<p>(A) Paraffin-embedded brain sections (40 <i>μ</i>m thick) of Tg and control mice were stained with a specific antibody for human L-ferritin chain. (B) Slices stained with DAB-enhanced Perl’s reaction showed a strong accumulation of ferritin/iron bodies in Tg-mouse brains. The quantitative evaluation of the percentage of brown staining in various fields showed the increase of the number and size of the granules with aging. At the optical microscope these granules seemed to be present mostly in neurons, and in the center of the cells in a nuclear/paranuclear position. (C) Mice were treated for 3 weeks with oral iron chelator Deferiprone (DFR) 1 mg/ml in drinking water ad libitum to reduce iron burden. The treatment reduced inclusion bodies...
<p>Increased DAB-enhanced Perls' iron stain is observed in small cells that have an eccentric nucleu...
Aberrant iron deposition in the brain is associated with aging and neurodegenerative disorders inclu...
Neuroferritinopathies are rare genetic diseases caused by mutations in the C−terminal domain of ferr...
Mutations in the ferritin light chain (FTL) gene cause the neurodegenerative disease neuroferritinop...
Huntington’s disease (HD) is a progressive neurodegenerative disorder caused by a polyglutamine-enco...
<p>Coronal sections from male <i>Irp2<sup>−/−</sup></i> and WT brains from rostral <i>(top</i>) to c...
<div><p>Huntington’s disease (HD) is a progressive neurodegenerative disorder caused by a polyglutam...
Huntington's disease (HD) is a progressive neurodegenerative disorder caused by a polyglutamine-enco...
Huntington's disease (HD) is a progressive neurodegenerative disorder caused by a polyglutamine-enco...
Impaired brain iron homeostatic mechanisms, independent of pathological hallmarks, are harmful to th...
Aberrant expression of ferritin, a major iron-binding protein, has shown to be involved in neurodege...
A number of neurodegenerative diseases like Multiple Sclerosis, Parkinson’s and Alzheimer’s have bee...
Ferritin is the main intracellular protein of iron storage with a central role in the regulation of ...
Iron homeostasis is tightly regulated by iron-binding proteins, as iron excess exhibits toxicity in ...
Mutations in the ferritin light chain (FTL) gene cause the neurodegenerative disease neuroferritinop...
<p>Increased DAB-enhanced Perls' iron stain is observed in small cells that have an eccentric nucleu...
Aberrant iron deposition in the brain is associated with aging and neurodegenerative disorders inclu...
Neuroferritinopathies are rare genetic diseases caused by mutations in the C−terminal domain of ferr...
Mutations in the ferritin light chain (FTL) gene cause the neurodegenerative disease neuroferritinop...
Huntington’s disease (HD) is a progressive neurodegenerative disorder caused by a polyglutamine-enco...
<p>Coronal sections from male <i>Irp2<sup>−/−</sup></i> and WT brains from rostral <i>(top</i>) to c...
<div><p>Huntington’s disease (HD) is a progressive neurodegenerative disorder caused by a polyglutam...
Huntington's disease (HD) is a progressive neurodegenerative disorder caused by a polyglutamine-enco...
Huntington's disease (HD) is a progressive neurodegenerative disorder caused by a polyglutamine-enco...
Impaired brain iron homeostatic mechanisms, independent of pathological hallmarks, are harmful to th...
Aberrant expression of ferritin, a major iron-binding protein, has shown to be involved in neurodege...
A number of neurodegenerative diseases like Multiple Sclerosis, Parkinson’s and Alzheimer’s have bee...
Ferritin is the main intracellular protein of iron storage with a central role in the regulation of ...
Iron homeostasis is tightly regulated by iron-binding proteins, as iron excess exhibits toxicity in ...
Mutations in the ferritin light chain (FTL) gene cause the neurodegenerative disease neuroferritinop...
<p>Increased DAB-enhanced Perls' iron stain is observed in small cells that have an eccentric nucleu...
Aberrant iron deposition in the brain is associated with aging and neurodegenerative disorders inclu...
Neuroferritinopathies are rare genetic diseases caused by mutations in the C−terminal domain of ferr...