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Quoted phrase not found in phrase index: "Combined oxidative phosphorylation defect type 9"
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Characterization of human myotubes from type 2 diabetic and nondiabetic subjects using complementary quantitative mass spectrometric methods.
Thingholm TE, Bak S, Beck-Nielsen H, Jensen ON, Gaster M. Thingholm TE, et al. Mol Cell Proteomics. 2011 Sep;10(9):M110.006650. doi: 10.1074/mcp.M110.006650. Epub 2011 Jun 22. Mol Cell Proteomics. 2011. PMID: 21697546 Free PMC article.
Several abnormalities have been identified in skeletal muscle from type 2 diabetic subjects, however, the exact molecular mechanisms leading to the diabetic phenotype has still not been found. ...Despite a clear diabetic phenotype in diabetic myotubes, the majority …
Several abnormalities have been identified in skeletal muscle from type 2 diabetic subjects, however, the exact molecular mech …
Cardiac manifestations in oxidative phosphorylation disorders of childhood.
Yaplito-Lee J, Weintraub R, Jamsen K, Chow CW, Thorburn DR, Boneh A. Yaplito-Lee J, et al. J Pediatr. 2007 Apr;150(4):407-11. doi: 10.1016/j.jpeds.2006.12.047. J Pediatr. 2007. PMID: 17382120
OBJECTIVE: To determine the frequency, type, and severity of cardiac involvement in pediatric patients with oxidative phosphorylation (OXPHOS) disorders. ...A change in the type of cardiomyopathy was noted on follow-up in 2 patients. Conduction and rhy …
OBJECTIVE: To determine the frequency, type, and severity of cardiac involvement in pediatric patients with oxidative phosp …
Development of a human mitochondrial oligonucleotide microarray (h-MitoArray) and gene expression analysis of fibroblast cell lines from 13 patients with isolated F1Fo ATP synthase deficiency.
Cízková A, Stránecký V, Ivánek R, Hartmannová H, Nosková L, Piherová L, Tesarová M, Hansíková H, Honzík T, Zeman J, Divina P, Potocká A, Paul J, Sperl W, Mayr JA, Seneca S, Houstĕk J, Kmoch S. Cízková A, et al. BMC Genomics. 2008 Jan 25;9:38. doi: 10.1186/1471-2164-9-38. BMC Genomics. 2008. PMID: 18221507 Free PMC article.
RESULTS: Molecular studies, in combination with unsupervised clustering methods, defined three subgroups of patient cell lines--M group with mtDNA mutation and N1 and N2 groups with nuclear defect. ...Evaluation of individual gene expression profiles confirmed alrea …
RESULTS: Molecular studies, in combination with unsupervised clustering methods, defined three subgroups of patient cell lines--M gro …