Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Stella Charalampopoulou"'
Autor:
Edurne San José-Enériz, Naroa Gimenez-Camino, Obdulia Rabal, Leire Garate, Estibaliz Miranda, Nahia Gómez-Echarte, Fernando García, Stella Charalampopoulou, Elena Sáez, Amaia Vilas-Zornoza, Patxi San Martín-Uriz, Luis V. Valcárcel, Naroa Barrena, Diego Alignani, Luis Esteban Tamariz-Amador, Ana Pérez-Ruiz, Sebastian Hilscher, Mike Schutkowski, Ana Alfonso-Pierola, Nicolás Martinez-Calle, María José Larrayoz, Bruno Paiva, María José Calasanz, Javier Muñoz, Marta Isasa, José Ignacio Martin-Subero, Antonio Pineda-Lucena, Julen Oyarzabal, Xabier Agirre, Felipe Prósper
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-23 (2024)
Abstract Despite the development of novel therapies for acute myeloid leukemia, outcomes remain poor for most patients, and therapeutic improvements are an urgent unmet need. Although treatment regimens promoting differentiation have succeeded in the
Externí odkaz:
https://doaj.org/article/c19f4277205c445384d53303bce19ff2
Autor:
Laura Ondrisova, Vaclav Seda, Eva Hoferkova, Giorgia Chiodin, Krystof Hlavac, Lenka Kostalova, Daniel Filip, Pedro Faria Zeni, Anna Panovska, Karla Plevova, Sarka Pospisilova, Martin Simkovic, Filip Vrbacky, Daniel Lysak, Stacey M. Fernandes, Matthew S. Davids, Alba Maiques-Diaz, Stella Charalampopoulou, Jose I Martin-Subero, Jennifer R Brown, Michael Doubek, Francesco Forconi, Jiri Mayer, Marek Mraz
Publikováno v:
HemaSphere, Vol 7, p e8228434 (2023)
Externí odkaz:
https://doaj.org/article/d170c389beac401f8b76921cc6daacb9
Autor:
Stella Charalampopoulou, Elise Chapiro, Ferran Nadeu, Thorsten Zenz, Silvia Beà, Damien Roos-Weil, Olivier Bernard, Santos A Susin, Estella Matutes, Elias Campo, Martí Duran-Ferrer, Florence Nguyen-Khac, José Ignacio Martín-Subero
Publikováno v:
HemaSphere, Vol 7, p e87988d2 (2023)
Externí odkaz:
https://doaj.org/article/6157ab0c4b8e4216a759aca26010a6d4
Autor:
Maurizio Mangolini, Alba Maiques-Diaz, Stella Charalampopoulou, Elena Gerhard-Hartmann, Johannes Bloehdorn, Andrew Moore, Giorgia Giachetti, Junyan Lu, Valar Nila Roamio Franklin, Chandra Sekkar Reddy Chilamakuri, Ilias Moutsopoulos, Andreas Rosenwald, Stephan Stilgenbauer, Thorsten Zenz, Irina Mohorianu, Clive D’Santos, Silvia Deaglio, Daniel J. Hodson, Jose I. Martin-Subero, Ingo Ringshausen
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-21 (2022)
NOTCH mutations are frequent in B cell malignancies. Here the authors use retroviral transduction of primary malignant B cells from Chronic Lymphocytic Leukemia (CLL) and Mantle Cell Lymphoma (MCL) patients to show that NOTCH1/2-mutations facilitate
Externí odkaz:
https://doaj.org/article/e779b836c8e440c8aa0f51dae36441ca
Autor:
Beatriz García-Torre, Marta Kulis, Mònica Romo, Anna Vidal, Stella Charalampopoulou, Vicente Chapaprieta, Martí Duran-Ferrer, Ferran Nadeu, Cristina López, Guillem Clot, Eva Giné, Armando Lopez-Guillermo, Sílvia Beà, Dolors Colomer, Elías Campo, José I. Martín-Subero
Publikováno v:
Blood. 140:1745-1746
Autor:
Vicente Chapaprieta, Alba Maiques-Diaz, Guillem Clot, Ferran Nadeu, Judith Mateos-Jaimez, Anna Vidal, Stella Charalampopoulou, Martí Duran-Ferrer, Romina Royo, Junyan Lu, Thorsten Zenz, Julio Delgado, Armando Lopez-Guillermo, Elías Campo, José I. Martín-Subero
Publikováno v:
Blood. 140:4123-4124
Autor:
Luis Vitores Valcárcel, Ane Amundarain, Francisco J. Planes, José I. Martín-Subero, Stella Charalampopoulou, Marta Kulis, Ari Melnick, Xabier Agirre, Jesús F. San Miguel, Felipe Prosper
Publikováno v:
Leukemia
Clinical and genetic risk factors are currently used in multiple myeloma (MM) to stratify patients and to design specific therapies. However, these systems do not capture the heterogeneity of the disease supporting the development of new prognostic f
Autor:
Elias Campo, Renée Beekman, Raquel Ordoñez, Cem Meydan, Teresa Ezponda, Stella Charalampopoulou, Guillem Clot, Ari Melnick, Bruno Paiva, Constantine S. Mitsiades, Ruba Y. Taha, Vicente Chapaprieta, Jesus San Miguel, Hendrik G. Stunnenberg, Beatriz García-Torre, Arantxa Carrasco-Leon, Felipe Prosper, Nuria Russiñol, Leire Garate, Halima El-Omri, Edurne San José-Enériz, José I. Martín-Subero, Joost H.A. Martens, Roser Vilarrasa-Blasi, Jonathan D. Licht, Amaia Vilas-Zornoza, Daphné Dupéré-Richer, Marta Kulis, Juan R. Rodriguez-Madoz, Ivo Gut, David Lara-Astiaso, Xabier Agirre, Paula Soler-Vila, Paul Flicek, Rebeca Martínez-Turrilas, Núria Verdaguer-Dot, Estíbaliz Miranda, Martí Duran-Ferrer, Maria J. Calasanz
Publikováno v:
Genome Research, 30, 9, pp. 1217-1227
Genome Res
Genome Research, 30, 1217-1227
Genome Res
Genome Research, 30, 1217-1227
Multiple myeloma (MM) is a plasma cell neoplasm associated with a broad variety of genetic lesions. In spite of this genetic heterogeneity, MMs share a characteristic malignant phenotype whose underlying molecular basis remains poorly characterized.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58806fdc212870e982fcf594422e8812
https://doi.org/10.1101/740027
https://doi.org/10.1101/740027
Akademický článek
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