UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Integrated Approach Reveals Role of Mitochondrial Germ-Line Mutation F18L in Respiratory Chain, Oxidative Alterations, Drug Sensitivity, and Patient Prognosis in Glioblastoma

International journal of molecular sciences, 2019-07, Vol.20 (13), p.3364

2019

Volltextzugriff (PDF)

Altered skeletal muscle insulin signaling and mitochondrial complex II-III linked activity in adult offspring of obese mice

American journal of physiology. Regulatory, integrative and comparative physiology, 2009-09, Vol.297 (3), p.R675-R681

2009

Volltextzugriff (PDF)

The coenzyme Q10 status of the brain regions of Parkinson's disease patients

Neuroscience letters, 2008-12, Vol.447 (1), p.17-19

2008

Volltextzugriff (PDF)

Ubiquinone: cholesterol's reclusive cousin

Annals of clinical biochemistry, 2003-05, Vol.40 (Pt 3), p.207-218

Hargreaves, Iain P

2003

Volltextzugriff (PDF)

Evidence of oxidative stress and mitochondrial dysfunction in spinocerebellar ataxia type 2 (SCA2) patient fibroblasts: Effect of coenzyme Q10 supplementation on these parameters

Mitochondrion, 2017-05, Vol.34, p.103-114

2017

Volltextzugriff (PDF)

Nutritional programming of coenzyme Q: potential for prevention and intervention?

The FASEB journal, 2014-12, Vol.28 (12), p.5398-5405

2014

Volltextzugriff (PDF)

Coenzyme Q10 in phenylketonuria and mevalonic aciduria

Mitochondrion, 2007-06, Vol.7 Suppl, p.S175-S180

Hargreaves, Iain P

2007

Volltextzugriff (PDF)

The effect of HMG-CoA Reductase inhibitors on Coenzyme Q10 : Possible biochemical/clinical implications

Drug safety, 2005, Vol.28 (8), p.659-676

2005

Volltextzugriff (PDF)

Phenotypic variability of mitochondrial disease caused by a nuclear mutation in complex II

Molecular genetics and metabolism, 2006-11, Vol.89 (3), p.214-221

2006

Volltextzugriff (PDF)

Decreased Ubiquinone Availability and Impaired Mitochondrial Cytochrome Oxidase Activity Associated With Statin Treatment

Toxicology mechanisms and methods, 2009-01, Vol.19 (1), p.44-50

2009

Volltextzugriff (PDF)

Coenzyme Q 10 Assessment and the Establishment of a Neuronal Cell Model of CoQ 10 Deficiency

Methods in molecular biology (Clifton, N.J.), 2020, Vol.2138, p.277

2020

Volltextzugriff (PDF)

The Effect of Organophosphate Exposure on Neuronal Cell Coenzyme Q 10 Status

Neurochemical research, 2021-01, Vol.46 (1), p.131

2021

Volltextzugriff (PDF)

The Effect of Methylmalonic Acid Treatment on Human Neuronal Cell Coenzyme Q 10 Status and Mitochondrial Function

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

2020

Volltextzugriff (PDF)

Cerebral mitochondrial electron transport chain dysfunction in multiple system atrophy and Parkinson's disease

Scientific reports, 2019-04, Vol.9 (1), p.6559, Article 6559

2019

Volltextzugriff (PDF)

Coenzyme Q10 Levels Are Decreased in the Cerebellum of Multiple-System Atrophy Patients

PloS one, 2016-02, Vol.11 (2), p.e0149557-e0149557

2016

Volltextzugriff (PDF)

Secondary coenzyme Q10 deficiency and oxidative stress in cultured fibroblasts from patients with riboflavin responsive multiple Acyl-CoA dehydrogenation deficiency

Human molecular genetics, 2013-10, Vol.22 (19), p.3819-3827

2013

Volltextzugriff (PDF)

1 – 18 von 18

Suche als RSS-Feed

Aktive Filter

ThemaUbiquinone - Metabolism

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(18)
Mit Volltextzugriff
(17)

Publikationsform

Artikel
(18)

Sprache

Englisch
(18)
Japanisch
(6)

Erscheinungsjahr

n.n

Thema

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

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

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

Integrated Approach Reveals Role of Mitochondrial Germ-Line Mutation F18L in Respiratory Chain, Oxidative Alterations, Drug Sensitivity, and Patient Prognosis in Glioblastoma

Altered skeletal muscle insulin signaling and mitochondrial complex II-III linked activity in adult offspring of obese mice

The coenzyme Q10 status of the brain regions of Parkinson's disease patients

Ubiquinone: cholesterol's reclusive cousin

Evidence of oxidative stress and mitochondrial dysfunction in spinocerebellar ataxia type 2 (SCA2) patient fibroblasts: Effect of coenzyme Q10 supplementation on these parameters

Nutritional programming of coenzyme Q: potential for prevention and intervention?

Coenzyme Q10 in phenylketonuria and mevalonic aciduria

The effect of HMG-CoA Reductase inhibitors on Coenzyme Q10 : Possible biochemical/clinical implications

Phenotypic variability of mitochondrial disease caused by a nuclear mutation in complex II

Decreased Ubiquinone Availability and Impaired Mitochondrial Cytochrome Oxidase Activity Associated With Statin Treatment

Coenzyme Q 10 Assessment and the Establishment of a Neuronal Cell Model of CoQ 10 Deficiency

The Effect of Organophosphate Exposure on Neuronal Cell Coenzyme Q 10 Status

The Effect of Methylmalonic Acid Treatment on Human Neuronal Cell Coenzyme Q 10 Status and Mitochondrial Function

Cerebral mitochondrial electron transport chain dysfunction in multiple system atrophy and Parkinson's disease

Coenzyme Q10 Levels Are Decreased in the Cerebellum of Multiple-System Atrophy Patients

Secondary coenzyme Q10 deficiency and oxidative stress in cultured fibroblasts from patients with riboflavin responsive multiple Acyl-CoA dehydrogenation deficiency

Aktive Filter

Suchergebnisse filtern