(Q43762848)

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Selective changes in mitochondria respiratory properties in oxidative or glycolytic muscle fibers isolated from G93AhumanSOD1 transgenic mice

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scholarly article

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Europe PubMed Central

PubMed publication ID

26 November 2017

Selective changes in mitochondria respiratory properties in oxidative or glycolytic muscle fibers isolated from G93AhumanSOD1 transgenic mice (English)

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Europe PubMed Central

PubMed publication ID

26 November 2017

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N Leclerc

1

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

F Ribera

2

1 reference

Europe PubMed Central

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26 November 2017

J Zoll

3

1 reference

Europe PubMed Central

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26 November 2017

J M Warter

4

1 reference

Europe PubMed Central

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26 November 2017

P Poindron

5

1 reference

Europe PubMed Central

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26 November 2017

E Lampert

6

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26 November 2017

J Borg

7

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26 November 2017

publication date

1 November 2001

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26 November 2017

Neuromuscular Disorders

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26 November 2017

11

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PubMed publication ID

26 November 2017

8

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Europe PubMed Central

PubMed publication ID

26 November 2017

722-727

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Europe PubMed Central

PubMed publication ID

26 November 2017

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

1 reference

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

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Decreased cerebrospinal-fluid superoxide dismutase in amyotrophic lateral sclerosis

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

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Copper/zinc superoxide dismutase mRNA levels are increased in sporadic amyotrophic lateral sclerosis motorneurons

1 reference

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Superoxide dismutase concentration and activity in familial amyotrophic lateral sclerosis

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Superoxide dismutase in familial amyotrophic lateral sclerosis: models for gain of function

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Copper, zinc superoxide dismutase catalyzes hydroxyl radical production from hydrogen peroxide

1 reference

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Altered reactivity of superoxide dismutase in familial amyotrophic lateral sclerosis

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A gain-of-function of an amyotrophic lateral sclerosis-associated Cu,Zn-superoxide dismutase mutant: An enhancement of free radical formation due to a decrease in Km for hydrogen peroxide

1 reference

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Oxidative damage and mitochondrial decay in aging

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Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases

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

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Ultrastructural study of synapses in the anterior horn neurons of patients with amyotrophic lateral sclerosis

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Progressive motor neuron impairment in an animal model of familial amyotrophic lateral sclerosis

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Muscle creatine kinase-deficient mice. II. Cardiac and skeletal muscles exhibit tissue-specific adaptation of the mitochondrial function

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Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation

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

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Mitochondrial respiratory parameters in cardiac tissue: a novel method of assessment by using saponin-skinned fibers

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Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B

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Spontaneous myopathy in the SJL/J mouse: pathology and strength loss

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CuZnSOD and MnSOD immunoreactivity in brain stem motor neurons from amyotrophic lateral sclerosis patients.

1 reference

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Oxidative stress mediates impairment of muscle function in transgenic mice with elevated level of wild-type Cu/Zn superoxide dismutase

1 reference

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Mitochondrial disease in superoxide dismutase 2 mutant mice

1 reference

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Maintained coupling of oxidative phosphorylation to creatine kinase activity in sarcomeric mitochondrial creatine kinase-deficient mice.

1 reference

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7 January 2021

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Impairment of mitochondrial function in skeletal muscle of patients with amyotrophic lateral sclerosis

1 reference

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7 January 2021

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Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis

1 reference

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Retarded diffusion of ADP in cardiomyocytes: possible role of mitochondrial outer membrane and creatine kinase in cellular regulation of oxidative phosphorylation.

1 reference

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Mitochondrial disease in mouse results in increased oxidative stress

1 reference

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7 January 2021

based on heuristic

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Early and selective loss of neuromuscular synapse subtypes with low sprouting competence in motoneuron diseases

1 reference

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The age-related accumulation of a mitochondrial DNA control region mutation in muscle, but not brain, detected by a sensitive PNA-directed PCR clamping based method

1 reference

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7 January 2021

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inferred from DOI database lookup

Identifiers

10.1016/S0960-8966(01)00240-1

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

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