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Haplotype variability in mitochondrial rRNA predisposes to metabolic syndrome.
- Published in:
- Communications Biology, 2024, v. 7, n. 1, p. 1, doi. 10.1038/s42003-024-06819-w
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- Article
Variability of Clinical Phenotypes Caused by Isolated Defects of Mitochondrial ATP Synthase.
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- Physiological Research, 2024, v. 73, p. S243, doi. 10.33549/physiolres.935407
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- Article
Czech Footprints in the Bioenergetics Research.
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- Physiological Research, 2024, v. 73, p. S23, doi. 10.33549/physiolres.935395
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- Article
Role of Mitochondrial Glycerol-3-Phosphate Dehydrogenase in Metabolic Adaptations of Prostate Cancer.
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- Cells (2073-4409), 2020, v. 9, n. 8, p. 1764, doi. 10.3390/cells9081764
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- Article
Cytochrome c Oxidase Subunit 4 Isoform Exchange Results in Modulation of Oxygen Affinity.
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- Cells (2073-4409), 2020, v. 9, n. 2, p. 443, doi. 10.3390/cells9020443
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- Article
Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 ε subunit.
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- Human Molecular Genetics, 2010, v. 19, n. 17, p. 3430, doi. 10.1093/hmg/ddq254
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- Article
POLRMT mutations impair mitochondrial transcription causing neurological disease.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-21279-0
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- Article
Mitochondrial targets of metformin—Are they physiologically relevant?
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- Biofactors, 2019, v. 45, n. 5, p. 703, doi. 10.1002/biof.1548
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- Article
Conplastic Strains for Identification of Retrograde Effects of Mitochondrial DNA Variation on Cardiometabolic Traits in the Spontaneously Hypertensive Rat.
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- Physiological Research, 2021, v. 70, p. S471, doi. 10.33549/physiolres.934740
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- Article
Genetic Complementation of ATP Synthase Deficiency Due to Dysfunction of TMEM70 Assembly Factor in Rat.
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- Biomedicines, 2022, v. 10, n. 2, p. 276, doi. 10.3390/biomedicines10020276
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- Article
Hypolipidemic Effects of Beetroot Juice in SHR-CRP and HHTg Rat Models of Metabolic Syndrome: Analysis of Hepatic Proteome.
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- Metabolites (2218-1989), 2023, v. 13, n. 2, p. 192, doi. 10.3390/metabo13020192
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- Article