Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Ianire, Astobiza"'
Autor:
Jana R. Crespo, Natalia Martín-Martín, Saioa Garcia-Longarte, Jon Corres-Mendizabal, Onintza Carlevaris, Ianire Astobiza, Amaia Zabala-Letona, Marc Guiu, Mikel Azkargorta, Monika Gonzalez-Lopez, Nuria Macías-Cámara, Phuong Doan, Félix Elortza, Isabel Mendizabal, Jukka Westermack, Roger R. Gomis, Amaia Ercilla, Arkaitz Carracedo
Publikováno v:
Cell Death and Disease, Vol 15, Iss 7, Pp 1-11 (2024)
Abstract Prostate cancer exhibits high prevalence and accounts for a high number of cancer-related deaths. The discovery and characterization of molecular determinants of aggressive prostate cancer represents an active area of research. The Immediate
Externí odkaz:
https://doaj.org/article/9d77cf5d40a74212b0e4aa7821487081
Autor:
Raquel García-Vílchez, Ana M. Añazco-Guenkova, Sabine Dietmann, Judith López, Virginia Morón-Calvente, Silvia D’Ambrosi, Paz Nombela, Kepa Zamacola, Isabel Mendizabal, Saioa García-Longarte, Amaia Zabala-Letona, Ianire Astobiza, Sonia Fernández, Alejandro Paniagua, Borja Miguel-López, Virginie Marchand, Diego Alonso-López, Angelika Merkel, Ignacio García-Tuñón, Aitziber Ugalde-Olano, Ana Loizaga-Iriarte, Isabel Lacasa-Viscasillas, Miguel Unda, Mikel Azkargorta, Félix Elortza, Laura Bárcena, Monika Gonzalez-Lopez, Ana M. Aransay, Tomás Di Domenico, Manuel A. Sánchez-Martín, Javier De Las Rivas, Sònia Guil, Yuri Motorin, Mark Helm, Pier Paolo Pandolfi, Arkaitz Carracedo, Sandra Blanco
Publikováno v:
Molecular Cancer, Vol 22, Iss 1, Pp 1-36 (2023)
Abstract Newly growing evidence highlights the essential role that epitranscriptomic marks play in the development of many cancers; however, little is known about the role and implications of altered epitranscriptome deposition in prostate cancer. He
Externí odkaz:
https://doaj.org/article/23776f080b2242829817059af1fa8867
Autor:
Arkaitz Carracedo, James D. Sutherland, Rosa Barrio, Antonio Gomez-Muñoz, Ana M. Aransay, Pilar Sánchez-Mosquera, Marco Piva, Amaia Arruabarrena-Aristorena, Lorea Valcárcel-Jiménez, Miguel Unda, Ana Loizaga-Iriarte, Aitziber Ugalde-Olano, Patricia Zúñiga-García, Ianire Astobiza, Verónica Torrano, Ana R. Cortazar, Mireia Castillo-Martin, Laura Camacho, Leire Arreal, Sonia Fernández-Ruiz, Amaia Zabala-Letona, Natalia Martín-Martín
The nuclear receptor PPAR-β/δ (PPARD) has essential roles in fatty acid catabolism and energy homeostasis as well as cell differentiation, inflammation, and metabolism. However, its contributions to tumorigenesis are uncertain and have been dispute
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::651724c4f1b416ceccd0e6bb409ff0f4
https://doi.org/10.1158/0008-5472.c.6509801
https://doi.org/10.1158/0008-5472.c.6509801
Autor:
Arkaitz Carracedo, James D. Sutherland, Rosa Barrio, Antonio Gomez-Muñoz, Ana M. Aransay, Pilar Sánchez-Mosquera, Marco Piva, Amaia Arruabarrena-Aristorena, Lorea Valcárcel-Jiménez, Miguel Unda, Ana Loizaga-Iriarte, Aitziber Ugalde-Olano, Patricia Zúñiga-García, Ianire Astobiza, Verónica Torrano, Ana R. Cortazar, Mireia Castillo-Martin, Laura Camacho, Leire Arreal, Sonia Fernández-Ruiz, Amaia Zabala-Letona, Natalia Martín-Martín
Suppl Table S1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f976bf0b2bc01cf063beb00531c5f74
https://doi.org/10.1158/0008-5472.22417259
https://doi.org/10.1158/0008-5472.22417259
Autor:
Arkaitz Carracedo, James D. Sutherland, Rosa Barrio, Antonio Gomez-Muñoz, Ana M. Aransay, Pilar Sánchez-Mosquera, Marco Piva, Amaia Arruabarrena-Aristorena, Lorea Valcárcel-Jiménez, Miguel Unda, Ana Loizaga-Iriarte, Aitziber Ugalde-Olano, Patricia Zúñiga-García, Ianire Astobiza, Verónica Torrano, Ana R. Cortazar, Mireia Castillo-Martin, Laura Camacho, Leire Arreal, Sonia Fernández-Ruiz, Amaia Zabala-Letona, Natalia Martín-Martín
Suppl Figures 1, 2, 3, 4, 5, 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c9e129764b7e01c5ddec24c8730111e
https://doi.org/10.1158/0008-5472.22417262
https://doi.org/10.1158/0008-5472.22417262
Autor:
A. Dessa Sadovnick, Anthony L. Traboulsee, Cecily Q. Bernales, Jay P. Ross, Amanda L. Forwell, Irene M. Yee, Lena Guillot-Noel, Bertrand Fontaine, Isabelle Cournu-Rebeix, Antonio Alcina, Maria Fedetz, Guillermo Izquierdo, Fuencisla Matesanz, Kelly Hilven, Bénédicte Dubois, An Goris, Ianire Astobiza, Iraide Alloza, Alfredo Antigüedad, Koen Vandenbroeck, Denis A. Akkad, Orhan Aktas, Paul Blaschke, Mathias Buttmann, Andrew Chan, Joerg T. Epplen, Lisa-Ann Gerdes, Antje Kroner, Christian Kubisch, Tania Kümpfel, Peter Lohse, Peter Rieckmann, Uwe K. Zettl, Frauke Zipp, Lars Bertram, Christina M Lill, Oscar Fernandez, Patricia Urbaneja, Laura Leyva, Jose Carlos Alvarez-Cermeño, Rafael Arroyo, Aroa M. Garagorri, Angel García-Martínez, Luisa M. Villar, Elena Urcelay, Sunny Malhotra, Xavier Montalban, Manuel Comabella, Thomas Berger, Franz Fazekas, Markus Reindl, Mascha C. Schmied, Alexander Zimprich, Carles Vilariño-Güell
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 6, Iss 7, Pp 2073-2079 (2016)
Multiple sclerosis (MS) is a prevalent neurological disease of complex etiology. Here, we describe the characterization of a multi-incident MS family that nominated a rare missense variant (p.G420D) in plasminogen (PLG) as a putative genetic risk fac
Externí odkaz:
https://doaj.org/article/ad94b930f9574b93ac8b8955b0887d3c
Autor:
Paloma Gómez-Fernández, Aitzkoa Lopez de Lapuente Portilla, Ianire Astobiza, Jorge Mena, Andoni Urtasun, Vivian Altmann, Fuencisla Matesanz, David Otaegui, Elena Urcelay, Alfredo Antigüedad, Sunny Malhotra, Xavier Montalban, Tamara Castillo-Triviño, Laura Espino-Paisán, Orhan Aktas, Mathias Buttmann, Andrew Chan, Bertrand Fontaine, Pierre-Antoine Gourraud, Michael Hecker, Sabine Hoffjan, Christian Kubisch, Tania Kümpfel, Felix Luessi, Uwe K. Zettl, Frauke Zipp, Iraide Alloza, Manuel Comabella, Christina M. Lill, Koen Vandenbroeck
Publikováno v:
Cells, Vol 9, Iss 1, p 175 (2020)
The IL22RA2 locus is associated with risk for multiple sclerosis (MS) but causative variants are yet to be determined. In a single nucleotide polymorphism (SNP) screen of this locus in a Basque population, rs28385692, a rare coding variant substituti
Externí odkaz:
https://doaj.org/article/d1ddca86ae88401eaffb82945a610542
Autor:
Manfred Spraul, Ana Loizaga-Iriarte, Aitziber Ugalde-Olano, Miguel Unda, Arkaitz Carracedo, Claire Cannet, Pilar Sanchez-Mosquera, Francisco J. Blanco, Oscar Millet, José M. Mato, Tammo Diercks, Ianire Astobiza, Hartmut Schäfer, Chiara Bruzzone, Nieves Embade, Ana R. Cortazar, Rubén Gil-Redondo
Publikováno v:
Journal of Proteome Research. 19:2419-2428
Prostate cancer is the second most common tumor and the fifth cause of cancer-related death among men worldwide. PC cells exhibit profound signaling and metabolic reprogramming that account for the acquisition of aggressive features. Although the met
Autor:
Ianire Astobiza, Antonio Gómez-Muñoz, Amaia Zabala-Letona, Laura Camacho, Cristina Viera, Amaia Ercilla, Arkaitz Carracedo, Jana Crespo, Verónica Torrano, Ainara Martinez-Gonzalez, Asier Dominguez-Herrera, Ana R. Cortazar, Sonia Fernández-Ruiz, Natalia Martín-Martín
Publikováno v:
Cancers
Volume 13
Issue 17
Addi. Archivo Digital para la Docencia y la Investigación
instname
Cancers, Vol 13, Iss 4307, p 4307 (2021)
Volume 13
Issue 17
Addi. Archivo Digital para la Docencia y la Investigación
instname
Cancers, Vol 13, Iss 4307, p 4307 (2021)
Prostate cancer (PCa) is one of the most prevalent cancers in men. Androgen receptor signaling plays a major role in this disease, and androgen deprivation therapy is a common therapeutic strategy in recurrent disease. Sphingolipid metabolism plays a
Autor:
Belén de la Hera, Jezabel Varadé, Marta García-Montojo, Antonio Alcina, María Fedetz, Iraide Alloza, Ianire Astobiza, Laura Leyva, Oscar Fernández, Guillermo Izquierdo, Alfredo Antigüedad, Rafael Arroyo, Roberto Álvarez-Lafuente, Koen Vandenbroeck, Fuencisla Matesanz, Elena Urcelay
Publikováno v:
PLoS ONE, Vol 9, Iss 3, p e90182 (2014)
BACKGROUND: Human endogenous retroviruses (HERVs) are repetitive sequences derived from ancestral germ-line infections by exogenous retroviruses and different HERV families have been integrated in the genome. HERV-Fc1 in chromosome X has been previou
Externí odkaz:
https://doaj.org/article/3c6e424e3fb445d695722351e38b30cc