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Neurodegeneration with brain iron accumulation: update on pathogenic mechanismsMutant ferritin L-chains that cause neurodegeneration act in a dominant-negative manner to reduce ferritin iron incorporationMitochondrial ferritin limits oxidative damage regulating mitochondrial iron availability: hypothesis for a protective role in Friedreich ataxiaNeuroferritinopathy: From ferritin structure modification to pathogenetic mechanismPantothenate kinase-associated neurodegeneration: altered mitochondria membrane potential and defective respiration in Pank2 knock-out mouse modelA human mitochondrial ferritin encoded by an intronless geneRole of intracellular labile iron, ferritin, and antioxidant defence in resistance of chronically adapted Jurkat T cells to hydrogen peroxideIron homeostasis in peripheral nervous system, still a black box?Mitochondrial ferritin expression in erythroid cells from patients with sideroblastic anemia.Structure, function, and evolution of ferritins.Crystal structure and biochemical properties of the human mitochondrial ferritin and its mutant Ser144Ala.The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload.The pathogenesis of cardiomyopathy in Friedreich ataxia.Over-expression of mitochondrial ferritin affects the JAK2/STAT5 pathway in K562 cells and causes mitochondrial iron accumulationMitochondrial ferritin.A novel neuroferritinopathy mouse model (FTL 498InsTC) shows progressive brain iron dysregulation, morphological signs of early neurodegeneration and motor coordination deficits.Immunochemical characterization of human liver and heart ferritins with monoclonal antibodies.Human L-ferritin deficiency is characterized by idiopathic generalized seizures and atypical restless leg syndrome.Coenzyme A corrects pathological defects in human neurons of PANK2-associated neurodegeneration.Mitochondrial ferritin expression in adult mouse tissues.Cytosolic and mitochondrial ferritins in the regulation of cellular iron homeostasis and oxidative damage.Microelectronic DNA chip for hereditary hyperferritinemia cataract syndrome, a model for large-scale analysis of disorders of iron metabolism.Characterization of human mitochondrial ferritin promoter: identification of transcription factors and evidences of epigenetic control.Oxidative stress and cell death in cells expressing L-ferritin variants causing neuroferritinopathy.Human mitochondrial ferritin expressed in HeLa cells incorporates iron and affects cellular iron metabolism.Relationship between TNF-alpha and iron metabolism in differentiating human monocytic THP-1 cells.Functional roles of the ferritin receptors of human liver, hepatoma, lymphoid and erythroid cells.Development of an immunoassay for all human isoferritins, and its application to serum ferritin evaluation.Skin fibroblasts from pantothenate kinase-associated neurodegeneration patients show altered cellular oxidative status and have defective iron-handling properties.Mitochondrial iron and energetic dysfunction distinguish fibroblasts and induced neurons from pantothenate kinase-associated neurodegeneration patients.Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3).Role of iron and ferritin in TNFalpha-induced apoptosis in HeLa cells.Analysis of the biologic functions of H- and L-ferritins in HeLa cells by transfection with siRNAs and cDNAs: evidence for a proliferative role of L-ferritin.Effects of mitochondrial ferritin overexpression in normal and sideroblastic erythroid progenitors.H ferritin silencing induces protein misfolding in K562 cells: A Raman analysis.Flow cytometry evaluation of erythroid dysplasia in patients with myelodysplastic syndrome.C29G in the iron-responsive element of L-ferritin: a new mutation associated with hyperferritinemia-cataract.The expression of human mitochondrial ferritin rescues respiratory function in frataxin-deficient yeast.Unexplained isolated hyperferritinemia without iron overload.The dentate nucleus in Friedreich's ataxia: the role of iron-responsive proteins.
P50
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P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Sonia Levi
@ast
Sonia Levi
@en
Sonia Levi
@es
Sonia Levi
@nl
Sonia Levi
@sl
type
label
Sonia Levi
@ast
Sonia Levi
@en
Sonia Levi
@es
Sonia Levi
@nl
Sonia Levi
@sl
prefLabel
Sonia Levi
@ast
Sonia Levi
@en
Sonia Levi
@es
Sonia Levi
@nl
Sonia Levi
@sl
P1053
A-3161-2015
P106
P1153
7102730658
P21
P31
P3829
P496
0000-0002-5092-0847