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Issue DateTitleAuthor(s)
16-Aug-2001¿Existe correlación entre la enfermedad de Alzheimer y defectos en el ADN mitocondrial?Rodríguez Santiago, Benjamín; Casademont i Pou, Jordi; Nunes Martínez, Virginia
15-Nov-2018TP53 aberrations in chronic lymphocytic leukemia: an overview of the clinical implications of improved diagnosticsCampo Güerri, Elias; Cymbalista, Florence; Ghia, Paolo; Jäger, Ulrich; Pospisilova, Sarka; Rosenquist, Richard; Schuh, Anna; Stilgenbauer, Stephan
25-Nov-2010Increased Cortical Thickness and Caudate Volume Precede Atrophy in PSEN1 Mutation CarriersFortea Ormaechea, Juan; Sala Llonch, Roser; Bartrés Faz, David; Bosch, Beatriz; Lladó Plarrumaní, Albert; Bargalló Alabart, Núria​; Molinuevo, José Luis; Sánchez del Valle Díaz, Raquel
1-Nov-2019Notch1 signaling in NOTCH1-mutated mantle cell lymphoma depends on Delta-Like ligand 4 and is a potential target for specific antibody therapy.Silkenstedt, Elisabeth; Arenas, Fabian; Colom-Sanmartí, Berta; Xargay i Torrent, Sílvia; Higashi, Morihiro; Giró, Ariadna; Rodríguez, Vanina; Fuentes, Patricia; Aulitzky, Walter E.; Kuip, Heiko van der; Beà Bobet, Sílvia M.; Toribio, María L.; Campo Güerri, Elias; López-Guerra, Mónica; Colomer Pujol, Dolors
13-May-2020Frequency and spectrum of PIK3CA somatic mutations in breast cancerMartínez Sáez, Olga; Chic, Núria; Pascual, Tomás; Adamo, Barbara; Vidal Losada, Maria Jesús; Gonzalez-Farre, Xavier; Sanfeliu, Esther; Schettini, Francesco; Conte, Benedetta; Brasó Maristany, Fara; Rodriguez, Adela; Martínez, Debora; Galván, Patricia; Rodríguez, Ana Belén; Martínez, Antonio; Muñoz Mateu, Montserrat; Prat Aparicio, Aleix
2-Jul-2021Parkinson’s disease patient-specific neuronal networks carrying the LRRK2 G2019S mutation unveil early functional alterations that predate neurodegenerationCarola, Giulia; Malagarriga, Daniel; Calatayud Aristoy, Carles; Pons-Espinal, Meritxell; Blasco Agell, Lucas; Richaud-Patin, Yvonne; Fernandez-Carasa, Irene; Baruffi, Valentina; Beltramone, Silvia; Molina, Elsa; Dell’Era, Patrizia; Toledo Aral, Juan J.; Tolosa, Eduardo; Muotri, Alysson R.; Garcia Ojalvo, Jordi; Soriano i Fradera, Jordi; Raya Chamorro, Ángel; Consiglio, Antonella
23-Dec-2022Identification of homologous GluN subunits variants accelerates GRIN variants stratificationSantos Gómez, Ana; García Recio, Adrián; Miguez Cabello, Federico; Soto del Cerro, David; Altafaj, Xavier; Olivella, Mireia
13-May-2021Molecular characterization of hepatocellular carcinoma in patients with nonalcoholic steatohepatitisPinyol, Roser; Torrecilla, Sara; Wang, Huan; Montironi, Carla; Piqué Gili, Marta; Torres Martín, Miguel; Wei-Qiang, Leow; Willoughby, Catherine E.; Ramadori, Pierluigi; Andreu Oller, Carmen; Taik, Patricia; Lee, Youngmin A.; Moeini, Agrin; Peix, Judit; Faure-Dupuy, Suzanne; Riedl, Tobias; Schuehle, Svenja; Oliveira, Claudia P.; Alves, Venancio A.; Boffetta, Paolo; Lachenmayer, Anja; Roessler, Sthephanie; Minguez, Beatriz; Schirmacher, Peter; Dufour, Jean François; Thung, Swan N.; Reeves, Helen L.; Carrilho, Flair J.; Chang, Charissa; Uzilov, Andrew V.; Heikenwalder, Mathias; Sanyal, Arun; Friedman, Scott L.; Sia, Daniela; Llovet i Bayer, Josep Maria
30-Nov-2022Mutational Status of SMAD4 and FBXW7 Affects Clinical Outcome in TP53-Mutated Metastatic Colorectal CancerLahoz, Sara; Rodríguez, Adela; Fernández, Laia; Gorría, Teresa; Moreno, Reinaldo; Esposito, Francis; Oliveres, Helena; Albiol, Santiago; Saurí, Tamara; Pesantez, David; Riu Viladoms, Gisela; Cuatrecasas Freixas, Miriam; Jares Gerboles, Pedro; Pedrosa, Leire; Pineda, Estela; Postigo, Antonio; Castells Garangou, Antoni; Prat Aparicio, Aleix; Maurel Santasusana, Joan; Camps, Jordi
26-Mar-2020Physiopathological bases of the disease caused by HACE1 mutations: alterations in autophagy, mitophagy and oxidative stress responseUgarteburu López, Olatz; Sánchez-Vilés, Marta; Ramos, Julio; Barcos Rodríguez, Tamara; Garrabou Tornos, Glòria; García Villoria, Judit; Ribes Rubió, Maria Antònia; Tort, Frederic