(FC) Bioquímica y Genética
Departamento académico
Iria
Vázquez Urio
Chercheuse jusqu' 2023
Publications dans lesquelles il/elle collabore avec Iria Vázquez Urio (33)
2024
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The genomic profiling of high-risk smoldering myeloma patients treated with an intensive strategy unveils potential markers of resistance and progression
Blood cancer journal, Vol. 14, Núm. 1, pp. 74
2023
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Integrated flow cytometry and sequencing to reconstruct evolutionary patterns from dysplasia to acute myeloid leukemia
Blood Advances, Vol. 7, Núm. 1, pp. 167-173
2022
2020
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Assessment of minimal residual disease by next generation sequencing in peripheral blood as a complementary tool for personalized transplant monitoring in myeloid neoplasms
Journal of Clinical Medicine, Vol. 9, Núm. 12, pp. 1-20
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Assessment of the clinical utility of four NGS panels in myeloid malignancies. Suggestions for NGS panel choice or design
PLoS ONE, Vol. 15, Núm. 1
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Biological and clinical significance of dysplastic hematopoiesis in patients with newly diagnosed multiple myeloma
Blood, Vol. 135, Núm. 26, pp. 2375-2387
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Networking for advanced molecular diagnosis in acute myeloid leukemia patients is possible: the PETHEMA NGS-AML project
Haematologica, Vol. Online ahead of print
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Spanish Guidelines for the use of targeted deep sequencing in myelodysplastic syndromes and chronic myelomonocytic leukaemia
British Journal of Haematology
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Strategy for identification of a potential inherited leukemia predisposition in a 299 patient's cohort with tumor-only sequencing data
Leukemia Research, Vol. 95
2017
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The MDS and EVI1 complex locus (MECOM) isoforms regulate their own transcription and have different roles in the transformation of hematopoietic stem and progenitor cells
Biochimica et Biophysica Acta - Gene Regulatory Mechanisms, Vol. 1860, Núm. 6, pp. 721-729
2016
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Use of human pharyngeal and palatine tonsils as a reservoir for the analysis of B-cell ontogeny in 10 paired samples
Clinical Otolaryngology, Vol. 41, Núm. 5, pp. 606-611
2013
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Erratum: ASPP1, a common activator of TP53, is inactivated by aberrant methylation of its promoter in acute lymphoblastic leukemia (Oncogene (2013) 32 (803) DOI: 10.1038/onc.2012.593)
Oncogene
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Functional characterization of the promoter region of the human EVI1 gene in acute myeloid leukemia: RUNX1 and ELK1 directly regulate its transcription
Oncogene, Vol. 32, Núm. 16, pp. 2069-2078
2011
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Down-regulation of EVI1 is associated with epigenetic alterations and good prognosis in patients with acute myeloid leukemia
Haematologica, Vol. 96, Núm. 10, pp. 1448-1456
2010
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EVI1 controls proliferation in acute myeloid leukaemia through modulation of miR-1-2
British Journal of Cancer, Vol. 103, Núm. 8, pp. 1292-1296
2009
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Mechanisms of overexpression of the EVI1 gene (3q26) and its role in the leukemic transformation of patients with acute myeloid leukemia
Mechanisms of overexpression of the EVI1 gene (3q26) and its role in the leukemic transformation of patients with acute myeloid leukemia
2007
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Duplication and rearrangement of the MYB oncogene in T-cell acute lymphoblastic leukemia
CELLULAR ONCOLOGY
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Erratum: JAK2-V617F activating mutation in acute myeloid leukemia: Prognostic impact and association with other molecular markers (Leukemia (2007) vol. 21 (2386-2390) 10.1038/sj.leu.2404812)
Leukemia