about
Expression and subcellular localization of NRAMP1 in human neutrophil granulesThe iron transport protein NRAMP2 is an integral membrane glycoprotein that colocalizes with transferrin in recycling endosomesSequential regulation of ferroportin expression after erythrophagocytosis in murine macrophages: early mRNA induction by haem, followed by iron-dependent protein expressionSuppression of hepcidin expression and iron overload mediate Salmonella susceptibility in ankyrin 1 ENU-induced mutantCharacterization of the iron transporter DMT1 (NRAMP2/DCT1) in red blood cells of normal and anemic mk/mk miceLack of the bone morphogenetic protein BMP6 induces massive iron overloadPresence of the iron exporter ferroportin at the plasma membrane of macrophages is enhanced by iron loading and down-regulated by hepcidinExpression of the DMT1 (NRAMP2/DCT1) iron transporter in mice with genetic iron overload disorders.Iron- and Hepcidin-Independent Downregulation of the Iron Exporter Ferroportin in Macrophages during Salmonella Infection.The Nramp1 protein and its role in resistance to infection and macrophage function.Lipid raft-dependent endocytosis: a new route for hepcidin-mediated regulation of ferroportin in macrophages.Benefits and risks of iron supplementation in anemic neonatal pigs.Characterization of nuclear proteins that bind to the regulatory TGATTGGC motif in the human immunodeficiency virus type 1 long terminal repeat.Copper deficiency leads to anemia, duodenal hypoxia, upregulation of HIF-2α and altered expression of iron absorption genes in mice.The microbiota shifts the iron sensing of intestinal cells.Pyruvate kinase deficiency confers susceptibility to Salmonella typhimurium infection in miceTransplantation of allogeneic T cells alters iron homeostasis in NOD/SCID mice.Novel Grb14-Mediated Cross Talk between Insulin and p62/Nrf2 Pathways Regulates Liver Lipogenesis and Selective Insulin Resistance.Acute loss of the hepatic endo-lysosomal system in vivo causes compensatory changes in iron homeostasis.Immune cells and hepatocytes express glycosylphosphatidylinositol-anchored ceruloplasmin at their cell surface.Pro-hepcidin is unable to degrade the iron exporter ferroportin unless maturated by a furin-dependent process.Comparative studies of duodenal and macrophage ferroportin proteins.Wild-type and mutant ferroportins do not form oligomers in transfected cells.Iron gene expression profile in atherogenic Mox macrophages.Mapping of Char10, a novel malaria susceptibility locus on mouse chromosome 9.Identification of a new chemically induced allele (Lp(m1Jus)) at the loop-tail locus: morphology, histology, and genetic mapping.Testosterone perturbs systemic iron balance through activation of epidermal growth factor receptor signaling in the liver and repression of hepcidin.Chronic hepcidin induction causes hyposideremia and alters the pattern of cellular iron accumulation in hemochromatotic mice.Haemolytic anaemia and alterations in hepatic iron metabolism in aged mice lacking Cu,Zn-superoxide dismutase.A physiological model to study iron recycling in macrophages.cAMP and bFGF negatively regulate tropomyosin expression in rat cultured astroblasts.Production of biologically active forms of recombinant hepcidin, the iron-regulatory hormone.The histone demethylase Phf2 acts as a molecular checkpoint to prevent NAFLD progression during obesity.Expression of the iron transporter DMT1 in kidney from normal and anemic mk miceEffect of Nramp1 on bacterial replication and on maturation of Mycobacterium avium-containing phagosomes in bone marrow-derived mouse macrophagesComparative capacities of the pig colon and duodenum for luminal iron absorption
P50
Q24299875-9803EC70-A363-4EA4-B28D-3E2626FB52DAQ24676869-D8DAE802-BE79-4016-86CC-26F49CBAF14DQ28260693-0402A95D-4EEE-4B61-985D-3B0E17F56F9FQ28505375-373DC762-A02B-420E-801C-B70748B461E4Q28507366-7BEBC8C8-C177-442E-AF47-2444AB41A963Q28510138-14B9C0BA-BA44-47B2-90E3-97F7674FF554Q28513640-223C0BC0-055F-4EA3-A8F1-CD54E8042EE3Q31835263-9216A43F-6C86-4D6C-8C58-E8D5928E0698Q33619541-062C66D0-478E-4727-91C4-EDD2EEC7B088Q33694066-67A6BF5D-E072-4D7C-94E1-D83E4C4DBF8AQ34032177-D4CC73F9-08A4-44ED-94D2-95AE6ABD6C0BQ34086911-4E9A6C09-559E-4835-9FAB-7C427B7A3B55Q34626810-74625F45-4EAD-411A-9EB6-6C38E56E2F16Q34651491-80DCBB19-2361-48A6-9578-B60DB25D42ABQ35775491-EA4C7B8A-5FE0-4D23-99F7-A258DF5AFE9CQ36229215-7B3C0D64-034A-4F85-AAB8-D327E82E0A85Q37109340-A81FE566-AFC9-452A-A006-4F23AFCABF6EQ37141714-8056B2B6-3E08-4856-BC08-15B2BD9790E0Q38713066-D8299063-AEC8-4E4A-B1C7-D05198E5B2D1Q39426768-40189783-174D-4C54-BD28-B2AA29B4ECAEQ39906904-25FADDFC-BFD2-41CA-9153-9CF7A73214AFQ40388518-F916F23D-8BEE-45E0-A966-162FB83A8CA3Q42026895-1D5232CA-99AA-49FC-B63B-F86E6095A72BQ42490391-65428E76-3054-4190-A855-130BF616478DQ43253103-2B2B7A02-2C9C-442A-AFE0-59D3584A47CFQ43636512-A093BE8F-F12F-49D7-877C-22C32A924FE0Q45282206-71702FD0-A2B6-4332-8E9F-D2C55960F139Q46843927-8B0CCED0-65A2-497C-9590-75BAB9D7F640Q50615560-468CD015-4AAF-40D9-8F53-3564B15AE52AQ50758548-1A9A8E1F-7581-4868-AA16-FA6A8FEB2637Q52212553-AE9AD64B-8557-4ECC-9A62-94EAAB6F4D09Q54420959-7FA88376-1B05-47E0-B9D9-463BDE732F11Q55297562-FA08ADD3-E22C-4E77-8BF3-29C88F247408Q74351886-D732F20F-5F90-4A2C-AB8D-F93C876363EEQ74601080-FF54021C-31B9-40AC-90CF-72890A4677C2Q80286250-7E59CB74-A480-48B5-B1B9-A296C5D2D3FA
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
François Canonne-Hergaux
@ast
François Canonne-Hergaux
@en
François Canonne-Hergaux
@es
François Canonne-Hergaux
@nl
type
label
François Canonne-Hergaux
@ast
François Canonne-Hergaux
@en
François Canonne-Hergaux
@es
François Canonne-Hergaux
@nl
prefLabel
François Canonne-Hergaux
@ast
François Canonne-Hergaux
@en
François Canonne-Hergaux
@es
François Canonne-Hergaux
@nl
P108
P106
P108
P31
P496
0000-0002-0621-2157