, Leticia, Rodríguez-Antona, Cristina, Letón, Rocío, Bernal, Carmen, de Campos, José M, Diez-Tascón, Cristina, Fraga, Mario F, Boullosa, Cesar, Pisano, David G, Opocher, Giuseppe, Robledo, Mercedes, Cascón, Alberto

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Whole-exome sequencing identifies MDH2 as a new familial paraganglioma gene von Cascón, Alberto, Comino-Méndez, Iñaki, Currás-Freixes, María, de Cubas, Aguirre A, Contreras, Laura, Richter, Susan, Peitzsch, Mirko, Mancikova, Veronika, Inglada-Pérez, Lucía, Pérez-Barrios, Andrés, Calatayud, María, Azriel, Sharona, Villar-Vicente, Rosa, Aller, Javier, Setién, Fernando, Moran, Sebastian, Garcia, Juan F, Río-Machín, Ana, Letón, Rocío, Gómez-Graña, Álvaro, Apellániz-Ruiz, María, Roncador, Giovanna, Esteller, Manel, Rodríguez-Antona, Cristina, Satrústegui, Jorgina, Eisenhofer, Graeme, Urioste, Miguel, Robledo, Mercedes

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Genetics of Pheochromocytoma and Paraganglioma in Spanish Patients von Cascón, Alberto, Pita, Guillermo, Burnichon, Nelly, Landa, Iñigo, López-Jiménez, Elena, Montero-Conde, Cristina, Leskelä, Susanna, Leandro-García, Luis Javier, Letón, Rocío, Rodríguez-Antona, Cristina, Díaz, José Ángel, López-Vidriero, Emilio, González-Neira, Anna, Velasco, Ana, Matias-Guiu, Xavier, Gimenez-Roqueplo, Anne-Paule, Robledo, Mercedes

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Identification of a Frameshift Mutation in Osterix in a Patient with Recessive Osteogenesis Imperfecta von Lapunzina, Pablo, Aglan, Mona, Temtamy, Samia, Caparrós-Martín, José A., Valencia, Maria, Letón, Rocío, Martínez-Glez, Victor, Elhossini, Rasha, Amr, Khalda, Vilaboa, Nuria, Ruiz-Perez, Victor L.

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Gain-of-function mutations in DNMT3A in patients with paraganglioma von Remacha, Laura, Currás-Freixes, Maria, Torres-Ruiz, Raúl, Schiavi, Francesca, Torres-Pérez, Rafael, Calsina, Bruna, Letón, Rocío, Comino-Méndez, Iñaki, Roldán-Romero, Juan M, Montero-Conde, Cristina, Santos, María, Pérez, Lucía Inglada, Pita, Guillermo, Alonso, María R., Honrado, Emiliano, Pedrinaci, Susana, Crespo-Facorro, Benedicto, Percesepe, Antonio, Falcioni, Maurizio, Rodríguez-Perales, Sandra, Korpershoek, Esther, Ramón-Maiques, Santiago, Opocher, Giuseppe, Rodríguez-Antona, Cristina, Robledo, Mercedes, Cascón, Alberto

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Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas von Remacha, Laura, Pirman, David, Mahoney, Christopher E., Coloma, Javier, Calsina, Bruna, Currás-Freixes, Maria, Letón, Rocío, Torres-Pérez, Rafael, Richter, Susan, Pita, Guillermo, Herráez, Belén, Cianchetta, Giovanni, Honrado, Emiliano, Maestre, Lorena, Urioste, Miguel, Aller, Javier, García-Uriarte, Óscar, Gálvez, María Ángeles, Luque, Raúl M., Lahera, Marcos, Moreno-Rengel, Cristina, Eisenhofer, Graeme, Montero-Conde, Cristina, Rodríguez-Antona, Cristina, Llorca, Óscar, Smolen, Gromoslaw A., Robledo, Mercedes, Cascón, Alberto

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Co-occurrence of mutations in NF1 and other susceptibility genes in pheochromocytoma and paraganglioma von Mellid, Sara, Gil, Eduardo, Letón, Rocío, Caleiras, Eduardo, Honrado, Emiliano, Richter, Susan, Palacios, Nuria, Lahera, Marcos, Galofré, Juan C, López-Fernández, Adriá, Calatayud, Maria, Herrera-Martínez, Aura D, Galvez, María A, Matias-Guiu, Xavier, Balbín, Milagros, Korpershoek, Esther, Lim, Eugénie S, Maletta, Francesca, Lider, Sofia, Fliedner, Stephanie M J, Bechmann, Nicole, Eisenhofer, Graeme, Canu, Letizia, Rapizzi, Elena, Bancos, Irina, Robledo, Mercedes, Cascón, Alberto

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Overexpression and activation of EGFR and VEGFR2 in medullary thyroid carcinomas is related to metastasis von Rodríguez-Antona, Cristina, Pallares, Judith, Montero-Conde, Cristina, Inglada-Pérez, Lucia, Castelblanco, Esmeralda, Landa, Iñigo, Leskelä, Susanna, Leandro-García, Luis J, López-Jiménez, Elena, Letón, Rocío, Cascón, Alberto, Lerma, Enrique, Martin, M Carmen, Carralero, M Carmen, Mauricio, Didac, Cruz Cigudosa, Juan, Matias-Guiu, Xavier, Robledo, Mercedes

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Tumoral and tissue-specific expression of the major human β-tubulin isotypes von Leandro-García, Luis J., Leskelä, Susanna, Landa, Iñigo, Montero-Conde, Cristina, López-Jiménez, Elena, Letón, Rocío, Cascón, Alberto, Robledo, Mercedes, Rodríguez-Antona, Cristina

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Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas von Remacha, Laura, Pirman, David, Mahoney, Christopher E., Coloma, Javier, Calsina, Bruna, Currás-Freixes, Maria, Letón, Rocío, Torres-Pérez, Rafael, Richter, Susan, Pita, Guillermo, Herráez, Belén, Cianchetta, Giovanni, Honrado, Emiliano, Maestre, Lorena, Urioste, Miguel, Aller, Javier, García-Uriarte, Óscar, Gálvez, María Ángeles, Luque, Raúl M., Lahera, Marcos, Moreno-Rengel, Cristina, Eisenhofer, Graeme, Montero-Conde, Cristina, Rodríguez-Antona, Cristina, Llorca, Óscar, Smolen, Gromoslaw A., Robledo, Mercedes, Cascón, Alberto

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Whole-Exome Sequencing Identifies MDH2 as a New Familial Paraganglioma Gene von Cascón, Alberto, Comino-Méndez, Iñaki, Currás-Freixes, María, de Cubas, Aguirre A., Contreras, Laura, Richter, Susan, Peitzsch, Mirko, Mancikova, Veronika, Inglada-Pérez, Lucía, Pérez-Barrios, Andrés, Calatayud, María, Azriel, Sharona, Villar-Vicente, Rosa, Aller, Javier, Setién, Fernando, Moran, Sebastian, Garcia, Juan F., Río-Machín, Ana, Letón, Rocío, Gómez-Graña, Álvaro, Apellániz-Ruiz, María, Roncador, Giovanna, Esteller, Manel, Rodríguez-Antona, Cristina, Satrústegui, Jorgina, Eisenhofer, Graeme, Urioste, Miguel, Robledo, Mercedes

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CD133 Expression in Medullary Thyroid Cancer Cells Identifies Patients with Poor Prognosis von Cordero-Barreal, Alfonso, Caleiras, Eduardo, López de Maturana, Evangelina, Monteagudo, María, Martínez-Montes, Ángel M, Letón, Rocío, Gil, Eduardo, Álvarez-Escolá, Cristina, Regojo, Rita M, Andía, Víctor, Marazuela, Mónica, Guadalix, Sonsoles, Calatayud, María, Robles-Díaz, Luis, Aguirre, Miguel, Cano, Juana M, Díaz, José Ángel, Saavedra, Pilar, Lamas, Cristina, Azriel, Sharona, Sastre, Julia, Aller, Javier, Leandro-García, Luis J, Calsina, Bruna, Roldán-Romero, Juan María, Santos, María, Lanillos, Javier, Cascón, Alberto, Rodríguez-Antona, Cristina, Robledo, Mercedes, Montero-Conde, Cristina

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Analysis of Telomere Maintenance Related Genes Reveals NOP10 as a New Metastatic-Risk Marker in Pheochromocytoma/Paraganglioma von Monteagudo, María, Martínez, Paula, Leandro-García, Luis J., Martínez-Montes, Ángel M., Calsina, Bruna, Pulgarín-Alfaro, Marta, Díaz-Talavera, Alberto, Mellid, Sara, Letón, Rocío, Gil, Eduardo, Pérez-Martínez, Manuel, Megías, Diego, Torres-Ruiz, Raúl, Rodriguez-Perales, Sandra, González, Patricia, Caleiras, Eduardo, Jiménez-Villa, Scherezade, Roncador, Giovanna, Álvarez-Escolá, Cristina, Regojo, Rita M., Calatayud, María, Guadalix, Sonsoles, Currás-Freixes, Maria, Rapizzi, Elena, Canu, Letizia, Nölting, Svenja, Remde, Hanna, Fassnacht, Martin, Bechmann, Nicole, Eisenhofer, Graeme, Mannelli, Massimo, Beuschlein, Felix, Quinkler, Marcus, Rodríguez-Antona, Cristina, Cascón, Alberto, Blasco, María A., Montero-Conde, Cristina, Robledo, Mercedes

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Detection of the first gross CDC73 germline deletion in an HPT-JT syndrome family von Cascón, Alberto, Huarte-Mendicoa, Carlos Vázquez, Javier Leandro-García, L., Letón, Rocío, Suela, Javier, Santana, Alfredo, Costa, Mauro Boronat, Comino-Méndez, Iñaki, Landa, Iñigo, Sánchez, Lydia, Rodríguez-Antona, Cristina, Cigudosa, Juan C., Robledo, Mercedes

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Genetics of pheochromocytoma and paraganglioma in Spanish pediatric patients von Cascón, Alberto, Inglada-Pérez, Lucía, Comino-Méndez, Iñaki, de Cubas, Aguirre A, Letón, Rocío, Mora, Jaume, Marazuela, Mónica, Galofré, Juan Carlos, Quesada-Charneco, Miguel, Robledo, Mercedes

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