Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Jesus M. Hernandez-Rivas"'
Autor:
Cristina Lugones-Sánchez, Sandra Santos-Mínguez, Rita Salvado, Susana González-Sánchez, Olaya Tamayo-Morales, Amaya Hoya-González, José I. Ramírez-Manent, Rosa Magallón-Botaya, José A. Quesada-Rico, Miriam D. Garcia-Cubillas, Emiliano Rodríguez-Sánchez, Manuel A. Gómez-Marcos, Rocío Benito-Sanchez, Alex Mira, Jesus M. Hernandez-Rivas, Luis Garcia-Ortiz, MIVAS III Researchers Group
Publikováno v:
Frontiers in Public Health, Vol 11 (2023)
BackgroundThe microbiota is increasingly recognized as a significant factor in the pathophysiology of many diseases, including cardiometabolic diseases, with lifestyles probably exerting the greatest influence on the composition of the human microbio
Externí odkaz:
https://doaj.org/article/efe9bb53a09040d69ed2a8e517b6668a
Autor:
Sara Aibar, Maria Abaigar, Francisco Jose Campos-Laborie, Jose Manuel Sánchez-Santos, Jesus M. Hernandez-Rivas, Javier De Las Rivas
Publikováno v:
BMC Bioinformatics, Vol 17, Iss S15, Pp 11-21 (2016)
Abstract Background In the study of complex diseases using genome-wide expression data from clinical samples, a difficult case is the identification and mapping of the gene signatures associated to the stages that occur in the progression of a diseas
Externí odkaz:
https://doaj.org/article/48a60fd2084f411dbf220bf2b218ca03
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:
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
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:
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
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