Cytochrome c association with the inner mitochondrial membrane is impaired in the CNS of G93A-SOD1 mice. (Q45213388)

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7 January 2020

title

Cytochrome c association with the inner mitochondrial membrane is impaired in the CNS of G93A-SOD1 mice (English)

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7 January 2020

author name string

Ilias G Kirkinezos

1

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7 January 2020

Sandra R Bacman

2

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7 January 2020

Dayami Hernandez

3

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7 January 2020

Jose Oca-Cossio

4

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7 January 2020

Laura J Arias

5

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7 January 2020

Miguel A Perez-Pinzon

6

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7 January 2020

Walter G Bradley

7

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7 January 2020

Carlos T Moraes

8

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7 January 2020

language of work or name

English

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publication date

1 January 2005

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7 January 2020

published in

Journal of Neuroscience

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7 January 2020

volume

25

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7 January 2020

issue

1

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7 January 2020

page(s)

164-172

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Neuroprotective effects of creatine in a transgenic animal model of amyotrophic lateral sclerosis.

7 January 2020

cites work

1 reference

12 December 2020

Loss of molecular interaction between cytochrome c and cardiolipin due to lipid peroxidation

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12 December 2020

Mitochondrial enzyme activity in amyotrophic lateral sclerosis: implications for the role of mitochondria in neuronal cell death

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12 December 2020

The roles of free radicals in amyotrophic lateral sclerosis: reactive oxygen species and elevated oxidation of protein, DNA, and membrane phospholipids

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12 December 2020

The effect of reactive oxygen species generated from the mitochondrial electron transport chain on the cytochrome c oxidase activity and on the cardiolipin content in bovine heart submitochondrial particles

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Cytochrome c nitration by peroxynitrite.

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Increased reactive oxygen species in familial amyotrophic lateral sclerosis with mutations in SOD1.

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Mitochondrial phospholipid hydroperoxide glutathione peroxidase inhibits the release of cytochrome c from mitochondria by suppressing the peroxidation of cardiolipin in hypoglycaemia-induced apoptosis

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Increased oxidative damage to DNA in ALS patients

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Dysfunctional mitochondrial respiration in the wobbler mouse brain

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Intrathecal cyclosporin prolongs survival of late-stage ALS mice

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Oxidative damage to mitochondrial DNA in spinal motoneurons of transgenic ALS mice.

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Amyotrophic lateral sclerosis: pathogenesis

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Recruitment of the mitochondrial-dependent apoptotic pathway in amyotrophic lateral sclerosis

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12 December 2020

Oxidative stress causes abnormal accumulation of familial amyotrophic lateral sclerosis-related mutant SOD1 in transgenic Caenorhabditis elegans

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12 December 2020

CuZn superoxide dismutase (SOD1) accumulates in vacuolated mitochondria in transgenic mice expressing amyotrophic lateral sclerosis-linked SOD1 mutations

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12 December 2020

Mutant Cu, Zn superoxide dismutase that causes motoneuron degeneration is present in mitochondria in the CNS

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12 December 2020

Mutant SOD1 causes motor neuron disease independent of copper chaperone-mediated copper loading

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12 December 2020

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

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12 December 2020

Mitochondrial dysfunction in a cell culture model of familial amyotrophic lateral sclerosis

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Is ALS caused by an altered oxidative activity of mutant superoxide dismutase?

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Update on the glutamatergic neurotransmitter system and the role of excitotoxicity in amyotrophic lateral sclerosis

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Mitochondrial electron transport chain complex dysfunction in a transgenic mouse model for amyotrophic lateral sclerosis

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12 December 2020

Mitochondrial localization of mutant superoxide dismutase 1 triggers caspase-dependent cell death in a cellular model of familial amyotrophic lateral sclerosis

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12 December 2020

Loss of cardiolipin and mitochondria during programmed neuronal death: evidence of a role for lipid peroxidation and autophagy

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12 December 2020

Cytochrome oxidase assembly does not require catalytically active cytochrome C.

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12 December 2020

Cardiolipin and apoptosis

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12 December 2020

ALS-associated mutant SOD1G93A causes mitochondrial vacuolation by expansion of the intermembrane space and by involvement of SOD1 aggregation and peroxisomes

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12 December 2020

Neurodegeneration in amyotrophic lateral sclerosis: the role of oxidative stress and altered homeostasis of metals

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12 December 2020

10N-nonyl acridine orange interacts with cardiolipin and allows the quantification of this phospholipid in isolated mitochondria

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12 December 2020

Wild-Type Nonneuronal Cells Extend Survival of SOD1 Mutant Motor Neurons in ALS Mice

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12 December 2020

Histological evidence of redox system breakdown caused by superoxide dismutase 1 (SOD1) aggregation is common to SOD1-mutated motor neurons in humans and animal models

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12 December 2020

Role of reactive oxygen species and cardiolipin in the release of cytochrome c from mitochondria

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12 December 2020

An ALS mouse model with a permeable blood-brain barrier benefits from systemic cyclosporine A treatment.

1 reference

12 December 2020

The cardiolipin-cytochrome c interaction and the mitochondrial regulation of apoptosis

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12 December 2020

Use of the fluorescent dye 10-N-nonyl acridine orange in quantitative and location assays of cardiolipin: a study on different experimental models

1 reference

12 December 2020

Initiation of apoptotic signal by the peroxidation of cardiolipin of mitochondria

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12 December 2020

Toxicity of familial ALS-linked SOD1 mutants from selective recruitment to spinal mitochondria.

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12 December 2020

Amyotrophic lateral sclerosis-associated SOD1 mutant proteins bind and aggregate with Bcl-2 in spinal cord mitochondria

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12 December 2020

Cardiolipins and biomembrane function

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12 December 2020

Cytochrome c dissociation and release from mitochondria by truncated Bid and ceramide

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12 December 2020

A double-blind study of the effectiveness of cyclosporine in amyotrophic lateral sclerosis

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12 December 2020

Comparative studies on the influence of decapitation, ketamine and thiopental anesthesia on rat heart mitochondria

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12 December 2020

An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria

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12 December 2020

Neuropathological changes in two lines of mice carrying a transgene for mutant human Cu,Zn SOD, and in mice overexpressing wild type human SOD: a model of familial amyotrophic lateral sclerosis (FALS).

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12 December 2020

Transgenic-mouse model of amyotrophic lateral sclerosis

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12 December 2020

Superoxide dismutase is an abundant component in cell bodies, dendrites, and axons of motor neurons and in a subset of other neurons

1 reference

12 December 2020

Parvalbumin and calbindin D-28k in the human motor system and in motor neuron disease.

1 reference

12 December 2020

Superoxide dismutase activity, oxidative damage, and mitochondrial energy metabolism in familial and sporadic amyotrophic lateral sclerosis

1 reference

12 December 2020

Decreased cytochrome c oxidase activity but unchanged superoxide dismutase and glutathione peroxidase activities in the spinal cords of patients with amyotrophic lateral sclerosis

1 reference

12 December 2020

Assessment of mitochondrial oxidative phosphorylation in patient muscle biopsies, lymphoblasts, and transmitochondrial cell lines

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12 December 2020

Mitochondrial dysfunction and calcium perturbation induced by traumatic brain injury.

1 reference

12 December 2020

Evidence of increased oxidative damage in both sporadic and familial amyotrophic lateral sclerosis.

1 reference

12 December 2020

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

1 reference

12 December 2020

Aberrant RNA processing in a neurodegenerative disease: the cause for absent EAAT2, a glutamate transporter, in amyotrophic lateral sclerosis

1 reference

12 December 2020

Massive mitochondrial degeneration in motor neurons triggers the onset of amyotrophic lateral sclerosis in mice expressing a mutant SOD1

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12 December 2020

Human xenomitochondrial cybrids. Cellular models of mitochondrial complex I deficiency

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12 December 2020

Aggregation and Motor Neuron Toxicity of an ALS-Linked SOD1 Mutant Independent from Wild-Type SOD1

1 reference

12 December 2020

10.1523/JNEUROSCI.3829-04.2005

Identifiers

DOI

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7 January 2020

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7 January 2020

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