Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Maria J Calasanz"'
Autor:
Jose I Martin-Subero, Ole Ammerpohl, Marina Bibikova, Eliza Wickham-Garcia, Xabier Agirre, Sara Alvarez, Monika Brüggemann, Stefanie Bug, Maria J Calasanz, Martina Deckert, Martin Dreyling, Ming Q Du, Jan Dürig, Martin J S Dyer, Jian-Bing Fan, Stefan Gesk, Martin-Leo Hansmann, Lana Harder, Sylvia Hartmann, Wolfram Klapper, Ralf Küppers, Manuel Montesinos-Rongen, Inga Nagel, Christiane Pott, Julia Richter, José Román-Gómez, Marc Seifert, Harald Stein, Javier Suela, Lorenz Trümper, Inga Vater, Felipe Prosper, Claudia Haferlach, Juan Cruz Cigudosa, Reiner Siebert
Publikováno v:
PLoS ONE, Vol 4, Iss 9, p e6986 (2009)
Alterations in the DNA methylation pattern are a hallmark of leukemias and lymphomas. However, most epigenetic studies in hematologic neoplasms (HNs) have focused either on the analysis of few candidate genes or many genes and few HN entities, and co
Externí odkaz:
https://doaj.org/article/245b34fbecf54135b42985c0a2339f84
Autor:
Mireia Ramos‐Muntada, Juan L. Trincado, Joan Blanco, Clara Bueno, Virginia C. Rodríguez‐Cortez, Alex Bataller, Belén López‐Millán, Claire Schwab, Margarita Ortega, Pablo Velasco, Maria L. Blanco, Josep Nomdedeu, Manuel Ramírez‐Orellana, Alfredo Minguela, Jose L. Fuster, Esther Cuatrecasas, Mireia Camós, Paola Ballerini, Gabriele Escherich, Judith Boer, Monique DenBoer, Jesús M. Hernández‐Rivas, Maria J. Calasanz, Giovanni Cazzaniga, Christine J. Harrison, Pablo Menéndez, Oscar Molina
Publikováno v:
Molecular Oncology, Vol 16, Iss 16, Pp 2899-2919 (2022)
B‐cell acute lymphoblastic leukemia (B‐ALL) is the commonest childhood cancer. High hyperdiploidy (HHD) identifies the most frequent cytogenetic subgroup in childhood B‐ALL. Although hyperdiploidy represents an important prognostic factor in ch
Externí odkaz:
https://doaj.org/article/c4efc3858e8a4dd59893e2d44eb72c0d
Autor:
Jose A. Martinez-Climent, Felipe Prosper, Oscar Yanes, Xabier Agirre, Maria D. Odero, Maria J. Moreno-Aliaga, Bruno Paiva, Alvaro Martinez-Baztan, Julen Oyarzabal, Ruben Pio, Puri Fortes, Celia Prior, Jiahuai Han, Alexandra Junza, Carlos Panizo, Maria J. Calasanz, Maria J. Larrayoz, Marta Fernandez-Galilea, Carmen Vicente, Jon Celay, Marta Larrayoz, Maria J. Garcia-Barchino, Vicente Fresquet
For millions of years, endogenous retroelements have remained transcriptionally silent within mammalian genomes by epigenetic mechanisms. Modern anticancer therapies targeting the epigenetic machinery awaken retroelement expression, inducing antivira
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fd38133a1d3d0fc69bfac72ef54132a
https://doi.org/10.1158/2159-8290.c.6549353.v1
https://doi.org/10.1158/2159-8290.c.6549353.v1
Autor:
Jose A. Martinez-Climent, Felipe Prosper, Oscar Yanes, Xabier Agirre, Maria D. Odero, Maria J. Moreno-Aliaga, Bruno Paiva, Alvaro Martinez-Baztan, Julen Oyarzabal, Ruben Pio, Puri Fortes, Celia Prior, Jiahuai Han, Alexandra Junza, Carlos Panizo, Maria J. Calasanz, Maria J. Larrayoz, Marta Fernandez-Galilea, Carmen Vicente, Jon Celay, Marta Larrayoz, Maria J. Garcia-Barchino, Vicente Fresquet
Supplementary Figures S1-S7 with legends
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04cd1ba7e34a4f91806bf9b7dfe5c665
https://doi.org/10.1158/2159-8290.22540328.v1
https://doi.org/10.1158/2159-8290.22540328.v1
Autor:
Jose A. Martinez-Climent, Felipe Prosper, Oscar Yanes, Xabier Agirre, Maria D. Odero, Maria J. Moreno-Aliaga, Bruno Paiva, Alvaro Martinez-Baztan, Julen Oyarzabal, Ruben Pio, Puri Fortes, Celia Prior, Jiahuai Han, Alexandra Junza, Carlos Panizo, Maria J. Calasanz, Maria J. Larrayoz, Marta Fernandez-Galilea, Carmen Vicente, Jon Celay, Marta Larrayoz, Maria J. Garcia-Barchino, Vicente Fresquet
Resources Table and Suppl. Tables. S1-S3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45c062deac21564ce858ab3b68ff8059
https://doi.org/10.1158/2159-8290.22540331
https://doi.org/10.1158/2159-8290.22540331
Autor:
Marta Larrayoz, Maria J. Garcia-Barchino, Jon Celay, Amaia Etxebeste, Maddalen Jimenez, Cristina Perez, Raquel Ordoñez, Cesar Cobaleda, Cirino Botta, Vicente Fresquet, Sergio Roa, Ibai Goicoechea, Catarina Maia, Miren Lasaga, Marta Chesi, P. Leif Bergsagel, Maria J. Larrayoz, Maria J. Calasanz, Elena Campos-Sanchez, Jorge Martinez-Cano, Carlos Panizo, Paula Rodriguez-Otero, Silvestre Vicent, Giovanna Roncador, Patricia Gonzalez, Satoru Takahashi, Samuel G. Katz, Loren D. Walensky, Shannon M. Ruppert, Elisabeth A. Lasater, Maria Amann, Teresa Lozano, Diana Llopiz, Pablo Sarobe, Juan J. Lasarte, Nuria Planell, David Gomez-Cabrero, Olga Kudryashova, Anna Kurilovich, Maria V. Revuelta, Leandro Cerchietti, Xabier Agirre, Jesus San Miguel, Bruno Paiva, Felipe Prosper, Jose A. Martinez-Climent
The historical lack of preclinical models reflecting the genetic heterogeneity of multiple myeloma (MM) hampers the advance of therapeutic discoveries. To circumvent this limitation, we screened mice engineered to carry eight MM lesions (NF-κB, KRAS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2563a745972cadf6c4af5126546113b9
https://hdl.handle.net/10171/65914
https://hdl.handle.net/10171/65914
Autor:
Eva Barragán, Pau Montesinos, Mireia Camos, Marcos González, Maria J. Calasanz, José Román-Gómez, Maria T. Gómez-Casares, Rosa Ayala, Javier López, Óscar Fuster, Dolors Colomer, Carmen Chillón, María J. Larrayoz, Pedro Sánchez-Godoy, José González-Campos, Félix Manso, Maria L. Amador, Edo Vellenga, Bob Lowenberg, Miguel A. Sanz
Publikováno v:
Haematologica, Vol 96, Iss 10 (2011)
Background Fms-like tyrosine kinase-3 (FLT3) gene mutations are frequent in acute promyelocytic leukemia but their prognostic value is not well established.Design and Methods We evaluated FLT3-internal tandem duplication and FLT3-D835 mutations in pa
Externí odkaz:
https://doaj.org/article/61645e85ddeb4ab1890368d26a4ce8fe
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
Autor:
Maria J, García-Barchino, Maria E, Sarasquete, Carlos, Panizo, Julie, Morscio, Antonio, Martinez, Miguel, Alcoceba, Vicente, Fresquet, Blanca, Gonzalez-Farre, Bruno, Paiva, Ken H, Young, Eloy F, Robles, Sergio, Roa, Jon, Celay, Marta, Larrayoz, Davide, Rossi, Gianluca, Gaidano, Santiago, Montes-Moreno, Miguel A, Piris, Ana, Balanzategui, Cristina, Jimenez, Idoia, Rodriguez, Maria J, Calasanz, Maria J, Larrayoz, Victor, Segura, Ricardo, Garcia-Muñoz, Maria P, Rabasa, Shuhua, Yi, Jianyong, Li, Mingzhi, Zhang, Zijun Y, Xu-Monette, Noemi, Puig-Moron, Alberto, Orfao, Sebastian, Böttcher, Jesus M, Hernandez-Rivas, Jesus San, Miguel, Felipe, Prosper, Thomas, Tousseyn, Xavier, Sagaert, Marcos, Gonzalez, Jose A, Martinez-Climent
Publikováno v:
The Journal of pathology. 245(1)
The increased risk of Richter transformation (RT) in patients with chronic lymphocytic leukaemia (CLL) due to Epstein-Barr virus (EBV) reactivation during immunosuppressive therapy with fludarabine other targeted agents remains controversial. Among 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::678609694b8a3c5ea5d4d16114e1d207
https://pubmed.ncbi.nlm.nih.gov/29464716
https://pubmed.ncbi.nlm.nih.gov/29464716
Autor:
Teresa Ezponda, Ari Melnick, Raquel Ordoñez, Hendrik G. Stunnenberg, Arantxa Carrasco, Halima El-Omri, Roser Vilarrasa-Blasi, Xabier Agirre, Estíbaliz Miranda, Núria Verdaguer-Dot, Ruba Y. Taha, Constantine S. Mitsiades, Marta Kulis, Martí Duran-Ferrer, Ivo Gut, Jesus San Miguel, Paul Flicek, Guillem Clot, José I. Martín-Subero, Jonathan D. Licht, Joost H.A. Martens, Bruno Paiva, Renée Beekman, Elias Campo, Vicente Chapaprieta, Leire Garate, Cem Meydan, Maria J. Calasanz, Nuria Russiñol, Felipe Prosper
Publikováno v:
HemaSphere. 3:236
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_________::aebb7594299e6307f316cdbad913ad0b
https://doi.org/10.1097/01.hs9.0000560560.72691.d3
https://doi.org/10.1097/01.hs9.0000560560.72691.d3