Coenzyme Q9

Coenzyme q9 is a lipid of Prenol Lipids (PR) class. The involved functions are known as Diastasis, Phosphorylation and Cardiac function.

Cross Reference

Introduction

To understand associated biological information of Coenzyme Q9, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.

What diseases are associated with Coenzyme Q9?

There are no associated biomedical information in the current reference collection.

No disease MeSH terms mapped to the current reference collection.

PubChem Associated disorders and diseases

What pathways are associated with Coenzyme Q9

There are no associated biomedical information in the current reference collection.

PubChem Biomolecular Interactions and Pathways

Link to PubChem Biomolecular Interactions and Pathways

What cellular locations are associated with Coenzyme Q9?

There are no associated biomedical information in the current reference collection.

What functions are associated with Coenzyme Q9?


Related references are published most in these journals:

Function Cross reference Weighted score Related literatures

What lipids are associated with Coenzyme Q9?

There are no associated biomedical information in the current reference collection.

What genes are associated with Coenzyme Q9?

There are no associated biomedical information in the current reference collection.

What common seen animal models are associated with Coenzyme Q9?

There are no associated biomedical information in the current reference collection.

NCBI Entrez Crosslinks

All references with Coenzyme Q9

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Authors Title Published Journal PubMed Link
Lekli I et al. Coenzyme Q9 provides cardioprotection after converting into coenzyme Q10. 2008 J. Agric. Food Chem. pmid:18543930
Rodríguez-Acuña R et al. Determination of coenzyme Q10 and Q9 in vegetable oils. 2008 J. Agric. Food Chem. pmid:18616270
Acworth IN et al. Determination of oxidized and reduced CoQ10 and CoQ9 in human plasma/serum using HPLC-ECD. 2008 Methods Mol. Biol. pmid:19082952
Li L et al. Analysis of CoQ10 in rat serum by ultra-performance liquid chromatography mass spectrometry after oral administration. 2008 J Pharm Biomed Anal pmid:18054195
Duncan AJ et al. A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease. 2009 Am. J. Hum. Genet. pmid:19375058
Shelley P et al. Altered skeletal muscle insulin signaling and mitochondrial complex II-III linked activity in adult offspring of obese mice. 2009 Am. J. Physiol. Regul. Integr. Comp. Physiol. pmid:19535678
Bae JS et al. Apoptotic cell death of human leukaemia U937 cells by ubiquinone-9 purified from Pleurotus eryngii. 2009 Nat. Prod. Res. pmid:19662576
Yang YY et al. The effect of different ubiquinones on lifespan in Caenorhabditis elegans. 2009 Mech. Ageing Dev. pmid:19428456
Sumien N et al. Prolonged intake of coenzyme Q10 impairs cognitive functions in mice. 2009 J. Nutr. pmid:19710165
Cano A et al. Hepatic VLDL assembly is disturbed in a rat model of nonalcoholic fatty liver disease: is there a role for dietary coenzyme Q? 2009 J. Appl. Physiol. pmid:19608932