Mitochondrial Mayhem: The Mitochondrion as a Modulator of Iron Metabolism and Its Role in Disease
Published 2011 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Mitochondrial Mayhem: The Mitochondrion as a Modulator of Iron Metabolism and Its Role in Disease
Authors
Keywords
-
Journal
ANTIOXIDANTS & REDOX SIGNALING
Volume 15, Issue 12, Pages 3003-3019
Publisher
Mary Ann Liebert Inc
Online
2011-03-01
DOI
10.1089/ars.2011.3921
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Mitochondrial Iron Metabolism and Its Role in Neurodegeneration
- (2017) Maxx P. Horowitz et al. JOURNAL OF ALZHEIMERS DISEASE
- Human MRCKα is regulated by cellular iron levels and interferes with transferrin iron uptake
- (2010) Radek Cmejla et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- Ferrochelatase forms an oligomeric complex with mitoferrin-1 and Abcb10 for erythroid heme biosynthesis
- (2010) W. Chen et al. BLOOD
- Glutaredoxin 5 deficiency causes sideroblastic anemia by specifically impairing heme biosynthesis and depleting cytosolic iron in human erythroblasts
- (2010) Hong Ye et al. JOURNAL OF CLINICAL INVESTIGATION
- Mitochondrial iron trafficking and the integration of iron metabolism between the mitochondrion and cytosol
- (2010) D. R. Richardson et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Iron–sulfur proteins in health and disease
- (2010) Alex Sheftel et al. TRENDS IN ENDOCRINOLOGY AND METABOLISM
- Hepcidin, the hormone of iron metabolism, is bound specifically to -2-macroglobulin in blood
- (2009) G. Peslova et al. BLOOD
- Clinical manifestation and a new ISCU mutation in iron–sulphur cluster deficiency myopathy
- (2009) Gittan Kollberg et al. BRAIN
- Function and biogenesis of iron–sulphur proteins
- (2009) Roland Lill NATURE
- Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia
- (2009) Duane L Guernsey et al. NATURE GENETICS
- Bacterial frataxin CyaY is the gatekeeper of iron-sulfur cluster formation catalyzed by IscS
- (2009) Salvatore Adinolfi et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- ABCs of erythroid mitochondrial iron uptake
- (2009) N. C. Andrews PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Elucidation of the mechanism of mitochondrial iron loading in Friedreich's ataxia by analysis of a mouse mutant
- (2009) M. L.-H. Huang et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Abcb10 physically interacts with mitoferrin-1 (Slc25a37) to enhance its stability and function in the erythroid mitochondria
- (2009) W. Chen et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- An E3 Ligase Possessing an Iron-Responsive Hemerythrin Domain Is a Regulator of Iron Homeostasis
- (2009) A. A. Salahudeen et al. SCIENCE
- Control of Iron Homeostasis by an Iron-Regulated Ubiquitin Ligase
- (2009) A. A. Vashisht et al. SCIENCE
- Splice Mutation in the Iron-Sulfur Cluster Scaffold Protein ISCU Causes Myopathy with Exercise Intolerance
- (2008) Fanny Mochel et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Systemic Iron Homeostasis and the Iron-Responsive Element/Iron-Regulatory Protein (IRE/IRP) Regulatory Network
- (2008) Martina U. Muckenthaler et al. Annual Review of Nutrition
- The role of iron in mitochondrial function
- (2008) Sonia Levi et al. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS
- Ferritins: A family of molecules for iron storage, antioxidation and more
- (2008) Paolo Arosio et al. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS
- Myopathy with lactic acidosis is linked to chromosome 12q23.3-24.11 and caused by an intron mutation in the ISCU gene resulting in a splicing defect
- (2008) A. Olsson et al. HUMAN MOLECULAR GENETICS
- Binding of Yeast Frataxin to the Scaffold for Fe-S Cluster Biogenesis, Isu
- (2008) Tao Wang et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Mitochondrial Dysfunction in Neurodegenerative Diseases
- (2008) Anthony H. V. Schapira NEUROCHEMICAL RESEARCH
- The MCK mouse heart model of Friedreich's ataxia: Alterations in iron-regulated proteins and cardiac hypertrophy are limited by iron chelation
- (2008) M. Whitnall et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Iron–sulfur cluster biogenesis and human disease
- (2008) Tracey A. Rouault et al. TRENDS IN GENETICS
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now