| P2093 | author name string | Li Yang | |
| | Taosheng Huang | |
| | Laura G Reinholdt | |
| | Yanyan Peng | |
| | Stacey J Sukoff Rizzo | |
| | Michael P Jankowski | |
| | Belinda Harris | |
| | Torrian Green | |
| | Luis F Queme | |
| | Jesse D Slone | |
| | Jennifer L Ryan | |
| P2860 | cites work | Presence of foveal bulge in optical coherence tomographic images in eyes with macular edema associated with branch retinal vein occlusion | Q87121266 |
| | A novel complex neurological phenotype due to a homozygous mutation in FDX2 | Q90237965 |
| | Biallelic mutations in FDXR cause neurodegeneration associated with inflammation | Q91704768 |
| | Fractalkine Induces Hepcidin Expression of BV-2 Microglia and Causes Iron Accumulation in SH-SY5Y Cells | Q92575793 |
| | Human adrenodoxin reductase: two mRNAs encoded by a single gene on chromosome 17cen----q25 are expressed in steroidogenic tissues | Q24293030 |
| | Regulation of cellular iron metabolism | Q24610063 |
| | Functional reconstitution of mitochondrial Fe/S cluster synthesis on Isu1 reveals the involvement of ferredoxin | Q27695962 |
| | Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder | Q28117097 |
| | Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia | Q28250989 |
| | Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion | Q28275699 |
| | Clinical and genetic abnormalities in patients with Friedreich's ataxia | Q28290611 |
| | Assembly and iron-binding properties of human frataxin, the protein deficient in Friedreich ataxia | Q28646412 |
| | Cerebellar pathology in Friedreich's ataxia: atrophied dentate nuclei with normal iron content. | Q30426640 |
| | Aggregation of actin and cofilin in identical twins with juvenile-onset dystonia | Q33649419 |
| | Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathy | Q33765243 |
| | Humans possess two mitochondrial ferredoxins, Fdx1 and Fdx2, with distinct roles in steroidogenesis, heme, and Fe/S cluster biosynthesis | Q33977876 |
| | Renin-angiotensin system regulates neurodegeneration in a mouse model of normal tension glaucoma | Q34007779 |
| | The pathogenesis of cardiomyopathy in Friedreich ataxia. | Q35147235 |
| | Deficit of in vivo mitochondrial ATP production in patients with Friedreich ataxia | Q35653693 |
| | Iron Toxicity in the Retina Requires Alu RNA and the NLRP3 Inflammasome | Q35782822 |
| | Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders | Q35793513 |
| | Relation of cytosolic iron excess to cardiomyopathy of Friedreich's ataxia | Q36438090 |
| | Both human ferredoxins 1 and 2 and ferredoxin reductase are important for iron-sulfur cluster biogenesis | Q36538094 |
| | Ferredoxin 1b (Fdx1b) Is the Essential Mitochondrial Redox Partner for Cortisol Biosynthesis in Zebrafish. | Q36625120 |
| | β-Propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulation | Q36904897 |
| | Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase gene | Q36926146 |
| | Neurodegeneration with Brain Iron Accumulation: Genetic Diversity and Pathophysiological Mechanisms | Q38479278 |
| | hGFRalpha-4: a new member of the GDNF receptor family and a candidate for NBIA. | Q40781259 |
| | 'Mitochondrial energy imbalance and lipid peroxidation cause cell death in Friedreich's ataxia'. | Q41827616 |
| | Individual dopaminergic neurons show raised iron levels in Parkinson disease. | Q45305197 |
| | Molecular recognition and electron transfer in mitochondrial steroid hydroxylase systems | Q46111671 |
| | Ferredoxin reductase is critical for p53-dependent tumor suppression via iron regulatory protein 2. | Q46234676 |
| | Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy | Q46282814 |
| | Loss of SLC25A46 causes neurodegeneration by affecting mitochondrial dynamics and energy production in mice. | Q47249910 |
| | FDXR Mutations Cause Sensorial Neuropathies and Expand the Spectrum of Mitochondrial Fe-S-Synthesis Diseases | Q47719193 |
| | Neurodegeneration Triggers Peripheral Immune Cell Recruitment into the Forebrain | Q48945835 |
| | Iron Overload Accelerates the Progression of Diabetic Retinopathy in Association with Increased Retinal Renin Expression | Q50333811 |
| | Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA). | Q51899563 |
| | Clinical, biochemical and molecular genetic correlations in Friedreich's ataxia | Q73295495 |
| | Blockade of mitochondrial calcium uniporter prevents cardiac mitochondrial dysfunction caused by iron overload | Q85766816 |
| P433 | issue | 6 | |
| P304 | page(s) | 423 | |
| P577 | publication date | 2020-06-04 | |
| P1433 | published in | Cell Death and Disease | Q2197222 |
| P1476 | title | Integrated analysis of the molecular pathogenesis of FDXR-associated disease | |
| P478 | volume | 11 | |