Search Results - "Alexandre, P.A."
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Humanized hemato-lymphoid system mice
Published in Haematologica (Roma) (01-01-2016)“…Over the last decades, incrementally improved xenograft mouse models, supporting the engraftment and development of a human hemato-lymphoid system, have been…”
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Pharmacological DNA demethylation restores SMAD1 expression and tumor suppressive signaling in diffuse large B-cell lymphoma
Published in Blood advances (22-10-2019)“…The sphingosine-1-phosphate (S1P) receptor S1PR2 and its downstream adaptor Gα13 are recurrently mutationally inactivated in the germinal center B-cell subtype…”
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A hierarchical neural model in short-term load forecasting
Published in Applied soft computing (01-09-2004)“…This paper proposes a novel neural model to the problem of short-term load forecasting (STLF). The neural model is made up of two self-organizing map (SOM)…”
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Sensitive Quantitative Proteomics of Human Hematopoietic Stem and Progenitor Cells by Data-independent Acquisition Mass Spectrometry[S]
Published in Molecular & cellular proteomics (01-07-2019)“…To date, technical limitations have precluded the robust quantitative proteomic analysis of rare cell types. We describe a highly sensitive mass…”
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Editorial: The therapeutic inhibition of macrophage checkpoints
Published in Frontiers in immunology (2024)Get full text
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Candida albicans -Induced NETosis Is Independent of Peptidylarginine Deiminase 4
Published in Frontiers in immunology (09-07-2018)“…Neutrophils are the most abundant innate immune cells and the first line of defense against many pathogenic microbes, including the human fungal pathogen …”
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Blocking the CD47-SIRPα interaction reverses the disease phenotype in a polycythemia vera mouse model
Published in Leukemia (01-06-2023)“…Polycythemia vera (PV) is a hematopoietic stem cell neoplasm driven by somatic mutations in JAK2 , leading to increased red blood cell (RBC) production…”
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Repurposing of glycine transport inhibitors for the treatment of erythropoietic protoporphyria
Published in Cell chemical biology (19-08-2021)“…Erythropoietic protoporphyria (EPP) is a rare disease in which patients experience severe light sensitivity. It is caused by a deficiency of ferrochelatase…”
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Bone marrow haematopoiesis in patients with COVID-19
Published in Histopathology (01-10-2023)“…Severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) infection broadly affects organ homeostasis, including the haematopoietic system. Autopsy…”
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Delivery of oligonucleotides to bone marrow to modulate ferrochelatase splicing in a mouse model of erythropoietic protoporphyria
Published in Nucleic acids research (21-05-2020)“…Abstract Erythropoietic protoporphyria (EPP) is a rare genetic disease in which patients experience acute phototoxic reactions after sunlight exposure. It is…”
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Disruption of SIRPα signaling in macrophages eliminates human acute myeloid leukemia stem cells in xenografts
Published in The Journal of experimental medicine (24-09-2012)“…Although tumor surveillance by T and B lymphocytes is well studied, the role of innate immune cells, in particular macrophages, is less clear. Moreover, the…”
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Proteogenetic drug response profiling elucidates targetable vulnerabilities of myelofibrosis
Published in Nature communications (12-10-2023)“…Myelofibrosis is a hematopoietic stem cell disorder belonging to the myeloproliferative neoplasms. Myelofibrosis patients frequently carry driver mutations in…”
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Finally: development of humanized lymph nodes
Published in Nature methods (01-08-2018)“…Overexpression of mouse thymic-stromal-cell-derived lymphopoietin in immune-compromised mice that harbor a reconstituted human immune system rescues lymph node…”
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Targeting the mevalonate or Wnt pathways to overcome CAR T-cell resistance in TP53-mutant AML cells
Published in EMBO molecular medicine (14-03-2024)“…TP53 -mutant acute myeloid leukemia (AML) and myelodysplastic neoplasms (MDS) are characterized by chemotherapy resistance and represent an unmet clinical…”
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Calreticulin mutations affect its chaperone function and perturb the glycoproteome
Published in Cell reports (Cambridge) (22-11-2022)“…Calreticulin (CALR) is an endoplasmic reticulum (ER)-retained chaperone that assists glycoproteins in obtaining their structure. CALR mutations occur in…”
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Homozygous calreticulin mutations in patients with myelofibrosis lead to acquired myeloperoxidase deficiency
Published in Blood (23-06-2016)“…The pathogenesis of acquired myeloperoxidase (MPO) deficiency, a rare phenomenon observed in patients with Philadelphia chromosome-negative myeloproliferative…”
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The sympathomimetic agonist mirabegron did not lower JAK2 -V617F allele burden, but restored nestin-positive cells and reduced reticulin fibrosis in patients with myeloproliferative neoplasms: results of phase II study SAKK 33/14
Published in Haematologica (Roma) (01-04-2019)“…The β-3 sympathomimetic agonist BRL37344 restored nestin-positive cells within the stem cell niche, and thereby normalized blood counts and improved…”
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Editorial: Advances in Human Immune System Mouse Models for Studying Human Hematopoiesis and Cancer Immunotherapy
Published in Frontiers in immunology (23-12-2021)Get full text
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Next Generation Humanized Mice Support Engraftment of Myelofibrosis CD34+ Cells
Published in Blood (06-12-2014)“…Introduction While the key transforming genetic events occur in the developing cancerous cell, this cell is dependent on its environmental context and…”
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