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Plos One|January 24, 2013
Genetic instability and intratumoral heterogeneity in neuroblastoma with MYCN amplification plus 11q deletionEva Villamón, Ana P Berbegall, Marta Piqueras, et al.Anticancer Research|September 15, 2019
Synergistic Antioncogenic Activity of Azacitidine and Curcumin in Myeloid Leukemia Cell Lines and Patient SamplesIván Martín, Blanca Navarro, Carlos Solano, et al.Human Reproduction (Oxford, England)|July 25, 2019
Dexamethasone does not prevent malignant cell reintroduction in leukemia patients undergoing ovarian transplant: risk assessment of leukemic cell transmission by a xenograft modelCésar Díaz-García, Sonia Herraiz, Esperanza Such, et al.Experimental and Molecular Pathology|July 19, 2018
Therapy-related acute myeloid leukemia developing 14 years after allogeneic hematopoietic stem cell transplantation, from a persistent R882H-DNMT3A mutated clone of patient originIván Martín, Blanca Navarro, Eva Villamón, et al.Annals of Hematology|January 29, 2020
Impact of clinical features, cytogenetics, genetic mutations, and methylation dynamics of CDKN2B and DLC-1 promoters on treatment response to azacitidineIván Martín, Blanca Navarro, Alicia Serrano, et al.Leukemia & Lymphoma|October 25, 2016
Negative impact on clinical outcome of the mutational co-occurrence of SF3B1 and DNMT3A in refractory anemia with ring sideroblasts (RARS)Iván Martín, Esperanza Such, Blanca Navarro, et al.The Journal of Molecular Diagnostics : JMD|April 16, 2025
Rapid Screening and Monitoring of UBA1 Mutations in VEXAS SyndromeIván Martín Castillo, Elvira Mora, Rafael Hernani, et al.Plos One|June 25, 2014
Single-nucleotide polymorphism array-based karyotyping of acute promyelocytic leukemiaInés Gómez-Seguí, Dolors Sánchez-Izquierdo, Eva Barragán, et al.American Journal of Cancer Research|March 10, 2023
Prognostic value of genetic alterations and 18F-FDG PET/CT imaging features in diffuse large B cell lymphomaBlanca Ferrer-Lores, Jose Lozano, Almudena Fuster-Matanzo, et al.British Journal of Haematology|July 23, 2021
Myelodysplastic syndromes with 20q deletion: incidence, prognostic value and impact on response to azacitidine of ASXL1 chromosomal deletion and genetic mutationsIván Martín, Eva Villamón, Rosario Abellán, et al.Pageof 4