(Q53232811)

12 May 2018

title

Effect of aluminium-induced Alzheimer like condition on oxidative energy metabolism in rat liver, brain and heart mitochondria. (English)

1 reference

12 May 2018

1 reference

Swegert CV

1

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12 May 2018

Dave KR

series ordinal

2

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12 May 2018

Katyare SS

series ordinal

3

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12 May 2018

publication date

1 December 1999

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12 May 2018

Mechanisms of Ageing and Development

published in

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12 May 2018

volume

112

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12 May 2018

issue

1

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12 May 2018

page(s)

27-42

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12 May 2018

Role of the beta-amyloid precursor protein in Alzheimer's disease.

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Mechanism of Alzheimer's disease: arguments for a neurotransmitter-aluminium complex implication

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Molecular determinants of amyloid deposition in Alzheimer's disease: conformational studies of synthetic beta-protein fragments.

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A mitochondrial DNA clone is associated with increased risk for Alzheimer disease

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Effect of corticosterone treatment on energy metabolism in rat liver mitochondria

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Is respiratory activity in the brain mitochondria responsive to thyroid hormone action?: a critical re-evaluation

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Effect of thyroid deficiency on oxidative phosphorylation in rat liver, kidney, and brain mitochondria.

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Brain Cytochrome Oxidase in Alzheimer's Disease

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Is Parkinson's disease a mitochondrial disorder?

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Oxidative energy deficiency. II. Human achondroplasia

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Brain aluminum in aging and Alzheimer disease

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Lipid fluidity and composition of the erythrocyte membrane from healthy dogs and Labrador retrievers with hereditary muscular dystrophy

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Mitochondrial ATPase: a target for paracetamol-induced hepatotoxicity

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Do mitochondrial DNA fragments promote cancer and aging?

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Membrane alterations as causes of impaired signal transduction in Alzheimer's disease and aging

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Effect of experimental thyrotoxicosis on oxidative phosphorylation in rat liver, kidney and brain mitochondria

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Mitochondrial complex I deficiency in Parkinson's disease

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Lipid composition of human serum lipoproteins

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Radical AGEing in Alzheimer's disease

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Multiple cytochrome deficiency and deteriorated mitochondrial polypeptide composition in fatal infantile mitochondrial myopathy and renal dysfunction

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Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

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7 January 2021

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7 January 2021

Evaluation of procedures for assaying oxidative phosphorylation enzyme activities in mitochondrial myopathy muscle biopsies

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7 January 2021

10.1016/S0047-6374(99)00051-2

Identifiers

DOI

1 reference

12 May 2018

PubMed ID

10656181

1 reference

12 May 2018