María Luz Sánchez

ORCID: 0009-0004-8048-4259
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Research Areas
  • Chronic Lymphocytic Leukemia Research
  • Lymphoma Diagnosis and Treatment
  • Multiple Myeloma Research and Treatments
  • T-cell and B-cell Immunology
  • Mast cells and histamine
  • Immunodeficiency and Autoimmune Disorders
  • Viral-associated cancers and disorders
  • Urticaria and Related Conditions
  • Immunotherapy and Immune Responses
  • Chronic Myeloid Leukemia Treatments
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Acute Myeloid Leukemia Research
  • Complement system in diseases
  • Asthma and respiratory diseases
  • Dialysis and Renal Disease Management
  • Amyloidosis: Diagnosis, Treatment, Outcomes
  • Immune Cell Function and Interaction
  • Protein Degradation and Inhibitors
  • Psoriasis: Treatment and Pathogenesis
  • Salivary Gland Disorders and Functions
  • Dermatology and Skin Diseases
  • Bone Metabolism and Diseases
  • Adenosine and Purinergic Signaling
  • Cancer Cells and Metastasis
  • Hematopoietic Stem Cell Transplantation

Administración Nacional de Laboratorios e Institutos de Salud
2025

Fundación Renal
2025

Hospital Universitario La Paz
2023

Centro de Investigación del Cáncer
2005-2015

Instituto de Investigación Biomédica de Salamanca
2013-2015

Universidad de Salamanca
2006-2015

Instituto de Biologia Molecular e Celular
2010-2013

Consejo Superior de Investigaciones Científicas
2008

Medicina
2008

Universidad de Murcia
2008

Abstract A heterogeneous spectrum of immunophenotypic abnormalities have been reported in myelodysplastic syndromes (MDS). However, most studies are restricted to the analysis CD34 + cells and/or other major subsets − cells, frequently not exploring diagnostic and prognostic impact immunophenotyping. Methods: We propose for first time an score (IS) based on altered distribution features maturing/mature compartments bone marrow (BM) hematopoietic 56 patients with MDS that could contribute a...

10.1002/cyto.b.20513 article EN Cytometry Part B Clinical Cytometry 2010-03-02

Abstract Background: Evaluation of the expression glycosylphosphatidylinositol‐anchored membrane proteins (GPI‐AP) is currently used for diagnosis paroxysmal nocturnal hemoglobinuria (PNH). In this study, we analyzed amount a wide variety GPI‐AP in different subsets hematopoietic cells present normal peripheral blood (PB), to establish their patterns and provide frame reference definition best combination PB cell be applied monitoring PNH. Results: Our results show variable distinct cells....

10.1002/cyto.b.20087 article EN Cytometry Part B Clinical Cytometry 2006-02-21

Abstract B‐cell chronic lymphocytic leukemia (B‐CLL) is a well‐defined clinical entity with heterogeneous molecular and cytogenetic features. Here, we analyze the impact of trisomy 12, del(13q), del(17p), del(11q) as determined by interphase fluorescence in situ hybridization analysis purified neoplastic B‐CLL cells on their immunophenotype, DNA ploidy status proliferative rate. Overall, 111 180 (62%) cases studied displayed one (50%) or more (12%) genetic abnormalities, del(13q) (35%) being...

10.1002/cyto.b.20390 article EN Cytometry Part B Clinical Cytometry 2007-12-05

SUMMARY Dendritic cells (DC) represent the most powerful professional antigen-presenting (APC) in immune system. The aim of present study was to analyse, on a single-cell basis by multiparametric flow cytometry with simultaneous four-colour staining and two-step acquisition procedure, immunophenotypic profile cytokine production DC from 67 normal whole peripheral blood (PB) samples. Two clearly different subsets HLA-II+/lineage− were identified their distinct phenotypic characteristics: one...

10.1046/j.1365-2249.1999.01078.x article EN Clinical & Experimental Immunology 1999-12-01

Abstract Background: Glycosylphosphatidylinositol‐anchored proteins (GPI‐AP) are a heterogeneous group of deficiently expressed in patients with paroxysmal nocturnal hemoglobinuria. Up till now, no study has been reported which the exact patterns expression large number GPI‐AP quantitatively evaluated normal bone marrow (BM) cells classified according to their lineage and maturation stage. Methods: In present study, we have analyzed eleven different (CD14, CD16, CD24, CD48, CD52, CD58, CD59,...

10.1002/cyto.b.20143 article EN Cytometry Part B Clinical Cytometry 2006-10-18

Background and Objectives Waldenström macroglobulinemia (WM) monoclonal gammopathy of undetermined significance (MGUS) are IgM-related disorders in which B cells harbor a unique clonotypic rearrangement the immunoglobulin heavy chain gene (IgH). The aim this study was to characterize IgH rearrangements larger series than any previously described.Design Methods Seventy-two patients with IgM (64 WM eight IgM-MGUS) were studied amplify sequence both VDJH DJH rearrangements. Twenty-nine them...

10.3324/haematol.10755 article EN cc-by-nc Haematologica 2007-05-01

La pandemia por COVID-19, como evento disruptivo y singular, puso en jaque mucho más que los sistemas de salud países a nivel global. misma afectó diferencialmente aquellos grupos definidos alto riesgo enfermedad muerte [entre se encuentran las personas con diabetes mellitus (DM)]. El objetivo principal esta investigación es indagar padecimientos DM, recabando percepciones sobre su proceso salud-enfermedad-atención-cuidado el contexto la última COVID-19. Se incluyeron diagnóstico DM...

10.36367/ntqr.21.1.2025.e1025 article ES cc-by-nc-nd New Trends in Qualitative Research 2025-01-17

Chronic kidney disease-associated pruritus (CKD-aP), a persistent itching sensation, is prevalent among hemodialysis patients. This study aims to understand its prevalence, possible association with selected solutes, and impact on quality of life (QoL) in Involving 434 patients Spain, this observational employed survey based validated assessment tools, alongside demographic, clinical, biochemical data collection. The used statistical analyses examine the correlation between CKD-aP various...

10.1038/s41598-024-83833-2 article EN cc-by-nc-nd Scientific Reports 2025-02-20

Information about maturation of plasmacytoid dendritic cell precursors (pre-pDCs) in normal bone marrow (BM) remains limited.Immunophenotypical, morphologic, and functional changes associated with pre-pDCs were analyzed adult human BM (n = 45).Three pre-pDC stages, an increasingly higher degree maturity, systematically identified: CD34++/HLA-DR++/+++/CD123++/CD45+/++ (Stage I), CD34+/HLA-DR+/++/CD123++/+++/CD45+/++ II), CD34-/HLA-DR++/CD123++/+++/CD45++ III) cells. Lymphoid- early...

10.1111/j.1537-2995.2009.02170.x article EN Transfusion 2009-04-21

// Paloma Bárcena 1 , María Jara-Acevedo Dolores Tabernero 2 Antonio López Luz Sánchez Andrés C. García-Montero Noemí Muñoz-García Belén Vidriales 3 Artur Paiva 4 Quentin Lecrevisse Margarida Lima 5 Anton W. Langerak 6 Sebastian Böttcher 7 Jacques J.M. van Dongen Alberto Orfao 1, * Julia Almeida Cancer Research Centre (IBMCC, CSIC-USAL), Institute of Biomedical Salamanca (IBSAL), (NUCLEUS) and Department Medicine, University Salamanca, Spain Unity IECSCYL, Hospital IBSAL, Hematology Unidade...

10.18632/oncotarget.5480 article EN Oncotarget 2015-11-06

Abstract Introduction Mesenchymal stem cells (MSCs) are multipotent capable of self-renewal and multilineage differentiation. Their multipotential capacity immunomodulatory properties have led to an increasing interest in their biological therapeutic applications. Currently, the definition MSCs relies on a combination phenotypic, morphological functional characteristics which typically evaluated upon vitro expansion, process that may ultimately lead modulation immunophenotypic, and/or...

10.1186/s13287-015-0152-8 article EN cc-by Stem Cell Research & Therapy 2015-09-07
Nuria Aresté Fosalba J. Emilio Sánchez-Álvarez Mario Prieto‐Velasco Pablo Molina Vicent Esteve-Simó and 94 more Raquel Ojeda Juan Manuel Buades Marián Goicoechea Rafael Sánchez Guillermo Alcalde Bezhold Rosa Elena Pérez-Morales Ana Blanco Santos Roser Peiró-Jordan María Dolores Arenas Ana Cristina Andrade Miguel Seras Mozas Paola Villabón José Luis Pérez Canga Natalia Andrés Torre Maria Jesús Moyano Franco Pablo Bouza Piñeiro María Fernanda Arrojo Alonso Willy Bernales Guerra Agustín Carreño Nerea Gómez Maria Slon Ramón González Joaquín Manrique I. Albo Castaño J.Tapia Sanz Edgardo Chacón J Solar Asuncion Ferrer‐Nadal Susana García Melendreras Jordi Soler Gregorio Romero Maribel Troya Fredzzia Graterol Francisco Henriquez Ortega Fernando Henríquez Isabel María Martín Báez Ana Isabel Martínez Puerto Elena Araceli Jiménez Vívora Silvia Benito García María Jesús Lloret Vanesa Martín Chica Victoria Mascarós Ferrer Catalina Beatriz Ulloa Clavijo Julia Mejido Moro María del Carmen Merino Bueno Belén Vizcaíno Belén Morales Franco Elba Díaz Ana María Oltra Benavent Sofía Ortego Sofía Palomo Aparicio Sara Piqueras Sánchez José Pórtoles Félix Valentín González Andrea Zapata Balcázar José Luis Rodriguez García F. González Sastre Manuel Fernández Martín Karina Furaz José C. De La Flor María Ortíz Sánchez Alfredo Cordón Nardeth Benavides Alicia González Mireilla Zeballos Ángel Méndez Mariano Acuña Daniel Galán Elena Guerrero Ana Botella Javier Naranjo Felipe Zalamea Paula Manso Delfina Yetman Damián Carneiro Mara Lisbet Cabana Carcasi Laura Beato Marina Burgos da Silva Marc Handel María Luz Sánchez Margarita Delgado Cerón María Melissa Vasquez Marta San Juan Luis Nieto Ramiro Cazar Jesús Hernández José Guerrero Carrillo María Isabel Martínez Araceli E. Rossignoli Maria Soledad Pizarro-Sánchez Lola Piña Emilio González‐Parra Mónica Pereira María Concepción Ferreira Feijoo

10.1093/ckj/sfac246 article EN cc-by-nc Clinical Kidney Journal 2023-03-23

Paroxysmal nocturnal hemoglobinuria (PNH) is characterized by a deficient expression of glycosylphosphatidylinositol-anchored proteins (GPI-APs), due to somatic mutations the phosphatidylinositolglycan complementation Class A (PIG-A) gene.In this study, high number GPI-APs on different subsets peripheral blood (PB) cells from 14 PNH patients and their potential association with underlying genetic abnormalities has been analyzed.This study confirms existence variable patterns both major minor...

10.1111/j.1537-2995.2008.01686.x article EN Transfusion 2008-04-16

The authors' objective was to determine by 2-dimensional echo Doppler (2DECHO) the cardiac abnormalities in juvenile onset ankylosing spondylitis (JOAS) and adult (AOAS) male patients with long-term disease. Twenty JOAS, 31 AOAS, 20 healthy controls of same age gender without cardiopulmonary symptoms were studied. Using 2DECHO, heart dimensions determined according American Society Echocardiography guidelines. left ventricle ejection fraction (LVEF) calculated Teichholz's formula....

10.1177/000331970105200806 article EN Angiology 2001-08-01

Summary Despite the effects of BCR ABL on cell proliferation, no study has compared proliferative rate different haematopoietic compartments from chronic myeloid leukaemia (CML) with those normal bone marrow (NBM). We comparatively analysed cycle distribution and / expression in BM cells 15 CML 11 NBM. Overall, our results showed similar indices patients However, CD34 + precursors displayed an increased proportion S G 2 /M‐phase ( P = 0·04), while significant differences were found between...

10.1111/j.1365-2141.2006.06265.x article EN British Journal of Haematology 2006-08-29

The coronavirus disease (COVID) pandemic has resulted in a major disruption healthcare that affected several medical and surgical specialties. European American Vascular Societies have proposed deferring the creation of an elective vascular access (VA) [autologous or prosthetic arteriovenous fistula (AVF) graft (AVG)] incident patients on haemodialysis (HD) era COVID pandemic. aim this study is to examine impact VA central venous catheter (CVC)-related hospitalizations complications HD...

10.1093/ckj/sfac094 article EN cc-by-nc Clinical Kidney Journal 2022-04-14
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