4.3 Review

SOD1 and mitochondria in ALS: a dangerous liaison

Related references

Note: Only part of the references are listed.
Review Biochemistry & Molecular Biology

Mitophagy and Parkinson's disease: The PINK1-parkin link

Emma Deas et al.

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2011)

Article Biophysics

Influence of aging on membrane permeability transition in brain mitochondria

Julia Toman et al.

JOURNAL OF BIOENERGETICS AND BIOMEMBRANES (2011)

Article Medicine, General & Internal

Amyotrophic lateral sclerosis

Matthew C. Kiernan et al.

LANCET (2011)

Review Biochemistry & Molecular Biology

The Intermembrane Space of Mitochondria

Johannes M. Herrmann et al.

ANTIOXIDANTS & REDOX SIGNALING (2010)

Article Biochemistry & Molecular Biology

In yeast redistribution of Sod1 to the mitochondrial intermembrane space provides protection against respiration derived oxidative stress

Christine Kloeppel et al.

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2010)

Review Biochemistry & Molecular Biology

Mitochondrial dysfunction in amyotrophic lateral sclerosis

Ping Shi et al.

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2010)

Review Cell Biology

Calcium dysregulation in amyotrophic lateral sclerosis

Julian Grosskreutz et al.

CELL CALCIUM (2010)

Article Biochemistry & Molecular Biology

Glutaredoxin 2 prevents aggregation of mutant SOD1 in mitochondria and abolishes its toxicity

Alberto Ferri et al.

HUMAN MOLECULAR GENETICS (2010)

Article Biochemistry & Molecular Biology

ALS-linked mutant SOD1 damages mitochondria by promoting conformational changes in Bcl-2

Steve Pedrini et al.

HUMAN MOLECULAR GENETICS (2010)

Review Cell Biology

Mitochondrial protein import: from proteomics to functional mechanisms

Oliver Schmidt et al.

NATURE REVIEWS MOLECULAR CELL BIOLOGY (2010)

Article Multidisciplinary Sciences

ALS-linked mutant superoxide dismutase 1 (SOD1) alters mitochondrial protein composition and decreases protein import

Quan Li et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)

Article Multidisciplinary Sciences

Altered distributions of Gemini of coiled bodies and mitochondria in motor neurons of TDP-43 transgenic mice

Xiu Shan et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)

Article Genetics & Heredity

Transgenic Rat Model of Neurodegeneration Caused by Mutation in the TDP Gene

Hongxia Zhou et al.

PLOS GENETICS (2010)

Article Clinical Neurology

Treatment with lithium carbonate does not improve disease progression in two different strains of SOD1 mutant mice

Chiara Pizzasegola et al.

AMYOTROPHIC LATERAL SCLEROSIS (2009)

Review Biochemistry & Molecular Biology

Mitochondrial Function, Morphology, and Axonal Transport in Amyotrophic Lateral Sclerosis

Jordi Magrane et al.

ANTIOXIDANTS & REDOX SIGNALING (2009)

Article Biochemistry & Molecular Biology

Oligomerization of Mutant SOD1 in Mitochondria of Motoneuronal Cells Drives Mitochondrial Damage and Cell Toxicity

Mauro Cozzolino et al.

ANTIOXIDANTS & REDOX SIGNALING (2009)

Article Biochemistry & Molecular Biology

Mutant SOD1 in neuronal mitochondria causes toxicity and mitochondrial dynamics abnormalities

Jordi Magrane et al.

HUMAN MOLECULAR GENETICS (2009)

Review Biochemistry & Molecular Biology

Mitochondrial dynamics-fusion, fission, movement, and mitophagy-in neurodegenerative diseases

Hsiuchen Chen et al.

HUMAN MOLECULAR GENETICS (2009)

Review Cell Biology

Non-cell autonomous toxicity in neurodegenerative disorders: ALS and beyond

Hristelina Ilieva et al.

JOURNAL OF CELL BIOLOGY (2009)

Article Biochemistry & Molecular Biology

The Disulfide Relay System of Mitochondria Is Required for the Biogenesis of Mitochondrial Ccs1 and Sod1

Silvia Reddehase et al.

JOURNAL OF MOLECULAR BIOLOGY (2009)

Review Neurosciences

Role of axonal transport in neurodegenerative diseases

Kurt J. De Vos et al.

ANNUAL REVIEW OF NEUROSCIENCE (2008)

Review Biochemistry & Molecular Biology

Amyotrophic lateral sclerosis: From current developments in the laboratory to clinical implications

Mauro Cozzolino et al.

ANTIOXIDANTS & REDOX SIGNALING (2008)

Article Biochemistry & Molecular Biology

Different regulation of wild-type and mutant Cu,Zn superoxide dismutase localization in mammalian mitochondria

Hibiki Kawamata et al.

HUMAN MOLECULAR GENETICS (2008)

Article Genetics & Heredity

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

Edor Kabashi et al.

NATURE GENETICS (2008)

Article Multidisciplinary Sciences

SOD1 and Amyotrophic Lateral Sclerosis: Mutations and Oligomerization

Lucia Banci et al.

PLOS ONE (2008)

Article Multidisciplinary Sciences

Selective assoction of misfolded ALS-linked mutant SOD1 with the cytoplasmic face of mitochondria

Christine Vande Velde et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)

Article Multidisciplinary Sciences

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

Jemeen Sreedharan et al.

SCIENCE (2008)

Article Biochemistry & Molecular Biology

Disulfide bond mediates aggregation, toxicity, and ubiquitylation of familial amyotrophic lateral sclerosis-linked mutant SOD1

Jun-ichi Niwa et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2007)

Article Neurosciences

Increased autophagy in transgenic mice with a G93A mutant SOD1 gene

Nobutoshi Morimoto et al.

BRAIN RESEARCH (2007)

Review Physiology

Mitochondrial membrane permeabilization in cell death

Guido Kroemer et al.

PHYSIOLOGICAL REVIEWS (2007)

Article Biochemistry & Molecular Biology

Bcl2a1 serves as a switch in death of motor neurons in amyotrophic lateral sclerosis

C. Crosio et al.

CELL DEATH AND DIFFERENTIATION (2006)

Article Multidisciplinary Sciences

Familial ALS-superoxide dismutases associate with mitochondria and shift their redox potentials

Alberto Ferri et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)

Article Multidisciplinary Sciences

Conversion to the amyotrophic lateral sclerosis phenotype is associated with intermolecular linked insoluble aggregates of SOD1 in mitochondria

HX Deng et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)

Article Multidisciplinary Sciences

Disulfide cross-linked protein represents a significant fraction of ALS-associated Cu, Zn-superoxide dismutase aggregates in spinal cords of model mice

Y Furukawa et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)

Review Pharmacology & Pharmacy

Targets in ALS:: designing multildrug therapies

Maria Teresa Carr et al.

TRENDS IN PHARMACOLOGICAL SCIENCES (2006)

Review Biochemistry & Molecular Biology

Lessons from models of SOD1-linked familial ALS

C Bendotti et al.

TRENDS IN MOLECULAR MEDICINE (2004)

Article Biochemistry & Molecular Biology

Factors controlling the uptake of yeast copper/zinc superoxide dismutase into mitochondria

LS Field et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2003)

Article Biochemistry & Molecular Biology

Mutated human SOD1 causes dysfunction of oxidative phosphorylation in mitochondria of transgenic mice

M Mattiazzi et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2002)

Article Biochemistry & Molecular Biology

Subcellular distribution of superoxide dismutases (SOD) in rat liver - Cu,Zn-SOD in mitochondria

A Okado-Matsumoto et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2001)

Article Multidisciplinary Sciences

Caspase-1 and-3 are Sequentially activated in motor neuron death in Cu,Zn superoxide dismutase-mediated familial amyotrophic lateral sclerosis

P Pasinelli et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)