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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
TMEM70 facilitates biogenesis of mammalian ATP synthase by promoting subunit c incorporation into the rotor structure of the enzyme.
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- FASEB Journal, 2019, v. 33, n. 12, p. 14103, doi. 10.1096/fj.201900685RR
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- Article
Sulforaphane Ameliorates Metabolic Changes Associated With Status Epilepticus in Immature Rats.
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- Frontiers in Cellular Neuroscience, 2022, v. 16, p. 1, doi. 10.3389/fncel.2022.855161
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- Article
Sex difference in the sensitivity of cardiac mitochondrial permeability transition pore to calcium load.
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- Molecular & Cellular Biochemistry, 2016, v. 412, n. 1/2, p. 147, doi. 10.1007/s11010-015-2619-4
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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
Acadian variant of Fanconi syndrome is caused by mitochondrial respiratory chain complex I deficiency due to a non-coding mutation in complex I assembly factor NDUFAF6.
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- Human Molecular Genetics, 2016, v. 25, n. 18, p. 4062, doi. 10.1093/hmg/ddw245
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- Article
Selective replacement of mitochondrial DNA increases the cardioprotective effect of chronic continuous hypoxia in spontaneously hypertensive rats.
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- Clinical Science, 2017, v. 131, n. 9, p. 865, doi. 10.1042/CS20170083
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- Article