Eva
Lumbreras González
Investigadora desde 2014
Hospital Universitario de Salamanca
Salamanca, EspañaPublicaciones en colaboración con investigadores/as de Hospital Universitario de Salamanca (20)
2022
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25-Hydroxyvitamin D Serum Levels Linked to Single Nucleotide Polymorphisms (SNPs) (rs2228570, rs2282679, rs10741657) in Skeletal Muscle Aging in Institutionalized Elderly Men Not Supplemented with Vitamin D
International Journal of Molecular Sciences, Vol. 23, Núm. 19
2021
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Clinical, biological, and prognostic implications of SF3B1 co-occurrence mutations in very low/low- and intermediate-risk MDS patients
Annals of Hematology, Vol. 100, Núm. 8, pp. 1995-2004
2020
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Comprehensive custom ngs panel validation for the improvement of the stratification of b-acute lymphoblastic leukemia patients
Journal of Personalized Medicine, Vol. 10, Núm. 3, pp. 1-21
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Genome-wide transcriptomics leads to the identification of deregulated genes after deferasirox therapy in low-risk MDS patients
Pharmacogenomics Journal, Vol. 20, Núm. 5, pp. 664-671
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Machine learning applied to gene expression analysis of T-lymphocytes in patients with cGVHD
Bone Marrow Transplantation
2019
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Chronic graft-versus-host disease could ameliorate the impact of adverse somatic mutations in patients with myelodysplastic syndromes and hematopoietic stem cell transplantation
Annals of Hematology, Vol. 98, Núm. 9, pp. 2151-2162
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Redefining synchronous colorectal cancers based on tumor clonality
International Journal of Cancer, Vol. 144, Núm. 7, pp. 1596-1608
2018
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Prospective randomized trial of 5 days azacitidine versus supportive care in patients with lower-risk myelodysplastic syndromes without 5q deletion and transfusion-dependent anemia
Leukemia and Lymphoma, Vol. 59, Núm. 5, pp. 1095-1104
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Transcriptomic rationale for synthetic lethality-targeting ERCC1 and CDKN1A in chronic myelomonocytic leukaemia
British Journal of Haematology, Vol. 182, Núm. 3, pp. 373-383
2016
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The presence of genomic imbalances is associated with poor outcome in patients with burkitt lymphoma treated with dose-intensive chemotherapy including rituximab
British journal of haematology, Vol. 172, Núm. 3, pp. 428-438
2013
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Alteration in Endoglin-Related Angiogenesis in Refractory Cytopenia with Multilineage Dysplasia
PLoS ONE, Vol. 8, Núm. 1
2012
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Expression of VAV1 in the tumour microenvironment of glioblastoma multiforme
Journal of Neuro-Oncology, Vol. 110, Núm. 1, pp. 69-77
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Imatinib therapy of chronic myeloid leukemia restores the expression levels of key genes for DNA damage and cell-cycle progression
Pharmacogenetics and Genomics, Vol. 22, Núm. 5, pp. 381-388
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Integration of global spectral karyotyping, CGH arrays, and expression arrays reveals important genes in the pathogenesis of glioblastoma multiforme
Annals of Surgical Oncology, Vol. 19, Núm. 7, pp. 2367-2379
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
2009
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Effects of imatinib mesylate on normal bone marrow cells from chronic myeloid leukemia patients in complete cytogenetic response
Leukemia Research, Vol. 33, Núm. 1, pp. 170-173
2006
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Analysis of chromosomal imbalances in an elderly woman with a giant cell tumour
Virchows Archiv, Vol. 448, Núm. 1, pp. 95-99
2005
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Characterization of chromosome 14 abnormalities by interphase in situ hybridization and comparative genomic hybridization in 124 meningiomas: Correlation with clinical, histopathologic, and prognostic features
American Journal of Clinical Pathology, Vol. 123, Núm. 5, pp. 744-751
2004
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Prognostic and biologic significance of chromosomal imbalances assessed by comparative genomic hybridization in multiple myeloma
Blood, Vol. 104, Núm. 9, pp. 2661-2666
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The value of flourescence in situ hybridization for the detection of 11q in multiple myeloma
Haematologica, Vol. 89, Núm. 10, pp. 1213-1218