Search Results - "Dolz, Sandra"
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Circulating MicroRNAs as Novel Biomarkers of Stenosis Progression in Asymptomatic Carotid Stenosis
Published in Stroke (1970) (01-01-2017)“…BACKGROUND AND PURPOSE—Progression of asymptomatic carotid artery stenosis (ACAS) in patients with >50% luminal narrowing is considered a potential risk factor…”
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Single-nucleotide polymorphism array-based karyotyping of acute promyelocytic leukemia
Published in PloS one (24-06-2014)“…Acute promyelocytic leukemia (APL) is characterized by the t(15;17)(q22;q21), but additional chromosomal abnormalities (ACA) and other rearrangements can…”
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Precision medicine in relapsed or refractory pediatric solid tumors: a collaborative Spanish initiative
Published in Translational medicine communications (02-07-2019)“…Background Understanding pediatric cancer biology is a huge challenge in continuous development that is currently being implemented into the clinical practice…”
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Rapid Screening of ASXL1, IDH1, IDH2, and c-CBL Mutations in de Novo Acute Myeloid Leukemia by High-Resolution Melting
Published in The Journal of molecular diagnostics : JMD (01-11-2012)“…Recently, many novel molecular abnormalities were found to be distinctly associated with acute myeloid leukemia (AML). However, their clinical relevance and…”
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Fragment length analysis screening for detection of CEBPA mutations in intermediate-risk karyotype acute myeloid leukemia
Published in Annals of hematology (01-01-2012)“…During last years, molecular markers have been increased as prognostic factors routinely screened in acute myeloid leukemia (AML). Recently, an increasing…”
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Analysis of SNP rs16754 of WT1 gene in a series of de novo acute myeloid leukemia patients
Published in Annals of hematology (01-12-2012)“…The single nucleotide polymorphism (SNP) rs16754 of the WT1 gene has been previously described as a possible prognostic marker in normal karyotype acute…”
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Germline variant in Ctcf links mental retardation to Wilms tumor predisposition
Published in European journal of human genetics : EJHG (01-11-2022)“…CTCF germline mutations have been related to MRD21. We report the first bilateral Wilms tumor suffered by a MRD21 patient carrying an unreported CTCF missense…”
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Germline Predisposition to Pediatric Cancer, from Next Generation Sequencing to Medical Care
Published in Cancers (24-10-2021)“…Knowledge about genetic predisposition to pediatric cancer is constantly expanding. The categorization and clinical management of the best-known syndromes has…”
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Adverse prognostic value of MYBL2 overexpression and association with microRNA-30 family in acute myeloid leukemia patients
Published in Leukemia research (01-12-2013)“…Abstract The MYBL2 gene encodes a transcription factor implicated in cell proliferation and maturation whose amplification or overexpression has been…”
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Study of the S427G polymorphism and of MYBL2 variants in patients with acute myeloid leukemia
Published in Leukemia & lymphoma (01-02-2016)“…Dysregulation of MYBL2 has been associated to tumorigenesis and the S427G polymorphism could induce partial inactivation of MYBL2, associating it with cancer…”
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Wilms’ Tumor 1 Expression Levels in Bone Marrow after Induction and/or Consolidation Therapy Allow a Better Stratification of Patients and Improves Treatment in Adult AML
Published in Blood (06-12-2014)“…Introduction: The Wilms’ tumor 1 (WT1) gene, located on chromosome 11p13, encodes a transcription factor. WT1 is overexpressed in 90% of patients with acute…”
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The Presence Of Residual Disease After Induction and/Or Consolidation Therapy Based On Wilms' Tumor 1 (WT1) Expression Is a Strong Prognostic Factor For Relapse and Survival In AML
Published in Blood (15-11-2013)“…The Wilms' tumor 1 (WT1) gene, located on chromosome 11p13, encodes a transcription factor with both oncogene and tumor suppressor functions. WT1 is reportedly…”
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Novel Real-Time Polymerase Chain Reaction Assay for Simultaneous Detection of Recurrent Fusion Genes in Acute Myeloid Leukemia
Published in The Journal of molecular diagnostics : JMD (01-09-2013)“…The recent World Health Organization classification recognizes different subtypes of acute myeloid leukemia (AML) according to the presence of several…”
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WT1 isoform expression pattern in acute myeloid leukemia
Published in Leukemia research (01-12-2013)“…Abstract WT1 plays a dual role in leukemia development, probably due to an imbalance in the expression of the 4 main WT1 isoforms. We quantify their expression…”
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Quantitative Expression Analysis of WT1 Main Isoforms in AML
Published in Blood (18-11-2011)“…Abstract 1469 The Wilms Tumor 1 (WT1) gene was first described as a tumour suppressor gene, but its accurate role in leukemia development has not been…”
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Analysis of ASXL1, IDH1, IDH2, c-CBL, and WT1 Mutations in De Novo Acute Myeloid Leukaemia
Published in Blood (18-11-2011)“…Abstract 1450 The clinical relevance and prognostic implications of some recently identified mutations in acute myeloid leukemia (AML) is not yet well…”
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Efecto del cizallamiento y del difosfato de adenosina sobre la activación plaquetaria y la formación de microagregados en controles sanos. Valoración mediante citometría de flujo
Published in Revista del laboratorio clínico (01-10-2009)“…Resumen Introducción Diversos estudios demuestran que las velocidades de cizallamiento elevadas provocan activación plaquetaria. Sin embargo, no está descrito…”
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