Zobrazeno 1 - 10
of 97
pro vyhledávání: '"Jesús M. Hernández‐Rivas"'
Autor:
Adrián Mosquera‐Orgueira, Eduardo Arellano‐Rodrigo, Marta Garrote, Iván Martín, Manuel Pérez‐Encinas, María‐Teresa Gómez‐Casares, Alberto Hernández‐Sánchez, Francisca Ferrer‐Marín, Elvira Mora, Patricia Velez, Rosa Ayala, Anna Angona, Natalia de las Heras, Elena Magro, Carlos Pérez‐Míguez, Davide Crucitti, María‐Isabel Mata‐Vázquez, María‐Laura Fox, Sonia González de Villambrosía, María‐José Ramírez, Ana García, Valentín García‐Gutiérrez, Amparo Cáceres, María‐Antonia Durán, María‐Alicia Senín, José‐María Raya, José A. González, Beatriz Cuevas, Blanca Xicoy, Jyoti Nangalia, Jesús M. Hernández‐Rivas, Beatriz Bellosillo, Alberto Álvarez‐Larrán, Juan C. Hernández‐Boluda, Spanish MPN Group (GEMFIN)
Publikováno v:
HemaSphere, Vol 8, Iss 3, Pp n/a-n/a (2024)
Externí odkaz:
https://doaj.org/article/c1c01a59ae404aefb27e5f7ada7bf978
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:
Paola E. Leone, Verónica Yumiceba, Ariana Jijón-Vergara, Andy Pérez-Villa, Isaac Armendáriz-Castillo, Jennyfer M. García-Cárdenas, Santiago Guerrero, Patricia Guevara-Ramírez, Andrés López-Cortés, Ana K. Zambrano, Jesús M. Hernández-Rivas, Juan Luis García, César Paz-y-Miño
Publikováno v:
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-9 (2020)
Abstract Background Turner syndrome is a genetic disorder that affects women. It is caused by an absent or incomplete X chromosome, which can be presented in mosaicism or not. There are 12 cases of Turner syndrome patients who present structural alte
Externí odkaz:
https://doaj.org/article/2c3597f4f75d4d4f90fb70e2316006d5
Autor:
Katharina M. Lang, Kathryn L. Harrison, Paula R. Williamson, Brian J. P. Huntly, Gert Ossenkoppele, Jan Geissler, Tamàs Bereczky, Jesús M. Hernández-Rivas, Hélène Chevrou-Séverac, Rory Goodbody, Renate Schulze-Rath, Lars Bullinger
Publikováno v:
Trials, Vol 21, Iss 1, Pp 1-6 (2020)
Abstract Background Acute myeloid leukemia (AML) is the most common acute leukemia in adults and has an unacceptably low cure rate. In recent years, a number of new treatment strategies and compounds were developed for the treatment of AML. There wer
Externí odkaz:
https://doaj.org/article/8ad59713feba49249b1b42326cc74e33
Autor:
Elena Vuelta, José L. Ordoñez, David J. Sanz, Sandra Ballesteros, Jesús M. Hernández-Rivas, Lucía Méndez-Sánchez, Manuel Sánchez-Martín, Ignacio García-Tuñón
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 12, p 6386 (2022)
Chronic myeloid leukaemia (CML) is a haematological neoplasm driven by the BCR/ABL fusion oncogene. The monogenic aspect of the disease and the feasibility of ex vivo therapies in haematological disorders make CML an excellent candidate for gene ther
Externí odkaz:
https://doaj.org/article/15d472f820954c5fab3388e1d2d5c3e9
Autor:
Maribel Forero-Castro, Adrián Montaño, Cristina Robledo, Alfonso García de Coca, José Luis Fuster, Natalia de las Heras, José Antonio Queizán, María Hernández-Sánchez, Luis A. Corchete-Sánchez, Marta Martín-Izquierdo, Jordi Ribera, José-María Ribera, Rocío Benito, Jesús M. Hernández-Rivas
Publikováno v:
Diagnostics, Vol 10, Iss 7, p 455 (2020)
The clonal basis of relapse in B-cell precursor acute lymphoblastic leukemia (BCP-ALL) is complex and not fully understood. Next-generation sequencing (NGS), array comparative genomic hybridization (aCGH), and multiplex ligation-dependent probe ampli
Externí odkaz:
https://doaj.org/article/8c7bfe55c6f543d1a24c92c9571527e1
Autor:
José M. Bastida, María L. Lozano, Rocío Benito, Kamila Janusz, Verónica Palma-Barqueros, Mónica Del Rey, Jesús M. Hernández-Sánchez, Susana Riesco, Nuria Bermejo, Hermenegildo González-García, Agustín Rodriguez-Alén, Carlos Aguilar, Teresa Sevivas, María F. López-Fernández, Anna E. Marneth, Bert A. van der Reijden, Neil V. Morgan, Steve P. Watson, Vicente Vicente, Jesús M. Hernández-Rivas, José Rivera, José R. González-Porras
Publikováno v:
Haematologica, Vol 103, Iss 1 (2018)
Inherited platelet disorders are a heterogeneous group of rare diseases, caused by inherited defects in platelet production and/or function. Their genetic diagnosis would benefit clinical care, prognosis and preventative treatments. Until recently, t
Externí odkaz:
https://doaj.org/article/e0ad23648fa549b5a1e7f34c2c654e55
Autor:
Iria Vázquez, Miren Maicas, José Cervera, Xabier Agirre, Oskar Marin-Béjar, Nerea Marcotegui, Carmen Vicente, Idoya Lahortiga, Maria Gomez-Benito, Claudia Carranza, Ana Valencia, Salut Brunet, Eva Lumbreras, Felipe Prosper, María T. Gómez-Casares, Jesús M. Hernández-Rivas, María J. Calasanz, Miguel A. Sanz, Jorge Sierra, María D. Odero
Publikováno v:
Haematologica, Vol 96, Iss 10 (2011)
Background The EVI1 gene (3q26) codes for a zinc finger transcription factor with important roles in both mammalian development and leukemogenesis. Over-expression of EVI1 through either 3q26 rearrangements, MLL fusions, or other unknown mechanisms c
Externí odkaz:
https://doaj.org/article/4e460ba7e7eb4f50b9be0966b0a12580
Autor:
Esperanza Such, José Cervera, Dolors Costa, Francesc Solé, Teresa Vallespí, Elisa Luño, Rosa Collado, María J. Calasanz, Jesús M. Hernández-Rivas, Juan C. Cigudosa, Benet Nomdedeu, Mar Mallo, Felix Carbonell, Javier Bueno, María T. Ardanaz, Fernando Ramos, Mar Tormo, Reyes Sancho-Tello, Consuelo del Cañizo, Valle Gómez, Victor Marco, Blanca Xicoy, Santiago Bonanad, Carmen Pedro, Teresa Bernal, Guillermo F. Sanz
Publikováno v:
Haematologica, Vol 96, Iss 3 (2011)
Background The prognostic value of cytogenetic findings in chronic myelomonocytic leukemia is unclear. Our purpose was to evaluate the independent prognostic impact of cytogenetic abnormalities in a large series of patients with chronic myelomonocyti
Externí odkaz:
https://doaj.org/article/aeb16864d3c2414aa60ca4fb5ab986f7
Autor:
José Cervera, Pau Montesinos, Jesús M. Hernández-Rivas, María J. Calasanz, Anna Aventín, María T. Ferro, Elisa Luño, Javier Sánchez, Edo Vellenga, Chelo Rayón, Gustavo Milone, Javier de la Serna, Concha Rivas, José D. González, Mar Tormo, Elena Amutio, Marcos González, Salut Brunet, Bob Lowenberg, Miguel A. Sanz
Publikováno v:
Haematologica, Vol 95, Iss 3 (2010)
Background Acute promyelocytic leukemia is a subtype of acute myeloid leukemia characterized by the t(15;17). The incidence and prognostic significance of additional chromosomal abnormalities in acute promyelocytic leukemia is still a controversial m
Externí odkaz:
https://doaj.org/article/0a22cbb8a141405286983a5878e2422c