[HTML][HTML] Cellular iron uptake, trafficking and metabolism: Key molecules and mechanisms and their roles in disease

DJR Lane, AM Merlot, MLH Huang, DH Bae… - … et Biophysica Acta (BBA …, 2015 - Elsevier
Iron is a crucial transition metal for virtually all life. Two major destinations of iron within
mammalian cells are the cytosolic iron-storage protein, ferritin, and mitochondria. In …

[HTML][HTML] Iron and diabetes risk

JA Simcox, DA McClain - Cell metabolism, 2013 - cell.com
Iron overload is a risk factor for diabetes. The link between iron and diabetes was first
recognized in pathologic conditions—hereditary hemochromatosis and thalassemia—but …

[HTML][HTML] Mammalian iron metabolism and its control by iron regulatory proteins

CP Anderson, M Shen, RS Eisenstein… - Biochimica et Biophysica …, 2012 - Elsevier
Cellular iron homeostasis is maintained by iron regulatory proteins 1 and 2 (IRP1 and IRP2).
IRPs bind to iron-responsive elements (IREs) located in the untranslated regions of mRNAs …

Basic principles and emerging concepts in the redox control of transcription factors

R Brigelius-Flohé, L Flohé - Antioxidants & redox signaling, 2011 - liebertpub.com
Convincing concepts of redox control of gene transcription have been worked out for
prokaryotes and lower eukaryotes, whereas the knowledge on complex mammalian systems …

Friedreich's ataxia: clinical features, pathogenesis and management

A Cook, P Giunti - British medical bulletin, 2017 - academic.oup.com
Introduction Friedreich's ataxia is the most common inherited ataxia. Sources of data
Literature search using PubMed with keywords Friedreich's ataxia together with published …

Compound heterozygous FXN mutations and clinical outcome in friedreich ataxia

CA Galea, A Huq, PJ Lockhart, G Tai… - Annals of …, 2016 - Wiley Online Library
Objective Friedreich ataxia (FRDA) is an inherited neurodegenerative disease characterized
by ataxia and cardiomyopathy. Homozygous GAA trinucleotide repeat expansions in the first …

Novel Nrf2-inducer prevents mitochondrial defects and oxidative stress in Friedreich's ataxia models

R Abeti, A Baccaro, N Esteras, P Giunti - Frontiers in cellular …, 2018 - frontiersin.org
Friedreich's Ataxia (FRDA) is an autosomal recessive neurodegenerative disorder, affecting
dorsal root ganglia (DRG), cerebellar dentate nuclei and heart. It is caused by a GAA repeat …

Frataxin and mitochondrial FeS cluster biogenesis

TL Stemmler, E Lesuisse, D Pain, A Dancis - Journal of Biological …, 2010 - ASBMB
Friedreich ataxia is an inherited neurodegenerative disease caused by frataxin deficiency.
Frataxin is a conserved mitochondrial protein that plays a role in FeS cluster assembly in …

The role of iron in Friedreich's ataxia: insights from studies in human tissues and cellular and animal models

JV Llorens, S Soriano, P Calap-Quintana… - Frontiers in …, 2019 - frontiersin.org
Friedreich's ataxia (FRDA) is a rare early-onset degenerative disease that affects both the
central and peripheral nervous systems, and other extraneural tissues, mainly the heart and …

Cytosolic iron-sulfur cluster assembly (CIA) system: factors, mechanism, and relevance to cellular iron regulation

AK Sharma, LJ Pallesen, RJ Spang… - Journal of Biological …, 2010 - ASBMB
FeS cluster biogenesis is an essential process in virtually all forms of life. Complex protein
machineries that are conserved from bacteria through higher eukaryotes facilitate assembly …