About: Loïc Garçon

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An Entity of Type : foaf:Person, within Data Space : data.idref.fr associated with source document(s)

Attributes	Values
type	Person
sameAs	Garçon, Loïc (1968-....) Garçon, Loïc (1968-....) Garçon, Loïc (1968-....)
Life Event	http://www.idref.fr/161279333/birth
preferred label	Garçon, Loïc (1968-....)
name	Loïc Garçon
dbpedia-owl:citizenship	http://sws.geonames.org/3017382/
Language	http://lexvo.org/id/iso639-3/fra
isni:identifierValid	0000000387287720
Given name	Loïc
familyName	Garçon
has biographical i...tion (Deprecated)	Titulaire d'une thèse de doctorat en Biologie des Cellules Sanguines à l'Université de Paris 7, 2008 Directeur de l'unité de recherche Hématopoïèse et immunologie (HEMATIM), Amiens Professeur des Universités - Praticien hospitalier à l'Université de Picardie (UPJV) à Amiens (en 2018)
gender	male
ORCID iD	0000-0002-1125-9355
org:hasMembership	http://www.idref.fr/161279333/affiliation/1 http://www.idref.fr/161279333/affiliation/2
org:memberOf	Université de Picardie Jules Verne Université de Picardie Jules Verne
ISI Researcher ID	FAZ-2732-2022
is sameAs of	Garçon, Loïc (1968-....) Garçon, Loïc (1968-....) Garçon, Loïc (1968-....)
is Thesis advisor of	http://www.sudoc.fr/235296899/id http://www.sudoc.fr/255363443/id http://www.sudoc.fr/238423239/id Corrélations phénotype/génotype dans la xérocytose héréditaire, étude d'une série de patients présentant une mutation au codon 598 http://www.sudoc.fr/235307637/id Intelligence artificielle et apprentissage profond appliqués à la reconnaissance d'images en cytogénétique http://www.sudoc.fr/252543580/id http://www.sudoc.fr/252542916/id http://www.sudoc.fr/256329346/id http://www.sudoc.fr/270074171/id http://www.sudoc.fr/269284249/id http://www.sudoc.fr/269716688/id Place des indices érythrocytaires (% HYPO et CHr) dans l'évaluation du statut martial de la femme enceinte
is Praeses of	http://www.sudoc.fr/269982396/id http://www.sudoc.fr/275989038/id http://www.sudoc.fr/260990760/id http://www.sudoc.fr/237815737/id http://www.sudoc.fr/256392579/id http://www.sudoc.fr/276459261/id
is Author of	http://www.sudoc.fr/161279147/id Hereditary Xerocytosis: Differential Behavior of PIEZO1 Mutations in the N-Terminal Extracellular Domain Between Red Blood Cells and HEK Cells Accurate classification of plasma cell dyscrasias is achieved by combining artificial intelligence and flow cytometry Recent advances in the pathophysiology of PIEZO1-related hereditary xerocytosis Mécanismes physiologiques de l'érythropoïèse, de STAT5 à Gfi-1B Hereditary stomatocytosis: advances in knowledge of forms with dehydrated red blood cells Orai3-Mediates Cisplatin-Resistance in Non-Small Cell Lung Cancer Cells by Enriching Cancer Stem Cell Population through PI3K/AKT Pathway Rapid Gardos Hereditary Xerocytosis Diagnosis in 8 Families Using Reticulocyte Indices HDAC6 regulates human erythroid differentiation through modulation of JAK2 signalling Multiple thrombosis in a patient with Gardos channelopathy and a new KCNN4 mutation Transgene-free hematopoietic stem and progenitor cells from human induced pluripotent stem cells A somatic mosaicism in the G6PD gene inducing a late onset chronic non-spherocytic hemolytic anemia Ascorbic acid (vitamin C) synergistically enhances the therapeutic effect of targeted therapy in chronic lymphocytic leukemia https://serval.unil.ch/notice/serval:BIB_101D14CABCC9#id Optical genome mapping, a promising alternative to gold standard cytogenetic approaches in a series of acute lymphoblastic leukemias https://archive-ouverte.unige.ch/unige:163869#id A new role of glutathione peroxidase 4 during human erythroblast enucleation Plasma Markers of Neutrophil Extracellular Trap Are Linked to Survival but Not to Pulmonary Embolism in COVID-19-Related ARDS Patients http://www.sudoc.fr/24800249X/id Agranulocytosis in Patients with Diamond-Blackfan Anaemia (DBA) Treated with Deferiprone for Post-Transfusion Iron Overload: A Retrospective Study of the French DBA Cohort. Acquired Spherocytosis Due to Somatic ANK1 Mutations as a Manifestation of Clonal Hematopoiesis in Elderly Patients. Long-term follow-up of subtotal splenectomy for hereditary spherocytosis: a single-center study TRIM37 is highly expressed during mitosis in CHON-002 chondrocytes cell line and is regulated by miR-223 Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels Immortalization of erythroid progenitors for in vitro large-scale red cell production Flow Cytometry as a Fast, Cost-Effective Tool to Assess IgHV Mutational Status in CLL. Clinical and biological features in PIEZO1-hereditary xerocytosis and Gardos channelopathy: a retrospective series of 126 patients Piezo1-xerocytosis red cell metabolome shows impaired glycolysis and increased hemoglobin oxygen affinity Immunomodulation with azacytidine and donor lymphocyte infusion following sequential conditioning allogenic stem cell transplantation improves outcome of unfavorable AML PIEZO1-gene gain-of-function mutations with lower limb lymphedema onset in an adult: Clinical, scintigraphic, and noncontrast magnetic resonance lymphography findings Indoxyl sulfate impairs erythropoiesis at BFU-E stage in chronic kidney disease PHYSIOPATHOLOGY OF HEREDITARY XEROCYTOSIS: PIEZO1 GAIN OF FUNCTION MUTATIONS IMPACT HEMOGLOBIN OXYGEN AFFINITY Optical Mapping, a Promising Alternative to Gold Standard Cytogenetic Approaches in Acute Lymphoblastic Leukemias: A Blind Comparison on 10 Patients Efficacy and Safety of Erythropoietic-Stimulating Agents with Ruxolitinib in Myelofibrosis Patients : A Retrospective Analysis on 45 Patients. on Behalf of the French Intergroup of Myeloproliferative Disorders (FIM) Red blood cell Gardos channel (KCNN4): the essential determinant of erythrocyte dehydration in hereditary xerocytosis The human spleen is a major reservoir for long-lived vaccinia virus-specific memory B cells. HEREDITARY XEROCYTOSIS: CLINICAL AND BIOLOGICAL PRESENTATION AT DIAGNOSIS IN A RETROSPECTIVE SERIES OF 103 PATIENTS In silico and Functional Studies for Classification of EPAS1/HIF2A Genetic Variants Identified in Patients with Erythrocytosis A New Role of Glutathion Peroxydase 4 in Human Erythroblast Enucleation Is Hematopoietic Clonality of Indetermined Potential a Risk Factor for Pulmonary Embolism? Hereditary Spherocytosis: Indication of splenectomy and its long-term complications Combining Imaging Flow Cytometry and Machine Learning for High-Throughput Schistocyte Quantification: A SVM Classifier Development and External Validation Cohort. PIEZO1 activation delays erythroid differentiation of normal and hereditary xerocytosis-derived human progenitor cells Hodgkin lymphoma infiltration with associated haemophagocytosis in bone marrow films New KCNN4 Variants Associated With Anemia: Stomatocytosis Without Erythrocyte Dehydration Myocardial infarction in women under 50: Possible implication of clonal haematopoiesis of indetermined potential PIEZO1, sensing the touch during erythropoiesis Utility of Assessing CD3(+) Cell Chimerism within the First Months after Allogeneic Hematopoietic Stem-Cell Transplantation for Acute Myeloid Leukemia. Histone Deacetylases Function in the Control of Early Hematopoiesis and Erythropoiesis Impact of MICA and NKG2D polymorphisms in HLA-fully matched related and unrelated hematopoietic stem cell transplantation SLEEP OBSTRUCTIVE APNEA SYNDROME (SOAS) IS NOT ASSOCIATED WITH MARKED ERYTHROCYTOSIS. A STUDY ON 337 PATIENTS Medical and Assistive Health Technology: Meeting the Needs of Aging Populations A simple score (Biovid-19) based on biological parameters predicts transfer to intensive care units and death in COVID-19 patients DHEA prevents ribavirin-induced anemia via inhibition of glucose-6-phosphate dehydrogenase Sequential conditioning in unfavorable AML: a single center experience INDOXYL SULFATE AFFECTS ERYTHROPOIESIS DURING THE COURSE OF CHRONIC KIDNEY DISEASE: A MOLECULAR STUDY

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