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Coenzyme Q10 and Autoimmune Disorders: An Overview

International journal of molecular sciences, 2024-04, Vol.25 (8), p.4576

2024

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Mitochondria and Quality Control Defects in a Mouse Model of Gaucher Disease—Links to Parkinson’s Disease

Cell metabolism, 2013-06, Vol.17 (6), p.941-953

2013

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The Ubiquinone-Ubiquinol Redox Cycle and Its Clinical Consequences: An Overview

International journal of molecular sciences, 2024-06, Vol.25 (12), p.6765

2024

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Targetable Pathways for Alleviating Mitochondrial Dysfunction in Neurodegeneration of Metabolic and Non-Metabolic Diseases

International journal of molecular sciences, 2021-10, Vol.22 (21), p.11444

2021

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Dysregulation of glucose metabolism is an early event in sporadic Parkinson's disease

Neurobiology of aging, 2014-05, Vol.35 (5), p.1111-1115

2014

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The ketogenic diet component decanoic acid increases mitochondrial citrate synthase and complex I activity in neuronal cells

Journal of neurochemistry, 2014-05, Vol.129 (3), p.426-433

2014

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Coenzyme Q10: Role in Less Common Age-Related Disorders

Antioxidants, 2022-11, Vol.11 (11), p.2293

2022

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The Effect of Neuronal CoQ10 Deficiency and Mitochondrial Dysfunction on a Rotenone-Induced Neuronal Cell Model of Parkinson’s Disease

International journal of molecular sciences, 2024-06, Vol.25 (12), p.6622

2024

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Secondary Mitochondrial Dysfunction as a Cause of Neurodegenerative Dysfunction in Lysosomal Storage Diseases and an Overview of Potential Therapies

International journal of molecular sciences, 2022-09, Vol.23 (18), p.10573

2022

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Coenzyme Q10 and Immune Function: An Overview

Antioxidants, 2021-05, Vol.10 (5), p.759

2021

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Assessment of Mitochondrial Dysfunction in Experimental Autoimmune Encephalomyelitis (EAE) Models of Multiple Sclerosis

International journal of molecular sciences, 2019-10, Vol.20 (20), p.4975

2019

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Primary Coenzyme Q10 Deficiency: An Update

Antioxidants, 2023-08, Vol.12 (8), p.1652

2023

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Depletion and Supplementation of Coenzyme Q10 in Secondary Deficiency Disorders

Frontiers in bioscience (Landmark. Print), 2022-12, Vol.27 (12), p.322-322

2022

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Coenzyme Q10, Ageing and the Nervous System: An Overview

Antioxidants, 2021-12, Vol.11 (1), p.2

2021

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The Biochemical Assessment of Mitochondrial Respiratory Chain Disorders

International journal of molecular sciences, 2022-07, Vol.23 (13), p.7487

2022

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A Nonsense Mutation in COQ9 Causes Autosomal-Recessive Neonatal-Onset Primary Coenzyme Q10 Deficiency: A Potentially Treatable Form of Mitochondrial Disease

American journal of human genetics, 2009-05, Vol.84 (5), p.558-566

2009

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Mitochondrial dysfunction is a key pathological driver of early stage Parkinson's

Acta neuropathologica communications, 2022-09, Vol.10 (1), p.134-134, Article 134

2022

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The Effect of Methylmalonic Acid Treatment on Human Neuronal Cell Coenzyme Q10 Status and Mitochondrial Function

International journal of molecular sciences, 2020-11, Vol.21 (23), p.9137

2020

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Zellweger syndrome and secondary mitochondrial myopathy

European journal of pediatrics, 2015-04, Vol.174 (4), p.557-563

2015

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ANO10 mutations cause ataxia and coenzyme Q10 deficiency

Journal of neurology, 2014-11, Vol.261 (11), p.2192-2198

2014

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Poor maternal nutrition and accelerated postnatal growth induces an accelerated aging phenotype and oxidative stress in skeletal muscle of male rats

Disease models & mechanisms, 2016-10, Vol.9 (10), p.1221-1229

2016

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Lyme Disease: A Role for Coenzyme Q10 Supplementation?

Antioxidants, 2022-03, Vol.11 (4), p.667

2022

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Current Strategies for the Biochemical Diagnosis and Monitoring of Mitochondrial Disease

Hargreaves, Iain

2018

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Potential Biomarkers of Mitochondrial Dysfunction Associated with COVID-19 Infection

Application of Omic Techniques to Identify New Biomarkers and Drug Targets for COVID-19, p.211-224

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Human neuronal coenzyme Q10 deficiency results in global loss of mitochondrial respiratory chain activity, increased mitochondrial oxidative stress and reversal of ATP synthase activity: implications for pathogenesis and treatment

Journal of inherited metabolic disease, 2013-01, Vol.36 (1), p.63-73

2013

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Coenzyme Q10 and Autoimmune Disorders: An Overview

Mitochondria and Quality Control Defects in a Mouse Model of Gaucher Disease—Links to Parkinson’s Disease

The Ubiquinone-Ubiquinol Redox Cycle and Its Clinical Consequences: An Overview

Targetable Pathways for Alleviating Mitochondrial Dysfunction in Neurodegeneration of Metabolic and Non-Metabolic Diseases

Dysregulation of glucose metabolism is an early event in sporadic Parkinson's disease

The ketogenic diet component decanoic acid increases mitochondrial citrate synthase and complex I activity in neuronal cells

Coenzyme Q10: Role in Less Common Age-Related Disorders

The Effect of Neuronal CoQ10 Deficiency and Mitochondrial Dysfunction on a Rotenone-Induced Neuronal Cell Model of Parkinson’s Disease

Secondary Mitochondrial Dysfunction as a Cause of Neurodegenerative Dysfunction in Lysosomal Storage Diseases and an Overview of Potential Therapies

Coenzyme Q10 and Immune Function: An Overview

Assessment of Mitochondrial Dysfunction in Experimental Autoimmune Encephalomyelitis (EAE) Models of Multiple Sclerosis

Primary Coenzyme Q10 Deficiency: An Update

Depletion and Supplementation of Coenzyme Q10 in Secondary Deficiency Disorders

Coenzyme Q10, Ageing and the Nervous System: An Overview

The Biochemical Assessment of Mitochondrial Respiratory Chain Disorders

A Nonsense Mutation in COQ9 Causes Autosomal-Recessive Neonatal-Onset Primary Coenzyme Q10 Deficiency: A Potentially Treatable Form of Mitochondrial Disease

Mitochondrial dysfunction is a key pathological driver of early stage Parkinson's

The Effect of Methylmalonic Acid Treatment on Human Neuronal Cell Coenzyme Q10 Status and Mitochondrial Function

Zellweger syndrome and secondary mitochondrial myopathy

ANO10 mutations cause ataxia and coenzyme Q10 deficiency

Poor maternal nutrition and accelerated postnatal growth induces an accelerated aging phenotype and oxidative stress in skeletal muscle of male rats

Lyme Disease: A Role for Coenzyme Q10 Supplementation?

Current Strategies for the Biochemical Diagnosis and Monitoring of Mitochondrial Disease

Potential Biomarkers of Mitochondrial Dysfunction Associated with COVID-19 Infection

Human neuronal coenzyme Q10 deficiency results in global loss of mitochondrial respiratory chain activity, increased mitochondrial oxidative stress and reversal of ATP synthase activity: implications for pathogenesis and treatment

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