Literature DB >> 5483633

Deficiency of coenzyme Q9 in mice having hereditary muscular dystrophy.

G P Littarru, D Jones, J Scholler, K Folkers.   

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Year:  1970        PMID： 5483633     DOI： 10.1016/0006-291x(70)90231-7

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN： 0006-291X            Impact factor:   3.575


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  5 in total

1.  Activity of 3-hydroxy-3-methylglutaryl-coenzyme A reductase does not respond to ubiquinone uptake in cultured cells.

Authors:  W A Maltese; J R Aprille; R A Green
Journal:  Biochem J       Date:  1987-09-01       Impact factor: 3.857

2.  Effect of coenzyme Q on serum levels of creatine phosphokinase in preclinical muscular dystrophy.

Authors:  K Folkers; R Nakamura; G P Littarru; H Zellweger; J B Brunkhorst; C W Williams; J H Langston
Journal:  Proc Natl Acad Sci U S A       Date:  1974-05       Impact factor: 11.205

3.  Biochemical rationale and the cardiac response of patients with muscle disease to therapy with coenzyme Q10.

Authors:  K Folkers; J Wolaniuk; R Simonsen; M Morishita; S Vadhanavikit
Journal:  Proc Natl Acad Sci U S A       Date:  1985-07       Impact factor: 11.205

4.  Breath isoprene: muscle dystrophy patients support the concept of a pool of isoprene in the periphery of the human body.

Authors:  J King; P Mochalski; K Unterkofler; G Teschl; M Klieber; M Stein; A Amann; M Baumann
Journal:  Biochem Biophys Res Commun       Date:  2012-06-05       Impact factor: 3.575

Review 5.  Metabogenic and Nutriceutical Approaches to Address Energy Dysregulation and Skeletal Muscle Wasting in Duchenne Muscular Dystrophy.

Authors:  Emma Rybalka; Cara A Timpani; Christos G Stathis; Alan Hayes; Matthew B Cooke
Journal:  Nutrients       Date:  2015-11-26       Impact factor: 5.717
  5 in total

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