Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Pablo Bousquets-Muñoz"'
Autor:
Ece Özoğul, Anna Montaner, Melina Pol, Gerard Frigola, Olga Balagué, Charlotte Syrykh, Pablo Bousquets-Muñoz, Romina Royo, Juliette Fontaine, Alexandra Traverse-Glehen, Marco M. Bühler, Luca Giudici, Marco Roncador, Thorsten Zenz, Sylvain Carras, Severine Valmary-Degano, Laurence de Leval, Jan Bosch-Schips, Fina Climent, Julia Salmeron-Villalobos, Melika Bashiri, Silvia Ruiz-Gaspà, Dolors Costa, Sílvia Beà, Itziar Salaverria, Eva Giné, Leticia Quintanilla-Martinez, Pierre Brousset, Mark Raffeld, Elaine S. Jaffe, Xose S. Puente, Cristina López, Ferran Nadeu, Elias Campo
Publikováno v:
Blood Cancer Journal, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract Mantle cell lymphoma (MCL) is genetically characterized by the IG::CCND1 translocation mediated by an aberrant V(D)J rearrangement. CCND1 translocations and overexpression have been identified in occasional aggressive B-cell lymphomas with u
Externí odkaz:
https://doaj.org/article/ebc32ff445d443efa40b812995ecadc9
Autor:
Pablo Bousquets-Muñoz, Ander Díaz-Navarro, Ferran Nadeu, Ana Sánchez-Pitiot, Sara López-Tamargo, Shimin Shuai, Milagros Balbín, Jose M. C. Tubio, Sílvia Beà, Jose I. Martin-Subero, Ana Gutiérrez-Fernández, Lincoln D. Stein, Elías Campo, Xose S. Puente
Publikováno v:
npj Genomic Medicine, Vol 7, Iss 1, Pp 1-12 (2022)
Abstract Current somatic mutation callers are biased against repetitive regions, preventing the identification of potential driver alterations in these loci. We developed a mutation caller for repetitive regions, and applied it to study repetitive no
Externí odkaz:
https://doaj.org/article/5f0f3806b2a34e4faaa729f3e687de20
Autor:
Raúl F. Pérez, Anna Yunuen Soto Fernández, Pablo Bousquets Muñoz, Marta I. Sierra, Juan Ramón Tejedor, Paula Morales-Sánchez, Adolfo F. Valdés, Ricardo Santamaría, Clara Blanco, Ramón Torrecillas, Mario F. Fraga, Agustín F. Fernández
Publikováno v:
Epigenetics, Vol 15, Iss 3, Pp 283-293 (2020)
The presence of nanomaterials in our everyday life is ever increasing, and so too are concerns about the possible health consequences of exposure to them. While evidence of their biological activity is growing, there is still scant knowledge of the e
Externí odkaz:
https://doaj.org/article/b24f321532884c4494a7246eb25681b2
Autor:
Binyamin A. Knisbacher, Ziao Lin, Cynthia K. Hahn, Ferran Nadeu, Martí Duran-Ferrer, Kristen E. Stevenson, Eugen Tausch, Julio Delgado, Alex Barbera-Mourelle, Amaro Taylor-Weiner, Pablo Bousquets-Muñoz, Ander Diaz-Navarro, Andrew Dunford, Shankara Anand, Helene Kretzmer, Jesus Gutierrez-Abril, Sara López-Tamargo, Stacey M. Fernandes, Clare Sun, Mariela Sivina, Laura Z. Rassenti, Christof Schneider, Shuqiang Li, Laxmi Parida, Alexander Meissner, François Aguet, Jan A. Burger, Adrian Wiestner, Thomas J. Kipps, Jennifer R. Brown, Michael Hallek, Chip Stewart, Donna S. Neuberg, José I. Martín-Subero, Xose S. Puente, Stephan Stilgenbauer, Catherine J. Wu, Elias Campo, Gad Getz
Publikováno v:
Nat Genet
Nature genetics, vol 54, iss 11
Nature Genetics
Nature genetics, vol 54, iss 11
Nature Genetics
Recent advances in cancer characterization have consistently revealed marked heterogeneity, impeding the completion of integrated molecular and clinical maps for each malignancy. Here, we focus on chronic lymphocytic leukemia (CLL), a B cell neoplasm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbcebcde5af0ed4f2d596ab3149447ab
https://europepmc.org/articles/PMC10084830/
https://europepmc.org/articles/PMC10084830/
Autor:
Ander Díaz-Navarro, Pablo Bousquets-Muñoz, Ferran Nadeu, Sara López-Tamargo, Silvia Beà, Elias Campo, Xose S. Puente
MotivationThe cost reduction in sequencing and the extensive genomic characterization of a wide variety of cancers is expanding the use of tumor sequencing approaches to a wide number of research groups and to the clinical practice. Although specific
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbf13378f4ce88db77b247673b8f10cb
https://doi.org/10.1101/2022.05.11.491496
https://doi.org/10.1101/2022.05.11.491496
Autor:
Pablo Bousquets-Muñoz, Ander Díaz-Navarro, Ferran Nadeu, Ana Sánchez-Pitiot, Sara López-Tamargo, Shimin Shuai, Milagros Balbín, Jose M. C. Tubio, Sílvia Beà, Jose I. Martin-Subero, Ana Gutiérrez-Fernández, Lincoln D. Stein, Elías Campo, Xose S. Puente
Publikováno v:
Scopus
RUO. Repositorio Institucional de la Universidad de Oviedo
instname
RUO. Repositorio Institucional de la Universidad de Oviedo
instname
Current somatic mutation callers are biased against repetitive regions, preventing the identification of potential driver alterations in these loci. We developed a mutation caller for repetitive regions, and applied it to study repetitive non protein
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::779db51463f337c2f8607f8a9face0d9
https://pubmed.ncbi.nlm.nih.gov/35288589
https://pubmed.ncbi.nlm.nih.gov/35288589
Autor:
Ricardo Santamaría, Mario F. Fraga, Ramón Torrecillas, Adolfo F. Valdes, Agustín F. Fernández, Raúl F. Pérez, Marta I. Sierra, Paula Morales-Sánchez, Anna Yunuen Soto Fernández, Clara Blanco, Juan Ramón Tejedor, Pablo Bousquets Muñoz
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Epigenetics
instname
Epigenetics
The presence of nanomaterials in our everyday life is ever increasing, and so too are concerns about the possible health consequences of exposure to them. While evidence of their biological activity is growing, there is still scant knowledge of the e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26d4f1fd449c969596b74a88525df1f7
https://doi.org/10.1080/15592294.2019.1666650
https://doi.org/10.1080/15592294.2019.1666650